[HTML][HTML] Physiological roles of zinc transporters: molecular and genetic importance in zinc homeostasis

T Hara, T Takeda, T Takagishi, K Fukue… - The Journal of …, 2017 - Springer
Zinc (Zn) is an essential trace mineral that regulates the expression and activation of
biological molecules such as transcription factors, enzymes, adapters, channels, and growth …

Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivity

A David, V Hwa, LA Metherell, I Netchine… - Endocrine …, 2011 - academic.oup.com
GH insensitivity (GHI) presents in childhood as growth failure and in its severe form is
associated with dysmorphic and metabolic abnormalities. GHI may be caused by genetic …

Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia

PQ Thomas, MT Dattani, JM Brickman… - Human molecular …, 2001 - academic.oup.com
We have previously shown that familial septo-optic dysplasia (SOD), a syndromic form of
congenital hypopituitarism involving optic nerve hypoplasia and agenesis of midline brain …

[HTML][HTML] The zinc transporter SLC39A14/ZIP14 controls G-protein coupled receptor-mediated signaling required for systemic growth

S Hojyo, T Fukada, S Shimoda, W Ohashi, BH Bin… - PloS one, 2011 - journals.plos.org
Aberrant zinc (Zn) homeostasis is associated with abnormal control of mammalian growth,
although the molecular mechanisms of Zn's roles in regulating systemic growth remain to be …

Isolated growth hormone deficiency (GHD) in childhood and adolescence: recent advances

KS Alatzoglou, EA Webb, P Le Tissier… - Endocrine …, 2014 - academic.oup.com
The diagnosis of GH deficiency (GHD) in childhood is a multistep process involving clinical
history, examination with detailed auxology, biochemical testing, and pituitary imaging, with …

Molecular mechanisms of pituitary organogenesis: in search of novel regulatory genes

SW Davis, F Castinetti, LR Carvalho… - Molecular and cellular …, 2010 - Elsevier
Defects in pituitary gland organogenesis are sometimes associated with congenital
anomalies that affect head development. Lesions in transcription factors and signaling …

Role of PROP1 in pituitary gland growth

RD Ward, LT Raetzman, H Suh, BM Stone… - Molecular …, 2005 - academic.oup.com
Mutations in the PROP1 transcription factor gene lead to reduced production of thyrotropin,
GH, prolactin, and gonadotropins as well as to pituitary hypoplasia in adult humans and …

Growth hormone deficiency with ectopic neurohypophysis: anatomical variations and relationship between the visibility of the pituitary stalk asserted by magnetic …

S Chen, J Léger, C Garel, M Hassan… - The Journal of …, 1999 - academic.oup.com
In GH-deficient children showing ectopic posterior pituitary hyperintense signal (EPP), the
anatomical details of the pituitary-hypothalamic region and the relationship between the …

Zinc transporters and signaling in physiology and pathogenesis

S Hojyo, T Fukada - Archives of biochemistry and biophysics, 2016 - Elsevier
Zinc (Zn) is an essential trace element that is vital in a wide range of cellular machineries
because of its effect on the expression and activity of various transcription factors and …

Lhx4 and Prop1 are required for cell survival and expansion of the pituitary primordia

LT Raetzman, R Ward, SA Camper - 2002 - journals.biologists.com
Deficiencies in the homeobox transcription factors LHX4 and PROP1 cause pituitary
hormone deficiency in both humans and mice. Lhx4 and Prop1 mutants exhibit severe …