(Q34550171)

English

Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty.

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

Genetic heterogeneity of constitutively activating mutations of the human luteinizing hormone receptor in familial male-limited precocious puberty (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

familial male-limited precocious puberty

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2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

author name string

L Laue

1

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28 October 2019

A J Hsueh

3

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28 October 2019

M Kudo

4

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28 October 2019

S Y Hsu

5

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28 October 2019

S M Wu

6

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28 October 2019

L Blomberg

7

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28 October 2019

G B Cutler

8

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28 October 2019

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publication date

1 March 1995

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28 October 2019

Proceedings of the National Academy of Sciences of the United States of America

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28 October 2019

92

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28 October 2019

6

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28 October 2019

1906-1910

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28 October 2019

Somatic mutations in the thyrotropin receptor gene cause hyperfunctioning thyroid adenomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Constitutively active mutants of the alpha 2-adrenergic receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Constitutive activation of opsin: influence of charge at position 134 and size at position 296.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

A mutation-induced activated state of the beta 2-adrenergic receptor. Extending the ternary complex model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Testicular leydig cell hyperplasia as a cause of familial sexual precocity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Gonadotropin-Independent Familial Sexual Precocity with Premature Leydig and Germinal Cell Maturation (Familial Testotoxicosis): Effects of a Potent Luteinizing Hormone-Releasing Factor Agonist and Medroxyprogesterone Acetate Therapy in Four Cases*

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

High-efficiency transformation of mammalian cells by plasmid DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Characterization of the cDNA encoding human nucleophosmin and studies of its role in normal and abnormal growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Treatment of familial male precocious puberty with spironolactone and testolactone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Expression of human luteinizing hormone (LH) receptor: interaction with LH and chorionic gonadotropin from human but not equine, rat, and ovine species

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Mechanism of activation and inactivation of opsin: role of Glu113 and Lys296

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Constitutively active mutants of rhodopsin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Sequence alignment of the G-protein coupled receptor superfamily

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=42391

7 July 2018

Hazards of ketoconazole therapy in testotoxicosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/7892197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vasoactive intestinal peptide: a novel stimulator of steroidogenesis by cultured rat granulosa cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7892197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Treatment of familial male precocious puberty with spironolactone, testolactone, and deslorelin

1 reference

https://pubmed.ncbi.nlm.nih.gov/7892197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of pregnancy-specific beta 1-glycoprotein genes in hematopoietic cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/7892197

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.92.6.1906

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

1995PNAS...92.1906L

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7892197%20AND%20SRC:MED&resulttype=core&format=json

28 October 2019

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