(Q36181703)

12 August 2017

1 reference

title

Clinical phenotypes and molecular genetic mechanisms of Carney complex (English)

1 reference

12 August 2017

David Wilkes

1

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12 August 2017

Deborah A McDermott

series ordinal

2

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12 August 2017

Craig T Basson

series ordinal

3

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12 August 2017

publication date

1 July 2005

1 reference

Lancet Oncology Commission

12 August 2017

published in

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12 August 2017

volume

6

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12 August 2017

issue

7

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12 August 2017

page(s)

501-508

1 reference

Comparative PRKAR1A genotype-phenotype analyses in humans with Carney complex and prkar1a haploinsufficient mice

12 August 2017

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

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7 January 2021

Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation

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7 January 2021

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7 January 2021

Primary adrenocortical nodular dysplasia with Cushing's syndrome and cardiac myxomas. A peculiar familial disease

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Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

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7 January 2021

"Syndrome myxoma": a subset of patients with cardiac myxoma associated with pigmented skin lesions and peripheral and endocrine neoplasms

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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.

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7 January 2021

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7 January 2021

Pituitary adenoma in Carney complex: an immunohistochemical, ultrastructural, and immunoelectron microscopic study

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7 January 2021

Sequence analysis of the PRKAR1A gene in sporadic somatotroph and other pituitary tumours

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7 January 2021

Thyroid gland abnormalities in patients with the syndrome of spotty skin pigmentation, myxomas, endocrine overactivity, and schwannomas (Carney complex)

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7 January 2021

Carney complex: report of three cases.

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7 January 2021

Testicular ultrasound in Carney complex: report of three cases

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7 January 2021

Cutaneous psammomatous melanotic schwannoma: non-recurrence with surgical excision

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7 January 2021

Ductal adenoma of the breast with tubular features. A probable component of the complex of myxomas, spotty pigmentation, endocrine overactivity, and schwannomas

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7 January 2021

Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complex.

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7 January 2021

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

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7 January 2021

Molecular analysis of the cyclic AMP-dependent protein kinase A (PKA) regulatory subunit 1A (PRKAR1A) gene in patients with Carney complex and primary pigmented nodular adrenocortical disease (PPNAD) reveals novel mutations and clues for pathophysio

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7 January 2021

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7 January 2021

Genetic heterogeneity and spectrum of mutations of the PRKAR1A gene in patients with the carney complex

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7 January 2021

Antisense protein kinase A RIalpha inhibits 7,12-dimethylbenz(a)anthracene-induction of mammary cancer: blockade at the initial phase of carcinogenesis

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7 January 2021

Antisense targeting protein kinase A type I as a drug for integrated strategies of cancer therapy.

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7 January 2021

Clinical studies in patients with solid tumors using a second-generation antisense oligonucleotide (GEM 231) targeted against protein kinase A type I.

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7 January 2021

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7 January 2021

A pleiomorphic GH pituitary adenoma from a Carney complex patient displays universal allelic loss at the protein kinase A regulatory subunit 1A (PRKARIA) locus

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7 January 2021

A transgenic mouse bearing an antisense construct of regulatory subunit type 1A of protein kinase A develops endocrine and other tumours: comparison with Carney complex and other PRKAR1A induced lesions.

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7 January 2021

The essential role of RI alpha in the maintenance of regulated PKA activity

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7 January 2021

Mutation of perinatal myosin heavy chain associated with a Carney complex variant

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7 January 2021

The distal arthrogryposes: delineation of new entities--review and nosologic discussion

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7 January 2021

No cytogenetic evidence for involvement of gene(s) at 2p16 in sporadic cardiac myxomas: cytogenetic changes in ten sporadic cardiac myxomas

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7 January 2021

Mutation and cancer: statistical study of retinoblastoma

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7 January 2021

Molecular genetic diagnosis of the familial myxoma syndrome (Carney complex).

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7 January 2021

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

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7 January 2021

Mutation of perinatal myosin heavy chain

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https://api.crossref.org/works/10.1016%2FS1470-2045%2805%2970244-8

7 January 2021

10.1016/S1470-2045(05)70244-8

Identifiers

DOI

1 reference

12 August 2017

1 reference