Literature DB >> 17336732

Genetics of growth hormone deficiency.

Primus E Mullis1.   

Abstract

When a child is not following the normal, predicted growth curve, an evaluation for underlying illness and central nervous system abnormalities is required and appropriate consideration should be given to genetic defects causing growth hormone (GH) deficiency. This article focuses on the GH gene, the various gene alterations, and their possible impact on the pituitary gland. Transcription factors regulating pituitary gland development may cause multiple pituitary hormone deficiency but may present initially as GH deficiency. The role of two most important transcription factors, POU1F1 (Pit-1) and PROP 1, is discussed.

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Year:  2007        PMID: 17336732     DOI: 10.1016/j.ecl.2006.11.010

Source DB:  PubMed          Journal:  Endocrinol Metab Clin North Am        ISSN: 0889-8529            Impact factor:   4.741


  14 in total

1.  Growth hormone (GH-1) gene deletions in children with isolated growth hormone deficiency (IGHD).

Authors:  Meena P Desai; Shilpa M Mithbawkar; Pradnya S Upadhye; Kavita K Shalia
Journal:  Indian J Pediatr       Date:  2011-10-21       Impact factor: 1.967

2.  Molecular genetic studies in isolated growth hormone deficiency (IGHD).

Authors:  Meena P Desai; Shilpa M Mithbawkar; Pradnya S Upadhye; Sudha C Rao; Vijayalakshmi Bhatia; Madhava Vijaykumar
Journal:  Indian J Pediatr       Date:  2013-02-23       Impact factor: 1.967

3.  Polymorphisms of caprine POU1F1 gene and their association with litter size in Jining Grey goats.

Authors:  T Feng; M X Chu; G L Cao; Q Q Tang; R Di; L Fang; N Li
Journal:  Mol Biol Rep       Date:  2011-07-17       Impact factor: 2.316

Review 4.  Phenotype-genotype correlations in congenital isolated growth hormone deficiency (IGHD).

Authors:  Kyriaki S Alatzoglou; Mehul T Dattani
Journal:  Indian J Pediatr       Date:  2011-12-03       Impact factor: 1.967

5.  A novel selection signature in stearoyl-coenzyme A desaturase (SCD) gene for enhanced milk fat content in Bubalus bubalis.

Authors:  J Maryam; M E Babar; Zhang Bao; A Nadeem
Journal:  Trop Anim Health Prod       Date:  2016-06-16       Impact factor: 1.559

6.  Rare diseases in clinical endocrinology: a taxonomic classification system.

Authors:  G Marcucci; L Cianferotti; P Beck-Peccoz; M Capezzone; F Cetani; A Colao; M V Davì; E degli Uberti; S Del Prato; R Elisei; A Faggiano; D Ferone; C Foresta; L Fugazzola; E Ghigo; G Giacchetti; F Giorgino; A Lenzi; P Malandrino; M Mannelli; C Marcocci; L Masi; F Pacini; G Opocher; A Radicioni; M Tonacchera; R Vigneri; M C Zatelli; M L Brandi
Journal:  J Endocrinol Invest       Date:  2014-11-07       Impact factor: 4.256

7.  Rescue of pituitary function in a mouse model of isolated growth hormone deficiency type II by RNA interference.

Authors:  Nikki Shariat; Robin C C Ryther; John A Phillips; Iain C A F Robinson; James G Patton
Journal:  Endocrinology       Date:  2007-11-15       Impact factor: 4.736

8.  Isolated growth hormone deficiency type II caused by a point mutation that alters both splice site strength and splicing enhancer function.

Authors:  N Shariat; C D Holladay; R K Cleary; J A Phillips; J G Patton
Journal:  Clin Genet       Date:  2008-06-11       Impact factor: 4.438

9.  p.R209H GH1 variant challenges short stature assessment.

Authors:  Nora Sanguineti; Debora Braslavsky; Paula A Scaglia; Ana Keselman; Maria G Ballerini; Maria G Ropelato; Sofia Suco; Sebastian Vishnopolska; Ariel J Berenstein; Héctor Jasper; Horacio M Domené; Rodolfo A Rey; Maria I Pérez Millán; Sally A Camper; Ignacio Bergadá
Journal:  Growth Horm IGF Res       Date:  2019-12-03       Impact factor: 2.372

10.  Highly conserved non-coding sequences and the 18q critical region for short stature: a common mechanism of disease?

Authors:  Flavio Rizzolio; Silvia Bione; Cinzia Sala; Carla Tribioli; Roberto Ciccone; Orsetta Zuffardi; Natascia di Iorgi; Mohamad Maghnie; Daniela Toniolo
Journal:  PLoS One       Date:  2008-01-23       Impact factor: 3.240

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