A case of isolated growth hormone deficiency associated with familial thyroxine binding globulin deficiency

Changes in serum insulin-like growth factor binding protein-2, -3, and -6 levels in patients with chronic renal failure following renal transplantation.

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society·2000

Interleukin-6 (IL-6) inhibits thyroid function in the presence of soluble IL-6 receptor in cultured human thyroid follicles.

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17 beta-estradiol increases calcium content in fetal mouse parietal bones cultured in serum-free medium only at physiological concentrations.

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Increase of vascular endothelial growth factor mRNA expression by 1,25-dihydroxyvitamin D3 in human osteoblast-like cells.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research·1996

Degradation of cell surface heparan sulfates decreases the high affinity binding of basic FGF to endothelial cells, but not to FRTL-5 rat thyroid cells.

Thyroid : official journal of the American Thyroid Association·1995

Stimulation by thyroid-stimulating hormone and Grave's immunoglobulin G of vascular endothelial growth factor mRNA expression in human thyroid follicles in vitro and flt mRNA expression in the rat thyroid in vivo.

The Journal of clinical investigation·1995

Anti-eye muscle antibodies and hypothyroid Graves' disease: a case report.

Endocrinologia japonica·1992

No inhibitory effects of gestrinone and medroxyprogesterone acetate on the estrogen production by ovaries of hypophysectomized rats stimulated by gonadotropins.

Endocrinologia japonica·1992

Immunohistochemical evidence that rat FSH cells contain beta II-subspecies of protein kinase C.

Endocrinologia japonica·1992

Source of prolactin in human follicular fluid.

Endocrinologia japonica·1992

Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.

Endocrinologia japonica·1992

Transient extreme insulin resistance in shock during diabetic ketoacidosis.

Endocrinologia japonica·1992

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

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Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.

The Journal of allergy and clinical immunology·2026

CRP-albumin-lymphocyte index and multisystem diseases: a phenome-wide Mendelian randomization study.

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A case of isolated growth hormone deficiency associated with familial thyroxine binding globulin deficiency

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Changes in serum insulin-like growth factor binding protein-2, -3, and -6 levels in patients with chronic renal failure following renal transplantation.

Interleukin-6 (IL-6) inhibits thyroid function in the presence of soluble IL-6 receptor in cultured human thyroid follicles.

17 beta-estradiol increases calcium content in fetal mouse parietal bones cultured in serum-free medium only at physiological concentrations.

Increase of vascular endothelial growth factor mRNA expression by 1,25-dihydroxyvitamin D3 in human osteoblast-like cells.

Degradation of cell surface heparan sulfates decreases the high affinity binding of basic FGF to endothelial cells, but not to FRTL-5 rat thyroid cells.

Stimulation by thyroid-stimulating hormone and Grave's immunoglobulin G of vascular endothelial growth factor mRNA expression in human thyroid follicles in vitro and flt mRNA expression in the rat thyroid in vivo.

Anti-eye muscle antibodies and hypothyroid Graves' disease: a case report.

No inhibitory effects of gestrinone and medroxyprogesterone acetate on the estrogen production by ovaries of hypophysectomized rats stimulated by gonadotropins.

Immunohistochemical evidence that rat FSH cells contain beta II-subspecies of protein kinase C.

Source of prolactin in human follicular fluid.

Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.

Transient extreme insulin resistance in shock during diabetic ketoacidosis.

Clinical and Molecular Spectrum of KBG Syndrome in the Largest Independent Turkish Cohort: Novel ANKRD11 Variants, 16q24.3 Deletions, and Structural Insights for Robust ANKRD11 Variant Interpretation.

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A case of isolated growth hormone deficiency associated with familial thyroxine binding globulin deficiency

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