Genetic disorders in the GH IGF-I axis in mouse and man.
about
The essential role of Mbd5 in the regulation of somatic growth and glucose homeostasis in miceThe systemic effects of platelet-rich plasma injectionSensational placodes: neurogenesis in the otic and olfactory systems.AKT signaling mediates IGF-I survival actions on otic neural progenitors.A comparative study of age-related hearing loss in wild type and insulin-like growth factor I deficient mice.Classic Case Report of Donohue Syndrome (Leprechaunism; OMIM *246200): The Impact of Consanguineous Mating.The role of insulin-like growth factor-I in the physiopathology of hearing.Gestational-neonatal iron deficiency suppresses and iron treatment reactivates IGF signaling in developing rat hippocampusGenetic evidence that thyroid hormone is indispensable for prepubertal insulin-like growth factor-I expression and bone acquisition in mice.The effect of two different GH dosages on final height and bone geometryRegulation of muscle mass by growth hormone and IGF-I.Expanding the mind: insulin-like growth factor I and brain development.Insulin growth factor 1 receptor/PI3K/AKT survival pathway in outer segment membranes of rod photoreceptors.Autophagy resolves early retinal inflammation in Igf1-deficient miceThe role of liver-derived insulin-like growth factor-I.Maternal high-fat diet promotes body length increases and insulin insensitivity in second-generation miceRole of insulin-like growth factor-1 in the regulation of skeletal growth.Progesterone regulates FGF10, MET, IGFBP1, and IGFBP3 in the endometrium of the ovine uterus.Pregnancy-associated plasma protein (PAPP)-A expressed in the mammary gland controls epithelial cell proliferation and differentiation.Skeletal effects of growth hormone and insulin-like growth factor-I therapy.Cre-mediated recombination in pituitary somatotropes.Three novel IGF1R mutations in microcephalic patients with prenatal and postnatal growth impairment.Familial short stature and intrauterine growth retardation associated with a novel mutation in the IGF-I receptor (IGF1R) gene.MRNA expression of members of the IGF system in the organ of Corti, the modiolus and the stria vascularis of newborn rats.Causality in biology has to answer 2 main questions--which and how: letter to the editor.
P2860
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P2860
Genetic disorders in the GH IGF-I axis in mouse and man.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Genetic disorders in the GH IGF-I axis in mouse and man.
@en
type
label
Genetic disorders in the GH IGF-I axis in mouse and man.
@en
prefLabel
Genetic disorders in the GH IGF-I axis in mouse and man.
@en
P356
P1476
Genetic disorders in the GH IGF-I axis in mouse and man.
@en
P2093
M J E Walenkamp
P304
P356
10.1530/EJE-07-0148
P478
157 Suppl 1
P577
2007-08-01T00:00:00Z