Associated Papers
STAT5b: A master regulator of key biological pathways.
Smith MR et al.
Frontiers in Immunology, 2022
Human growth disorders associated with impaired GH action: Defects in STAT5B and JAK2.
Hwa V
Molecular and Cellular Endocrinology, 2021
Nonclassical GH Insensitivity: Characterization of Mild Abnormalities of GH Action.
Storr HL et al.
Endocrine Reviews, 2019
STAT5B mutations in heterozygous state have negative impact on height: another clue in human stature heritability.
Scalco RC et al.
European Journal of Endocrinology, 2015
Current issues on molecular diagnosis of GH signaling defects.
Feigerlova E et al.
Endocrine Development, 2013
Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivity.
David A et al.
Endocrine Reviews, 2011
STAT5b deficiency: lessons from STAT5b gene mutations.
Hwa V et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2011
Genetic Defects in the Growth Hormone-IGF-I Axis Causing Growth Hormone Insensitivity and Impaired Linear Growth.
Savage MO et al.
Frontiers in Endocrinology, 2011
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