Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CNOT3[original query] |
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A high density SNP genotyping approach within the 19q13 chromosome region identifies an association of a CNOT3 polymorphism with ankylosing spondylitis. Annals of the rheumatic diseases 2012 May 71 (5): 714-7. Díaz-Peña Roberto, Aransay Ana M, Suárez-Álvarez Beatriz, Bruges-Armas Jacome, Rodríguez-Ezpeleta Naiara, Regueiro María, Pimentel-Santos Fernando M, Mulero Juan, Sánchez Alejandra, Collantes Eduardo, Queiro Rubén, Ballina Javier, Alves Helena, López-Larrea Carl |
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia. Haematologica 2016 May . La Starza Roberta, Barba Gianluca, Demeyer Sofie, Pierini Valentina, Di Giacomo Danika, Gianfelici Valentina, Schwab Claire, Matteucci Caterina, Vicente Carmen, Cools Jan, Messina Monica, Crescenzi Barbara, Chiaretti Sabina, Foa' Robin, Basso Giuseppe, Harrison Christine J, Mecucci Cristi |
Identification of a genetically defined ultra-high-risk group in relapsed pediatric T-lymphoblastic leukemia. Blood cancer journal 2017 Feb 7 (2): e523. Richter-Pecha?ska P, Kunz J B, Hof J, Zimmermann M, Rausch T, Bandapalli O R, Orlova E, Scapinello G, Sagi J C, Stanulla M, Schrappe M, Cario G, Kirschner-Schwabe R, Eckert C, Benes V, Korbel J O, Muckenthaler M U, Kulozik A |
Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008.
British journal of haematology 2019 Feb 184 (3): 405-417. Højfeldt Sofie G, Wolthers Benjamin O, Tulstrup Morten, Abrahamsson Jonas, Gupta Ramneek, Harila-Saari Arja, Heyman Mats, Henriksen Louise T, Jónsson Òlafur G, Lähteenmäki Päivi M, Lund Bendik, Pruunsild Kaie, Vaitkeviciene Goda, Schmiegelow Kjeld, Albertsen Birgitte K, |
The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy. Genetics in medicine : official journal of the American College of Medical Genetics 2019 9 22 (2): 427-431. Pinard Amélie, Guey Stéphanie, Guo Dongchuan, Cecchi Alana C, Kharas Natasha, Wallace Stephanie, Regalado Ellen S, Hostetler Ellen M, Sharrief Anjail Z, Bergametti Françoise, Kossorotoff Manoelle, Hervé Dominique, Kraemer Markus, Bamshad Michael J, Nickerson Deborah A, Smith Edward R, Tournier-Lasserve Elisabeth, Milewicz Dianna |
A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. Genes 2021 May 12 (6): . Vattathil Selina M, Liu Yue, Harerimana Nadia V, Lori Adriana, Gerasimov Ekaterina S, Beach Thomas G, Reiman Eric M, De Jager Philip L, Schneider Julie A, Bennett David A, Seyfried Nicholas T, Levey Allan I, Wingo Aliza P, Wingo Thomas |
Determinants of Disease Penetrance in PRPF31-Associated Retinopathy. Genes 2021 10 12 (10): . McLenachan Samuel, Zhang Dan, Grainok Janya, Zhang Xiao, Huang Zhiqin, Chen Shang-Chih, Zaw Khine, Lima Alanis, Jennings Luke, Roshandel Danial, Moon Sang Yoon, Heath Jeffery Rachael C, Attia Mary S, Thompson Jennifer A, Lamey Tina M, McLaren Terri L, De Roach John, Fletcher Sue, Chen Fred |
Targeted sequencing to identify genetic alterations and prognostic markers in pediatric T-cell acute lymphoblastic leukemia. Scientific reports 2021 Jan 11 (1): 769. Chang Ya-Hsuan, Yu Chih-Hsiang, Jou Shiann-Tarng, Lin Chien-Yu, Lin Kai-Hsin, Lu Meng-Yao, Wu Kang-Hsi, Chang Hsiu-Hao, Lin Dong-Tsamn, Lin Shu-Wha, Chen Hsuan-Yu, Yang Yung- |
Genetic Modifiers of Non-Penetrance and RNA Expression Levels in PRPF31-Associated Retinitis Pigmentosa in a Danish Cohort. Genes 2023 2 14 (2): . Lisbjerg Kristian, Grønskov Karen, Bertelsen Mette, Møller Lisbeth Birk, Kessel Li |
Clinical features of CNOT3-associated neurodevelopmental disorder in three Chinese patients. Neurogenetics 2023 2 . Zhao Peiwei, Meng Qingjie, Wan Chunhui, Lei Tao, Zhang Lei, Zhang Xiankai, Tan Li, Zhu Hongmin, He Xueli |
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- Page last updated:Apr 16, 2024
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