Point substitutions in albumin genetic variants from Asia. - Wikidata - awgldk - TriplyDB

Point substitutions in albumin genetic variants from Asia.

Point substitutions in albumin genetic variants from Asia.

http://www.wikidata.org/entity/Q30353686

about

Hypermutability of CpG dinucleotides in the propeptide-encoding sequence of the human albumin gene.Mutations in genetic variants of human serum albumin found in Italy.Genetic variants of human serum albumin in Italy: point mutants and a carboxyl-terminal variant.cDNA and protein sequence of polymorphic macaque albumins that differ in bilirubin binding.Alloalbuminemia in Sweden: structural study and phenotypic distribution of nine albumin variants A donor splice mutation and a single-base deletion produce two carboxyl-terminal variants of human serum albumin.Genetic variants of serum albumin in Americans and Japanese.A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia

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P2860

Point substitutions in albumin genetic variants from Asia.

http://www.wikidata.org/entity/Q30353686

description

1990 nî lūn-bûn

@nan

1990 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

1990 թվականի հունվարին հրատարակված գիտական հոդված

@hy

1990年の論文

@ja

1990年学术文章

@wuu

1990年学术文章

@zh-cn

1990年学术文章

@zh-hans

1990年学术文章

@zh-my

1990年学术文章

@zh-sg

1990年學術文章

@yue

name

Point substitutions in albumin genetic variants from Asia.

@ast

Point substitutions in albumin genetic variants from Asia.

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type

label

Point substitutions in albumin genetic variants from Asia.

@ast

Point substitutions in albumin genetic variants from Asia.

@en

prefLabel

Point substitutions in albumin genetic variants from Asia.

@ast

Point substitutions in albumin genetic variants from Asia.

@en

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P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

Point substitutions in albumin genetic variants from Asia.

@en

P2093

A Shimizu

http://www.w3.org/2001/XMLSchema#string

F W Putnam

http://www.w3.org/2001/XMLSchema#string

J Madison

http://www.w3.org/2001/XMLSchema#string

K Arai

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P2860

The same substitution, glutamic acid----lysine at position 501, occurs in three alloalbumins of Asiatic origin: albumins Vancouver, Birmingham, and Adana

Identical structural changes in inherited albumin variants from different populations

Amino acid substitutions in albumin variants found in Brazil.

Point substitutions in Japanese alloalbumins

Structural changes and metal binding by proalbumins and other amino-terminal genetic variants of human serum albumin

Amino acid substitutions in inherited albumin variants from Amerindian and Japanese populations.

Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning.

Additional data on the population distribution of human serum albumin genes; three new variants.

Albumin Redhill (-1 Arg, 320 Ala----Thr): a glycoprotein variant of human serum albumin whose precursor has an aberrant signal peptidase cleavage site.

Genetic and drug-induced variation in serum albumin.

P304

497-501

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scholarly article

P356

10.1073/PNAS.87.1.497

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P433

1

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87

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1990-01-01T00:00:00Z

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2404284

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53291

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