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Title: Molecular basis of Bardet-Biedl syndrome caused by defects of intraflagellar transport complex IFT-B
Other Titles: 繊毛内タンパク質輸送複合体IFT-Bの欠陥に起因する繊毛病バルデー・ビードル症候群の発症の分子基盤
Authors: Zhou, Zhuang
Author's alias: 周, 壮
Keywords: Cilia
Bardet-Biedl Syndrome
IFT-B complex
intraflagellar transport
Issue Date: 26-Sep-2022
Publisher: Kyoto University
Conferring University: 京都大学
Degree Level: 新制・課程博士
Degree Discipline: 博士(薬科学)
Degree Report no.: 甲第24205号
Degree no.: 薬科博第158号
Conferral date: 2022-09-26
Degree Call no.: 新制||薬科||17(附属図書館)
Degree Affiliation: 京都大学大学院薬学研究科薬科学専攻
Examination Committee members: (主査)教授 中山 和久, 教授 井垣 達吏, 教授 土居 雅夫
Provisions of the Ruling of Degree: 学位規則第4条第1項該当
Rights: 許諾条件により本文は2023-09-26に公開
This research was partly published in Human Molecular Genetics. Impaired cooperation between IFT74/BBS22–IFT81 and IFT25–IFT27/BBS19 causes Bardet-Biedl syndrome. Zhuang Zhou, Hantian Qiu, Roiner-Francisco Castro-Araya, Ryota Takei, Kazuhisa Nakayama, and Yohei Katoh Human Molecular Genetics (2022) 31, 1681–1693. doi:10.1093/hmg/ddab354.
DOI: 10.14989/doctor.k24205
Appears in Collections:080_1 Doctoral Dissertation (Pharmaceutical Sciences)

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