[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 …
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
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 …
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
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 …
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
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 …
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 …
history, examination with detailed auxology, biochemical testing, and pituitary imaging, with …
Molecular mechanisms of pituitary organogenesis: in search of novel regulatory genes
Defects in pituitary gland organogenesis are sometimes associated with congenital
anomalies that affect head development. Lesions in transcription factors and signaling …
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 …
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 …
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 …
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 …
hormone deficiency in both humans and mice. Lhx4 and Prop1 mutants exhibit severe …