Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus (Q28183211)

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17 September 2022

author name string

M F Arthus

5

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G N Hendy

6

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D G Bichet

8

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Rosenthal W

1

1 reference

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17 September 2022

Seibold A

2

1 reference

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17 September 2022

Antaramian A

3

1 reference

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17 September 2022

Lonergan M

4

1 reference

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17 September 2022

Arthus MF

5

1 reference

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17 September 2022

Hendy GN

6

1 reference

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17 September 2022

Birnbaumer M

7

1 reference

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Hemodynamic and coagulation responses to 1-desamino[8-D-arginine] vasopressin in patients with congenital nephrogenic diabetes insipidus

17 September 2022

language of work or name

English

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publication date

17 September 1992

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published in

Nature

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volume

359

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issue

6392

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page(s)

233-5

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cites work

1 reference

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

7 January 2021

Molecular cloning of the receptor for human antidiuretic hormone

1 reference

7 January 2021

Chimeric alpha 2-,beta 2-adrenergic receptors: delineation of domains involved in effector coupling and ligand binding specificity

1 reference

7 January 2021

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

7 January 2021

Linkage of X-linked nephrogenic diabetes insipidus with DXS52, a polymorphic DNA marker

1 reference

7 January 2021

Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus

1 reference

7 January 2021

A simple method for displaying the hydropathic character of a protein

1 reference

7 January 2021

Epinephrine and dDAVP administration in patients with congenital nephrogenic diabetes insipidus. Evidence for a pre-cyclic AMP V2 receptor defective mechanism

1 reference

7 January 2021

Absence of overlapping resistance to vasopressin and parathyroid hormone in patients with nephrogenic diabetes insipidus and pseudohypoparathyroidism

1 reference

7 January 2021

Mutation in the gene encoding the stimulatory G protein of adenylate cyclase in Albright's hereditary osteodystrophy

1 reference

7 January 2021

Cloning large segments of genomic DNA using cosmid vectors

1 reference

7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/359233A0

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1023279299

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Fatcat ID

release_yup7e3u6bvarfnroszefducuzu

1 reference

Fatcat

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24 November 2022

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