(Q34510622)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex (English)

1 reference

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9 November 2019

0 references

3

1 reference

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9 November 2019

author name string

Kirschner LS

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Carney JA

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Taymans SE

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Giatzakis C

5

1 reference

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9 November 2019

Cho YS

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Cho-Chung YS

7

1 reference

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9 November 2019

Stratakis CA

8

1 reference

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9 November 2019

language of work or name

English

0 references

publication date

1 September 2000

1 reference

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9 November 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

26

1 reference

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9 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

89-92

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https://scigraph.springernature.com/pub.10.1038/79238

9 November 2019

exact match

0 references

cites work

Carney complex: the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas.

1 reference

7 January 2021

Carney complex: diagnosis and management of the complex of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas

1 reference

7 January 2021

Dominant inheritance of the complex of myxomas, spotty pigmentation, and endocrine overactivity

1 reference

7 January 2021

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

1 reference

7 January 2021

Identification of a novel genetic locus for familial cardiac myxomas and Carney complex

1 reference

7 January 2021

Activating mutations of the stimulatory G protein in the McCune-Albright syndrome

1 reference

7 January 2021

Paradoxical response to dexamethasone in the diagnosis of primary pigmented nodular adrenocortical disease

1 reference

7 January 2021

Sporadic cardiac myxomas and tumors from patients with Carney complex are not associated with activating mutations of the Gsα gene

1 reference

7 January 2021

Adrenocortical micronodular dysplasia, cardiac myxomas, lentigines, and spindle cell tumors. Report of a kindred

1 reference

7 January 2021

The Human Gene for the Regulatory Subunit RIα of Cyclic Adenosine 3′,5′-Monophosphate-Dependent Protein Kinase: Two Distinct Promoters Provide Differential Regulation of Alternately Spliced Messenger Ribonucleic Acids1

1 reference

7 January 2021

A mutated human homologue to yeast Upf1 protein has a dominant-negative effect on the decay of nonsense-containing mRNAs in mammalian cells

1 reference

7 January 2021

Hypervariabflity of simple sequences as a general source for polymorphic DNA markers

1 reference

7 January 2021

Genetically lean mice result from targeted disruption of the RII beta subunit of protein kinase A

1 reference

7 January 2021

Compensatory regulation of RIalpha protein levels in protein kinase A mutant mice

1 reference

7 January 2021

Cyclic nucleotide-dependent protein kinases

1 reference

7 January 2021

Mutations in the catalytic subunit of cAMP-dependent protein kinase result in unregulated biological activity

1 reference

7 January 2021

Carney Complex, Peutz-Jeghers Syndrome, Cowden Disease, and Bannayan-Zonana Syndrome Share Cutaneous and Endocrine Manifestations, But Not Genetic Loci

1 reference

7 January 2021

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

1 reference

7 January 2021

Identifiers

DOI

10.1038/79238

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10973256%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference