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Article

Cloning of a human GHF-1/Pit-1 cDNA variant.

Nucleic acids research - 25 Jul 1993

Pernasetti F, Wera S, Belayew A, Martial J A

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 8346040
DOI: 10.1093/nar/21.15.3584
PMCID: PMC331470

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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Cloning of a human GHF-1/Pit-1 cDNA variant.PMID 8346040Read ↗

Differential splicing of the GHF1 primary transcript gives rise to two functionally distinct homeodomain proteins.Semantic proximity Read ↗

PIT1 abnormality.Semantic proximity Read ↗

A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency.Semantic proximity Read ↗

Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency.Semantic proximity Read ↗

[The pituitary specific transcription factor Pit-1/GHF-1 and PIT1 abnormality].Semantic proximity Read ↗

Identification of the human pituitary tumor transforming gene (hPTTG) family: molecular structure, expression, and chromosomal localizationSemantic proximity Read ↗

Dissection of functional domains of the pituitary-specific transcription factor GHF-1.Semantic proximity Read ↗

Functional characterization of a human <i>POU1F1</i> mutation associated with isolated growth hormone deficiency: a novel etiology for IGHDSemantic proximity Read ↗

Identification of a novel mutation in the exon 2 splice donor site of the POU1F1/PIT-1 gene in Japanese identical twins with mild combined pituitary hormone deficiency.Semantic proximity Read ↗

[Pituitary specific transcription factor Pit-1/GHF-1 and combined pituitary hormone deficiency].Semantic proximity Read ↗

The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutationSemantic proximity Read ↗

Genomic structure of the human M6P/IGF2 receptorSemantic proximity Read ↗

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