Zoekresultaten - "mutation"

GATA2 mutations and overexpression in pediatric acute myeloid leukemia door Zhenzhen Yang, Xingjuan Wang, Xi Chen, Hu Dou, Yi Huang, Ling Lu, Lin Zou, Junqin Bi, Meng Su, Jie Yu, Liming Bao

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Elastin genetic point mutation and the risk of pelvic organ prolapse door N. Haya, I. Feferkorn, F. Fares, N. Azzam, R. Auslender, Y. Abramov

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ACTA2 mutation and postpartum hemorrhage: a case report door Kylie Cooper, Stephen Brown

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Gene Mutation Spectrum of Thalassemia Among Children in Yunnan Province door Ti-Long Huang, Tian-Yao Zhang, Chun-Yan Song, Yun-Bi Lin, Bao-Hua Sang, Qing-Ling Lei, Yu Lv, Chun-Hui Yang, Na Li, Xin Tian, Yue-Huang Yang, Xian-Wen Zhang

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Discovery of aminopyridine-containing spiro derivatives as EGFR mutations inhibitors door Lianbao Ye, Tao Zhao, Wenjun Du, Anhu Li, Wei Gao, Jingrong Li, Ling Wang, Weiqiang Chen

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Phenotypic variations in X chromosome mutations: Two case reports door Josette C. Dawkins, Olivia Carpinello, Micah Hill, Alan H. DeCherney

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A Negative Correlation Between MEFV Mutations and Allergic Diseases door Malik Ejder Yıldırım, Hande Küçük Kurtulgan, Hasan Kılıçgün, Fatma Duksal

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MEFV gene mutation spectrum in patients with familial mediterranean fever door Hsin-Hui Wang

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PSENEN mutation in coexistent hidradenitis suppurativa and dowling-degos disease door Dincy C. V Peter, Frances J. D Smith, Neil J Wilson, Sumita Danda

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Dyskeratosis congenita with DKC1 mutation: A case report door Xing-Yun Zhao, Wei-Long Zhong, Jie Zhang, Gang Ma, Hao Hu, Bo Yu

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The role of IDH1/2 mutations in the pathogenesis of secondary glioblastomas door Eduardo Cambruzzi

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Treatment of BRAF-Mutated Metastatic Melanoma: Immunotherapy or Target Therapy? door Ana Sofia Rodrigues, Ana Brinca

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Mutation Detection in the Menkes Gene Using the Protein Truncation Test door Lisbeth Birk Møller, Nina Horn

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Familial Hemiplegic Migraine With ATP1A2 Mutations door J Gordon Millichap

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Treatment of TRPV3 mutation-associated Olmsted syndrome with erlotinib door Kathleen E. Spitz, MD, MBA, Lena Chu, BS, Leslie P. Lawley, MD

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Idiopathic Infantile Nystagmus, With and Without FRMD7 Gene Mutations door J Gordon Millichap

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The prognostic value of p53 mutation in pediatric marrow hypoplasia door Sharaf Alzahraa EA, Attia Fadia M, Abo-Elwafa Hasnaa A

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Expanding the genetic and clinical characteristics of Protocadherin 19 gene mutations door Giovanni Battista Dell'Isola, Elisabetta Mencaroni, Antonella Fattorusso, Giorgia Tascini, Paolo Prontera, Valentina Imperatore, Giuseppe Di Cara, Pasquale Striano, Alberto Verrotti

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Molecular Mutations and Their Cooccurrences in Cytogenetically Normal Acute Myeloid Leukemia door Mengning Wang, Chuanwei Yang, Le Zhang, Dale G. Schaar

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Potassium channel gene mutations rarely cause atrial fibrillation door Nam Edwin G, Zakharova Elena, Petrov-Kondratov Vadim I, Ellinor Patrick T, MacRae Calum A

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