The growth hormone receptor gene deleted for exon three ( GHRd3 ) polymorphism is associated with birth and placental weight
Author:
Affiliation:
1. Developmental Endocrinology Research Group
2. Clinical & Molecular Genetics Unit, UCL Institute of Child Health, University College London, London, UK
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2265.2011.04207.x
Reference21 articles.
1. Species-specific Alternative Splice Mimicry at the Growth Hormone Receptor Locus Revealed by the Lineage of Retroelements during Primate Evolution
2. Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism.
3. Expression of exon 3-retaining and exon 3-excluding isoforms of the human growth hormone-receptor is regulated in an interindividual, rather than a tissue-specific, manner
4. Alternative splicing of exon 3 of the human growth hormone receptor is the result of an unusual genetic polymorphism.
5. The Roles of Placental Growth Hormone and Placental Lactogen in the Regulation of Human Fetal Growth and Development
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1. The Exon 3-Deleted Growth Hormone Receptor (d3GHR) Polymorphism—A Favorable Backdoor Mechanism for the GHR Function;International Journal of Molecular Sciences;2023-09-10
2. Sex-specific phenotypic effects and evolutionary history of an ancient polymorphic deletion of the human growth hormone receptor;Science Advances;2021-09-24
3. A common deletion in the growth hormone receptor gene (d3-GHR) in the offspring is related to maternal placental GH levels during pregnancy;Growth Hormone & IGF Research;2020-12
4. Whole genome analysis of water buffalo and global cattle breeds highlights convergent signatures of domestication;Nature Communications;2020-09-21
5. Sex-specific phenotypic effects and evolutionary history of an ancient polymorphic deletion of the human growth hormone receptor;2019-10-01
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