Gotowe bibliografie tematyczne / Hereditary effect

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji

Gotowa bibliografia na temat „Hereditary effect”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Hereditary effect"

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Шахназаров, К. Ю. "The «fluid memory» effect in steel, cast iron and silumin." Informacionno-technologicheskij vestnik, no. 2(24) (June 17, 2020): 179–85. http://dx.doi.org/10.21499/2409-1650-2020-24-2-179-185.

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Явление структурной наследственности получило промышленное применение, несмотря на то что «механизм передачи наследственных признаков расплаву, их сохранение, зарождение в нем новых признаков и передача их твердому металлу - все это сложные, во многом неизученные вопросы» (Б.А. Баум с коллегами). На примерах стали, чугуна и алюминия предпринята попытка обоснования предположения, что одним из механизмов передачи наследственных признаков может быть эффект «памяти жидкости», который заключается в сохранении ее свойств при очень сильном разбавлении. The phenomenon of structural heredity is used by
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DURU, FERIDE, and AYTEMIZ GÜRGEY. "Effect of corticosteroids in hereditary spherocytosis." Pediatrics International 36, no. 6 (1994): 666–68. http://dx.doi.org/10.1111/j.1442-200x.1994.tb03266.x.

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Myslyakova, Yu G. "Developing a Typology of Regions Based on Their Predisposition to Scientific and Technological Development." Economics and Management 27, no. 10 (2021): 775–85. http://dx.doi.org/10.35854/1998-1627-2021-10-775-785.

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Aim. The presented study aims to describe the proposed typology of regions based on their predisposition to scientific and technological development in the context of hereditary industrial, social, and institutional determinants of economic territorial development. Tasks. The authors develop a methodological approach to forming a basic criterion for the classification of regions; develop a methodology for the classification of regions based on their predisposition to scientific and technological development with allowance for the economic impact of their hereditary core; test the authors’ deve
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Baskerville, Richard, Nykle Krijgsveld, Patrick Esser, Glen Jeffery, and Joanna Poulton. "The Effect of Photobiomodulation on the Treatment of Hereditary Mitochondrial Diseases." Journal of Lasers in Medical Sciences 14 (October 10, 2023): e41. http://dx.doi.org/10.34172/jlms.2023.41.

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Introduction: Despite a wide variety of clinical presentations in hereditary Mitochondrial Diseases, muscle fatigue is a common theme and impairs a patient’s quality of life and ability to function. Current treatments are only supportive and include nutritional supplementation and physical therapy. Photobiomodulation therapy (PBMT) using low-intensity, narrow spectrum light in the red/near infrared (NIR) range, from a low-level laser or light-emitting diode sources, enhances mitochondrial function in preclinical and clinical studies on a range of conditions. However, little research has been d
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Major, Tamás, Réka Gindele, Gábor Balogh, Péter Bárdossy, and Zsuzsanna Bereczky. "Founder Effects in Hereditary Hemorrhagic Telangiectasia." Journal of Clinical Medicine 10, no. 8 (2021): 1682. http://dx.doi.org/10.3390/jcm10081682.

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A founder effect can result from the establishment of a new population by individuals from a larger population or bottleneck events. Certain alleles may be found at much higher frequencies because of genetic drift immediately after the founder event. We provide a systematic literature review of the sporadically reported founder effects in hereditary hemorrhagic telangiectasia (HHT). All publications from the ACVRL1, ENG and SMAD4 Mutation Databases and publications searched for terms “hereditary hemorrhagic telangiectasia” and “founder” in PubMed and Scopus, respectively, were extracted. Follo
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Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.1124.

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Abstract Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect
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Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.bloodjournal7141124.

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Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect in heredi
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Can, Ferda, Tansu Büyükgül, Nuray Yılmaz Cakmak, et al. "EFFECT OF HEREDITARY THROMBOPHILIA ON ARTERIAL THROMBOSIS." Hematology, Transfusion and Cell Therapy 46 (May 2024): 3–4. http://dx.doi.org/10.1016/j.htct.2024.04.006.

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Tverdyi, Dmitrii, Evgeny Makarov, and Roman Parovik. "Hereditary Mathematical Model of the Dynamics of Radon Accumulation in the Accumulation Chamber." Mathematics 11, no. 4 (2023): 850. http://dx.doi.org/10.3390/math11040850.

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Mathematical modeling is used to study the hereditary mechanism of the accumulation of radioactive radon gas in a chamber with gas-discharge counters at several observation points in Kamchatka. Continuous monitoring of variations in radon volumetric activity in order to identify anomalies in its values is one of the effective methods for studying the stress–strain state of the geo-environment with the possibility of building strong earthquake forecasts. The model equation of radon transfer, taking into account its accumulation in the chamber and the presence of the hereditary effect (heredity
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Murtazina, Aysylu F., Olga A. Shchagina, Sergey S. Nikitin, Elena L. Dadali, and Alexander V. Polyakov. "Current view on phenotypic and genetic features of autosomal recessive inherited peripheral neuropathies." Annals of Clinical and Experimental Neurology 13, no. 1 (2019): 55–69. https://doi.org/10.25692/acen.2019.1.7.

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Inherited peripheral neuropathies (IPNs) are a heterogeneous group of hereditary motor and sensory neuropathies (HMSN), hereditary motor neuropathies, and hereditary sensory neuropathies. IPNs can be inherited in autosomal dominant, autosomal recessive or X-linked manner. In clinical practice, isolated cases are more common, and the absence of genealogical data significantly complicates differential diagnosis. About 45% of HMSN cases lack genetic confirmation. For a number of autosomal recessive IPNs, peculiar clinical, electrophysiological and histological features can be distinguished, howev
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Rozprawy doktorskie na temat "Hereditary effect"

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Norgren, Nina. "Hereditary transthyretin amyloidosis (ATTR V30M) : from genes to genealogy." Doctoral thesis, Umeå universitet, Medicin, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-84494.

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Background: Hereditary transthyretin amyloidosis is an autosomal dominant disease with a reduced penetrance. The most common mutation in Sweden is the V30M mutation in the transthyretin gene. Clustering areas of the disease can be found in Northern Sweden, Portugal, Brazil and Japan, although sporadic cases exist worldwide. Despite being caused by the same mutation, there are large differences in onset, penetrance and symptoms of the disease. Swedish V30M patients typically have a later onset with a lower penetrance compared to those from the clustering Portuguese V30M areas. The reasons for t
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KREKEL, CHRISTINE ELIZABETH. "THE EFFECT OF CLINICAL PRACTICE LOCATION ON PHYSICIAN REFERRAL PRACTICES AND ATTITUDES FOR HEREDITARY BREAST CANCER." University of Cincinnati / OhioLINK, 2002. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1025639885.

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Perrier-Trudova, Victoria. "Molecular characterization of hereditary and sporadic papillary renal cell carcinoma type 2 (PRCC2)." Thesis, Paris, EPHE, 2015. http://www.theses.fr/2015EPHE3085.

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Le cancer du rein papillaire de type 2 (PRCC2) est un cancer très agressif avec un potentiel métastatique élevé et pour lequel il n’y a pas de traitement efficace. La forme héréditaire de PRCC2 est associée au syndrome rare de la léiomyomatose cutanéo-utérine héréditaire (HLRCC). HLRCC est due à une mutation germinale hétérozygote du gène Fumarate Hydratase (FH) qui code l'enzyme du cycle de Krebs, la Fumarase. Le déficit en fumarase induit l’accumulation de fumarate et active les voies de signalisation du facteur de transcription inductible par l’hypoxie (HIF) et des espèces réactives de l’ox
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Hept, Megan A. "ANALYZING THE PHENOTYPIC EFFECT OF THREE CANDIDATE GENES ASSOCIATED WITH NONSYNDROMIC CRANIOSYNOSTOSIS USING A ZEBRAFISH MODEL." VCU Scholars Compass, 2017. http://scholarscompass.vcu.edu/etd/5021.

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In normal cranial suture development, the cranial sutures close at predetermined periods of development to allow the brain the capability to grow in a malleable environment. However, in craniosynostosis, cranial sutures prematurely fuse before birth which can lead to a wide range of developmental issues and complications. Craniosynostosis can be categorized as nonsyndromic which involves the sole fusion of one or more of the cranial sutures, or syndromic in which cranial sutures fuse as well as other abnormalities associated with a genetic disorder. Past research has identified three candidate
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Rocheleau, Jessica Marie. "Effect of KCNE1 and KCNE3 Accessory Subunits on KCNQ1 Potassium Channel Function: A Dissertation." eScholarship@UMMS, 2008. https://escholarship.umassmed.edu/gsbs_diss/397.

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The KCNE1 and KCNE3 type I transmembrane-spanning β-subunits assemble with the KCNQ1 voltage-gated K+ channel to afford membrane-embedded complexes with dramatically different properties. Assembly with KCNE1 produces the very slowly activating and deactivating IKs current that shapes the repolarization phase of cardiac action potentials. Genetic mutations in KCNQ1 or KCNE1 that reduce IKs current cause long QT syndrome and predispose affected individuals to potentially fatal cardiac arrhythmias. In contrast, complexes formed between KCNQ1 and KCNE3 produce rapidly activating and mostly voltage
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Stone, Elizabeth Anne. "Multilevel Model Selection: A Regularization Approach Incorporating Heredity Constraints." Diss., Temple University Libraries, 2013. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/234414.

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Statistics<br>Ph.D.<br>This dissertation focuses on estimation and selection methods for a simple linear model with two levels of variation. This model provides a foundation for extensions to more levels. We propose new regularization criteria for model selection, subset selection, and variable selection in this context. Regularization is a penalized-estimation approach that shrinks the estimate and selects variables for structured data. This dissertation introduces a procedure (HM-ALASSO) that extends regularized multilevel-model estimation and selection to enforce principles of fixed heredit
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Simons, Andrew M. (Andrew Michael). "The effect of environmental variability on heritabilities and genetic correlations of traits in the field cricket, Gryllus pennsylvanicus /." Thesis, McGill University, 1993. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=69659.

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The amount of heritable variation and the pattern of genetic covariation in traits are the chief determinants in the evolution of a population, at least over the short term. A preponderance of heritability (h$ sp2)$ and genetic (r$ rm sb g)$ experiments are performed under laboratory conditions which are characterized by low levels of environmental variability. This thesis describes the investigation of the effects of environmental heterogeneity on phenotypic components of variance and covariance. Full-sib families of the field cricket, Gryllus pennsylvanicus, were split between a homogeneous
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Dinkelborg, Katja [Verfasser]. "Investigation of genetic and translational effects of tumor suppressor proteins in two hereditary forms of renal cell carcinoma / Katja Dinkelborg." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2021. http://d-nb.info/1235756866/34.

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Sahenk, Zarife. "The effects of mutant Schwann Cells on the Axonal Cytoskeleton and regeneration-associated myelination in hereditary neuropathies : studies on nerve xenografts /." The Ohio State University, 1998. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487951907960135.

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Wassmer, Sarah. "The Effects of XIAP Gene Therapy in a Murine Model of Leber’s Hereditary Optic Neuropathy and a Feline Model of Retinal Detachment." Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/35774.

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In Canada alone, there were an estimated 800,000 visually impaired people in 2007, costing the federal government an annual amount of $15.8 billion in services, treatments and lost revenue. These costs are estimated to double by the year 2032, as the population ages. The leading causes of visual impairment and blindness is retinal degeneration, characterized by the progressive death of retinal cells. The research presented in this PhD thesis aimed to prevent retinal degeneration by over-expressing the X-linked Inhibitor of Apoptosis (XIAP) in retinal cells using plasmid and adeno-associated
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Książki na temat "Hereditary effect"

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Jakob, Claude Adrian. Expression of 5'-cytosine-DNA-methyltransferase in hereditary colon-cancer syndromes and effect of sulindac, a nonsteroidal anti-inflammatory drug. [s.n.], 1996.

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Radiation, United Nations Scientific Committee on the Effects of Atomic. Sources, effects and risks of ionizing radiation: 1988 report to the General Assembly, with annexes. United Nations, 1988.

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Laureno, Robert. Selective Vulnerability. Edited by Robert Laureno. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190607166.003.0006.

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This chapter on “Selective Vulnerability” examines the selective vulnerability of different parts of the brain to particular diseases. In one disease, certain areas of brain are particularly vulnerable. In other diseases, different parts of the brain are more susceptible. The concept of selective vulnerability was originally applied to toxic/metabolic and hereditary disorders, but it is also useful in thinking about other neuropathologic processes including neoplastic, infectious, demyelinative, vascular, and traumatic diseases. Diseases can selectively affect brain systems, brain structures,
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Pattenden, Miles. The New Pope. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198797449.003.0006.

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This chapter explains the difficulties facing a new pope after his election. Once the shine had worn off his elevation he had to find ways to assert his authority over his former peers. The principle routes were: symbolic display, patronage, and coercion. All had shortcomings which were greater in an elective monarchy like the papacy than in hereditary institutions. Different popes tried different balances of the three, with varying degrees of success. However, none found a winning formula for long because the nature of the pope’s authority—diminishing constantly from the moment of election—me
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Lippmann, Morton, and Richard B. Schlesinger. Effects of Contaminants on Human Health. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190688622.003.0006.

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This chapter describes the methodology used for evaluating potential human health effects resulting from exposure to environmental chemicals. It discusses the concept of the dose-response relationship, and reviews the processes by which chemicals may be delivered to and absorbed by the body. Concepts of the metabolic transformation of absorbed chemical are provided, as are the potential for storage and excretion. It explores the biological mechanisms and pathways underlying specific responses to chemical contaminants, which range from disruption of physiology to alteration of biochemical pathw
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Hereditary Effects of Radiation, United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) 2001 Report. UN, 2001. http://dx.doi.org/10.18356/bca3dbad-en.

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Hereditary Effects of Radiation: Unscear 2001 Report to the General Assembly, with Scientific Annex. United Nations Publications, 2001.

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Hirntod einer Idee: Die Erblichkeit der Intelligenz. V&R Unipress, 2013.

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Deb, Rabindra Narayan. Effects of Heredity on Reaction to Skin-Grafts in Guinea Pigs. Creative Media Partners, LLC, 2021.

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Romagnolo, ​. Cesare, and Tiziano Maggino, eds. NEOPLASIA and FERTILITY. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/97898150501411220101.

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Research on young individuals and childbearing adults being treated for neoplasia has revealed a rising number of requests for treatments aimed to maintain the possibility to conceive. To answer such requests, it is important for medical professionals to consider the necessity to cure the woman, to preserve her fertility, to give information both on the effect of neoplasia and treatments on pregnancy. Patients have to be informed on the possible treatment alternatives that are less aggressive towards the reproductive function, but at the same time, give desirable results in terms of survival.
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Części książek na temat "Hereditary effect"

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Takada, Hideho, Toshiyuki Minoura, Toshiyuki Takata, et al. "Inhibitory Effect of Eicosapentaenoic Acid on Colon Carcinogenesis." In Hereditary Colorectal Cancer. Springer Japan, 1990. http://dx.doi.org/10.1007/978-4-431-68337-7_37.

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Torra, R., C. Badenas, L. P�rez, X. Estivill, and A. Darnell. "Hypertension in Polycystic Kidney Disease Types 1 and 2 and Its Effect on the Age of Onset of End-Stage Renal Disease." In Hereditary Kidney Diseases. KARGER, 1997. http://dx.doi.org/10.1159/000059886.

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Mateos, Felicitas A., Juan G. Puig, Teresa H. Ramos, and Irving H. Fox. "Effect of Fructose Infusion in Hereditary Xanthinuria." In Purine and Pyrimidine Metabolism in Man V. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5104-7_18.

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Stern, Hartley S., Roger C. Gregoire, Hanoch Kashtan, Teri Berk, and W. Robert Bruce. "Long-Term Effects of Dietary Calcium on Risk Markers for Colon Cancer in Familial Polyposis Patients." In Hereditary Colorectal Cancer. Springer Japan, 1990. http://dx.doi.org/10.1007/978-4-431-68337-7_42.

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Moss, A. J., W. Zareba, W. J. Hall, J. L. Robinson, and M. L. Andrews. "Effect of β-Blocker Therapy on the Frequency and Type of Cardiac Events in Patients with the Hereditary Long QT Syndrome." In Cardiac Arrhythmias 1999 - Vol.1. Springer Milan, 2000. http://dx.doi.org/10.1007/978-88-470-2139-6_39.

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Earnest, David L., David S. Alberts, Lee J. Hixson, and Frank L. Meyskens. "Dietary Fiber or Piroxicam as Potential Cancer Prevention Agents: Effects on Rectal Epithelial Cell Proliferation in Humans at Increased Risk of Colon Cancer." In Hereditary Colorectal Cancer. Springer Japan, 1990. http://dx.doi.org/10.1007/978-4-431-68337-7_41.

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Friedman, Eileen A. "Dietary Fat Diglycerides Activate by Tyrosine Phosphorylation a pp63 Membrane Protein Only in Colon Tumors and not in Normal Colonocytes, Leading to Selective Biological Effects." In Hereditary Colorectal Cancer. Springer Japan, 1990. http://dx.doi.org/10.1007/978-4-431-68337-7_81.

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Moini, Jahangir, Oyindamola Akinso, and Raheleh Ahangari. "Nutritional Effects on Hereditary Metabolic Disorders." In Global Malnutrition. CRC Press, 2023. http://dx.doi.org/10.1201/b22969-23.

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Noguchi, Hidehisa, Yoshikazu Ojima, and Seiichi Yasui. "Bayesian Lasso with Effect Heredity Principle." In Frontiers in Statistical Quality Control 11. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-12355-4_21.

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Fan, X. L., and Y. K. Li. "Effect of drought stress and drought tolerance heredity on nitrogen efficiency of winter wheat." In Plant Nutrition. Springer Netherlands, 2001. http://dx.doi.org/10.1007/0-306-47624-x_29.

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Streszczenia konferencji na temat "Hereditary effect"

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Adachi, Tomohide, and Nobuaki Ozaki. "04103 Effect of Givosiran for hereditary coproporphyria: 2 cases report." In Abstracts of the International Conference of Porphyrins and Porphyrias, Pamplona, Spain, 21–25 September 2024. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/bmjgast-2024-icpp.40.

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Horio, Y., T. Suzuki, K. Shima, et al. "The Effect of Pulmonary Macrophage Transplantation Therapy on Bacterial Infection in Hereditary Pulmonary Alveolar Proteinosis." In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a1170.

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Sepahi, I., U. Faust, M. Sturm, et al. "Truncating variants in DNA-repair genes and their effect on AAO of hereditary breast cancer." In 38. Jahrestagung der Deutschen Gesellschaft für Senologie. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1651801.

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Atasay, Elif Bilge, İlayda Altun, Sude Çavdaroğlu, and Gülbüz Sezgin. "04122 Coexistence of Wilson’s disease and hereditary coproporphyria: effect of copper on the heme pathway." In Abstracts of the International Conference of Porphyrins and Porphyrias, Pamplona, Spain, 21–25 September 2024. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/bmjgast-2024-icpp.90.

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Swanson, William H., and Gary E. Fish. "Cone Optical Density and Foveal Architecture in Patients with Hereditary Photoreceptor Degenerations." In Noninvasive Assessment of the Visual System. Optica Publishing Group, 1993. http://dx.doi.org/10.1364/navs.1993.nmb.2.

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A century has passed since it was first reported that an observer's anomaloscope setting (Rayleigh match) can be affected by field size, with less red light required for smaller fields. This phenomenon, known as the color-match area effect, appears to be due to longer cone outer segments in the foveola than in the parafovea, which results in higher effective optical density of foveolar cone photopigments. Since Rayleigh match midpoints are determined by ratio of quantal catches in the cone outer segments for the different wavelengths, they will not be affected by reduced numbers of cones, chan
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Bork, K., and G. Witzke. "LCNG-TEFM SUBSTITUTION WITH Cl-INACTIVATOR IN PATIENTS WITH HEREDITARY AND ACQUIRED Cl-INH DEFICIENCY AND LIFE-THREATENING ANGIOEDEMA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644329.

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Patients with hereditary car acquired cl-inactivator (Cl-INH) deficiency suffer frcm repeated episodes of oedema of the skin and internal organs, which often constitute a threat to life (laryngeal, pulmonary and brain oedama). The treatment which is rapidly effective in the other, much more common, forms of angio-oedema (idiopathic, allergic or anaphylactoid, often associated with urticaria) has little or no effect in these cases. This applies particularly to treatment with antihistamin agents and corticosteroids. However, in patients with hereditary angiooedana (HAE) Danazol is effective for
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Gandrille, S., P. Priollet, L. Capron, M. Roncato, J. N. Fiessinger, and M. Aiach. "ASSOCIATION OF HEREDITARY DYSFIBRINOGENEMIA WITH PROTEIN C DEFICIENCY IN TWO PATIENTS WITH THROMBOTIC TENDENCY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644309.

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An abnormal fibrinogen was found to be associated with protein C deficiency in two unrelated patients. Both were symptomatic, one having severe complicated atherosclerosis, the other recurrent venous thrombosis. In both cases, the two abnormalities coexisted in several members of the family. The two abnormal fibrinogens (Poitiers and Argenteuil) were purified from the patients' plasma and compared to fibrinogens purified from several normal subjects. Polymerisation was abnormal in both cases in presence of reptilase and thrombin.The kinetic of proteolysis by plasmin was studied during 24 hours
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Fukunaga, Masataka, and Nobuyuki Shimizu. "Nonlinear Fractional Derivative Stress-Strain Relations for Polymer Gels Based on the Generalized Maxwell Model." In ASME 2009 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/detc2009-87283.

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In this paper, we formulate two nonlinear stress-strain relations including memory effect in the dynamical behavior of gels that are the kind of viscoelastic materials. The basic assumption of the model is made that the gels consist of blobs of high polymers. Hereditary response of blobs to the stress determines the average stress-strain relation of the material. Two stress-strain relations are derived for different models of gels. These stress-strain relations are compared with the fractional derivative version of Lodge’s rubber-like liquids and the empirical nonlinear fractional derivative m
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BRINK, K., F. DERKX, E. BROMMER, J. STIBBE, H. KOLSTEE, and M. SCHALEKAMP. "THE FIBRINOLYTIC, FACTOR VIII:C, VON WILLEBRAND FACTOR AND HEMODYNAMIC RESPONSES TO DDAVP IN PATIENTS WITH HEREDITARY NEPHROGENIC DIABETES INSIPIDUS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644709.

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The pressor response of vasopressin (AVP) is mediated by a calcium-dependent mechanism (VI-receptor), whereas its antidiuretic effect depends on c-ANP (V2-receptor). DDAVP (1-desamino-8-D-arginine vasopressin) is a synthetic V2 analog of AVP. AVP and DDAVP also increase FVIII:C vWF:Ag and tissue-type plasminogen activator (t-PA) in plasma. The mechanism by which AVP and DDAVP elevate these factors is unclear. Patients with X-linked nephrogenic diabetes insipidus (NDI) are resistant to the V2-mediated antidiuretic action of AVP and DDAVP. We therefore have studied the effect of DDAVP (0.4 ug/kg
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Schäfer, E., N. Rotter, D. Häussler, and H. Sadick. "Intranasal submucosal application of Bevacizumab in hereditary hemorrhagic telangiectasia (HHT) – the effect on endothelial cell proliferation and VEGF expression – an in vitro study." In Abstract- und Posterband – 91. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Welche Qualität macht den Unterschied. © Georg Thieme Verlag KG, 2020. http://dx.doi.org/10.1055/s-0040-1711350.

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