Found: 13
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Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 6, p. 1287, doi. 10.1093/hmg/ddr558
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- Publication type:
- Article
The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.
- Published in:
- Clinical Genetics, 2021, v. 99, n. 5, p. 684, doi. 10.1111/cge.13927
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- Publication type:
- Article
Genomic duplication in the 19q13.42 imprinted region identified as a new genetic cause of intrauterine growth restriction.
- Published in:
- Clinical Genetics, 2018, v. 94, n. 6, p. 575, doi. 10.1111/cge.13449
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- Publication type:
- Article
Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome.
- Published in:
- Human Genetics, 2021, v. 140, n. 7, p. 1031, doi. 10.1007/s00439-021-02270-7
- By:
- Publication type:
- Article
Escherichia coli Producing CNF1 Toxin Hijacks Tollip to Trigger Rac1-Dependent Cell Invasion.
- Published in:
- Traffic, 2011, v. 12, n. 5, p. 579, doi. 10.1111/j.1600-0854.2011.01174.x
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- Publication type:
- Article
Activated Rac1, but not the tumorigenic variant Rac1b, is ubiquitinated on Lys 147 through a JNK-regulated process.
- Published in:
- FEBS Journal, 2008, v. 275, n. 2, p. 386, doi. 10.1111/j.1742-4658.2007.06209.x
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- Publication type:
- Article
BAF60A mediates interactions between the microphthalmia‐associated transcription factor and the BRG1‐containing SWI/SNF complex during melanocyte differentiation.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 7, p. 11780, doi. 10.1002/jcp.27840
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- Publication type:
- Article
Enhanced apoptosis in the thymus of transgenic mice expressing constitutively activated forms of human Rac2GTPase.
- Published in:
- Oncogene, 1997, v. 15, n. 5, p. 601, doi. 10.1038/sj.onc.1201378
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- Publication type:
- Article
Corrigendum: Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.
- Published in:
- Human Molecular Genetics, 2019, v. 28, n. 6, p. 1052, doi. 10.1093/hmg/ddy368
- By:
- Publication type:
- Article
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 7, p. 1196, doi. 10.1093/hmg/ddy034
- By:
- Publication type:
- Article
The SWI/SNF protein BAF60b is ubiquitinated through a signalling process involving Rac GTPase and the RING finger protein Unkempt.
- Published in:
- FEBS Journal, 2010, v. 277, n. 6, p. 1453, doi. 10.1111/j.1742-4658.2010.07575.x
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- Publication type:
- Article