Found: 24
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RFX transcription factors are essential for hearing in mice.
- Published in:
- Scientific Reports, 2015, p. 8549, doi. 10.1038/ncomms9549
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- Publication type:
- Article
Dissection of epistasis in oligogenic Bardet–Biedl syndrome.
- Published in:
- Nature, 2006, v. 439, n. 7074, p. 326, doi. 10.1038/nature04370
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- Publication type:
- Article
Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome.
- Published in:
- Nature, 2003, v. 425, n. 6958, p. 628, doi. 10.1038/nature02030
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- Publication type:
- Article
FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1.
- Published in:
- Nature Communications, 2016, v. 7, n. 4, p. 1, doi. 10.1038/ncomms10953
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- Publication type:
- Article
RFX transcription factors are essential for hearing in mice.
- Published in:
- Nature Communications, 2015, v. 6, n. 10, p. 8549, doi. 10.1038/ncomms9549
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- Publication type:
- Article
Genome-Wide Screen Identifies Drug-Induced Regulation of the Gene Giant Axonal Neuropathy (Gan) in a Mouse Model of Antiretroviral-Induced Painful Peripheral Neuropathy.
- Published in:
- Biological Research for Nursing, 2009, v. 11, n. 1, p. 7, doi. 10.1177/1099800409332726
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- Publication type:
- Article
Brain-derived neurotrophic factor modulates antiretroviral-induced mechanical allodynia in the mouse.
- Published in:
- Journal of Neuroscience Research, 2011, v. 89, n. 10, p. 1551, doi. 10.1002/jnr.22685
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- Publication type:
- Article
Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio.
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- G3: Genes | Genomes | Genetics, 2018, v. 8, n. 7, p. 2215, doi. 10.1534/g3.118.200144
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- Publication type:
- Article
Corrigendum: Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
- Published in:
- 2008
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- Correction notice
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome.
- Published in:
- Nature Genetics, 2008, v. 40, n. 4, p. 443, doi. 10.1038/ng.97
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- Publication type:
- Article
Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response.
- Published in:
- Nature Genetics, 2007, v. 39, n. 11, p. 1350, doi. 10.1038/ng.2007.12
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- Publication type:
- Article
BBS10 encodes a vertebrate-specific chaperonin-like protein and is a major BBS locus.
- Published in:
- Nature Genetics, 2006, v. 38, n. 5, p. 521, doi. 10.1038/ng1771
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- Publication type:
- Article
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.
- Published in:
- Nature Genetics, 2005, v. 37, n. 10, p. 1135, doi. 10.1038/ng1644
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- Publication type:
- Article
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.
- Published in:
- Nature Genetics, 2005, v. 37, n. 3, p. 275, doi. 10.1038/ng1511
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- Publication type:
- Article
Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse.
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- Nature Genetics, 2004, v. 36, n. 9, p. 994, doi. 10.1038/ng1418
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- Publication type:
- Article
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.
- Published in:
- Nature Genetics, 2004, v. 36, n. 5, p. 462, doi. 10.1038/ng1352
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- Publication type:
- Article
An Essential Role for DYF-11/MIP-T3 in Assembling Functional Intraflagellar Transport Complexes.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 3, p. 1, doi. 10.1371/journal.pgen.1000044
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- Publication type:
- Article
A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 2, p. 318, doi. 10.1111/cge.13878
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- Publication type:
- Article
<i>BBS4</i> Is Necessary for Ciliary Localization of TrkB Receptor and Activation by BDNF.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098687
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- Publication type:
- Article
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators.
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- 2014
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- Publication type:
- journal article
Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators.
- Published in:
- Journal of Clinical Investigation, 2014, v. 124, n. 5, p. 2059, doi. 10.1172/JCI71898
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- Publication type:
- Article
ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response.
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- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-10967-7
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- Publication type:
- Article
Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 13, p. 2212, doi. 10.1093/hmg/ddz053
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- Publication type:
- Article
Differential effects on β-cell mass by disruption of Bardet--Biedl syndrome or Alstrom syndrome genes.
- Published in:
- Human Molecular Genetics, 2016, v. 25, n. 1, p. 57, doi. 10.1093/hmg/ddv447
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- Publication type:
- Article