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Article

Development of a model for mapping cryptorchidism in sheep and initial evidence for association of INSL3 with the defect.

Animal genetics - 1 Apr 2007

Williams G A, Ott T L, Michal J J, Gaskins C T, Wright R W, Daniels T F, Jiang Z

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Identifiers

PMID: 17355391
DOI: 10.1111/j.1365-2052.2007.01585.x

Genes

INSL3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Development of a model for mapping cryptorchidism in sheep and initial evidence for association of INSL3 with the defect.PMID 17355391Read ↗

Targeted Disruption of the Insl3 Gene Causes Bilateral CryptorchidismSemantic proximity Read ↗

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The molecular basis of cryptorchidism.Semantic proximity Read ↗

INSL3/LGR8 role in testicular descent and cryptorchidism.Semantic proximity Read ↗

The INSL3-LGR8/GREAT ligand-receptor pair in human cryptorchidism.Semantic proximity Read ↗

Genetic alterations associated with cryptorchidism.Semantic proximity Read ↗

Analysis of transcript and methylation levels of INSL3 and RXFP2 in undescended and descended dog testes suggested promising biomarkers associated with cryptorchidismSemantic proximity Read ↗

Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresiaSemantic proximity Read ↗

Role of Hormones, Genes, and Environment in Human CryptorchidismSemantic proximity Read ↗

Familial bilateral cryptorchidism is caused by recessive variants in RXFP2Semantic proximity Read ↗

Lack of LGR8 gene mutation in Finnish patients with a family history of cryptorchidism.Semantic proximity Read ↗

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