(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

https://scigraph.springernature.com/pub.10.1038/ng0995-76

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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page(s)

76-82

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issue

1

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exact match

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cites work

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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

21 April 2017

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

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

21 April 2017

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Epithelial sodium channel related to proteins involved in neurodegeneration

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

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Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

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

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Cosmid vectors for genomic walking and rapid restriction mapping

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

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7 January 2021

Mutation of a mutL homolog in hereditary colon cancer

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Membrane topology of the epithelial sodium channel in intact cells

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

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

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

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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

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

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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

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

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Identifiers

DOI

10.1038/NG0995-76

1 reference

Consolidated OpenCitations Corpus – April 2017

2420221

2420221

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference