Results 121 to 130 of about 4,171 (132)

Molecular characterization of G6PD deficiency in Southern Italy: heterogeneity, correlation genotype–phenotype and description of a new variant (G6PD Neapolis)

British Journal of Haematology, 1997
Maria Vittoria Cubellis, Amelia Cimmino, Stefania Filosa   +2 more
exaly  

Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017

Human Mutation, 2020
Qing Lu, Jingkun Miao, Xiaoli Shu
exaly  

Concordance between glucose-6-phosphate dehydrogenase (G6PD) genotype and phenotype and rasburicase use in patients with hematologic malignancies

Pharmacogenomics Journal, 2018
Jeffrey Rubnitz, Mary Relling, Wenjian Yang   +2 more
exaly  

Functional and structural analysis of double and triple mutants reveals the contribution of protein instability to clinical manifestations of G6PD variants

International Journal of Biological Macromolecules, 2020
USA Boonyuen, Mallika Imwong
exaly  

Corrigendum to “G6PD deficiency: The genotype-phenotype association” [Blood Rev. 21 (2007) 267–283]

Blood Reviews, 2010
JOSÉ M Bautista
exaly  

Human Papillomavirus Genotype Distributions Inform Screening and Vaccination Policy

Ca-A Cancer Journal for Clinicians, 2009
M D Pinkowish
exaly  

Molecular basis of G6PD deficiency in India

Blood Cells, Molecules, and Diseases, 2004
Malay Mukherjee, Dipika Mohanty
exaly  

A trade off between catalytic activity and protein stability determines the clinical manifestations of glucose-6-phosphate dehydrogenase (G6PD) deficiency

International Journal of Biological Macromolecules, 2017
Nicholas White, USA Boonyuen, Mallika Imwong   +2 more
exaly  

Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind)

Blood Cells, Molecules, and Diseases, 2005
Chayamon Takpradit, Taku Shirakawa
exaly  

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guidelines for Rasburicase Therapy in the Context of G6PD Deficiency Genotype

Clinical Pharmacology and Therapeutics, 2014
exaly