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The tumor suppressor protein menin interacts with NF-κB proteins and inhibits NF-κB-mediated transactivation.
- Published in:
- Oncogene, 2001, v. 20, n. 36, p. 4917, doi. 10.1038/sj.onc.1204529
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- Article
Identification of G Protein α-Subunits in RINm5F Cells and Their Selective Interaction With Galanin Receptor.
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- Diabetes, 1991, v. 40, n. 9, p. 1170, doi. 10.2337/diab.40.9.1170
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- Article
Heterotrimeric GTP-binding proteins: An expanding family of signal transducers.
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- Medicinal Research Reviews, 1992, v. 12, n. 1, p. 55, doi. 10.1002/med.2610120105
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- Article
Technetium-99m-Sestamibi Imaging before Reoperation for Primary Hyperparathyroidism.
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- Journal of Nuclear Medicine, 1995, v. 36, n. 12, p. 2186
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- Publication type:
- Article
MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 28, n. 1, p. 58, doi. 10.1002/(SICI)1098-2264(200005)28:1<58::AID-GCC7>3.0.CO;2-2
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- Article
Genome-Wide Analysis of Menin Binding<br /> Provides Insights into MEN1 Tumorigenesis.
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- PLoS Genetics, 2006, v. 2, n. 4, p. e51, doi. 10.1371/journal.pgen.0020051
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- Article
Multiple endocrine neoplasia type 1: clinical and genetic topics.
- Published in:
- 1998
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- Publication type:
- journal article
THE JEREMIAH METZGER LECTURE: A BRIEF HISTORY OF EUGENICS IN AMERICA: IMPLICATIONS FOR MEDICINE IN THE 21<sup>ST</sup> CENTURY.
- Published in:
- Transactions of the American Clinical & Climatological Association, 2019, v. 130, p. 216
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- Publication type:
- Article
Homozygous loss of menin is well tolerated in liver, a tissue not affected in MEN1.
- Published in:
- Mammalian Genome, 2004, v. 15, n. 11, p. 872, doi. 10.1007/s00335-004-2395-z
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- Article
Abolition of the expression of inhibitory guanine nucleotide regulatory protein G<sub>i</sub> activity in diabetes.
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- Nature, 1987, v. 327, n. 6119, p. 229, doi. 10.1038/327229a0
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- Article
Olfactory dysfunction in humans with deficient guanine nucleotide-binding protein.
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- Nature, 1986, v. 322, n. 6080, p. 635, doi. 10.1038/322635a0
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- Publication type:
- Article
2020 Extra: More NIH Heads View the Future.
- Published in:
- JAMA: Journal of the American Medical Association, 2000, v. 283, n. 6, p. 733, doi. 10.1001/jama.283.6.733
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- Publication type:
- Article
Functional Effects of Monoclonal Antibodies to the Purified Amino-Terminal Extracellular Domain of the Human Ca<sup>2+</sup> Receptor.
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- Journal of Bone & Mineral Research, 2007, v. 22, n. 4, p. 601, doi. 10.1359/JBMR.070111
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- Publication type:
- Article
Autosomal Dominant Hypocalcemia in Monozygotic Twins Caused by a De Novo Germline Mutation Near the Amino-Terminus of the Human Calcium Receptor.
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- Journal of Bone & Mineral Research, 2004, v. 19, n. 4, p. 578, doi. 10.1359/JBMR.040106
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- Article
Autosomal Dominant Hypocalcemia Caused by a Novel Mutation in the Loop 2 Region of the Human Calcium Receptor Extracellular Domain.
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- Journal of Bone & Mineral Research, 2002, v. 17, n. 8, p. 1461, doi. 10.1359/jbmr.2002.17.8.1461
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- Article
Monoclonal Antibodies Against Synthetic Peptides Corresponding to the Extracellular Domain of the Human Ca<sup>2+</sup> Receptor: Characterization and Use in Studying Concanavalin A Inhibition.
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- Journal of Bone & Mineral Research, 1997, v. 12, n. 11, p. 1780, doi. 10.1359/jbmr.1997.12.11.1780
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- Article
Discussion section I.
- Published in:
- Journal of Bone & Mineral Research, 1991, v. 6, n. S2, p. S31, doi. 10.1002/jbmr.5650061410
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- Publication type:
- Article
Pathophysiology of primary hyperparathyroidism.
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- Journal of Bone & Mineral Research, 1991, v. 6, n. S2, p. S15, doi. 10.1002/jbmr.5650061407
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- Publication type:
- Article
The Parathyroid/Pituitary Variant of Multiple Endocrine Neoplasia Type 1 Usually Has Causes Other than p27<sup>Kip1</sup> Mutations.
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- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 5, p. 1948, doi. 10.1210/jc.2006-2563
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- Article
Expression of the Calcium-Sensing Receptor in Gastrinomas.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 11, p. 4131, doi. 10.1210/jcem.85.11.6963
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- Article
Genotype/Phenotype Correlation of Multiple Endocrine Neoplasia Type 1 Gene Mutations in Sporadic Gastrinomas.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 1, p. 116, doi. 10.1210/jcem.85.1.6260
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- Publication type:
- Article
MEN1 Gene Analysis in Sporadic Adrenocortical Neoplasms*.
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- Journal of Clinical Endocrinology & Metabolism, 1999, v. 84, n. 1, p. 216, doi. 10.1210/jcem.84.1.5388
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- Article
Treatment of Hypercalcemia Secondary to Parathyroid Carcinoma with a Novel Calcimimetic Agent.
- Published in:
- 1998
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- Publication type:
- journal article
Sporadic Hypoparathyroidism Caused by de Novo Gain- of-Function Mutations of the Ca<sup>2+</sup>-Sensing Receptor.
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- Journal of Clinical Endocrinology & Metabolism, 1997, v. 82, n. 8, p. 2710, doi. 10.1210/jc.82.8.2710
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- Article
Heterogeneous size of the parathyroid glands in familial multiple endocrine neoplasia type 1.
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- Clinical Endocrinology, 1991, v. 35, n. 6, p. 521, doi. 10.1111/j.1365-2265.1991.tb00938.x
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- Article
Familial hypocalciuric hypercalcemia: recognition among patients referred after unsuccessful parathyroid exploration.
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- 1980
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- Publication type:
- journal article
Diagnosis of radiosensitive hypothalamic tumors without craniotomy: endocrine and neuroradiologic studies of intracranial atypical teratomas.
- Published in:
- 1976
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- Publication type:
- journal article
A double negative: inhibition of hepatic Gi signaling improves glucose homeostasis.
- Published in:
- 2018
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- Publication type:
- journal article
Spontaneous Intracellular Calcium Oscillations and G<sup>s</sup>α Subunit Expression are Inversely Correlated with Secretory Granule Content in Pituitary Cells.
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- Journal of Neuroendocrinology, 1992, v. 4, n. 4, p. 473, doi. 10.1111/j.1365-2826.1992.tb00195.x
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- Article
Following in the Footsteps of a "Neuroscience" Giant.
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- Einstein Journal of Biology & Medicine, 2006, v. 22, n. 2, p. 96
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- Article
Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.
- Published in:
- Human Mutation, 1998, v. 12, n. 2, p. 75, doi. 10.1002/(SICI)1098-1004(1998)12:2<75::AID-HUMU1>3.0.CO;2-T
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- Article
Common ancestral mutations in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1<sub>Burin</sub>) in four kindreds from Newfoundland.
- Published in:
- Human Mutation, 1998, v. 11, n. 4, p. 264, doi. 10.1002/(SICI)1098-1004(1998)11:4<264::AID-HUMU2>3.0.CO;2-V
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- Article
Structure and function of the human calcium-sensing receptor: insights from natural and engineered mutations and allosteric modulators.
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- Journal of Cellular & Molecular Medicine, 2007, v. 11, n. 5, p. 908, doi. 10.1111/j.1582-4934.2007.00096.x
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- Article
NIH research on obesity and type 2 diabetes: providing the scientific evidence base for actions to improve health.
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- Nature Medicine, 2006, v. 12, n. 1, p. 67, doi. 10.1038/nm0106-67
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- Article
Isolation, characterization, expression and functional analysis of the zebrafish ortholog of MEN1.
- Published in:
- Mammalian Genome, 2000, v. 11, n. 6, p. 448, doi. 10.1007/s003350010085
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- Article
Identification of MEN1 Gene Mutations in Sporadic Carcinoid Tumors of the Lung.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 13, p. 2285, doi. 10.1093/hmg/6.13.2285
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- Article
Germline Mutations of the MEN1 Gene in Familial Multiple Endocrine Neoplasia Type 1 and Related States.
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- Human Molecular Genetics, 1997, v. 6, n. 7, p. 1169, doi. 10.1093/hmg/6.7.1169
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- Publication type:
- Article
Novel mutations in the V2 vasopressin receptor gene of patients with X-linked nephrogenic diabetes insipidus.
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- Human Molecular Genetics, 1994, v. 3, n. 8, p. 1429
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- Publication type:
- Article
The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gsα gene: site-specific patterns and recurrent histological hallmarks.
- Published in:
- Journal of Pathology, 1999, v. 187, n. 2, p. 249, doi. 10.1002/(SICI)1096-9896(199901)187:2<249::AID-PATH222>3.0.CO;2-J
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- Publication type:
- Article