Peter Sadow
0000-0003-1036-6367
Harvard Medical School
129 papers found
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Angiogenin-Stimulated rRNA Transcription Is Essential for Initiation and Survival of AKT-Induced Prostate Intraepithelial Neoplasia
Intraoperative diagnosis of a functional paraganglioma presenting as a gastrointestinal stromal cell tumor (GIST)
Vitamin D-Mediated Hypercalcemia and Cushing Syndrome as Manifestations of Malignant Pleural Mesothelioma
A patient with ectopic cortisol production derived from malignant testicular masses
Malignant struma ovarii
Stathmin Expression in Pheochromocytomas, Paragangliomas, and in other Endocrine Tumors
Klebsiella PneumoniaeNecrotizing Fasciitis And Septic Arthritis: An Appearance in The Western Hemisphere
Cleft of the secondary palate without cleft lip diagnosed with three-dimensional ultrasound and magnetic resonance imaging in a fetus with Fryns' syndrome
Tissue responses to thyroid hormone in a kindred with resistance to thyroid hormone harboring a commonly occurring mutation in the thyroid hormone receptor β gene (P453T)
Thyroid Hormone Receptor-Specific Interactions with Steroid Receptor Coactivator-1 in the Pituitary
Regulation of expression of thyroid hormone receptor isoforms and coactivators in liver and heart by thyroid hormone
Specificity of thyroid hormone receptor subtype and steroid receptor coactivator-1 on thyroid hormone action
Thyroid hormone and cardiac function in mice deficient in thyroid hormone receptor-α or -β: An echocardiograph study
Thyroid function in mice with compound heterozygous and homozygous disruptions of SRC-1 and TIF-2 coactivators: Evidence for haploinsufficiency
Steroid receptor coactivator-1 deficiency causes variable alterations in the modulation of t3-regulated transcription of genes in vivo
Resistance to thyroid hormones without thyroid hormone receptor genes mutation | Résistance aux hormones thyroïdiennes sans mutation des gènes des récepteurs aux hormones thyroïdiennes
Congenital hypothyroidism in a child with unsuspected familial dysalbuminemic hyperthyroxinemia caused by a mutation (R218H) in the human albumin gene
Resistance to Thyroid Hormone in the Absence of Mutations in the Thyroid Hormone Receptor Genes
A Novel Point Mutation in Cluster 3 of the Thyroid Hormone Receptor β Gene (P247L) Causing Mild Resistance to Thyroid Hormone
Differential inhibition of collagenase and interleukin-1α gene expression in cultured corneal fibroblasts by TGF-β, dexamethasone, and retinoic acid
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