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Most of the coding region of rat ACTHβ-LPH precursor gene lacks intervening sequences.
- Published in:
- Nature, 1980, v. 288, n. 5791, p. 610, doi. 10.1038/288610a0
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- Publication type:
- Article
Ptx1 regulates SF-1 activity by an interaction that mimics the role of the ligand-binding domain.
- Published in:
- EMBO Journal, 1999, v. 18, n. 12, p. 3431, doi. 10.1093/emboj/18.12.3431
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- Publication type:
- Article
Molecular Determinants for Cell Specificity and Glucocorticoid Repression of the Proopiomelanocortin Gene<sup>a</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1993, v. 680, n. 1, p. 663, doi. 10.1111/j.1749-6632.1993.tb19768.x
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- Publication type:
- Article
Récepteurs à la Provençale.
- Published in:
- 2003
- By:
- Publication type:
- Report
Control of mouse limb initiation and antero-posterior patterning by Meis transcription factors.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23373-9
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- Publication type:
- Article
The Cables1 Gene in Glucocorticoid Regulation of Pituitary Corticotrope Growth and Cushing Disease.
- Published in:
- 2016
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- Publication type:
- journal article
Severe Cortisol Deficiency Associated with Reversible Growth Hormone Deficiency in Two Infants: What Is the Link?
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 9, p. 2670, doi. 10.1210/jc.2011-0129
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- Publication type:
- Article
Formation and Differentiation of Multiple Mesenchymal Lineages during Lung Development Is Regulated by β-catenin Signaling.
- Published in:
- PLoS ONE, 2008, v. 3, n. 1, p. 1, doi. 10.1371/journal.pone.0001516
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- Publication type:
- Article
The TPIT Gene Mutation M86R Associated with Isolated Adrenocorticotropin Deficiency Interferes with Protein: Protein Interactions.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 10, p. 3991, doi. 10.1210/jc.2007-0284
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- Publication type:
- Article
Differential Regulation of Proopiomelanocortin and Pituitary-Restricted Transcription Factor (TPIT), a New Marker of Normal and Adenomatous Human Corticotrophs.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 7, p. 3050, doi. 10.1210/jc.2002-021934
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- Publication type:
- Article
Gene structure of human cardiac hormone precursor, pronatriodilatin.
- Published in:
- Nature, 1984, v. 312, n. 5995, p. 654, doi. 10.1038/312654a0
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- Publication type:
- Article
Pituitary cell translation and secretory capacities are enhanced cell autonomously by the transcription factor Creb3l2.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11894-3
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- Publication type:
- Article
Pioneer and nonpioneer factor cooperation drives lineage specific chromatin opening.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11791-9
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- Publication type:
- Article
Pioneer transcription factors in pituitary development and tumorigenesis.
- Published in:
- European Journal of Endocrinology, 2021, v. 184, n. 1, p. R1, doi. 10.1530/EJE-20-0866
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- Publication type:
- Article
Pro-opiomelanocortin gene: A model for negative regulation of transcription by glucocorticoids.
- Published in:
- Journal of Cellular Biochemistry, 1987, v. 35, n. 4, p. 293, doi. 10.1002/jcb.240350404
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- Publication type:
- Article
The transcription factor Pitx3 is expressed selectively in midbrain dopaminergic neurons susceptible to neurodegenerative stress.
- Published in:
- Journal of Neurochemistry, 2013, v. 125, n. 6, p. 932, doi. 10.1111/jnc.12160
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- Publication type:
- Article
Human iPSC-derived Down syndrome astrocytes display genome-wide perturbations in gene expression, an altered adhesion profile, and increased cellular dynamics.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 5, p. 785, doi. 10.1093/hmg/ddaa003
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- Publication type:
- Article
Pitx1 in vivo Promoter Activity and Mechanisms of Positive Autoregulation.
- Published in:
- Neuroendocrinology, 2003, v. 78, n. 3, p. 129, doi. 10.1159/000072794
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- Publication type:
- Article
Transcriptional Properties of Ptx1 and Ptx2 Isoforms.
- Published in:
- Neuroendocrinology, 2000, v. 71, n. 5, p. 277, doi. 10.1159/000054547
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- Publication type:
- Article
Chromatin opening ability of pioneer factor Pax7 depends on unique isoform and C-terminal domain.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. 14, p. 7254, doi. 10.1093/nar/gkad520
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- Publication type:
- Article
Pax7 pioneer factor action requires both paired and homeo DNA binding domains.
- Published in:
- Nucleic Acids Research, 2021, v. 49, n. 13, p. 7424, doi. 10.1093/nar/gkab561
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- Publication type:
- Article
Rgs6 is Required for Adult Maintenance of Dopaminergic Neurons in the Ventral Substantia Nigra.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 12, p. 1, doi. 10.1371/journal.pgen.1004863
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- Publication type:
- Article
Regulatory Network Analyses Reveal Genome-Wide Potentiation of LIF Signaling by Glucocorticoids and Define an Innate Cell Defense Response.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 10, p. 1, doi. 10.1371/journal.pgen.1000224
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- Publication type:
- Article
Neuroendocrine dysplasia in mice lacking protein tyrosine phosphatase σ.
- Published in:
- Nature Genetics, 1999, v. 21, n. 3, p. 330, doi. 10.1038/6859
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- Publication type:
- Article
Striatal neuroadaptation and rescue of locomotor deficit by l-dopa in aphakia mice, a model of Parkinson's disease.
- Published in:
- Journal of Neurochemistry, 2006, v. 96, n. 1, p. 160, doi. 10.1111/j.1471-4159.2005.03522.x
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- Publication type:
- Article
Pitx3 activates mouse tyrosine hydorxylase promoter via at high-affinity binding site.
- Published in:
- Journal of Neurochemistry, 2001, v. 77, n. 2, p. 558, doi. 10.1046/j.1471-4159.2001.00257.x
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- Publication type:
- Article
Specificity of Pitx3-Dependent Gene Regulatory Networks in Subsets of Midbrain Dopamine Neurons.
- Published in:
- Molecular Neurobiology, 2017, v. 54, n. 7, p. 4921, doi. 10.1007/s12035-016-0040-y
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- Publication type:
- Article
HOX13-dependent chromatin accessibility underlies the transition towards the digit development program.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16317-2
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- Publication type:
- Article
Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.
- Published in:
- BMC Medical Genetics, 2014, v. 15, n. 1, p. 156, doi. 10.1186/s12881-014-0139-9
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- Publication type:
- Article