A 1.5-Mb PAC/BAC Contig Spanning the Prader-Willi Syndrome Critical Region (PWCR)
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概要
- 論文の詳細を見る
Prader-Willi syndrome (PWS) is a multiple anomalies/mental retardation syndrome. The putative PWS gene(s) remains unknown, and its occurrence is based on genomic imprinting at chromosome 15q11-q13. We have constructed a 1.5- Mb, fine, physical map of PWS critical region (PWCR) between two markers, D15S9 and D15S174 at 15q11-q13. The map is composed of 32 PAC and 3 BAC clones without any gaps. By the PAC/BAC-end sequencing procedure, a total of 26 sequence tag site (STS) markers were newly generated, and 5 expressed sequence tags (ESTs) were mapped in the region. The contig map was verified by both STS and fluorescence in situ hybridization analyses. Our map has higher resolution, compared with a previous YAC-based map of PWCR. It is useful for further genome analysis, especially on genomic imprinting of this region.
- 長崎大学の論文
著者
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Kishino T
Department Of Pediatrics Nagasaki University School Of Medicine
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Kondoh Tatsuro
長崎大学 医学部小児科
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Kondoh Tatsuro
長崎大学 看
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Kondoh Tatsuro
長崎大学 医歯薬学研究科人類遺伝学
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Kondoh Tatsuro
東北大学 医学部遺伝病学分野
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Yoshiura Koh-ichiro
長崎大学 医歯薬学総合研究科人類遺伝学
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Yoshiura Koh‐ichiro
Jst‐sorst Kawaguchi Jpn
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Niikawa Norio
長崎大学 医歯薬学総合研究科人類遺伝学
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Niikawa N
The Research Institute Of Personalized Health Sciences Health Sciences University Of Hokkaido
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KONDO Shinji
Department of Pediatrics, The University of Iowa, Iowa City
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Matsumoto Naomichi
長崎大学 医歯薬学研究科人類遺伝学
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Yoshimura Shuichiro
長崎大学 医歯薬学総合研究科人類遺伝学
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Kondo Shinji
Division Of Functional Genomics Center For Frontier Life Sciences Nagasaki University
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Kondoh Shinji
長崎大学 大学院生物医学科学
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Kudo T
Department Of Medical Genetics Tohoku University School Of Medicine
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Tomita Hiro-Aki
Department of Plastic and Reconstructive Surgery, Nagasaki University School of Medicine
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Kishino Tatsuya
Department of Ophthalmology, Nagasaki University School of Medicine
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Yoshiura Koh-ichiro
RIKEN Gene Bank, Institute of Physical and Chemical Research
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Yamada Koki
Department of Human Genetics, University of Chicago
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Soeda Eiichi
Department of Genetics, Case Western Reserve University
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Kudo Takayuki
Department Of Otorhinolaryngology Tohoku University School Of Medicine
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Ohta T
Sorst Japan Science And Technology Agency
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YAMASAKI Kentaro
Department of Obstetrics and Gynecology, Nagasaki University Graduate School of Biomedical Sciences
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Kayashima Tomohiko
Department Of Human Genetics Nagasaki University School Of Medicine
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Tomita Hiro-aki
Nagasaki Prefectural Medical Health Center
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Yamada Koki
Department Of Human Genetics University Of Chicago
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Soeda Eiichi
Department Of Applied Microbial Technology Kumamoto Institute Of Technology
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Soeda Eiichi
Department Of Genetics Case Western Reserve University
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Tomita Hiro-aki
Department Of Physiology And Biophysics Med Sci I D-335 University Of California
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Yoshiura Koh-ichiro
Department Of Human Genetics Nagasaki University Graduate School Of Biomedical Sciences
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Kondoh Tatsuro
Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences
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Kondo Shinji
Department Of Pediatrics The University Of Iowa Iowa City
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Ozawa Hiroki
Department Of Psychiatry Nagasaki University Hospital
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Tomita Hiroaki
Department Of Biological Psychiatry Tohoku University Graduate School Of Medicine
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Yoshiura Kohichiro
RIKEN Gene Bank, Institute of Physical and Chemical Research
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KONDO Shinji
Department of Applied Chemistry, Muroran Institute of Technology
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