Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism (Q24307650)

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English	Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism	scientific article

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scholarly article

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Heparan sulfate 6-O-sulfotransferase 1, a gene involved in extracellular sugar modifications, is mutated in patients with idiopathic hypogonadotrophic hypogonadism (English)

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1 reference

based on heuristic

inferred from title

neuron development

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GOA release 2020-03-11

Gerasimos P Sykiotis

object named as

Gerasimos P Sykiotis

2

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Nelly Pitteloud

15

object named as

Nelly Pitteloud

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4

object named as

Lacey Plummer

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Stephanie B Seminara

8

object named as

Stephanie B Seminara

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William F. Crowley

12

object named as

William F Crowley

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10

object named as

Guy Van Vliet

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author name string

Janne Tornberg

1

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Kimberly Keefe

3

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Xuan Hoang

5

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Janet E Hall

6

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Richard Quinton

7

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Virginia Hughes

9

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Stan Van Uum

11

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Hiroko Habuchi

13

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Koji Kimata

14

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Hannes E Bülow

16

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language of work or name

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publication date

12 July 2011

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

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108

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28

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11524-9

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Novel mechanisms of fibroblast growth factor receptor 1 regulation by extracellular matrix protein anosmin-1

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

The endocrine-gland-derived VEGF homologue Bv8 promotes angiogenesis in the testis: Localization of Bv8 receptors to endothelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Redirecting the substrate specificity of heparan sulfate 2-O-sulfotransferase by structurally guided mutagenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Regulated diversity of heparan sulfate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan Sulfate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

The occurrence of three isoforms of heparan sulfate 6-O-sulfotransferase having different specificities for hexuronic acid adjacent to the targeted N-sulfoglucosamine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

19 March 2017

Order out of chaos: assembly of ligand binding sites in heparan sulfate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

7 April 2017

Oligogenic basis of isolated gonadotropin-releasing hormone deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Impaired fibroblast growth factor receptor 1 signaling as a cause of normosmic idiopathic hypogonadotropic hypogonadism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

The molecular diversity of glycosaminoglycans shapes animal development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

A protein canyon in the FGF-FGF receptor dimer selects from an à la carte menu of heparan sulfate motifs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Sugar codes for axons?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

A window of opportunity: the diagnosis of gonadotropin deficiency in the male infant

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Molecular mechanisms of gonadotropin-releasing hormone neuronal migration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Cell signaling events: a view from the matrix

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Heparin/Heparan sulfate domains in binding and signaling of fibroblast growth factor 8b.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Development. The decade of the developing brain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

egl-17 encodes an invertebrate fibroblast growth factor family member required specifically for sex myoblast migration in Caenorhabditis elegans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

cis regulatory requirements for hypodermal cell-specific expression of the Caenorhabditis elegans cuticle collagen gene dpy-7.

1 reference

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27 September 2017

Guanylyl cyclase expression in specific sensory neurons: a new family of chemosensory receptors.

1 reference

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27 September 2017

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

27 September 2017

Extracellular sugar modifications provide instructive and cell-specific information for axon-guidance choices

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

30 May 2018

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

Differential expression of heparan sulfate 6-O-sulfotransferase isoforms in the mouse embryo suggests distinctive roles during organogenesis

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

An FGF receptor signaling pathway is required for the normal cell migrations of the sex myoblasts in C. elegans hermaphrodites

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

let-756, a C. elegans fgf essential for worm development.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

Reversal of idiopathic hypogonadotropic hypogonadism

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1102284108

21 January 2018

Differential functions of the C. elegans FGF receptor in axon outgrowth and maintenance of axon position.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

29 November 2018

Differential sulfations and epimerization define heparan sulfate specificity in nervous system development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3136273

29 November 2018

Alternative splicing affecting a novel domain in the C. elegans EGL-15 FGF receptor confers functional specificity

1 reference

https://pubmed.ncbi.nlm.nih.gov/21700882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glycosaminoglycans in the olfactory epithelium and nerve of chick embryos: an immunocytochemical study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21700882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gonadotropin-releasing hormone deficiency in the human (idiopathic hypogonadotropic hypogonadism and Kallmann's syndrome): pathophysiological and genetic considerations

1 reference

https://pubmed.ncbi.nlm.nih.gov/21700882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.1102284108

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2011PNAS..10811524T

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OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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