Статті в журналах з теми "C16orf35"
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Ознайомтеся з топ-48 статей у журналах для дослідження на тему "C16orf35".
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Zhou, Guo-Ling, Li Xin, Wei Song, Li-Jun Di, Guang Liu, Xue-Song Wu, De-Pei Liu та Chih-Chuan Liang. "Active Chromatin Hub of the Mouse α-Globin Locus Forms in a Transcription Factory of Clustered Housekeeping Genes". Molecular and Cellular Biology 26, № 13 (1 липня 2006): 5096–105. http://dx.doi.org/10.1128/mcb.02454-05.
Повний текст джерелаKowalczyk, Monika S., Jim R. Hughes, Jacqueline A. Sharpe, Jill M. Brown, Veronica J. Buckle, William G. Wood та Douglas R. Higgs. "Does Transcription of Remote α-Globin Regulatory Elements Affect Their Function?." Blood 114, № 22 (20 листопада 2009): 4060. http://dx.doi.org/10.1182/blood.v114.22.4060.4060.
Повний текст джерелаLunardi, Andrea, Fulvio Chiacchiera, Elisa D’Este, Marcello Carotti, Marco Dal Ferro, Giulio Di Minin, Giannino Del Sal, and Licio Collavin. "The evolutionary conserved gene C16orf35 encodes a nucleo-cytoplasmic protein that interacts with p73." Biochemical and Biophysical Research Communications 388, no. 2 (October 2009): 428–33. http://dx.doi.org/10.1016/j.bbrc.2009.08.027.
Повний текст джерелаDu, Xinna, Wei Xia, Weiping Fan, Xuan Shen, Hongyan Wu, and Hu Zhang. "Integrated Analysis of C16orf54 as a Potential Prognostic, Diagnostic, and Immune Marker across Pan-Cancer." Disease Markers 2022 (September 9, 2022): 1–25. http://dx.doi.org/10.1155/2022/9365046.
Повний текст джерелаNakamura, Toru, Toyomasa Katagiri, Shoki Sato, Toshihiro Kushibiki, Koji Hontani, Takahiro Tsuchikawa, Satoshi Hirano, and Yusuke Nakamura. "Overexpression of C16orf74 is involved in aggressive pancreatic cancers." Oncotarget 8, no. 31 (July 28, 2016): 50460–75. http://dx.doi.org/10.18632/oncotarget.10912.
Повний текст джерелаAfink, Gijs B., Geertruda Veenboer, Janine de Randamie, Remco Keijser, Christof Meischl, Hans Niessen, and Carrie Ris-Stalpers. "Initial Characterization of C16orf89, A Novel Thyroid-Specific Gene." Thyroid 20, no. 7 (July 2010): 811–21. http://dx.doi.org/10.1089/thy.2009.0366.
Повний текст джерелаLi, Tingting, Fei Li, Jia Lin, Yinglan Zhang, Qi Zhang, Yanhe Sun, Xudong Chen, Mingqing Xu, Xu Wang, and Qiang Li. "Deletion of c16orf45 in zebrafish results in a low fertilization rate and increased thigmotaxis." Developmental Psychobiology 62, no. 8 (May 18, 2020): 1003–10. http://dx.doi.org/10.1002/dev.21984.
Повний текст джерелаBhalla, Kavita, Helen J. Eyre, Scott A. Whitmore, Grant R. Sutherland, and David F. Callen. "C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain." Journal of Human Genetics 44, no. 6 (October 1999): 383–87. http://dx.doi.org/10.1007/s100380050183.
Повний текст джерелаArnold, A. W., P. H. Itin, M. Pigors, J. Kohlhase, L. Bruckner-Tuderman, and C. Has. "Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria." British Journal of Dermatology 163, no. 4 (July 2, 2010): 866–69. http://dx.doi.org/10.1111/j.1365-2133.2010.09929.x.
Повний текст джерелаLu, Meng, Qin Xueying, Peng Hexiang, Gao Wenjing, Sara Hägg, Cao Weihua, Li Chunxiao, et al. "Genome-wide associations between alcohol consumption and blood DNA methylation: evidence from twin study." Epigenomics 13, no. 12 (June 2021): 939–51. http://dx.doi.org/10.2217/epi-2021-0039.
Повний текст джерелаKushibiki, Toshihiro, Toru Nakamura, Masumi Tsuda, Takahiro Tsuchikawa, Koji Hontani, Kazuho Inoko, Mizuna Takahashi, et al. "Role of Dimerized C16orf74 in Aggressive Pancreatic Cancer: A Novel Therapeutic Target." Molecular Cancer Therapeutics 19, no. 1 (October 9, 2019): 187–98. http://dx.doi.org/10.1158/1535-7163.mct-19-0491.
Повний текст джерелаVolpi, Ludovica, Gaia Roversi, Elisa Adele Colombo, Nico Leijsten, Daniela Concolino, Andrea Calabria, Maria Antonietta Mencarelli, et al. "Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene." American Journal of Human Genetics 86, no. 1 (January 2010): 72–76. http://dx.doi.org/10.1016/j.ajhg.2009.11.014.
Повний текст джерелаVolpi, Ludovica, Gaia Roversi, Elisa Adele Colombo, Nico Leijsten, Daniela Concolino, Andrea Calabria, Maria Antonietta Mencarelli, et al. "Targeted Next-Generation Sequencing Appoints C16orf57 as Clericuzio-Type Poikiloderma with Neutropenia Gene." American Journal of Human Genetics 87, no. 3 (September 2010): 445. http://dx.doi.org/10.1016/j.ajhg.2010.08.012.
Повний текст джерелаSakka, Rania, Bahri Mahjoub, Emna Kerkeni, Amina Werdani, Raoudha Boussoffara, Hassen Ben Cheikh, Ridha M'rad, and Mohamed Taher Sfar. "Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation." Pediatric Blood & Cancer 65, no. 9 (May 24, 2018): e27262. http://dx.doi.org/10.1002/pbc.27262.
Повний текст джерелаClericuzio, Carol, Karine Harutyunyan, Weidong Jin, Robert P. Erickson, Alan D. Irvine, W. H. Irwin McLean, Yaran Wen, et al. "Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia." American Journal of Medical Genetics Part A 155, no. 2 (December 22, 2010): 337–42. http://dx.doi.org/10.1002/ajmg.a.33807.
Повний текст джерелаKilic, Sara S., and Sukru Cekic. "Juvenile Idiopathic Inflammatory Myopathy in a Patient With Dyskeratosis Congenita Due to C16orf57 Mutation." Journal of Pediatric Hematology/Oncology 38, no. 2 (March 2016): e75-e77. http://dx.doi.org/10.1097/mph.0000000000000455.
Повний текст джерелаCarvalho, M. E., F. S. Baldi, M. H. A. Santana, R. V. Ventura, G. A. Oliveira, R. S. Bueno, M. N. Bonin, et al. "Identification of genomic regions related to tenderness in Nellore beef cattle." Advances in Animal Biosciences 8, s1 (October 2017): s42—s44. http://dx.doi.org/10.1017/s2040470017001674.
Повний текст джерелаPhillips-Krawczak, Christine A., Amika Singla, Petro Starokadomskyy, Zhihui Deng, Douglas G. Osborne, Haiying Li, Christopher J. Dick, et al. "COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the copper transporter ATP7A." Molecular Biology of the Cell 26, no. 1 (January 2015): 91–103. http://dx.doi.org/10.1091/mbc.e14-06-1073.
Повний текст джерелаKim, Won Tae, Seok Joong Yun, Cheol Park, Isaac Yi Kim, Sung-Kwon Moon, Tae Gyun Kwon, Yung Hyun Choi, and Wun-Jae Kim. "Identification of C16orf74 as a Marker of Progression in Primary Non-Muscle Invasive Bladder Cancer." PLoS ONE 5, no. 12 (December 21, 2010): e15260. http://dx.doi.org/10.1371/journal.pone.0015260.
Повний текст джерелаSrivastava, Shalini, and Dulal Panda. "A centrosomal protein FOR20 regulates microtubule assembly dynamics and plays a role in cell migration." Biochemical Journal 474, no. 16 (August 10, 2017): 2841–59. http://dx.doi.org/10.1042/bcj20170303.
Повний текст джерелаSuter, Aude-Annick, Peter Itin, Karl Heinimann, Munaza Ahmed, Tazeen Ashraf, Helen Fryssira, Usha Kini, et al. "Rothmund-Thomson Syndrome: novel pathogenic mutations and frequencies of variants in the RECQL4 and USB1 (C16orf57) gene." Molecular Genetics & Genomic Medicine 4, no. 3 (February 24, 2016): 359–66. http://dx.doi.org/10.1002/mgg3.209.
Повний текст джерелаKojima, Waka, Koji Yamano, Hidetaka Kosako, Kenichiro Imai, Reika Kikuchi, Keiji Tanaka, and Noriyuki Matsuda. "Mammalian BCAS3 and C16orf70 associate with the phagophore assembly site in response to selective and non-selective autophagy." Autophagy 17, no. 8 (January 26, 2021): 2011–36. http://dx.doi.org/10.1080/15548627.2021.1874133.
Повний текст джерелаGong, Junling, Haiying Fan, Jing Deng, and Qiumei Zhang. "LncRNA HAND2‐AS1 represses cervical cancer progression by interaction with transcription factor E2F4 at the promoter of C16orf74." Journal of Cellular and Molecular Medicine 24, no. 11 (April 21, 2020): 6015–27. http://dx.doi.org/10.1111/jcmm.15117.
Повний текст джерелаFernández, María, Alicia de Coo, Inés Quintela, Eliane García, Márcio Diniz-Freitas, Jacobo Limeres, Pedro Diz, Juan Blanco, Ángel Carracedo, and Raquel Cruz. "Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study." International Journal of Molecular Sciences 22, no. 12 (June 10, 2021): 6274. http://dx.doi.org/10.3390/ijms22126274.
Повний текст джерелаNazarian, Alireza, Anatoliy I. Yashin, and Alexander M. Kulminski. "Summary-Based Methylome-Wide Association Analyses Suggest Potential Genetically Driven Epigenetic Heterogeneity of Alzheimer’s Disease." Journal of Clinical Medicine 9, no. 5 (May 15, 2020): 1489. http://dx.doi.org/10.3390/jcm9051489.
Повний текст джерелаDokal, Inderjeet. "Dyskeratosis Congenita." Hematology 2011, no. 1 (December 10, 2011): 480–86. http://dx.doi.org/10.1182/asheducation-2011.1.480.
Повний текст джерелаConcolino, D., G. Roversi, G. L. Muzzi, S. Sestito, E. A. Colombo, L. Volpi, L. Larizza, and P. Strisciuglio. "Clericuzio-type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: Delineation of the phenotype." American Journal of Medical Genetics Part A 152A, no. 10 (August 23, 2010): 2588–94. http://dx.doi.org/10.1002/ajmg.a.33600.
Повний текст джерелаMroczek, S., J. Krwawicz, J. Kutner, M. Lazniewski, I. Kucinski, K. Ginalski, and A. Dziembowski. "C16orf57, a gene mutated in poikiloderma with neutropenia, encodes a putative phosphodiesterase responsible for the U6 snRNA 3' end modification." Genes & Development 26, no. 17 (August 16, 2012): 1911–25. http://dx.doi.org/10.1101/gad.193169.112.
Повний текст джерелаDanuta, Galetzka, Müller Tobias, Dittrich Marcus, Endres Miriam, Kartal Nergiz, Sinizyn Olesja, Rapp Steffen, et al. "Molecular karyotyping and gene expression analysis in childhood cancer patients." Journal of Molecular Medicine 98, no. 8 (June 23, 2020): 1107–23. http://dx.doi.org/10.1007/s00109-020-01937-4.
Повний текст джерелаLu, Li, Huiyu Li, Xiaomei Chen, Wei Xiong, and Shiang Huang. "The Chromosome Open Reading Frame Genes Targeted By Abnormal Micrornas in Microvesicles from Chronic Myeloid Leukemia." Blood 124, no. 21 (December 6, 2014): 5509. http://dx.doi.org/10.1182/blood.v124.21.5509.5509.
Повний текст джерелаColombo, Elisa A., J. Fernando Bazan, Gloria Negri, Cristina Gervasini, Nursel H. Elcioglu, Deniz Yucelten, Ilknur Altunay, et al. "Novel C16orf57 mutations in patients with Poikiloderma with Neutropenia: bioinformatic analysis of the protein and predicted effects of all reported mutations." Orphanet Journal of Rare Diseases 7, no. 1 (2012): 7. http://dx.doi.org/10.1186/1750-1172-7-7.
Повний текст джерелаWalne, Amanda J., Tom Vulliamy, Richard Beswick, Michael Kirwan, and Inderjeet Dokal. "Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome." Human Molecular Genetics 19, no. 22 (September 3, 2010): 4453–61. http://dx.doi.org/10.1093/hmg/ddq371.
Повний текст джерелаDereure, O. "Des mutations du gène C16orf57 sont impliquées dans le syndrome poïkilodermie – neutropénie et dans une variété particulière de dyskératose congénitale à télomères normaux." Annales de Dermatologie et de Vénéréologie 138, no. 4 (April 2011): 362–63. http://dx.doi.org/10.1016/j.annder.2011.01.026.
Повний текст джерелаYoung, Corey D., Eric B. Dammer, Ti'ara L. Griffen, Sha'kayla K. Nunez, Courtney Dill, Kaylin M. Carey, and James W. Lillard. "Abstract 2950: Coexpression networks of miRNAs and gene transcripts coinciding with lung adenocarcinoma progression and survival." Cancer Research 82, no. 12_Supplement (June 15, 2022): 2950. http://dx.doi.org/10.1158/1538-7445.am2022-2950.
Повний текст джерелаJeong, Ho-Chang, Siddharth Shukla, Roy Parker, and Luis Batista. "USB1 Is a miRNA Deadenylase That Regulates Hematopoietic Development." Blood 138, Supplement 1 (November 5, 2021): 2191. http://dx.doi.org/10.1182/blood-2021-146115.
Повний текст джерелаBaratti, Mariana O., Yuri B. Moreira, Fabiola Traina, Luciene Borges, Fernando F. Costa, Sergio Verjovski-Almeida, and Sara T. O. Saad. "Identification of Intronic RNA Expression in CD34+ Cells of Patients with Myelodysplatic Syndrome by RNA Microarray Analysis." Blood 110, no. 11 (November 16, 2007): 2423. http://dx.doi.org/10.1182/blood.v110.11.2423.2423.
Повний текст джерелаWestin, Erik, Larisa Pereboeva, Divya Devadasan, Tim M. Townes, and Frederick D. Goldman. "Suppression of Antioxidant Responses in Dyskeratosis Congenita Cells." Blood 126, no. 23 (December 3, 2015): 2412. http://dx.doi.org/10.1182/blood.v126.23.2412.2412.
Повний текст джерелаJansen, Iris E., Sven J. van der Lee, Duber Gomez-Fonseca, Itziar de Rojas, Maria Carolina Dalmasso, Benjamin Grenier-Boley, Anna Zettergren, et al. "Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers." Acta Neuropathologica, September 6, 2022. http://dx.doi.org/10.1007/s00401-022-02454-z.
Повний текст джерелаBenslimane, Yahya, María Sánchez‐Osuna, Jasmin Coulombe‐Huntington, Thierry Bertomeu, Danielle Henry, Caroline Huard, Éric Bonneil, Pierre Thibault, Mike Tyers, and Lea Harrington. "A novel p53 regulator, C16ORF72/TAPR1, buffers against telomerase inhibition." Aging Cell 20, no. 4 (March 4, 2021). http://dx.doi.org/10.1111/acel.13331.
Повний текст джерелаAmici, David R., Harun Cingoz, Milad J. Alasady, Sammy Alhayek, Claire M. Phoumyvong, Nidhi Sahni, S. Stephen Yi, and Marc L. Mendillo. "The HAPSTR2 retrogene buffers stress signaling and resilience in mammals." Nature Communications 14, no. 1 (January 11, 2023). http://dx.doi.org/10.1038/s41467-022-35697-1.
Повний текст джерелаAmici, David R., Daniel J. Ansel, Kyle A. Metz, Roger S. Smith, Claire M. Phoumyvong, Sitaram Gayatri, Tomasz Chamera, et al. "C16orf72/HAPSTR1 is a molecular rheostat in an integrated network of stress response pathways." Proceedings of the National Academy of Sciences 119, no. 27 (July 2022). http://dx.doi.org/10.1073/pnas.2111262119.
Повний текст джерелаNisar, Haider, Memoona Khan, Qamar Un Nisa Chaudhry, Raheel Iftikhar, and Tariq Ghafoor. "Case report: A novel mutation in RTEL1 gene in dyskeratosis congenita." Frontiers in Oncology 13 (March 2, 2023). http://dx.doi.org/10.3389/fonc.2023.1098876.
Повний текст джерелаLee, Chanjae, Rachael M. Cox, Ophelia Papoulas, Amjad Horani, Kevin Drew, Caitlin C. Devitt, Steven L. Brody, Edward M. Marcotte, and John B. Wallingford. "Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins." eLife 9 (December 2, 2020). http://dx.doi.org/10.7554/elife.58662.
Повний текст джерелаAbolnezhadian, Farhad, and Sara Iranparast. "Identification of a Novel C16orf57 Mutation in Iranian Patient With Clericuzio-type Poikiloderma with Neutropenia (CPN): A Case Report." Iranian Journal of Allergy, Asthma and Immunology, September 4, 2019. http://dx.doi.org/10.18502/ijaai.v18i4.1424.
Повний текст джерелаTanaka, Akio, Fanny Morice-Picard, Didier Lacombe, Nikoletta Nagy, Michihiro Hide, Alain Taïeb, and John McGrath. "Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia." American Journal of Medical Genetics Part A, 2010, n/a. http://dx.doi.org/10.1002/ajmg.a.33455.
Повний текст джерелаPim, David, Justyna Broniarczyk, Abida Siddiqa, Paola Massimi, and Lawrence Banks. "Human Papillomavirus type 16 L2 recruits both retromer and retriever complexes during retrograde trafficking of the viral genome to the cell nucleus." Journal of Virology, November 11, 2020. http://dx.doi.org/10.1128/jvi.02068-20.
Повний текст джерелаCade, Brian E., Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen, Sina A. Gharib, et al. "Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program." Genome Medicine 13, no. 1 (August 26, 2021). http://dx.doi.org/10.1186/s13073-021-00917-8.
Повний текст джерелаTaylor, Laura W., John E. French, Zachary G. Robbins, and Leena A. Nylander-French. "Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-Painters." Frontiers in Genetics 12 (July 14, 2021). http://dx.doi.org/10.3389/fgene.2021.700636.
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