Relevant bibliographies by topics / Kiaa1217

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Kiaa1217'

Author: Grafiati
Published: 22 February 2025
Last updated: 31 July 2025

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Journal articles on the topic "Kiaa1217"

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Wang, Yanhong, Na Li, Yanping Zheng, et al. "KIAA1217 Promotes Epithelial-Mesenchymal Transition and Hepatocellular Carcinoma Metastasis by Interacting with and Activating STAT3." International Journal of Molecular Sciences 23, no. 1 (2021): 104. http://dx.doi.org/10.3390/ijms23010104.

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The survival and prognosis of hepatocellular carcinoma (HCC) are poor, mainly due to metastasis. Therefore, insights into the molecular mechanisms underlying HCC invasion and metastasis are urgently needed to develop a more effective antimetastatic therapy. Here, we report that KIAA1217, a functionally unknown macromolecular protein, plays a crucial role in HCC metastasis. KIAA1217 expression was frequently upregulated in HCC cell lines and tissues, and high KIAA1217 expression was closely associated with shorter survival of patients with HCC. Overexpression and knockdown experiments revealed
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Al Dhaheri, Noura, Nan Wu, Sen Zhao, et al. "KIAA1217 : A novel candidate gene associated with isolated and syndromic vertebral malformations." American Journal of Medical Genetics Part A 182, no. 7 (2020): 1664–72. http://dx.doi.org/10.1002/ajmg.a.61607.

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Karasugi, Tatsuki, Kei Semba, Yuichiro Hirose, et al. "Association of the Tag SNPs in the HumanSKTGene (KIAA1217) With Lumbar Disc Herniation." Journal of Bone and Mineral Research 24, no. 9 (2009): 1537–43. http://dx.doi.org/10.1359/jbmr.090314.

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Lee, Mi-Sook, Ryong Nam Kim, Hoseok I, et al. "Identification of a novel partner gene, KIAA1217, fused to RET: Functional characterization and inhibitor sensitivity of two isoforms in lung adenocarcinoma." Oncotarget 7, no. 24 (2016): 36101–14. http://dx.doi.org/10.18632/oncotarget.9137.

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Knyazeva, E. A., S. V. Nikulin, A. Yu Khristichenko, V. A. Petrov, A. Turchinovich та A. A. Sergievich. "HIF-1α Activation Reduces Expression of the microRNA hsa-miR-603 Host Gene KIAA1217 and Increases Expression of the Target CCND1 Gene in BeWo b30 Cells". Biotekhnologiya 35, № 6 (2019): 80–86. http://dx.doi.org/10.21519/0234-2758-2019-35-6-80-86.

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The model of the placental barrier based on the human choriocarcinoma cell line BeWo b30 allows studying the effect of hypoxia on trophoblast cells. The effect of the oxyquinoline derivative inhibiting HIF-prolyl hydroxylases was studied on this model. Inhibition of these enzymes leads to an increase in the HIF-1α subunit in the cytoplasm, mimicking the cell response to hypoxia. Incubation of the cells with the drug at a concentration of 10 uM for 24 h did not affect the paracellular transport, but reduced the transport of glucose through the cell barrier. The transcriptome analysis after the
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Kuroda, Naoto, Kiril Trpkov, Yuan Gao, et al. "ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217." Modern Pathology 33, no. 12 (2020): 2564–79. http://dx.doi.org/10.1038/s41379-020-0578-0.

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Mohammadi, Ali, Sadegh Alijani, Seyed Abbas Rafat, and Rostam Abdollahi-Arpanahi. "Genome-Wide Association Study and Pathway Analysis for Female Fertility Traits in Iranian Holstein Cattle." Annals of Animal Science 20, no. 3 (2020): 825–51. http://dx.doi.org/10.2478/aoas-2020-0031.

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AbstractFemale fertility is an important trait that contributes to cow’s profitability and it can be improved by genomic information. The objective of this study was to detect genomic regions and variants affecting fertility traits in Iranian Holstein cattle. A data set comprised of female fertility records and 3,452,730 pedigree information from Iranian Holstein cattle were used to predict the breeding values, which were then employed to estimate the de-regressed proofs (DRP) of genotyped animals. A total of 878 animals with DRP records and 54k SNP markers were utilized in the genome-wide ass
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Iwadate, Manabu, Norisato Mitsutake, Michiko Matsuse, et al. "The Clinicopathological Results of Thyroid Cancer With BRAF V600E Mutation in the Young Population of Fukushima." Journal of Clinical Endocrinology & Metabolism 105, no. 12 (2020): e4328-e4336. http://dx.doi.org/10.1210/clinem/dgaa573.

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Abstract Background Thyroid ultrasound screening for children aged 0 to 18 years was performed in Fukushima following the accident at the Fukushima Daiichi Nuclear Power Plant. As a result, many thyroid cancer cases were detected. To explore the carcinogenic mechanisms of these cancers, we analyzed their clinicopathological and genetic features. Methods We analyzed 138 cases (52 males and 86 females) who had undergone surgery between 2013 and 2016 at Fukushima Medical University Hospital. Postoperative pathological diagnosis revealed 136 (98.6%) cases of papillary thyroid cancer (PTC). Results
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Lin, Rongbo, Shen Zhao, Lisheng Cai, et al. "Real-world fusion landscape in advanced Chinese gastric cancer using next generation sequencing: A multicenter study." Journal of Clinical Oncology 37, no. 4_suppl (2019): 51. http://dx.doi.org/10.1200/jco.2019.37.4_suppl.51.

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51 Background: Gastric cancer (GC) is a highly heterogeneous disease. Cell-free DNA (cfDNA) has been a research hotspot in molecular tumor profiling. In advanced GC patients, malignant pleural effusion (MPE) and ascites provide a wealth of tumor cells that can be investigated. The aim of this study is to investigate fusion landscape in advanced GC. Methods: A multicenter study in China was initiated from Aug. 2016, and GC patients have been enrolled as of Aug. 2018. To determine the fusion frequency in GC, we analyzed data from 371clinical GC cases, each of which had results from next-generati
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Cleary, James M., Martin Henner Voss, Funda Meric-Bernstam, et al. "Safety and efficacy of the selective FGFR inhibitor debio 1347 in phase I study patients with FGFR genomically activated advanced biliary tract cancer (BTC)." Journal of Clinical Oncology 36, no. 4_suppl (2018): 447. http://dx.doi.org/10.1200/jco.2018.36.4_suppl.447.

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447 Background: BTC are aggressive tumors with limited treatment options and poor overall survival. Aberrant FGFR signaling has been implicated in BTC carcinogenesis. Debio 1347 is an orally available selective FGFRi with potent antitumor effect in preclinical model bearing FGFR alterations. Debio 1347 showed encouraging preliminary clinical activity and manageable treatment-emergent adverse events (TEAE) in its first-in-human (FIH) ph1 study (NCT1948297) dose-escalating part. Here we report only results from the BTC pts of this study. Methods: This FIH study enrolled pts with advanced solid m
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Dissertations / Theses on the topic "Kiaa1217"

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Greibill, Logan. "Analyse fonctionnelle de la protéine centriolaire KIAA1217, un nouveau régulateur de la ciliogenèse par la voie de signalisation de la famille SRC." Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASL123.

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Les cils, retrouvés à la surface de la majorité des cellules humaines, possèdent de nombreuses fonctions tant sensorielles que motiles. Des défauts dans leurs fonctions ou leurs formations entrainent des pathologies multisystémiques graves, appelées ciliopathies, dont la prévalence cumulée est de 1:2000. La formation des cils est appelée ciliogenèse et requiert des mécanismes complexes séquentiellement organisés. Elle débute par la maturation et la migration du centriole père, afin qu'il s'ancre à une membrane et devienne un corps basal (CB). La migration est assurée par les cytosquelettes d'a
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Yoshikiyo, Kazunori. "KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents." Kyoto University, 2013. http://hdl.handle.net/2433/180458.

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Kazunori Yoshikiyo, Katja Kratz, Kouji Hirota, Kana Nishihara, Minoru Takata, Hitoshi Kurumizaka, Satoshi Horimoto, Shunichi Takeda, and Josef Jiricny "KIAA1018/FAN1 nuclease protects cells against genomic instability induced by interstrand cross-linking agents" PNAS 2010 107 (50) 21553-21557; published ahead of print November 29, 2010, doi:10.1073/pnas.1011081107<br>Kyoto University (京都大学)<br>0048<br>新制・論文博士<br>博士(医学)<br>乙第12772号<br>論医博第2063号<br>新制||医||1000(附属図書館)<br>30755<br>(主査)教授 小松 賢志, 教授 小川 誠司, 教授 松本 智裕<br>学位規則第4条第2項該当
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Khorasani, Abraham J. "Examining the function of KIAA1310/NSL3, a member of the NSL, TET2 and TET3 epigenetic complexes." Thesis, Boston University, 2012. https://hdl.handle.net/2144/12444.

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Thesis (M.A.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.<br>Eukaryotic gene expression is regulated by a number of factors. Transcription initiation can be modulated by the binding of protein factors to specific sequences of DNA in the promoter of a gene. In addition, no
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Schwartz, Lisa. "Proteomic analysis of a novel protein complex KIAA1310 and studying the roles of DNA hydroxymethylation in diabetic patients." Thesis, Boston University, 2013. https://hdl.handle.net/2144/12218.

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Thesis (M.A.)--Boston University<br>Epigenetic modifications affect the genome without directly affecting the genetic code within the DNA. There are many different types of these modifications and they can last for just a few cell replications or for many generations of cells. Many of them involve covalent modifications of histone proteins, affecting the packing of the chromatin and therefore regulating the transcription and expression of different genes. One epigenetic modification that has been considered more permanent is the methylation of the 5' carbon on cytosine. DNA methylation is perf
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Dubos, Aline Hanauer André. "Identification de nouveaux gènes de retard mental par la caractérisation de translocations (X;Autosome) KIAA1202 et CDKL3, deux nouveaux gènes candidats pour le retard mental /." Strasbourg : Université Louis Pasteur, 2007. http://eprints-scd-ulp.u-strasbg.fr:8080/secure/00000646/01/Dubos2006.pdf.

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Dubos, Aline. "Identification de nouveaux gènes de retard mental par la caractérisation de translocations (X;Autosome) : KIAA1202 et CDKL3, deux nouveaux gènes candidats pour le retard mental." Strasbourg 1, 2006. https://publication-theses.unistra.fr/restreint/theses_doctorat/2006/DUBOS_Aline_2006.pdf.

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Les retards mentaux (RM) concernent 1 à 2% de la population et représentent un véritable problème de santé publique. Ils se définissent comme une limitation significative à la fois du fonctionnement intellectuel général et des capacités d’adaptation. Ils sont divisés en deux groupes : les RM syndromiques (RM associé à d’autres signes cliniques) et les RM non syndromiques (RM isolé). L’objectif de ma thèse était d’identifier de nouveaux gènes responsables de RM lié au chromosome X (RMLX) non syndromiques et de comprendre leur implication dans le RM. Pour cela, nous avons étudié plusieurs patien
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PARISI, BARBARA. "Role of the novel neuronal protein APache in autophagy." Doctoral thesis, Università degli studi di Genova, 2022. http://hdl.handle.net/11567/1090471.

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The central event driving neuronal activity is represented by synaptic transmission, a process that relies on regulated cycles of synaptic vesicle (SV) exocytosis and endocytosis at presynaptic terminal level. Neurons, polarized and perennial cells, to guarantee an efficient neurotransmitter release, to maintain cellular homeostasis and promote neuronal survival, are particularly dependent on efficient quality control pathways to continuously remove dysfunctional presynaptic proteins and organelles. The main mechanisms used by neurons to achieve these goals are endosomal sorting and autophagy,
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Chang, Hao-Yen, and 張皓衍. "Studies on an ALK related novel protein KIAA1618." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/72821539212040955976.

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碩士<br>臺灣大學<br>生化科學研究所<br>98<br>KIAA1618/ALO17 is a novel protein discovered from the cases of the anaplastic large cell lymphoma (ALCL). A chimeric protein created due to a translocation of the N-terminal KIAA1618 protein (a.a. 1-1008) fused with the C-terminal truncated anaplastic lymphoma kinase (ALK, a.a. 1058-1620). According to the reported cases of ALCL, the oncogenesis is highly correlated with this chimeric protein. Nonetheless, the physiological function of KIAA1618 is still remained unclear. Using HA-tagged KIAA1618 to transfect HEK293 cells, silver-stain and Western blotting results
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Hagens, Olivier [Verfasser]. "Search for genes involved in human cognition : molecular characterisation of two novel genes, FBXO25 and KIAA1202, disrupted by a translocation in a mentally retarded patient / vorgelegt Olivier Hagens." 2007. http://d-nb.info/985002883/34.

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Book chapters on the topic "Kiaa1217"

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Gewies, Andreas, Jürgen Ruland, Alexey Kotlyarov, et al. "MARK1: EMK3, hPAR-1c, KIAA1477." In Encyclopedia of Signaling Molecules. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100767.

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"KIAA1415." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_105431.

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"KIAA1415." In Encyclopedia of Signaling Molecules. Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100685.

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Brooks, Alice S., and Robert M. W. Hofstra. "KIAA1279 and Goldberg–Shprintzen Syndrome." In Inborn Errors Of Development. Oxford University PressNew York, NY, 2008. http://dx.doi.org/10.1093/oso/9780195306910.003.0182.

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Abstract Goldberg–Shprintzen syndrome or Goldberg–Shprintzen megacolon syndrome (GOSHS) (MIM 609460) is a rare autosomal recessive syndrome with only seven families described in the literature (Goldberg et al., 1981; Hurst et al., 1988; Kumasaka et al., 1988; Yomo et al., 1991; Fryer, 1998; Brooks et al., 1999; Murphy et al., 2006). GOSHS is best characterized as a Hirschsprung dis- ease–mental retardation–microcephaly syndrome. Distinctive associated facial features include high-arched eyebrows, synophrys, hypertelorism, cleft palate/bifid uvula, and clouding of the cornea related to a primar
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"MARK1: EMK3, hPAR-1c, KIAA1477." In Encyclopedia of Signaling Molecules. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_102181.

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Brooks, Alice S., and Robert M. W. Hofstra. "KIAA1279 and Goldberg-Shprintzen Syndrome." In Epstein's Inborn Errors of Development. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199934522.003.0217.

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Conference papers on the topic "Kiaa1217"

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Kim, Young Min, Sae Won Kim, Seungwon Lee, et al. "Abstract B012: Preclinical study of Kiatomab, a novel monoclonal antibody to the cancer stem cell surface marker KIAA1114, for anti-cancer therapy in colorectal carcinoma." In Abstracts: Second CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; September 25-28, 2016; New York, NY. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/2326-6066.imm2016-b012.

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Reports on the topic "Kiaa1217"

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Weller, Joel I., Harris A. Lewin, and Micha Ron. Determination of Allele Frequencies for Quantitative Trait Loci in Commercial Animal Populations. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7586473.bard.

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Individual loci affecting economic traits in dairy cattle (ETL) have been detected via linkage to genetic markers by application of the granddaughter design in the US population and the daughter design in the Israeli population. From these analyses it is not possible to determine allelic frequencies in the population at large, or whether the same alleles are segregating in different families. We proposed to answer this question by application of the "modified granddaughter design", in which granddaughters with a common maternal grandsire are both genotyped and analyzed for the economic traits.
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