The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families-Reference-Cited by-同舟云学术

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The 1591C Mutation in Triosephosphate Isomerase (TPI) Deficiency. Tightly Linked Polymorphisms and a Common Haplotype in All Known Families

Published:1996-08 Issue:2 Volume:22 Page:115-125
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Schneider Arthur,Westwood Beryl,Yim Catherine,Cohen-Solal Michel,Rosa Raymonde,Labotka Richard,Eber Stefan,Wolf Raoul,Lammi Ahti,Beutler Ernest

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Discovery and characterization of a novel highly potent and selective type II native and drug-resistant V299L mutant BCR-ABL inhibitor (CHMFL-ABL-039) for Chronic Myeloid Leukemia (CML);Cancer Biology & Therapy;2019-03-20

2. Structural analysis on mutation residues and interfacial water molecules for human TIM disease understanding;BMC Bioinformatics;2013-10

3. Enzymes of the Red Blood Cell;Tietz Textbook of Clinical Chemistry and Molecular Diagnostics;2012

4. Triosephosphate isomerase: a highly evolved biocatalyst;Cellular and Molecular Life Sciences;2010-08-07

5. Sequencing and genotypic analysis of the triosephosphate isomerase (TPI1) locus in a large sample of long-lived Germans;BMC Genetics;2008-05-29

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