Artículos de revistas sobre el tema "C16orf35"
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Zhou, Guo-Ling, Li Xin, Wei Song, Li-Jun Di, Guang Liu, Xue-Song Wu, De-Pei Liu y 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, n.º 13 (1 de julio de 2006): 5096–105. http://dx.doi.org/10.1128/mcb.02454-05.
Texto completoKowalczyk, Monika S., Jim R. Hughes, Jacqueline A. Sharpe, Jill M. Brown, Veronica J. Buckle, William G. Wood y Douglas R. Higgs. "Does Transcription of Remote α-Globin Regulatory Elements Affect Their Function?." Blood 114, n.º 22 (20 de noviembre de 2009): 4060. http://dx.doi.org/10.1182/blood.v114.22.4060.4060.
Texto completoLunardi, Andrea, Fulvio Chiacchiera, Elisa D’Este, Marcello Carotti, Marco Dal Ferro, Giulio Di Minin, Giannino Del Sal y Licio Collavin. "The evolutionary conserved gene C16orf35 encodes a nucleo-cytoplasmic protein that interacts with p73". Biochemical and Biophysical Research Communications 388, n.º 2 (octubre de 2009): 428–33. http://dx.doi.org/10.1016/j.bbrc.2009.08.027.
Texto completoDu, Xinna, Wei Xia, Weiping Fan, Xuan Shen, Hongyan Wu y Hu Zhang. "Integrated Analysis of C16orf54 as a Potential Prognostic, Diagnostic, and Immune Marker across Pan-Cancer". Disease Markers 2022 (9 de septiembre de 2022): 1–25. http://dx.doi.org/10.1155/2022/9365046.
Texto completoNakamura, Toru, Toyomasa Katagiri, Shoki Sato, Toshihiro Kushibiki, Koji Hontani, Takahiro Tsuchikawa, Satoshi Hirano y Yusuke Nakamura. "Overexpression of C16orf74 is involved in aggressive pancreatic cancers". Oncotarget 8, n.º 31 (28 de julio de 2016): 50460–75. http://dx.doi.org/10.18632/oncotarget.10912.
Texto completoAfink, Gijs B., Geertruda Veenboer, Janine de Randamie, Remco Keijser, Christof Meischl, Hans Niessen y Carrie Ris-Stalpers. "Initial Characterization of C16orf89, A Novel Thyroid-Specific Gene". Thyroid 20, n.º 7 (julio de 2010): 811–21. http://dx.doi.org/10.1089/thy.2009.0366.
Texto completoLi, Tingting, Fei Li, Jia Lin, Yinglan Zhang, Qi Zhang, Yanhe Sun, Xudong Chen, Mingqing Xu, Xu Wang y Qiang Li. "Deletion of c16orf45 in zebrafish results in a low fertilization rate and increased thigmotaxis". Developmental Psychobiology 62, n.º 8 (18 de mayo de 2020): 1003–10. http://dx.doi.org/10.1002/dev.21984.
Texto completoBhalla, Kavita, Helen J. Eyre, Scott A. Whitmore, Grant R. Sutherland y David F. Callen. "C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain". Journal of Human Genetics 44, n.º 6 (octubre de 1999): 383–87. http://dx.doi.org/10.1007/s100380050183.
Texto completoArnold, A. W., P. H. Itin, M. Pigors, J. Kohlhase, L. Bruckner-Tuderman y C. Has. "Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria". British Journal of Dermatology 163, n.º 4 (2 de julio de 2010): 866–69. http://dx.doi.org/10.1111/j.1365-2133.2010.09929.x.
Texto completoLu, 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, n.º 12 (junio de 2021): 939–51. http://dx.doi.org/10.2217/epi-2021-0039.
Texto completoKushibiki, 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, n.º 1 (9 de octubre de 2019): 187–98. http://dx.doi.org/10.1158/1535-7163.mct-19-0491.
Texto completoVolpi, 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, n.º 1 (enero de 2010): 72–76. http://dx.doi.org/10.1016/j.ajhg.2009.11.014.
Texto completoVolpi, 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, n.º 3 (septiembre de 2010): 445. http://dx.doi.org/10.1016/j.ajhg.2010.08.012.
Texto completoSakka, Rania, Bahri Mahjoub, Emna Kerkeni, Amina Werdani, Raoudha Boussoffara, Hassen Ben Cheikh, Ridha M'rad y Mohamed Taher Sfar. "Poikiloderma with neutropenia in a Tunisian patient with a novel C16orf57 gene mutation". Pediatric Blood & Cancer 65, n.º 9 (24 de mayo de 2018): e27262. http://dx.doi.org/10.1002/pbc.27262.
Texto completoClericuzio, 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, n.º 2 (22 de diciembre de 2010): 337–42. http://dx.doi.org/10.1002/ajmg.a.33807.
Texto completoKilic, Sara S. y Sukru Cekic. "Juvenile Idiopathic Inflammatory Myopathy in a Patient With Dyskeratosis Congenita Due to C16orf57 Mutation". Journal of Pediatric Hematology/Oncology 38, n.º 2 (marzo de 2016): e75-e77. http://dx.doi.org/10.1097/mph.0000000000000455.
Texto completoCarvalho, 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 (octubre de 2017): s42—s44. http://dx.doi.org/10.1017/s2040470017001674.
Texto completoPhillips-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, n.º 1 (enero de 2015): 91–103. http://dx.doi.org/10.1091/mbc.e14-06-1073.
Texto completoKim, Won Tae, Seok Joong Yun, Cheol Park, Isaac Yi Kim, Sung-Kwon Moon, Tae Gyun Kwon, Yung Hyun Choi y Wun-Jae Kim. "Identification of C16orf74 as a Marker of Progression in Primary Non-Muscle Invasive Bladder Cancer". PLoS ONE 5, n.º 12 (21 de diciembre de 2010): e15260. http://dx.doi.org/10.1371/journal.pone.0015260.
Texto completoSrivastava, Shalini y Dulal Panda. "A centrosomal protein FOR20 regulates microtubule assembly dynamics and plays a role in cell migration". Biochemical Journal 474, n.º 16 (10 de agosto de 2017): 2841–59. http://dx.doi.org/10.1042/bcj20170303.
Texto completoSuter, 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, n.º 3 (24 de febrero de 2016): 359–66. http://dx.doi.org/10.1002/mgg3.209.
Texto completoKojima, Waka, Koji Yamano, Hidetaka Kosako, Kenichiro Imai, Reika Kikuchi, Keiji Tanaka y Noriyuki Matsuda. "Mammalian BCAS3 and C16orf70 associate with the phagophore assembly site in response to selective and non-selective autophagy". Autophagy 17, n.º 8 (26 de enero de 2021): 2011–36. http://dx.doi.org/10.1080/15548627.2021.1874133.
Texto completoGong, Junling, Haiying Fan, Jing Deng y 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, n.º 11 (21 de abril de 2020): 6015–27. http://dx.doi.org/10.1111/jcmm.15117.
Texto completoFernández, María, Alicia de Coo, Inés Quintela, Eliane García, Márcio Diniz-Freitas, Jacobo Limeres, Pedro Diz, Juan Blanco, Ángel Carracedo y Raquel Cruz. "Genetic Susceptibility to Periodontal Disease in Down Syndrome: A Case-Control Study". International Journal of Molecular Sciences 22, n.º 12 (10 de junio de 2021): 6274. http://dx.doi.org/10.3390/ijms22126274.
Texto completoNazarian, Alireza, Anatoliy I. Yashin y Alexander M. Kulminski. "Summary-Based Methylome-Wide Association Analyses Suggest Potential Genetically Driven Epigenetic Heterogeneity of Alzheimer’s Disease". Journal of Clinical Medicine 9, n.º 5 (15 de mayo de 2020): 1489. http://dx.doi.org/10.3390/jcm9051489.
Texto completoDokal, Inderjeet. "Dyskeratosis Congenita". Hematology 2011, n.º 1 (10 de diciembre de 2011): 480–86. http://dx.doi.org/10.1182/asheducation-2011.1.480.
Texto completoConcolino, D., G. Roversi, G. L. Muzzi, S. Sestito, E. A. Colombo, L. Volpi, L. Larizza y 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, n.º 10 (23 de agosto de 2010): 2588–94. http://dx.doi.org/10.1002/ajmg.a.33600.
Texto completoMroczek, S., J. Krwawicz, J. Kutner, M. Lazniewski, I. Kucinski, K. Ginalski y 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, n.º 17 (16 de agosto de 2012): 1911–25. http://dx.doi.org/10.1101/gad.193169.112.
Texto completoDanuta, 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, n.º 8 (23 de junio de 2020): 1107–23. http://dx.doi.org/10.1007/s00109-020-01937-4.
Texto completoLu, Li, Huiyu Li, Xiaomei Chen, Wei Xiong y Shiang Huang. "The Chromosome Open Reading Frame Genes Targeted By Abnormal Micrornas in Microvesicles from Chronic Myeloid Leukemia". Blood 124, n.º 21 (6 de diciembre de 2014): 5509. http://dx.doi.org/10.1182/blood.v124.21.5509.5509.
Texto completoColombo, 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, n.º 1 (2012): 7. http://dx.doi.org/10.1186/1750-1172-7-7.
Texto completoWalne, Amanda J., Tom Vulliamy, Richard Beswick, Michael Kirwan y 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, n.º 22 (3 de septiembre de 2010): 4453–61. http://dx.doi.org/10.1093/hmg/ddq371.
Texto completoDereure, 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, n.º 4 (abril de 2011): 362–63. http://dx.doi.org/10.1016/j.annder.2011.01.026.
Texto completoYoung, Corey D., Eric B. Dammer, Ti'ara L. Griffen, Sha'kayla K. Nunez, Courtney Dill, Kaylin M. Carey y James W. Lillard. "Abstract 2950: Coexpression networks of miRNAs and gene transcripts coinciding with lung adenocarcinoma progression and survival". Cancer Research 82, n.º 12_Supplement (15 de junio de 2022): 2950. http://dx.doi.org/10.1158/1538-7445.am2022-2950.
Texto completoJeong, Ho-Chang, Siddharth Shukla, Roy Parker y Luis Batista. "USB1 Is a miRNA Deadenylase That Regulates Hematopoietic Development". Blood 138, Supplement 1 (5 de noviembre de 2021): 2191. http://dx.doi.org/10.1182/blood-2021-146115.
Texto completoBaratti, Mariana O., Yuri B. Moreira, Fabiola Traina, Luciene Borges, Fernando F. Costa, Sergio Verjovski-Almeida y Sara T. O. Saad. "Identification of Intronic RNA Expression in CD34+ Cells of Patients with Myelodysplatic Syndrome by RNA Microarray Analysis." Blood 110, n.º 11 (16 de noviembre de 2007): 2423. http://dx.doi.org/10.1182/blood.v110.11.2423.2423.
Texto completoWestin, Erik, Larisa Pereboeva, Divya Devadasan, Tim M. Townes y Frederick D. Goldman. "Suppression of Antioxidant Responses in Dyskeratosis Congenita Cells". Blood 126, n.º 23 (3 de diciembre de 2015): 2412. http://dx.doi.org/10.1182/blood.v126.23.2412.2412.
Texto completoJansen, 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, 6 de septiembre de 2022. http://dx.doi.org/10.1007/s00401-022-02454-z.
Texto completoBenslimane, Yahya, María Sánchez‐Osuna, Jasmin Coulombe‐Huntington, Thierry Bertomeu, Danielle Henry, Caroline Huard, Éric Bonneil, Pierre Thibault, Mike Tyers y Lea Harrington. "A novel p53 regulator, C16ORF72/TAPR1, buffers against telomerase inhibition". Aging Cell 20, n.º 4 (4 de marzo de 2021). http://dx.doi.org/10.1111/acel.13331.
Texto completoAmici, David R., Harun Cingoz, Milad J. Alasady, Sammy Alhayek, Claire M. Phoumyvong, Nidhi Sahni, S. Stephen Yi y Marc L. Mendillo. "The HAPSTR2 retrogene buffers stress signaling and resilience in mammals". Nature Communications 14, n.º 1 (11 de enero de 2023). http://dx.doi.org/10.1038/s41467-022-35697-1.
Texto completoAmici, 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, n.º 27 (julio de 2022). http://dx.doi.org/10.1073/pnas.2111262119.
Texto completoNisar, Haider, Memoona Khan, Qamar Un Nisa Chaudhry, Raheel Iftikhar y Tariq Ghafoor. "Case report: A novel mutation in RTEL1 gene in dyskeratosis congenita". Frontiers in Oncology 13 (2 de marzo de 2023). http://dx.doi.org/10.3389/fonc.2023.1098876.
Texto completoLee, Chanjae, Rachael M. Cox, Ophelia Papoulas, Amjad Horani, Kevin Drew, Caitlin C. Devitt, Steven L. Brody, Edward M. Marcotte y John B. Wallingford. "Functional partitioning of a liquid-like organelle during assembly of axonemal dyneins". eLife 9 (2 de diciembre de 2020). http://dx.doi.org/10.7554/elife.58662.
Texto completoAbolnezhadian, Farhad y 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, 4 de septiembre de 2019. http://dx.doi.org/10.18502/ijaai.v18i4.1424.
Texto completoTanaka, Akio, Fanny Morice-Picard, Didier Lacombe, Nikoletta Nagy, Michihiro Hide, Alain Taïeb y 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.
Texto completoPim, David, Justyna Broniarczyk, Abida Siddiqa, Paola Massimi y 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, 11 de noviembre de 2020. http://dx.doi.org/10.1128/jvi.02068-20.
Texto completoCade, 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, n.º 1 (26 de agosto de 2021). http://dx.doi.org/10.1186/s13073-021-00917-8.
Texto completoTaylor, Laura W., John E. French, Zachary G. Robbins y Leena A. Nylander-French. "Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-Painters". Frontiers in Genetics 12 (14 de julio de 2021). http://dx.doi.org/10.3389/fgene.2021.700636.
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