Dmrt1 is necessary for male sexual development in zebrafish
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چکیده
منابع مشابه
Zebrafish pitx3 is necessary for normal lens and retinal development
The human PITX3 gene encodes a bicoid-like homeodomain transcription factor associated with a variety of congenital ocular conditions, including anterior segment dysgenesis, Peter's anomaly, and cataracts. We identified a zebrafish pitx3 gene encoding a protein (Pitx3) that possesses 63% amino acid identity with human PITX3. The zebrafish pitx3 gene encompasses approximately 16.5kb on chromosom...
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Urodele amphibians and teleost fish regenerate amputated body parts via a process called epimorphic regeneration. A hallmark of this phenomenon is the reactivation of silenced developmental regulatory genes that previously functioned during embryonic patterning. We demonstrate that histone modifications silence promoters of numerous genes involved in zebrafish caudal fin regeneration. Silenced ...
متن کامل03-P091 COPII-dependent vesicular traffic is necessary for normal eye development in zebrafish
03-P089 A simple leaf with compound gene expression: Indeterminate leaves co-express ARP and KNOX genes Kanae Nishii, Michael Moeller, Catherine Kidner, Alberto Spada, Raffaella Mantegazza, Hao-Chun Hsu, Toshiyuki Nagata, Chun-Neng Wang 1 National Taiwan University, Taipei, Taiwan 2 Royal Botanic Garden Edinburgh, Edinburgh, United Kingdom 3 Milan University, Milan, Italy 4 Hosei University, To...
متن کاملcsrnp1a Is Necessary for the Development of Primitive Hematopoiesis Progenitors in Zebrafish
The CSRNP (cystein-serine-rich nuclear protein) transcription factors are conserved from Drosophila to human. Functional studies in mice, through knockout for each of their paralogs, have resulted insufficient to elucidate the function of this family of proteins in vertebrate development. Previously, we described the function of the zebrafish ortholog, Csnrp1/Axud1, showing its essential role i...
متن کاملWnt5a is necessary for normal kidney development in zebrafish and mice.
BACKGROUND Wnt5a is important for the development of various organs and postnatal cellular function. Little is known, however, about the role of Wnt5a in kidney development, although WNT5A mutations were identified in patients with Robinow syndrome, a genetic disease which includes developmental defects in kidneys. Our goal in this study was to determine the role of Wnt5a in kidney development....
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ژورنال
عنوان ژورنال: Developmental Biology
سال: 2017
ISSN: 0012-1606
DOI: 10.1016/j.ydbio.2016.12.008