Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shinji Saitoh"'
Autor:
Yongming Sun, Shinji Saitoh, Bryan E. Hainline, Catherine G. Palmer, Robert D. Nicholls, Merlin G. Butler
Publikováno v:
Human Molecular Genetics. 5:517-524
A patient with Prader-Willi syndrome (PWS) was found to carry a de novo balanced reciprocal translocation, t(15;19)(q12;q13.41), which disrupted the small nuclear ribonucleoprotein N (SNRPN) locus. The translocation chromosome 15 was found to be pate
Autor:
Akira Kuwano, David H. Ledbetter, N. Niikawa, Shinji Saitoh, Apiwat Mutirangura, Karin Buiting, Bernhard Horsthemke, Bärbel Dittrich, A.C. Chinault, Frank Greenberg, Susan A. Ledbetter
Publikováno v:
Human Molecular Genetics. 1:417-425
Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct mental retardation disorders associated with deletions of proximal 15q (q11-q13) of different parental origin. Yeast artificial chromosome (YAC) clones were isolated for 9 previously
Autor:
Shinji Saitoh, Yonggang Ji, Daniel J. Driscoll, Michelle T.C. Jong, Todd A. Gray, Robert D. Nicholls, Christopher C. Glenn
Publikováno v:
Human molecular genetics. 8(5)
We describe a complex imprinted locus in chromosome 15q11-q13 that encodes two genes, ZNF127 and ZNF127AS. The ZNF127 gene encodes a protein with a RING (C3HC4) zinc-finger and multiple C3H zinc-finger motifs, the former being closely related to a pr
Publikováno v:
Human Molecular Genetics. 3:1912-1912