Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q34289994)
Watch
English
Inherited disorders of the gonadotropin hormones.
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 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
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author
John C. Achermann
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Eun Jig Lee
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
J. Larry Jameson
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
author name string
J Weiss
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
publication date
1 June 2001
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Molecular and Cellular Endocrinology
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
179
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
1-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
89-96
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impairing follicle-stimulating hormone (FSH) signaling in vivo: targeted disruption of the FSH receptor leads to aberrant gametogenesis and hormonal imbalance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic Variability in Familial Combined Pituitary Hormone Deficiency Caused by a PROP1 Gene Mutation Resulting in the Substitution of Arg->Cys at Codon 120 (R120C)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
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%2801%2900474-9
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%2801%2900474-9
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Obesity and impaired prohormone processing associated with mutations in the human prohormone convertase 1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Follicle stimulating hormone is required for ovarian follicle maturation but not male fertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Delayed puberty and hypogonadism caused by mutations in the follicle-stimulating hormone beta-subunit gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A new molecular variant of luteinizing hormone associated with female infertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Follitropin (FSH) deficiency in an infertile male due to FSHbeta gene mutation. A syndrome of normal puberty and virilization but underdeveloped testicles with azoospermia, low FSH but high lutropin and normal serum testosterone concentrations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolated deficiency of follicle-stimulating hormone re-revisited
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypogonadotropic hypogonadism in a female caused by an X-linked recessive mutation in the DAX1 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Steroidogenic factor 1: a key determinant of endocrine development and function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Male hypogonadism due to a mutation in the gene for the beta-subunit of follicle-stimulating hormone
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A leptin missense mutation associated with hypogonadism and morbid obesity.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in DAX1 causes delayed-onset adrenal insufficiency and incomplete hypogonadotropic hypogonadism
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Men homozygous for an inactivating mutation of the follicle-stimulating hormone (FSH) receptor gene present variable suppression of spermatogenesis and fertility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
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%2801%2900474-9
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in PROP1 cause familial combined pituitary hormone deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Role of Ahch in gonadal development and gametogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900474-9
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%2801%2900474-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0303-7207(01)00474-9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
11420133
1 reference
stated in
Europe PubMed Central
PubMed publication ID
11420133
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420133%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit