The human mitochondrial transport/carrier protein family. Nonsynonymous single nucleotide polymorphisms (nsSNPs) and mutations that lead to human diseases-Reference-Cited by-同舟云学术

The human mitochondrial transport/carrier protein family. Nonsynonymous single nucleotide polymorphisms (nsSNPs) and mutations that lead to human diseases

Published:2006-09 Issue:9-10 Volume:1757 Page:1263-1270
ISSN:0005-2728
Container-title:Biochimica et Biophysica Acta (BBA) - Bioenergetics
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Bioenergetics

Author:

Wohlrab Hartmut

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry,Biophysics

Reference42 articles.

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3. Mrs2p is an essential component of the major electrophoretic Mg2+ influx system in mitochondria;Kolisek;EMBO J.,2003

4. Sequence of the N-terminal formic acid fragment and location of the N-ethylmaleimide-binding site of the phosphate transport protein from beef heart mitochondria;Kolbe;J. Biol. Chem.,1985

5. Single replacement constructs of all hydroxyl, basic, and acidic amino acids identify new function and structure-sensitive regions of the mitochondrial phosphate transport protein;Wohlrab;Biochemistry,2002

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