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Journal articles on the topic 'XP'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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1

Cowham, R. "To XP or not to XP?" ITNOW 47, no. 2 (2005): 16. http://dx.doi.org/10.1093/itnow/bwi030.

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2

Fischer, R., M. Uhl, and H. Vonach. "Nb93(n,xp),Agnat(n,xp), andInnat(n,xp) reactions at 14.1 MeV." Physical Review C 37, no. 2 (1988): 578–86. http://dx.doi.org/10.1103/physrevc.37.578.

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3

Sonia, Archana Singhal, and Hema Banati. "FISA-XP." ACM SIGSOFT Software Engineering Notes 39, no. 3 (2014): 1–14. http://dx.doi.org/10.1145/2597716.2597728.

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4

Litts, Thom, and Jeff Kopaska. "RIP XP." Fisheries 39, no. 4 (2014): 151. http://dx.doi.org/10.1080/03632415.2014.893871.

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5

Ivorra, Wilfrid. "Sur les équations xp+2βyp= z2et xp+2βyp= 2z2". Acta Arithmetica 108, № 4 (2003): 327–38. http://dx.doi.org/10.4064/aa108-4-3.

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6

Lee, Jeeyun, Do Hoon Lim, Sung Kim, et al. "Phase III Trial Comparing Capecitabine Plus Cisplatin Versus Capecitabine Plus Cisplatin With Concurrent Capecitabine Radiotherapy in Completely Resected Gastric Cancer With D2 Lymph Node Dissection: The ARTIST Trial." Journal of Clinical Oncology 30, no. 3 (2012): 268–73. http://dx.doi.org/10.1200/jco.2011.39.1953.

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Purpose The ARTIST (Adjuvant Chemoradiation Therapy in Stomach Cancer) trial was the first study to our knowledge to investigate the role of postoperative chemoradiotherapy therapy in patients with curatively resected gastric cancer with D2 lymph node dissection. This trial was designed to compare postoperative treatment with capecitabine plus cisplatin (XP) versus XP plus radiotherapy with capecitabine (XP/XRT/XP). Patients and Methods The XP arm received six cycles of XP (capecitabine 2,000 mg/m2 per day on days 1 to 14 and cisplatin 60 mg/m2 on day 1, repeated every 3 weeks) chemotherapy. T

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7

Fassihi, Hiva, Mieran Sethi, Heather Fawcett, et al. "Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect." Proceedings of the National Academy of Sciences 113, no. 9 (2016): E1236—E1245. http://dx.doi.org/10.1073/pnas.1519444113.

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Xeroderma pigmentosum (XP) is a rare DNA repair disorder characterized by increased susceptibility to UV radiation (UVR)-induced skin pigmentation, skin cancers, ocular surface disease, and, in some patients, sunburn and neurological degeneration. Genetically, it is assigned to eight complementation groups (XP-A to -G and variant). For the last 5 y, the UK national multidisciplinary XP service has provided follow-up for 89 XP patients, representing most of the XP patients in the United Kingdom. Causative mutations, DNA repair levels, and more than 60 clinical variables relating to dermatology,

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8

Abid, Kalthoum, Jihene Bettaieb, Faouzi El Mezni, and Hamouda Boussen. "Proinflammatory cytokines in xeroderma pigmentosum (XP) and non-XP cancer patients—a pilot study." Exploration of Immunology 4, no. 4 (2024): 557–67. http://dx.doi.org/10.37349/ei.2024.00159.

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Aim: Testing the feasibility of the determination to what extent the inability to repair DNA lesions in xeroderma pigmentosum (XP) patients, contributes to the alteration of immune responses, in the course of skin carcinogenesis. Methods: Serum samples from 11 (five XP, six non-XP) bearing skin carcinomas and from three healthy donors, were available for the quantification of IL-2, IL-4, IL-10, IFN‐γ and TNF-α cytokines concentrations. We used kits for ELISA test, by a non-competitive sandwich method. Statistical analysis of the results was performed, using non-parametric Mann-Whitney U test,

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9

Maxmen, Amy. "XP mutant power!" Journal of Experimental Medicine 206, no. 13 (2009): 2856. http://dx.doi.org/10.1084/jem.20613iti2.

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10

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi та ін. "Общие аспекты пигментной ксеродермии: обзор". Núcleo do Conhecimento 11, № 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/ru/70626.

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Xeroderma Pigmentoso (XP) является редким, рецессивным и аутосомно-генетическим заболеванием, которое также поражает как пол, так и все этнические группы, тесно связанные с общинами с высоким уровнем инбридинга. Целью данного обзора было подробно основные маршруты восстановления ДНК XP, различные функциональные дефекты, которые приводят к развитию 8 типов XP, основные характеристики клинической картины пациента с XP, основные сопутствующие заболевания, связанные с XP, и методы лечения доступны или которые все еще находятся в исследованиях для лиц, пострадавших от XP. Библиографические исследов

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11

Kunwar, Sundar. "Enabling and Limiting factors in eXtreme Programming (XP) with Evaluation Framework." SCITECH Nepal 14, no. 1 (2019): 50–62. http://dx.doi.org/10.3126/scitech.v14i1.25534.

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As agile software development methodologies are used in many domains and come with different shapes and sizes, it is one of the complex human endeavors. Extreme Programming (XP) is one of the well-known agile software development methodologies and is driven by a set of values including simplicity, communication, feedback and courage, but lacks the mechanism to measure these values demanding the evaluation framework to make it measurable and attainable. The main aim of this study is to build the software process improvement model that can be used for evaluating XP values and practices. The prop

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12

RapićOtrin, Vesna, Isao Kuraoka, Tiziana Nardo, et al. "Relationship of the Xeroderma Pigmentosum Group E DNA Repair Defect to the Chromatin and DNA Binding Proteins UV-DDB and Replication Protein A." Molecular and Cellular Biology 18, no. 6 (1998): 3182–90. http://dx.doi.org/10.1128/mcb.18.6.3182.

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ABSTRACT Cells from complementation groups A through G of the heritable sun-sensitive disorder xeroderma pigmentosum (XP) show defects in nucleotide excision repair of damaged DNA. Proteins representing groups A, B, C, D, F, and G are subunits of the core recognition and incision machinery of repair. XP group E (XP-E) is the mildest form of the disorder, and cells generally show about 50% of the normal repair level. We investigated two protein factors previously implicated in the XP-E defect, UV-damaged DNA binding protein (UV-DDB) and replication protein A (RPA). Three newly identified XP-E c

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13

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "Allgemeine Aspekte von Xeroderma pigmentosum: Eine Übersicht." Núcleo do Conhecimento 11, no. 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/gesundheit/aspekte-von-xeroderma.

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Xeroderma Pigmentoso (XP) ist eine seltene, rezessive und autosomal genetische Erkrankung, die auch sowohl Das Geschlechter als auch alle Ethnien betrifft und eng mit Gemeinschaften mit einer hohen Inzuchtrate verbunden ist. Ziel dieser Überprüfung war es, die Hauptwege der DNA-Reparatur von XP, die verschiedenen funktionellen Defekte, die zur Entwicklung der 8 XP-Typen führen, die Hauptmerkmale des klinischen Bildes eines Patienten mit XP, die wichtigsten Komorbiditäten im Zusammenhang mit XP und die verfügbaren Behandlungen oder die noch in Studien für Personen von XP durchgeführt werden. Di

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14

Stanojevic, Jelena. "On estimation of high quantiles for certain classes of distributions." Yugoslav Journal of Operations Research 25, no. 2 (2015): 299–312. http://dx.doi.org/10.2298/yjor130606013s.

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We investigate the rate of convergence of the direct-simulation estimator ? ?xp(n) of a large quantile xp of the Pareto and Gamma distributions. The upper bound of the probability P{|?xp(n)- xp|>? is determined.

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15

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "Aspectos gerais do xeroderma pigmentoso: Uma revisão." Núcleo do Conhecimento 11, no. 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/saude/aspectos-gerais-do-xeroderma.

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O Xeroderma Pigmentoso (XP) é uma doença genética rara, de caráter recessivo e autossômico, que afeta igualmente os dois sexos e todas as etnias, estando associado intimamente a comunidades com alta taxa de consanguinidade. O objetivo desta revisão foi detalhar as principais vias de reparo do DNA do XP, os diferentes defeitos funcionais que resultam no desenvolvimento dos 8 tipos de XP, as principais características do quadro clínico de um paciente com XP, as principais comorbidades associadas ao XP, e os tratamentos disponíveis ou que ainda estão em estudos para indivíduos acometidos pelo XP.

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16

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "Aspetti generali dello xeroderma pigmentoso: una revisione." Núcleo do Conhecimento 11, no. 03 (2022): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/salute/generali-dello-xeroderma.

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Xeroderma Pigmentoso (XP) è una malattia genetica rara, recessiva e autosomica che colpisce anche sia i sessi che tutte le etnie, essendo strettamente associata alle comunità con un alto tasso di consanguineità. Lo scopo di questa revisione era quello di dettagliare le principali vie di riparazione del DNA di XP, i diversi difetti funzionali che si traducono nello sviluppo degli 8 tipi di XP, le caratteristiche principali del quadro clinico di un paziente con XP, le principali comorbilità associate a XP e i trattamenti disponibili o che sono ancora in studi per individui affetti da XP. La rice

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17

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "General aspects of xeroderma pigmentosum: A review." Núcleo do Conhecimento 11, no. 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/health/xeroderma-pigmentosum.

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Xeroderma Pigmentoso (XP) is a rare, recessive and autosomal genetic disease that also affects both sexes and all ethnicities, being closely associated with communities with a high rate of inbreeding. The aim of this review was to detail the main routes of DNA repair of XP, the different functional defects that result in the development of the 8 types of XP, the main characteristics of the clinical picture of a patient with XP, the main comorbidities associated with XP, and the treatments available or that are still in studies for individuals affected by XP. The bibliographic research was carr

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18

Kim, Jinsu, and Wonho Lee. "Flood Inundation Analysis in Urban Area Using XP-SWMM." Journal of the Korean Geoenvironmental Society 16, no. 1 (2015): 29–36. http://dx.doi.org/10.14481/jkges.2015.16.1.29.

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19

Suman, AHM Khairul Imam, Khadija Begum, Kaniz Rahman, et al. "Association of Xanthelasma palpebrarum (XP) with cardiovascular disease (CVD) risk factors." Asian Journal of Medical and Biological Research 5, no. 4 (2020): 324–29. http://dx.doi.org/10.3329/ajmbr.v5i4.45271.

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Xanthelasma palpebrarum (XP) is the most common cutaneous xanthoma occurs over or surrounding the eyelids in yellowish color and various shapes. The objective of this study was to describe the status of cardiovascular disease risk factors in XP patients and determine their association with XP. A case-control study was conducted among 81 cases (have XP) and 81 controls (no XP) among patients attended for cardiac check-up between January 2019 to July 2019 at Ad-Din Women's Medical College Hospital, Dhaka, Bangladesh. Among 162 subjects were interviewed in our study, majority were female (62.3%).

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20

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "Aspectos generales del xeroderma pigmentoso: una revisión." Núcleo do Conhecimento 11, no. 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/salud/xeroderma-pigmentoso.

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Xeroderma Pigmentoso (XP) es una enfermedad genética rara, recesiva y autosómica que también afecta tanto a los sexos como a todas las etnias, estando estrechamente asociada con las comunidades con una alta tasa de endogamia. El objetivo de esta revisión fue detallar las principales rutas de reparación del ADN de LA XP, los diferentes defectos funcionales que dan lugar al desarrollo de los 8 tipos de XP, las principales características del cuadro clínico de un paciente con XP, las principales comorbilidades asociadas con XP, y los tratamientos disponibles o que todavía están en estudios para i

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21

Vaz-Garcia, Eduarda Santiago, Victor Talarico Leal Vieira, Natasha Pereira da Silva Ferreira Petitet, et al. "Mechanical Properties of Anatomic Finishing Files: XP-Endo Finisher and XP-Clean." Brazilian Dental Journal 29, no. 2 (2018): 208–13. http://dx.doi.org/10.1590/0103-6440201801903.

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Abstract The aim of the present study was to evaluate the cyclic fatigue of two anatomic finishing files: XP-Endo Finisher and XP-Clean. Roughness pattern and the micro-hardness of the files were also assessed. Instruments were subjected to cyclic fatigue resistance measuring the time to fracture in an artificial stainless-steel canal with a 60° angle and a 5-mm radius of curvature. The fracture surface of all fragments was examined with a scanning electron microscope. The roughness of the working parts was quantified by using a profilometer and the micro-hardness test was carried out using a

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22

Gambichler, Thilo, Julia Hyun, Frank Oellig, Jürgen C. Becker, and Alexander Kreuter. "Immuncheckpoint‐Inhibitoren bei Kindern mit Xeroderma pigmentosum und fortgeschrittenem kutanen Plattenepithelkarzinom: Fallvorstellung und kurzer Überblick." JDDG: Journal der Deutschen Dermatologischen Gesellschaft 23, no. 3 (2025): 303–10. https://doi.org/10.1111/ddg.15648_g.

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ZusammenfassungPatienten mit Xeroderma pigmentosum (XP) entwickeln häufig bereits in jungen Jahren Hautkrebs, darunter auch kutane Plattenepithelkarzinome (cSCC). Das mediane Sterbealter liegt bei 32 Jahren, und 60% der XP‐Patienten versterben vor dem 20. Lebensjahr. cSSC bei XP‐Patienten weisen eine außergewöhnlich hohe Mutationslast auf, was für eine gute Ansprechrate auf Immuncheckpoint‐Inhibitoren (ICI) spricht. Wir berichten über einen 7‐jährigen Jungen mit XP und einem großflächigen cSCC im Gesicht, das durch Metastasen in die Halslymphknoten kompliziert wurde. Auf Empfehlung des Tumorbo

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23

Webster, Mark A., Benjamin J. Brown, and Stephen D. Bartlett. "The XP Stabiliser Formalism: a Generalisation of the Pauli Stabiliser Formalism with Arbitrary Phases." Quantum 6 (September 22, 2022): 815. http://dx.doi.org/10.22331/q-2022-09-22-815.

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We propose an extension to the Pauli stabiliser formalism that includes fractional 2&#x03C0;/N rotations around the Z axis for some integer N. The resulting generalised stabiliser formalism – denoted the XP stabiliser formalism – allows for a wider range of states and codespaces to be represented. We describe the states which arise in the formalism, and demonstrate an equivalence between XP stabiliser states and 'weighted hypergraph states' – a generalisation of both hypergraph and weighted graph states. Given an arbitrary set of XP operators, we present algorithms for determining the code

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24

Kim, Young Geun, Jae Wook Oh, Keun Cheol Lee, and Sung Ho Yoon. "Clinical association between serum cholesterol level and the size of xanthelasma palpebrarum." Archives of Craniofacial Surgery 23, no. 2 (2022): 71–76. http://dx.doi.org/10.7181/acfs.2022.00185.

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Background: Xanthelasma palpebrarum (XP) is a benign periorbital lesion. The relationship between xanthelasma lesion size and serum cholesterol levels has been poorly studied. In this study, we investigated this relationship in the context of the clinical etiology of XP. Methods: We retrospectively reviewed medical records and pathology reports of all patients treated for XP at our hospital between June 2014 and June 2021; the data were used to analyze lesion size, underlying disease, serum cholesterol, and disease recurrence.Results: The mean values for patient age, serum cholesterol, and les

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25

Phillies, George David Joseph. "Simulational Tests of the Rouse Model." Polymers 15, no. 12 (2023): 2615. http://dx.doi.org/10.3390/polym15122615.

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An extensive review of literature simulations of quiescent polymer melts is given, considering results that test aspects of the Rouse model in the melt. We focus on Rouse model predictions for the mean-square amplitudes ⟨(Xp(0))2⟩ and time correlation functions ⟨Xp(0)Xp(t)⟩ of the Rouse mode Xp(t). The simulations conclusively demonstrate that the Rouse model is invalid in polymer melts. In particular, and contrary to the Rouse model, (i) mean-square Rouse mode amplitudes ⟨(Xp(0))2⟩ do not scale as sin−2(pπ/2N), N being the number of beads in the polymer. For small p (say, p≤3) ⟨(Xp(0))2⟩ scal

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26

Price, Vera H. "Trichothiodystrophy: Current Concepts." Journal of Cutaneous Medicine and Surgery 1, no. 1 (1996): 45–49. http://dx.doi.org/10.1177/120347549600100113.

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Background: Trichothiodystrophy (TTD) is a rare, autosomal recessive disorder in which the hair identifies a group of genetic disorders with deficient high-sulfur matrix proteins, and a defect in excision repair of ultraviolet damage in fibroblasts of most patients. TTD patients may be grouped as follows: (1) the major group with defects in the excision repair cross-complementing gene ERCC2, the gene for xeroderma pigmentosum group D (XP-D); (2) those with defects in ERCC3, the gene for XP-B; and (3) those with a repair defect distinct from those in XP-D and XP-B. In contrast to XP patients, T

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27

Miao, Junjie, Changchun Chai, Wei Zhang, Yanxing Song, and Yintang Yang. "First-Principles Study on Structural, Mechanical, Anisotropic, Electronic and Thermal Properties of III-Phosphides: XP (X = Al, Ga, or In) in the P6422 Phase." Materials 13, no. 3 (2020): 686. http://dx.doi.org/10.3390/ma13030686.

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The structural, mechanical, electronic, and thermal properties, as well as the stability and elastic anisotropy, of XP (X = Al, Ga, or In) in the P6422 phase were studied via density functional theory (DFT) in this work. P6422-XP (X = Al, Ga, or In) are dynamically and thermodynamically stable via phonon spectra and enthalpy. At 0 GPa, P6422-XP (X = Al, Ga, or In) are more rigid than F 4 ¯ 3 m-XP (X = Al, Ga, or In), of which P6422-XP (X = Al or Ga) are brittle and P6422-InP is ductile. In the same plane (except for (001)-plane), P6422-AlP and P6422-InP exhibit the smallest and the largest ani

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28

Lee, J., W. Kang, D. Lim, et al. "Phase III trial of adjuvant capecitabine/cisplatin (XP) versus capecitabine/cisplatin/RT (XPRT) in resected gastric cancer with D2 nodal dissection (ARTIST trial): Safety analysis." Journal of Clinical Oncology 27, no. 15_suppl (2009): 4537. http://dx.doi.org/10.1200/jco.2009.27.15_suppl.4537.

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4537 Background: Although the adjuvant chemoradiation therapy has gained popularity and has become the standard of care in patients with resected gastric cancer in U.S., the role of chemoradiation therapy after extended D2 dissection has been questioned. We conducted a phase III trial to compare capecitabine/cisplatin (XP) vs XP + radiotherapy (RT) in curatively D2 resected gastric cancer patients in terms of disease free survival and overall survival. Methods: Eligibility criteria were as follows: stage Ib (T1N1, T2bN0) - IV (M1 excluded), curatively ≥ D2 resected gastric adenocarcinoma. XP o

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29

Fernández-Sánchez, Javier. "Against a clausal ellipsis account of all stripping strings in Spanish." Poznan Studies in Contemporary Linguistics 55, no. 1 (2018): 53–87. http://dx.doi.org/10.1515/psicl-2019-0003.

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Abstract Stripping is a phenomenon whereby a full clause is coordinated with a phrase (XP) and an adverb, typically NEG(ation) (e.g. John read Hamlet but not Othello). As noted previously in the literature (e.g. Bosque 1984), while in English NEG must precede XP, Spanish allows the reverse order as well (XP-NEG). This paper examines these two strings (i.e. XP-NEG and NEG-XP) in Spanish and compares them with respect to a number of properties. The major goal of this paper is to show that, despite the appearances, the two strings constitute radically distinct phenomena. Analytically, I defend, i

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30

Reifer, D. J. "XP and the CMM." IEEE Software 20, no. 3 (2003): 14–15. http://dx.doi.org/10.1109/ms.2003.1196314.

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31

Torre, Alberto C. de la. "The ubiquitous XP commutator." European Journal of Physics 27, no. 2 (2006): 225–30. http://dx.doi.org/10.1088/0143-0807/27/2/005.

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32

Fraser, Steven, and Giancarlo Succi. "XP requirement negotiation workshop." ACM SIGAPP Applied Computing Review 10, no. 1 (2002): 26–31. http://dx.doi.org/10.1145/568235.568239.

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33

Schwarz, Diemo, and Etienne Brunet. "theconcatenator: Placard XP edit." Leonardo Music Journal 18 (December 2008): 89–90. http://dx.doi.org/10.1162/lmj.2008.18.89b.

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34

J.-M.M. "XP Centaur en majesté." Revue Francophone des Laboratoires 2007, no. 388 (2007): 10. http://dx.doi.org/10.1016/s1773-035x(07)80003-7.

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35

Gengler, Barbara. "XP a National Threat?" Network Security 2001, no. 11 (2001): 5. http://dx.doi.org/10.1016/s1353-4858(01)01111-4.

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36

Sundar, Kunwar. "Extreme Programming (XP) Simplified." European Journal of Advances in Engineering and Technology 5, no. 3 (2018): 198–206. https://doi.org/10.5281/zenodo.10702437.

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<strong>ABSTRACT </strong> Agile software development methods have drawn the attention of software development professionals in the past few years. Agile software development methods use iterative and incremental approaches to address the changing requirements of customers. One of the well-known agile software development methods is extreme Programming (XP) and is derived by sets of values including simplicity, communication, feedback and courage. The extreme practices, variation in composition and interaction between values and the feedback in XP has made the software system more complex and

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37

Beroual, Nabil, and Ahmed Bendjeddou. "On a Predator–Prey System with Holling Functional Response: xp/(a + xp)." National Academy Science Letters 39, no. 1 (2015): 43–46. http://dx.doi.org/10.1007/s40009-015-0400-6.

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38

Sarasin, Alain. "The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies." Cancers 15, no. 10 (2023): 2706. http://dx.doi.org/10.3390/cancers15102706.

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Background: Xeroderma pigmentosum (XP) is a rare genetic disorder characterized by a high incidence of skin cancers. These patients are deficient in nucleotide excision repair caused by mutations in one of the 7 XP genes. Methods: We diagnosed 181 XP patients using UV-induced DNA repair measurements and/or DNA sequencing from 1982 to 2022 in France. Results: As all XP patients, the French ones are very sensitive to UV exposure but since they are usually very well protected, they develop relatively few skin cancers. A majority of French XP patients originate from North Africa and bear a founder

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39

Moreira, Danilo José Silva, Juliana Brito da Fonseca, Karoline Rossi, et al. "Aspects généraux de Xeroderma pigmentosum: un examen." Núcleo do Conhecimento 11, no. 03 (2020): 114–26. https://doi.org/10.32749/nucleodoconhecimento.com.br/sante/generaux-de-xeroderma.

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Xeroderma Pigmentoso (XP) est une maladie génétique rare, récessive et autosomique qui affecte également les deux sexes et toutes les ethnies, étant étroitement associée aux communautés avec un taux élevé de consanguinité. L'objectif de cet examen était de détailler les principales voies de réparation de l'ADN de XP, les différents défauts fonctionnels qui entraînent le développement des 8 types d'XP, les principales caractéristiques de l'image clinique d'un patient atteint d'XP, les principales comorbidités associées à XP, et les traitements disponibles ou qui sont encore en études pour les p

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40

Rana, MS, MM Rahman, UK Rima, and NS Juyena. "General anaesthesia of indigenous pigs in Bangladesh." Bangladesh Veterinarian 30, no. 2 (2014): 46–53. http://dx.doi.org/10.3329/bvet.v30i2.18254.

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Anaesthetic trials were conducted with propofol (P), xylazine-propofol (XP), xylazine-ketamine (XK), xylazine-thiopentone (XT) in 16 healthy indigenous pigs. Respiration rate decreased significantly (P < 0.01) five minutes after induction, and during maximum depth of anaesthesia, and had not returned to control value after recovery from anaesthesia with all anaesthetic combinations. Heart rate with P increased significantly (P<0.01) five minutes after induction, whereas it decreased significantly (P < 0.01) with XP, XK and XT during anaesthesia and remained below the normal range afte

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Karentz, D., and J. E. Cleaver. "Repair-deficient xeroderma pigmentosum cells made UV light resistant by fusion with X-ray-inactivated Chinese hamster cells." Molecular and Cellular Biology 6, no. 10 (1986): 3428–32. http://dx.doi.org/10.1128/mcb.6.10.3428-3432.1986.

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Xeroderma pigmentosum (XP) is an autosomal recessive human disease, characterized by an extreme sensitivity to sunlight, caused by the inability of cells to repair UV light-induced damage to DNA. Cell fusion was used to transfer fragments of Chinese hamster ovary (CHO) chromosomes into XP cells. The hybrid cells exhibited UV resistance and DNA repair characteristics comparable to those expressed by CHO cells, and their DNA had greater homology with CHO DNA than did the DNA from XP cells. Control experiments consisted of fusion of irradiated and unirradiated XP cells and repeated exposure of un

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Karentz, D., and J. E. Cleaver. "Repair-deficient xeroderma pigmentosum cells made UV light resistant by fusion with X-ray-inactivated Chinese hamster cells." Molecular and Cellular Biology 6, no. 10 (1986): 3428–32. http://dx.doi.org/10.1128/mcb.6.10.3428.

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Xeroderma pigmentosum (XP) is an autosomal recessive human disease, characterized by an extreme sensitivity to sunlight, caused by the inability of cells to repair UV light-induced damage to DNA. Cell fusion was used to transfer fragments of Chinese hamster ovary (CHO) chromosomes into XP cells. The hybrid cells exhibited UV resistance and DNA repair characteristics comparable to those expressed by CHO cells, and their DNA had greater homology with CHO DNA than did the DNA from XP cells. Control experiments consisted of fusion of irradiated and unirradiated XP cells and repeated exposure of un

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Martens, M. C., L. Boeckmann, and S. Emmert. "Genetisch bedingte Hauterkrankungen – Xeroderma pigmentosum und das CEDNIK-Syndrom." Aktuelle Dermatologie 46, no. 08/09 (2020): 375–78. http://dx.doi.org/10.1055/a-1148-3867.

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ZusammenfassungDie Rostocker Hautklinik ist Europäisches Referenznetzwerkzentrum für seltene Hauterkrankungen mit den besonderen Schwerpunkten Xeroderma pigmentosum und Ichthyosen. Diese Themen vertreten wir auch in der medizinischen Grundlagenforschung.Xeroderma pigmentosum (XP) ist eine seltene, autosomal-rezessive Erkrankung, die entsprechend der Gendefekte in 7 Komplementationsgruppen – XP-A bis XP-G sowie die sog. XP-Variante (XP-V) – eingeteilt wird. XP ist ein Nukleotid-Exzisions-Reparatur-Defektsyndrom und äußert sich v. a. durch vorzeitige Hautalterung und frühzeitige Entwicklung von

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Hajar Tahiri, Fatima zahra El Fatoiki, Meriem Regragui, Fouzia. Hali, and Soumiya .Chiheb. "A rare occurrence of Hodgkin lymphoma in a Xeroderma pigmentosum patient: A case report and literature review." World Journal of Advanced Research and Reviews 22, no. 1 (2024): 1484–86. http://dx.doi.org/10.30574/wjarr.2024.22.1.1179.

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Xeroderma pigmentosum (XP) is a rare genetic disorder characterized by extreme sensitivity to ultraviolet (UV) radiation, resulting in an increased risk of skin cancer and other UV-induced malignancies. Reports of hematological malignancies occurring in patients with XP are found in the literature, but they seem to be quite rare. This report describes a 29-year-old male patient with XP who developed Hodgkin lymphoma. The potential increased risk of lymphoma in XP patients is highlighted in this paper; however, further studies are needed to better understand the underlying mechanisms of lymphom

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Hajar, Tahiri, zahra El Fatoiki Fatima, Regragui Meriem, Hali Fouzia., and .Chiheb Soumiya. "A rare occurrence of Hodgkin lymphoma in a Xeroderma pigmentosum patient: A case report and literature review." World Journal of Advanced Research and Reviews 22, no. 1 (2024): 1484–86. https://doi.org/10.5281/zenodo.14225598.

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Xeroderma pigmentosum (XP) is a rare genetic disorder characterized by extreme sensitivity to ultraviolet (UV) radiation, resulting in an increased risk of skin cancer and other UV-induced malignancies. Reports of hematological malignancies occurring in patients with XP are found in the literature, but they seem to be quite rare. This report describes a 29-year-old male patient with XP who developed Hodgkin lymphoma. The potential increased risk of lymphoma in XP patients is highlighted in this paper; however, further studies are needed to better understand the underlying mechanisms of lymphom

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Alakshar, Asmaa, Abdul Rahman Mohammed Saleh, and Mehmet Omer Gorduysus. "Debris and Smear Layer Removal from Oval Root Canals Comparing XP-Endo Finisher, EndoActivator, and Manual Irrigation: A SEM Evaluation." European Journal of Dentistry 14, no. 04 (2020): 626–33. http://dx.doi.org/10.1055/s-0040-1714762.

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Abstract Objective This study aimed to assess and compare XP-Endo Finisher (XP) cleaning efficiency with respect to the amount of remaining debris and smear layer versus Max-I-Probe needle (CI), EndoActivator device (EA), and combination of XP-Endo Finisher file with EndoActivator device (XP+EA) in oval root canals. Materials and Methods This in vitro study was performed on 36 extracted single root/canal mandibular premolars. Radiographic images were taken in buccolingual and mesiodistal projections to evaluate the shape of the root canal and determine whether it met exclusion criteria. All te

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Rothkopf, Michael. "An Algorithmic Approach for Lipid Metabolism and Management of Patients with Xanthelasma Palpebrarum (XP)." Current Developments in Nutrition 4, Supplement_2 (2020): 1140. http://dx.doi.org/10.1093/cdn/nzaa055_025.

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Abstract Objectives XP (flat, yellowish plaques around the eyes) is difficult to treat and often recurs. We describe an algorithmic approach to explore the lipid metabolism and management of XP. Methods A 64 yo female with hypothyroidism, obesity, and metabolic syndrome was successful with weight loss and glycemia but noted recurrence of XP after a surgical excision. Her lipid profile (on rosuvastatin) revealed: total cholesterol 150 mg/dL, LDL 54 mg/dL, triglycerides 74 mg/dL, HDL 81 mg/dL. Apolipoprotein (Apo) A1 was 213 mg/dL (nl female &gt; 140). Apo B100 was 63 mg/dL (nl &lt; 130)

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Sugimoto, Naotoshi, Tetsuhiro Yoshinami, Sachiko Yamamoto, Toshinari Yagi, and Fumio Imamura. "Does capecitabine plus cisplatin (XP) give advanced or recurrent gastric cancer (AGC) patients higher early tumor shrinkage (ETS) rate than S1 plus cisplatin (SP) with safety?" Journal of Clinical Oncology 33, no. 3_suppl (2015): 172. http://dx.doi.org/10.1200/jco.2015.33.3_suppl.172.

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172 Background: Capecitabine plus cisplatin (XP) is defined as the platform regimen in many global trials (ex: ToGA, AVAGAST) for AGC in first-line setting. But in the Japanese Gastric Cancer Treatment Guideline (4th edition), S-1 plus cisplatin (SP) is mentioned the standard (recommendation 1), XP is considered as recommendation 2. Few reports were existed about the comparison between XP and SP. So we retrospectively compared the efficacy and toxicity of XP and SP for patients with AGC in our hospital. Methods: The selection criteria were pathologically proven AGC (HER2 negative or unknown);

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Takeno, Atsushi, Youichi Makari, Shunji Endo, et al. "Randomized, open-label, phase II study comparing five-weekly S-1 plus cisplatin (SP) with tri-weekly capecitabine plus cisplatin (XP) in chemotherapy-naïve patients with HER2 negative advanced gastric cancer (AGC): OGSG 1105 HERBIS-4A trial." Journal of Clinical Oncology 36, no. 4_suppl (2018): 102. http://dx.doi.org/10.1200/jco.2018.36.4_suppl.102.

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102 Background: This phase II study aimed to investigate the safety and efficacy of XP compared to SP in the first-line treatment of HER2 negative AGC. Methods: Patients were randomly assigned to receive either SP (S-1 at 40–60 mg twice daily for 21 days plus cisplatin at 60 mg/ m2 on day 8, every 5 weeks) or XP (capecitabine 1,000 mg/m2 twice daily for 14 days plus cisplatin 80 mg/m2 on day 1, every 3 weeks). Primary endpoint was response rate (RR), and secondary endpoints were progression-free survival (PFS), overall survival (OS), time to treatment failure (TTF), and adverse events. Results

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Bahrudin, Ida Aryanie, Rafizah Mohd Hanifa, Mohd Ezree Abdullah, and Muhammad Firdaus Kamarudin. "Adapting eXtreme Programming Approach in Developing Electronic Document Online System (eDoc)." Applied Mechanics and Materials 321-324 (June 2013): 2938–41. http://dx.doi.org/10.4028/www.scientific.net/amm.321-324.2938.

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eXtreme Programming (XP) is one of new discipline of software development methodology on values of simplicity, communication, feedback and also courage. XP is an explorative and agile development method that seeks to satisfy the customer through early and continuous delivery of valuable software. XP software development process starts with planning, and all iterations consist of four basic phases in its life cycle: designing, coding, testing, and listening. This paper tends to report the experience in adapting XP in developing electronic document online system for the use of Centre for Diploma

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