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Disruptive innovation as a driver of science and medicine.
- Published in:
- 2014
- By:
- Publication type:
- Speech
Introduction of John T. Potts Jr.
- Published in:
- Journal of Clinical Investigation, 2013, v. 123, n. 11, p. 4971, doi. 10.1172/JCI73227
- By:
- Publication type:
- Article
Genetic rescue of nonclassical ERα signaling normalizes energy balance in obese Erα-null mutant mice.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Harrison's Principles of Internal Medicine 19th Edition, Vols I & II.
- Published in:
- 2015
- By:
- Publication type:
- Book Review
Skeletal Effects of Estrogen Are Mediated by Opposing Actions of Classical and Nonclassical Estrogen Receptor Pathways.
- Published in:
- Journal of Bone & Mineral Research, 2005, v. 20, n. 11, p. 1992, doi. 10.1359/JBMR.050713
- By:
- Publication type:
- Article
Dax1 is required for testis determination.
- Published in:
- Nature Genetics, 2003, v. 34, n. 1, p. 32, doi. 10.1038/ng1141
- By:
- Publication type:
- Article
A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans.
- Published in:
- Nature Genetics, 1999, v. 22, n. 2, p. 125, doi. 10.1038/9629
- By:
- Publication type:
- Article
Splice Variants of the Forkhead Box Protein AFX Exhibit Dominant Negative Activity and Inhibit AFXα-Mediated Tumor Cell Apoptosis.
- Published in:
- PLoS ONE, 2008, v. 3, n. 7, p. 1, doi. 10.1371/journal.pone.0002743
- By:
- Publication type:
- Article
Syndrome of Resistance to Thyroid Hormone: Insights into Thyroid Hormone Action.
- Published in:
- Proceedings of the Society for Experimental Biology & Medicine, 1996, v. 211, n. 1, p. 49, doi. 10.3181/00379727-211-43951
- By:
- Publication type:
- Article
Heterozygous missense mutations in steroidogenic factor 1 (SF1/Ad4BP, NR5A1) are associated with 46,XY disorders of sex development with normal adrenal function.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Analysis of DAX1 (NR0B1) and steroidogenic factor-1 (NR5A1) in children and adults with primary adrenal failure: ten years' experience.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Phenotypic Features Associated with Mutations in Steroidogenic Acute Regulatory Protein.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 11, p. 6303, doi. 10.1210/jc.2005-0434
- By:
- Publication type:
- Article
Editorial: Of Mice and Men: The Tale of Steroidogenic Factor-1.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 12, p. 5927, doi. 10.1210/jc.2004-2047
- By:
- Publication type:
- Article
X-Linked Sex-Determining Region Y Box 3 (SOX3) Gene Mutations Are Uncommon in Men with Idiopathic Oligoazoospermic Infertility.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 8, p. 4146, doi. 10.1210/jc.2004-0191
- By:
- Publication type:
- Article
An Alternate Translation Initiation Site Circumvents an Amino-Terminal DAX1 Nonsense Mutation Leading to a Mild Form of X-Linked Adrenal Hypoplasia Congenita.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 1, p. 417, doi. 10.1210/jc.2002-021034
- By:
- Publication type:
- Article
Adenovirus-Mediated Targeted Expression of Toxic Genes to Adrenocorticotropin-Producing Pituitary Tumors Using the Proopiomelanocortin Promoter.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 7, p. 3400
- By:
- Publication type:
- Article
Genetic Causes of Human Reproductive Disease.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2447, doi. 10.1210/jcem.87.6.8622
- By:
- Publication type:
- Article
Gonadal Determination and Adrenal Development Are Regulated by the Orphan Nuclear Receptor Steroidogenic Factor-1, in a Dose-Dependent Manner.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 4, p. 1829, doi. 10.1210/jcem.87.4.8376
- By:
- Publication type:
- Article
Effects of aging on vasopressin production in a kindred with autosomal dominant neurohypophyseal diabetes insipidus due to the DeltaE47 neurophysin mutation.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 2, p. 870, doi. 10.1210/jcem.87.2.8270
- By:
- Publication type:
- Article
Hypogonadotropic Hypogonadism as a Presenting Feature of Late-Onset X-Linked Adrenal Hypoplasia Congenita.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 1, p. 44, doi. 10.1210/jcem.87.1.8163
- By:
- Publication type:
- Article
Absence of Constitutively Activating Mutations in the GHRH Receptor in GH-Producing Pituitary Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 8, p. 3989, doi. 10.1210/jcem.86.8.7732
- By:
- Publication type:
- Article
Missense Mutations Cluster within the Carboxyl-Terminal Region of DAX-1 and Impair Transcriptional Repression.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 7, p. 3171, doi. 10.1210/jcem.86.7.7660
- By:
- Publication type:
- Article
X-Linked Adrenal Hypoplasia Congenita: A Mutation in DAX1 Expands the Phenotypic Spectrum in Males and Females.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Mutational Analysis of DAX1 in Patients with Hypogonadotropic Hypogonadism or Pubertal Delay.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Targeted Expression of Toxic Genes Directed by Pituitary Hormone Promoters: A Potential Strategy for Adenovirus-Mediated Gene Therapy of Pituitary Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 2, p. 786, doi. 10.1210/jcem.84.2.5504
- By:
- Publication type:
- Article
Clinical and Functional Effects of Mutations in the DAX-1 Gene in Patients with Adrenal Hypoplasia Congenita.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 2, p. 504, doi. 10.1210/jcem.84.2.5468
- By:
- Publication type:
- Article
G Protein and Thyrotropin Receptor Mutations in Thyroid Neoplasia.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 2, p. 493, doi. 10.1210/jcem.82.2.3719
- By:
- Publication type:
- Article
Introducing Expert Endocrine Consult.
- Published in:
- Journal of the Endocrine Society, 2020, v. 4, n. 8, p. 1, doi. 10.1210/jendso/bvaa070
- By:
- Publication type:
- Article
Regulation of Kiss1 and Dynorphin Gene Expression in the Murine Brain by Classical and Nonclassical Estrogen Receptor Pathways.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 29, p. 9390, doi. 10.1523/JNEUROSCI.0763-09.2009
- By:
- Publication type:
- Article
Variable Presentation of X-linked Adrenal Hypoplasia Congenita.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 8, p. 1093, doi. 10.1515/jpem-2001-0804
- By:
- Publication type:
- Article
Advances in the Molecular Genetics of Hypogonadotropic Hypogonadism.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2001, v. 14, n. 1, p. 3
- By:
- Publication type:
- Article
LEWIS LANDSBERG, MD 1938 - 2021.
- Published in:
- 2022
- By:
- Publication type:
- Obituary
A tribute to Jean D. Wilson (1932-2021).
- Published in:
- 2021
- By:
- Publication type:
- journal article
Resveratrol acts as an estrogen receptor (ER) agonist in breast cancer cells stably transfected with ER α.
- Published in:
- International Journal of Cancer, 2003, v. 104, n. 5, p. 587, doi. 10.1002/ijc.10992
- By:
- Publication type:
- Article
Research in academic medical centers: Two threats to sustainable support.
- Published in:
- Science Translational Medicine, 2015, v. 7, n. 289, p. 1, doi. 10.1126/scitranslmed.aac5200
- By:
- Publication type:
- Article
A novel loss of function mutation in exon 10 of the FSH receptor gene causing hypergonadotrophic hypogonadism: clinical and molecular characteristics.
- Published in:
- 2003
- By:
- Publication type:
- journal article
A missense mutation in LRR8 of RXFP2 is associated with cryptorchidism.
- Published in:
- Mammalian Genome, 2010, v. 21, n. 9/10, p. 442, doi. 10.1007/s00335-010-9291-5
- By:
- Publication type:
- Article
Classification and Proposed Nomenclature for Inherited Defects of Thyroid Hormone Action, Cell Transport, and Metabolism.
- Published in:
- Thyroid, 2014, v. 24, n. 3, p. 407, doi. 10.1089/thy.2013.3393.nomen
- By:
- Publication type:
- Article
Serum from Methimazole-Treated Patients Induces Activation of Aryl Hydrocarbon Receptor, a Transcription Factor That Binds to Dioxin-Response Elements.
- Published in:
- Thyroid, 2012, v. 22, n. 8, p. 769, doi. 10.1089/thy.2012.0057
- By:
- Publication type:
- Article
Substitutions of Tyrosine 601 in the Human Thyrotropin Receptor Result in Increase or Loss of Basal Activation of the Cyclic Adenosine Monophosphate Pathway and Disrupt Coupling to G<sub>q</sub>/11.
- Published in:
- Thyroid, 2000, v. 10, n. 1, p. 3, doi. 10.1089/thy.2000.10.3
- By:
- Publication type:
- Article
Thyrotropin Receptor Mutations in Hyperfunctioning Thyroid Adenomas from Brazil.
- Published in:
- Thyroid, 1999, v. 9, n. 11, p. 1063, doi. 10.1089/thy.1999.9.1063
- By:
- Publication type:
- Article
Structural Analysis of the Thyrotropin Receptor in Four Patients with Congenital Hypothyroidism Due to Thyroid Hypoplasia.
- Published in:
- Thyroid, 1999, v. 9, n. 6, p. 523, doi. 10.1089/thy.1999.9.523
- By:
- Publication type:
- Article
Congenital Nonautoimmune Hyperthyroidism in a Nonidentical Twin Caused by a Sporadic Germline Mutation in the Thyrotropin Receptor Gene.
- Published in:
- Thyroid, 1997, v. 7, n. 5, p. 765, doi. 10.1089/thy.1997.7.765
- By:
- Publication type:
- Article
Dominant Negative and DNA-Binding Properties of Mutant Thyroid Hormone Receptors That Are Defective in Homodimerization But Not Heterodimerization.
- Published in:
- Thyroid, 1995, v. 5, n. 5, p. 343, doi. 10.1089/thy.1995.5.343
- By:
- Publication type:
- Article
Mechanisms by Which Thyroid Hormone Receptor Mutations Cause Clinical Syndromes of Resistance to Thyroid Hormone.
- Published in:
- Thyroid, 1994, v. 4, n. 4, p. 485, doi. 10.1089/thy.1994.4.485
- By:
- Publication type:
- Article
Role of Ahch in gonadal development and gametogenesis.
- Published in:
- Nature Genetics, 1998, v. 20, n. 4, p. 353, doi. 10.1038/3822
- By:
- Publication type:
- Article
Absence of activating mutations of CXCR4 in pituitary tumours.
- Published in:
- Clinical Endocrinology, 2010, v. 72, n. 2, p. 209, doi. 10.1111/j.1365-2265.2009.03629.x
- By:
- Publication type:
- Article