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Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders.
- Published in:
- 2021
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- Publication type:
- journal article
Conditional Gata2 inactivation results in HSC loss and lymphatic mispatterning.
- Published in:
- Journal of Clinical Investigation, 2012, v. 122, n. 10, p. 3705, doi. 10.1172/JCI61619
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- Publication type:
- Article
PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells.
- Published in:
- eLife, 2016, p. 1, doi. 10.7554/eLife.14470
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- Publication type:
- Article
The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing.
- Published in:
- eLife, 2015, p. 1, doi. 10.7554/eLife.08627
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- Publication type:
- Article
Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21712-4
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- Publication type:
- Article
Sox3 and sexual dysfunction: it's in the head.
- Published in:
- Nature Genetics, 2004, v. 36, n. 3, p. 217, doi. 10.1038/ng0304-217
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- Publication type:
- Article
β-catenin is required in the neural crest and mesencephalon for pituitary gland organogenesis.
- Published in:
- BMC Developmental Biology, 2016, v. 16, p. 1, doi. 10.1186/s12861-016-0118-9
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- Publication type:
- Article
The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model
- Published in:
- BMC Developmental Biology, 2015, v. 15, n. 1, p. 30, doi. 10.1186/s12861-015-0080-y
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- Publication type:
- Article
The pattern of congenital heart defects arising from reduced Tbx5 expression is altered in a Down syndrome mouse model.
- Published in:
- BMC Developmental Biology, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12861-015-0080-y
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- Publication type:
- Article
Multi-omic profiling of pituitary thyrotropic cells and progenitors.
- Published in:
- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01009-0
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- Publication type:
- Article
Efficient, specific, developmentally appropriate cre-mediated recombination in anterior pituitary gonadotropes and thyrotropes.
- Published in:
- Genesis: The Journal of Genetics & Development, 2013, v. 51, n. 11, p. 785, doi. 10.1002/dvg.22425
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- Publication type:
- Article
Hypomorphic phenotype in mice with pituitary-specific knockout of steroidogenic factor 1.
- Published in:
- Genesis: The Journal of Genetics & Development, 2001, v. 30, n. 2, p. 65, doi. 10.1002/gene.1034
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- Publication type:
- Article
Cre-mediated recombination in the pituitary gland.
- Published in:
- Genesis: The Journal of Genetics & Development, 2000, v. 28, n. 3/4, p. 167, doi. 10.1002/1526-968X(200011/12)28:3/4<167::AID-GENE120>3.0.CO;2-N
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- Publication type:
- Article
Knockout mice with pituitary malformations help identify human cases of hypopituitarism.
- Published in:
- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01347-y
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- Publication type:
- Article
Aged PROP1 Deficient Dwarf Mice Maintain ACTH Production.
- Published in:
- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0028355
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- Publication type:
- Article
A Transient Transgenic RNAi Strategy for Rapid Characterization of Gene Function during Embryonic Development.
- Published in:
- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014375
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- Publication type:
- Article
SnoRNA Snord116 (Pwcr1/MBII-85) Deletion Causes Growth Deficiency and Hyperphagia in Mice.
- Published in:
- PLoS ONE, 2008, v. 3, n. 3, p. 1, doi. 10.1371/journal.pone.0001709
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- Publication type:
- Article
Pituitary Neoplasm Nomenclature Workshop: Does Adenoma Stand the Test of Time?
- Published in:
- Journal of the Endocrine Society, 2021, v. 5, n. 3, p. 1, doi. 10.1210/jendso/bvaa205
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- Publication type:
- Article
Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid Pit1<sup>dw</sup> Mutants.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 4, p. 1212, doi. 10.1523/JNEUROSCI.4957-08.2009
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- Publication type:
- Article
Novel mechanism of pituitary hormone deficiency: genetic variants shift splicing to produce a dominant negative transcription factor isoform.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 6, p. C19, doi. 10.1530/EJE-21-0949
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- Publication type:
- Article
The phenotypic spectrum associated with OTX2 mutations in humans.
- Published in:
- European Journal of Endocrinology, 2021, v. 185, n. 1, p. 121, doi. 10.1530/EJE-20-1453
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- Publication type:
- Article
Novel Candidate Regulators and Developmental Trajectory of Pituitary Thyrotropes.
- Published in:
- Endocrinology, 2023, v. 164, n. 6, p. 1, doi. 10.1210/endocr/bqad076
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- Publication type:
- Article
Disruption of RNA Splicing Is an Important Contributor to Congenital Hypopituitarism and Other Human Genetic Diseases.
- Published in:
- Endocrinology, 2023, v. 164, n. 5, p. 1, doi. 10.1210/endocr/bqad039
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- Publication type:
- Article
Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling.
- Published in:
- Endocrinology, 2023, v. 164, n. 3, p. 1, doi. 10.1210/endocr/bqad016
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- Publication type:
- Article
Pituitary Tumors and Immortalized Cell Lines Generated by Cre-Inducible Expression of SV40 T Antigen.
- Published in:
- Endocrinology, 2021, v. 162, n. 7, p. 1, doi. 10.1210/endocr/bqab073
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- Publication type:
- Article
PROP1-Dependent Retinoic Acid Signaling Regulates Developmental Pituitary Morphogenesis and Hormone Expression.
- Published in:
- Endocrinology, 2020, v. 161, n. 2, p. 1, doi. 10.1210/endocr/bqaa002
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- Publication type:
- Article
Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors.
- Published in:
- 2020
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- Publication type:
- journal article
Ash1l controls quiescence and self-renewal potential in hematopoietic stem cells.
- Published in:
- Journal of Clinical Investigation, 2015, v. 125, n. 5, p. 2007, doi. 10.1172/JCI78124
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- Publication type:
- Article
Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 3, p. 367, doi. 10.1093/hmg/ddac192
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- Publication type:
- Article
WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth.
- Published in:
- Developmental Dynamics, 2008, v. 237, n. 6, p. spc1, doi. 10.1002/dvdy.21603
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- Publication type:
- Article
WNT signaling affects gene expression in the ventral diencephalon and pituitary gland growth.
- Published in:
- Developmental Dynamics, 2008, v. 237, n. 4, p. 1006, doi. 10.1002/dvdy.21511
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- Publication type:
- Article
Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.
- Published in:
- 2012
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- Publication type:
- journal article
Genetic Background of Prop1 Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment.
- Published in:
- JARO - Journal of the Association for Research in Otolaryngology, 2012, v. 13, n. 2, p. 173, doi. 10.1007/s10162-011-0302-3
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- Publication type:
- Article
Age-Related Changes in Cochlear Gene Expression In Normal and Shaker 2 Mice.
- Published in:
- JARO - Journal of the Association for Research in Otolaryngology, 2006, v. 7, n. 3, p. 317, doi. 10.1007/s10162-006-0046-7
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- Publication type:
- Article
Next generation sequencing panel based on single molecule molecular inversion probes for detecting genetic variants in children with hypopituitarism.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 4, p. 514, doi. 10.1002/mgg3.395
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- Publication type:
- Article
Otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 10, p. 1648, doi. 10.1093/hmg/ddaa064
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- Publication type:
- Article
Deletion of OTX2 in neural ectoderm delays anterior pituitary development.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 4, p. 939, doi. 10.1093/hmg/ddu506
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- Publication type:
- Article
A novel loss-of-function mutation in Npr2 clarifies primary role in female reproduction and reveals a potential therapy for acromesomelic dysplasia, Maroteaux type.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 2, p. 345, doi. 10.1093/hmg/dds432
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- Publication type:
- Article
Cocaine-and Amphetamine Regulated Transcript (CART) Peptide Is Expressed in Precursor Cells and Somatotropes of the Mouse Pituitary Gland.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0160068
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- Publication type:
- Article
Transgenic mice expressing LHX3 transcription factor isoforms in the pituitary: Effects on the gonadotrope axis and sex-specific reproductive disease.
- Published in:
- Journal of Cellular Physiology, 2007, v. 212, n. 1, p. 105, doi. 10.1002/jcp.21010
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- Publication type:
- Article
Genetic variation in thyroid folliculogenesis influences susceptibility to hypothyroidism-induced hearing impairment.
- Published in:
- Mammalian Genome, 2019, v. 30, n. 1/2, p. 5, doi. 10.1007/s00335-019-09792-6
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- Publication type:
- Article
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.
- Published in:
- Mammalian Genome, 2007, v. 18, n. 8, p. 596, doi. 10.1007/s00335-007-9038-0
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- Publication type:
- Article
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line.
- Published in:
- Mammalian Genome, 2007, v. 18, n. 8, p. 549, doi. 10.1007/s00335-007-9054-0
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- Publication type:
- Article
Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene.
- Published in:
- Mammalian Genome, 2007, v. 18, n. 6/7, p. 521, doi. 10.1007/s00335-007-9008-6
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- Publication type:
- Article
19th International Mouse Genome Conference.
- Published in:
- Mammalian Genome, 2006, v. 17, n. 5, p. 355, doi. 10.1007/s00335-005-1900-3
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- Publication type:
- Article
Identification of members of the Wnt signaling pathway in the embryonic pituitary gland.
- Published in:
- Mammalian Genome, 2001, v. 12, n. 11, p. 843, doi. 10.1007/s00335-001-2076-0
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- Publication type:
- Article
Molecular basis of pituitary dysfunction in mouse and human.
- Published in:
- Mammalian Genome, 2001, v. 12, n. 7, p. 485, doi. 10.1007/s003350040002
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- Publication type:
- Article
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 01, doi. 10.3389/fendo.2022.1008306
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- Publication type:
- Article
Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system.
- Published in:
- European Journal of Neuroscience, 2007, v. 25, n. 4, p. 999, doi. 10.1111/j.1460-9568.2007.05332.x
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- Publication type:
- Article