Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 39 Records) |
Query Trace: GATA1[original query] |
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The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes. British journal of haematology 2016 Mar . Olsson Linda, Zettermark Sofia, Biloglav Andrea, Castor Anders, Behrendtz Mikael, Forestier Erik, Paulsson Kajsa, Johansson Bert |
GATA1 gene variants associated with thrombocytopenia and anemia. Platelets 2017 11 28 (7): 731-734. Freson Kathleen, Wijgaerts Anouck, Van Geet Chr |
Implications of mutational spectrum in myelodysplastic syndromes based on targeted next-generation sequencing. Oncotarget 2017 Oct 8 (47): 82475-82490. Xu Yuanyuan, Li Yan, Xu Qingyu, Chen Yuelong, Lv Na, Jing Yu, Dou Liping, Bo Jian, Hou Guangyuan, Guo Jing, Wang Xiuli, Wang Lili, Li Yonghui, Chen Chongjian, Yu |
Disruption of a GATA1-binding motif upstream of XG/PBDX abolishes Xg expression and resolves the Xg blood group system. Blood 2018 5 132 (3): 334-338. Möller Mattias, Lee Yan Quan, Vidovic Karina, Kjellström Sven, Björkman Linda, Storry Jill R, Olsson Martin |
GATA1 Expression in BCR/ABL1-negative Myeloproliferative Neoplasms. Annals of laboratory medicine 2018 Jul 38 (4): 296-305. Yang Naery, Park Sholhui, Cho Min Sun, Lee Miae, Hong Ki Sook, Mun Yeung Chul, Seong Chu Myong, Huh Hee Jin, Huh Jungw |
Comprehensive blood group antigen profile predictions for Western Desert Indigenous Australians from whole exome sequence data. Transfusion 2018 12 59 (2): 768-778. Schoeman Elizna M, Roulis Eileen V, Perry Maree A, Flower Robert L, Hyland Catherine |
ARHGEF12 regulates erythropoiesis and is involved in erythroid regeneration after chemotherapy in acute lymphoblastic leukemia patients. Haematologica 2019 8 105 (4): 925-936. Xie Yangyang, Gao Li, Xu Chunhui, Chu Liming, Gao Lei, Wu Ruichi, Liu Yu, Liu Ting, Sun Xiao-Jian, Ren Ruibao, Tang Jingyan, Zheng Yi, Zhou Yong, Shen Shuho |
[Somatic Mutations Associated with Metastasis in Acral Melanoma]. Molekuliarnaia biologiia 2019 8 53 (4): 648-653. Abramov I S, Emelyanova M A, Ryabaya O O, Krasnov G S, Zasedatelev A S, Nasedkina T |
[Clinical and laboratory analysis of a neonate with Down syndrome and a novel GATA1 gene mutation]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 4 36 (4): 322-326. Zheng Rui, Zhang Weiqing, Chen Baoguo, Shen Zhiying, Lin Aif |
Two Novel GATA1 Mutations in Transient Abnormal Myelopoiesis of Thai Neonates with Down Syndrome. Journal of pediatric genetics 2019 11 8 (4): 187-192. Chukua Kanokporn, Netsawang Chayanont, Padungthai Kittipoom, Khetkham Thanitchet, Chokevittaya Piyaporn, Poonjearansilp Onapinya, Prachuktum Sariya, Kositamongkol Sudatip, Techasatit Wiliporn, Silapamongkolkul Phakatip, Satayasai Wallee, Pusongchai Tasama, Surapolchai Pacharapan, Rojnueangnit Kitiw |
Panel-based next-generation sequencing facilitates the characterization of childhood acute myeloid leukemia in clinical settings. Biomedical reports 2020 9 13 (5): 46. Ishida Hisashi, Iguchi Akihiro, Aoe Michinori, Nishiuchi Ritsuo, Matsubara Takehiro, Keino Dai, Sanada Masashi, Shimada Aki |
Retrospective Analysis of the Treatment Outcome in Myeloid Leukemia of Down Syndrome in Polish Pediatric Leukemia and Lymphoma Study Group From 2005 to 2019. Frontiers in pediatrics 2020 7 8 277. Czogala Malgorzata, Pawinska-Wasikowska Katarzyna, Ksiazek Teofila, Sikorska-Fic Barbara, Matysiak Michal, Skalska-Sadowska Jolanta, Wachowiak Jacek, Rodziewicz-Konarska Anna, Chybicka Alicja, Myszynska-Roslan Katarzyna, Krawczuk-Rybak Maryna, Grabowski Dominik, Kowalczyk Jerzy, Maciejka-Kemblowska Lucyna, Adamkiewicz-Drozynska Elzbieta, Bobeff Katarzyna, Mlynarski Wojciech, Tomaszewska Renata, Szczepanski Tomasz, Pohorecka Joanna, Chodala-Grzywacz Agnieszka, Karolczyk Grazyna, Mizia-Malarz Agnieszka, Mycko Katarzyna, Badowska Wanda, Zielezinska Karolina, Urasinski Tomasz, Nykiel Magdalena, Woszczyk Mariola, Ciebiera Malgorzata, Chaber Rados?aw, Skoczen Szymon, Balwierz Walenty |
Complete blood count differences in a cohort of Down syndrome neonates with transient abnormal myelopoiesis screened for GATA1 pathogenic variants. American journal of medical genetics. Part A 2020 Jul . Orozco-Vela Mireya, Corona-Rivera Alfredo, Cruz-Osorio Rosa Margarita, Mendoza-Maldonado Lucero, Márquez-Mora Aurea, Barba-Barba César Cenobio, Peña-Padilla Christian, Baldomero-López Alejandra, Bobadilla-Morales Lucina, Corona-Rivera Jorge Rom |
A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling.
American journal of human genetics 2020 Jul . Rodriguez Benjamin A T, Bhan Arunoday, Beswick Andrew, Elwood Peter C, Niiranen Teemu J, Salomaa Veikko, , Trégouët David-Alexandre, Morange Pierre-Emmanuel, Civelek Mete, Ben-Shlomo Yoav, Schlaeger Thorsten, Chen Ming-Huei, Johnson Andrew |
Genomic and Transcriptomic Analyses of Breast Cancer Primaries and Matched Metastases in AURORA, the Breast International Group (BIG) Molecular Screening Initiative. Cancer discovery 2021 6 11 (11): 2796-2811. Aftimos Philippe, Oliveira Mafalda, Irrthum Alexandre, Fumagalli Debora, Sotiriou Christos, Gal-Yam Einav Nili, Robson Mark E, Ndozeng Justin, Di Leo Angelo, Ciruelos Eva M, de Azambuja Evandro, Viale Giuseppe, Scheepers Elsemieke D, Curigliano Giuseppe, Bliss Judith M, Reis-Filho Jorge S, Colleoni Marco, Balic Marija, Cardoso Fatima, Albanell Joan, Duhem Caroline, Marreaud Sandrine, Romagnoli Dario, Rojas Beatriz, Gombos Andrea, Wildiers Hans, Guerrero-Zotano Angel, Hall Peter, Bonetti Andrea, Larsson Karolina Fs, Degiorgis Martina, Khodaverdi Silvia, Greil Richard, Sverrisdóttir Ásgerdur, Paoli Marta, Seyll Ethel, Loibl Sibylle, Linderholm Barbro, Zoppoli Gabriele, Davidson Nancy E, Johannsson Oskar Th, Bedard Philippe L, Loi Sherene, Knox Susan, Cameron David A, Harbeck Nadia, Montoya Maite Lasa, Brandão Mariana, Vingiani Andrea, Caballero Carmela, Hilbers Florentine S, Yates Lucy R, Benelli Matteo, Venet David, Piccart Martine |
Mechanistic insights into the CYP2C19 genetic variants prevalent in the Indian population. Gene 2021 Mar 784 145592. Naushad Shaik Mohammad, Vattam Kiran Kumar, Devi Yadamreddy Kanaka Durga, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum |
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling. Neuroscience letters 2021 04 750 135802. Naushad Shaik Mohammad, Hussain Tajamul, Alrokayan Salman, Kutala Vijay Kum |
Clinically significant genomic alterations in the Chinese and Western patients with intrahepatic cholangiocarcinoma. BMC cancer 2021 Feb 21 (1): 152. Xu Shifeng, Guo Yuan, Zeng Yanwu, Song Zhijian, Zhu Xiaodan, Fan Ning, Zhang Zhilei, Ren Guibing, Zang Yunjin, Rao W |
GATA1 mutation analysis and molecular landscape characterization in acute myeloid leukemia with trisomy 21 in pediatric patients. International journal of laboratory hematology 2021 1 43 (4): 713-723. Panferova Agnesa, Gaskova Marina, Nikitin Eugenyi, Baryshev Pavel, Timofeeva Natalia, Kazakova Anna, Matveev Viktor, Mikhailova Ekaterina, Popov Alexander, Kalinina Irina, Hachatrian Lili, Maschan Aleksey, Maschan Michael, Novichkova Galina, Olshanskaya Yul |
G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1.
Blood advances 2021 9 6 (7): 2319-2330. Downes Kate, Zhao Xuefei, Gleadall Nicholas S, McKinney Harriet, Kempster Carly, Batista Joana, Thomas Patrick L, Cooper Matthew, Michael James V, Kreuzhuber Roman, Wedderburn Katherine, Waller Kathryn, Varney Bianca, Verdier Hippolyte, Kriek Neline, Ashford Sofie E, Stirrups Kathleen E, Dunster Joanne L, McKenzie Steven E, Ouwehand Willem H, Gibbins Jonathan M, Yang Jing, Astle William J, Ma Peiso |
Molecular evaluation of gene mutation profiles and copy number variations in pediatric acute myeloid leukemia. Leukemia research 2022 9 122 106954. Meena Jagdish Prasad, Pathak Nivedita, Gupta Aditya Kumar, Bakhshi Sameer, Gupta Ritu, Makkar Harshita, Seth Rach |
By characterizing metabolic and immune microenvironment reveal potential prognostic markers in the development of colorectal cancer. Frontiers in bioengineering and biotechnology 2022 8 10 822835. Liao Liangliang, Gao Yongjian, Su Jie, Feng |
Accelerated epigenetic aging in newborns with Down syndrome. Aging cell 2022 6 21 (7): e13652. Xu Keren, Li Shaobo, Muskens Ivo S, Elliott Natalina, Myint Swe Swe, Pandey Priyatama, Hansen Helen M, Morimoto Libby M, Kang Alice Y, Ma Xiaomei, Metayer Catherine, Mueller Beth A, Roberts Irene, Walsh Kyle M, Horvath Steve, Wiemels Joseph L, de Smith Adam |
A family case series of inherited thrombocytopenia. Proceedings (Baylor University. Medical Center) 2022 12 36 (1): 93-95. Borkowski Artur, Gawry? Jakub, Iwanek Gracjan, Dybko Jaros? |
Genomic characterization of intracranial teratomas using whole genome sequencing. Frontiers in oncology 2022 12 12 1013722. Zhang Chao, Zhou Xiaoyu, Huang Xiang, Ding Xinghua, Wang Yang, Zhang Ro |
Generation of CHOPi-008-B, a euploid iPSC line from a patient with Trisomy 21 and a GATA1 mutation. Stem cell research 2023 9 72 103198. Kaoru Takasaki, Sara S Kumar, Alyssa Gagne, Deborah L French, Stella T Ch |
In silico genotyping of blood group alleles using WGS data: a comparative study of the Orang Asli in Peninsular Malaysia. Journal of genetics 2023 9 102 . Mercy Rophina, Teh Lay Kek, Sridhar Sivasubbu, Vinod Scaria, Mohd Zaki Sall |
Elucidation of the low-expressing erythroid CR1 phenotype by bioinformatic mining of the GATA1-driven blood-group regulome. Nature communications 2023 8 14 (1): 5001. Ping Chun Wu, Yan Quan Lee, Mattias Möller, Jill R Storry, Martin L Olss |
Identification of mutations in porcine STAT5A that contributes to the transcription of CISH. Frontiers in veterinary science 2023 2 9 1090833. Yao Diwen, Guo Dongchun, Zhang Yingkun, Chen Zhihua, Gao Xiaowen, Xing Guiling, Yang Xiuqin, Wang Xibiao, Di Shengwei, Cai Jiancheng, Niu Buy |
Novel Candidate loci and Pathogenic Germline Variants Involved in Familial Hematological Malignancies Revealed by Whole-Exome Sequencing. Cancers 2023 2 15 (3): . Andrés-Zayas Cristina, Suárez-González Julia, Chicano-Lavilla María, Bastos Oreiro Mariana, Rodríguez-Macías Gabriela, Font López Patricia, Osorio Prendes Santiago, Oarbeascoa Royuela Gillen, García Ramírez Patricia, Nieves Salgado Rocío, Gómez-Centurión Ignacio, Carbonell Muñoz Diego, Muñiz Paula, Kwon Mi, Díez-Martín José Luis, Buño Ismael, Martínez-Laperche Caroli |
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