(Q28288744)

2

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H Suzuki

3

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L Schild

4

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R Shimkets

5

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Y Lu

6

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C Canessa

7

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T Iwasaki

8

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B Rossier

9

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R P Lifton

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

10

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language of work or name

English

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publication date

September 1995

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published in

Nature Genetics

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volume

11

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issue

1

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page(s)

76-82

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Epithelial sodium channel related to proteins involved in neurodegeneration

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Human hypertension caused by mutations in the kidney isozyme of 11β–hydroxysteroid dehydrogenase

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

The 1993-94 Généthon human genetic linkage map

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0995-76

Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

A first-generation physical map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

Molecular basis of human hypertension: role of angiotensinogen

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

The molecular genetics of human hemoglobins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

SA gene and blood pressure cosegregation using Dahl salt-sensitive rats

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

Evaluation of the SA locus in human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

Cosmid vectors for genomic walking and rapid restriction mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Mutation of a mutL homolog in hereditary colon cancer

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Membrane topology of the epithelial sodium channel in intact cells

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

A mutation in the epithelial sodium channel causing Liddle disease increases channel activity in the Xenopus laevis oocyte expression system

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

[A case of Liddle's syndrome with familial occurrence]

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0995-76

7 January 2021

Identifiers

DOI

10.1038/NG0995-76

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

7550319

1 reference

Consolidated OpenCitations Corpus – April 2017