Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH) (Q28281736)

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English	Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)	scientific article

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instance of

scholarly article

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title

Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH) (English)

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main subject

idiopathy

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patient

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hypogonadism

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based on heuristic

inferred from title

hypogonadotropic hypogonadism

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based on heuristic

inferred from title

author

Stephanie B Seminara

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3

object named as

Stephanie B Seminara

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Kiyonori Miura

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1

object named as

Kiyonori Miura

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author name string

James S Acierno

series ordinal

2

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language of work or name

English

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publication date

2004

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published in

Journal of Human Genetics

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volume

49

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issue

5

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page(s)

265-8

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cites work

Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel interstitial deletion of KAL1 in a Japanese family with Kallmann syndrome.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked adrenal hypoplasia congenita: a mutation in DAX1 expands the phenotypic spectrum in males and females

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

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The genetic and clinical heterogeneity of gonadotropin-releasing hormone deficiency in the human

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

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Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Normal reference laboratory values

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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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

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

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Molecular mechanisms for migration of placodally derived GnRH neurons

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel gene expressed in nasal region influences outgrowth of olfactory axons and migration of luteinizing hormone-releasing hormone (LHRH) neurons

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Kallmann syndrome: towards molecular pathogenesis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biology of normal luteinizing hormone-releasing hormone neurons during and after their migration from olfactory placode

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15362570

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S10038-004-0137-4

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3232781

OpenCitations bibliographic resource ID

3232781

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3232781

PubMed publication ID

15362570

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3232781

ResearchGate publication ID

8351244

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