Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene. (Q33593778)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

review article

1 reference

title

Menstrual disorders and infertility caused by inactivating mutations of the luteinizing hormone receptor gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference

Ana Claudia Latronico Xavier

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

Berenice Bilharinho Mendonça

4 December 2019

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

author name string

I J Arnhold

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

M C Batista

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

language of work or name

English

0 references

publication date

1 April 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

published in

Fertility and Sterility

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

volume

71

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

page(s)

597-601

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

Receptors and G proteins as primary components of transmembrane signal transduction. Part 1. G-protein-coupled receptors: structure and function.

4 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Leydig-cell agenesis: a cause of male pseudohermaphroditism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

A clinico-genetic investigation of Leydig cell hypoplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Comparison of immunocytochemical and molecular features with the phenotype in a case of incomplete male pseudohermaphroditism associated with a mutation of the luteinizing hormone receptor.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Ovarian resistance to luteinizing hormone: a novel cause of amenorrhea and infertility.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

17β-Estradiol Biosynthesis in Cultured Granulosa and Thecal Cells of Human Ovarian Follicles: Stimulation by Follicle-Stimulating Hormone*

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Immunohistochemical localization of pituitary gonadotrophins and gonadal steroids confirms the 'two-cell, two-gonadotrophin' hypothesis of steroidogenesis in the human ovary

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Stimulation of ovarian follicular maturation with pure follicle-stimulating hormone in women with gonadotropin deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

The Production of Progesterone, Androgens, and Estrogens by Granulosa Cells, Thecal Tissue, and Stromal Tissue from Human Ovaries in Vitro *

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Human Chorionic Gonadotropin-Secreting Pineal Tumors Relation to Pathogenesis and Sex Limitation of Sexual Precocity*

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Clinical features of primary ovarian failure caused by a point mutation in the follicle-stimulating hormone receptor gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failure

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

An activating mutation of the follicle-stimulating hormone receptor autonomously sustains spermatogenesis in a hypophysectomized man.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0015-0282%2898%2900517-2

10.1016/S0015-0282(98)00517-2

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10202864%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

1 reference