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English
Inherited disorders of the gonadotropin hormones
scientific article published on 01 December 1996
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
review article
1 reference
stated in
Europe PubMed Central
title
Inherited disorders of the gonadotropin hormones
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
author
J. Larry Jameson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
publication date
1 December 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
published in
Molecular and Cellular Endocrinology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
volume
125
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
page(s)
143-149
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
cites work
Primary amenorrhoea and infertility due to a mutation in the beta-subunit of follicle-stimulating hormone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypogonadism in a Male with Immunologically Active, Biologically Inactive Luteinizing Hormone: An Exception to a Venerable Rule*
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypogonadism Caused by a Single Amino Acid Substitution in the β Subunit of Luteinizing Hormone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypogonadism in a male with an immunologically active, biologically inactive luteinizing hormone: characterization of the abnormal hormone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ontogeny of pituitary-gonadal interactions: current advances and controversies
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Brief report: testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Glycoprotein Hormones: Structure and Function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Crystal structure of human chorionic gonadotropin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Antigenic alteration of an anomalous human luteinizing hormone caused by two chorionic gonadotropin-type amino-acid substitutions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evolution of the genes for the beta subunits of human chorionic gonadotropin and luteinizing hormone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A deletion truncating the gonadotropin-releasing hormone gene is responsible for hypogonadism in the hpg mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal structure of the gonadotropin-releasing hormone (GnRH) gene in patients with GnRH deficiency and idiopathic hypogonadotropic hypogonadism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normal Sequence of the Gonadotropin-Releasing Hormone Gene in Patients with Idiopathic Hypogonadotropic Hypogonadism1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Analysis of gonadotropin-releasing hormone gene structure in families with familial central precocious puberty and idiopathic hypogonadotropic hypogonadism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A cell-specific nuclear receptor is essential for adrenal and gonadal development and sexual differentiation.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The nuclear receptor steroidogenic factor 1 acts at multiple levels of the reproductive axis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The nuclear receptor steroidogenic factor 1 is essential for the formation of the ventromedial hypothalamic nucleus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: evidence that DAX-1 mutations lead to combined hypothalmic and pituitary defects in gonadotropin production
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2896%2903950-0
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0303-7207(96)03950-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
PubMed publication ID
9027352
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9027352
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9027352%20AND%20SRC:MED&resulttype=core&format=json
retrieved
31 October 2019
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