HASHIMURA Yuya 橋村裕也

Researcher Number	80457077
Affiliation (based on the past Project Information) *help	2010: 神戸大学, 大学院・医学研究科, 助教
Review Section/Research Field	Except Principal Investigator Kidney internal medicine
Keywords	Except Principal Investigator 多嚢胞性異形成腎(MCDK) / TCF2 / genome-wide CNV array / copy number variation(CNV) / microduplication / microdeletion / copy number variation (CNV) / 先天性腎尿路奇形(CAKUT) / 原因遺伝子 / CNV解析 / 先天性腎尿路奇形

Identification of novel genes for congenital anomalies of Kidney and urinary tract (CAKUT) by CNV analyses and development of comprehensive gene testing for CAKUT
- Principal Investigator
  
  IIJIMA Kazumoto
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Kobe University

All 2011 2010 2009 2008

All Journal Article Presentation

[Journal Article] The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies.2010
- Author(s)
  Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M.
- Journal Title
  
  J Clin Endocrinol Metab. 95(12)
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 集学的治療により救命しえたPotter sequenceの1例2010
- Author(s)
  忍頂寺毅史, 藤岡一路, 橋村裕也, 貝藤裕史, 森岡一朗, 野津寛大, 横山直樹, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎不全学会雑誌
  
  Volume: 30 Pages: 178-180
- NAID
  10027697824
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 24(6)
  
  Pages: 1181-1186
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 溶血性尿毒症症候群発症8年後より高度蛋白尿を呈し、糸球体硬化および著明な間質の線維化を認めた1例2009
- Author(s)
  橋村裕也, 野津寛大, 忍頂寺毅史, 貝藤裕史, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 183-187
- NAID
  10026411977
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009
- Author(s)
  Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Hum Genet 126
  
  Pages: 533-538
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.2009
- Author(s)
  Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
- Journal Title
  
  BMC Nephrol 14
  
  Pages: 10-37
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] IPEX症候群と腎疾患2009
- Author(s)
  橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 金兼弘和, 宮脇利男, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 131-135
- NAID
  10026411780
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene2009
- Author(s)
  Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
- Journal Title
  
  BMC Nephrol 10
  
  Pages: 37-37
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Minimal change nephrotic syndrome associated with IPEX syndrome.2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iiiima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 偽性低アルドステロン症I型2009
- Author(s)
  神田杏子, 野津寛大, 橋村裕也, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 123-125
- NAID
  10026411765
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.2009
- Author(s)
  Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Hum Genet 126(4)
  
  Pages: 533-538
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 1181-1186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008
- Author(s)
  Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iiiima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 23
  
  Pages: 2085-2090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008
- Author(s)
  Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol. 23(11)
  
  Pages: 2085-2090
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Nutcracker症候群を合併した軽症IgA腎症の1例2011
- Author(s)
  石森真吾、大坪裕美、橋本総子、橋村裕也、貝藤裕史、森貞直哉、飯島一誠、松尾雅文
- Organizer
  第24回近畿小児科学会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2011-03-12
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] レシピエント選定基準改定後に経験した小児献腎移植の5例2010
- Author(s)
  忍頂寺毅史、橋村裕也、貝藤裕史、野津寛大、飯島一誠、松尾雅文
- Organizer
  第113回日本小児科学会学術集会
- Place of Presentation
  いわて県民情報交流センター(岩手県)
- Year and Date
  2010-04-25
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 常染色体性Alport症候群の臨床および分子生物学的検討2010
- Author(s)
  岡政史、野津寛大、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical Characteristics of Genetically-Proven Gitelman's Syndrome2010
- Author(s)
  Kaito H,Nozu N,Hashimura Y,Oka M,Ninchoji T,Nakanishi K,Yoshikawa N,Iijima K,Matsuo M
- Organizer
  the 15th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  New York Hilton(アメリカ)
- Year and Date
  2010-08-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝子解析で確定診断しえたGitelman症候群31例の臨床的検討2010
- Author(s)
  貝藤裕史、野津寛大、橋村裕也、岡政史、忍頂寺毅史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Treatment Strategy and Outcome for Henoch-Schonlein Purpura Nephritis2010
- Author(s)
  Ninchoj T, Hashimura Y, Kaito H, Nozu N, Kanda, K, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Iijima K, Yoshikawa N, Matsuo M
- Organizer
  the 15th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  New York Hilton(アメリカ)
- Year and Date
  2010-08-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome2010
- Author(s)
  Iijima K, Oka M, Hashimura Y, Otsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M
- Organizer
  Renal Week 2010
- Place of Presentation
  Colorado Convention Center(アメリカ)
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome.2010
- Author(s)
  Iijima K, Oka M, Hashimura Y, Ohtsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M.
- Organizer
  American Society of Nephrology 2010 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型Alport症候群の臨床的検討2010
- Author(s)
  橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、中西浩一、吉川徳茂、松尾雅文
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 平滑筋腫合併アルポート症候群(DL-AS)の遺伝学的検討2010
- Author(s)
  岡政史、野津寛大、森貞直哉、平野大志、藤永周一郎、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型Alport症候群と血友病Aを合併した一男児例-同胞男児間における表現型の差異についての分子遺伝学的検討-2010
- Author(s)
  橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] A Deep Intronic Mutation in the SLC12A3 Gene leads to Gitelman Syndrome.2009
- Author(s)
  Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M.
- Organizer
  American Society of Nephrology 2009 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome2009
- Author(s)
  Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M
- Organizer
  American Society of Nephrology 2009 Annual Meeting
- Place of Presentation
  San Diego Convention Center(America)
- Year and Date
  2009-10-30
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための in vivo および in vitro の実験系の確立2009
- Author(s)
  野津寛大, 野津圭美, 齋木加代子, 西田篤丈, 貝藤裕史, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 河井和夫, 竹島泰弘, 飯島一誠, 松尾雅文
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] IPEX 症候群に微小変化型ネフローゼ症候群を合併した1症例2009
- Author(s)
  橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] NR3C2遺伝子変異に伴いmRNAに splicing 異常を認めたにも関わらず軽症であった偽性低アルドステロン症1型の親子例2009
- Author(s)
  神田杏子, 野津寛大, 橋村裕也, 三輪明弘, 森岡一朗, 横山直樹, 飯島一誠, 松尾雅文
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群(XLAS)の分子遺伝学的検討2009
- Author(s)
  野津寛大, 貝藤裕史, 神田杏子, 橋村裕也, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための実験系の確立2009
- Author(s)
  野津寛大, 貝藤裕史, 橋村裕也, 忍頂寺毅史, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第39回日本腎臓学会西部学術大会
- Place of Presentation
  和歌山県民文化会館(和歌山県)
- Year and Date
  2009-10-17
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討2009
- Author(s)
  野津寛大, Krol Rafal, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
- Organizer
  第112回日本小児科学会学術集会
- Place of Presentation
  奈良県立文化会館(奈良県)
- Year and Date
  2009-04-17
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 等張性輸液は手術後の低ナトリウム(Na)血症を防止する2009
- Author(s)
  橋村裕也, 神田杏子, 野津寛大, 飯島一誠, 松尾雅文
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-03
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 腎不全に至ったステロイド感受性微小変化型ネフローゼ症候群の1例2009
- Author(s)
  橋村裕也, 忍頂寺毅史, 貝藤裕史, 野津寛大, 飯島一誠, 中西浩一, 吉川徳茂, 松尾雅文
- Organizer
  第39回日本腎臓学会西部学術大会
- Place of Presentation
  和歌山県民文化会館(和歌山県)
- Year and Date
  2009-10-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討.2008
- Author(s)
  野津寛大, KrolRafal, 貝藤裕史, 神田杏子, 橋村裕也, 松尾雅文, 中西浩一, 吉川徳茂, 飯島一誠.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Somatic Mosaicism for a Mutation of the COL4A5 Gene in Three Sporadic X-Linked Alport Syndrome Cases.2008
- Author(s)
  Nozu K, Krol PR, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Hashimura Y, Iijima K, Matsuo M.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-08
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome2008
- Author(s)
  Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-06
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.2008
- Author(s)
  Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240

1. IIJIMA Kazumoto (00240854)

# of Collaborated Projects: 1 results

# of Collaborated Products: 39 results
2. NAGATA Michio (10192238)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. NAKAYAMA Makioko (80469999)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. MORISADA Naoya (00389446)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. NOZU Kandai (70362796)

# of Collaborated Projects: 1 results

# of Collaborated Products: 38 results

HASHIMURA Yuya 橋村 裕也

Research Projects

Research Products

Co-Researchers

Identification of novel genes for congenital anomalies of Kidney and urinary tract (CAKUT) by CNV analyses and development of comprehensive gene testing for CAKUT

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies.2010

Author(s)

Journal Title

Data Source

[Journal Article] 集学的治療により救命しえたPotter sequenceの1例2010

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.2009

Author(s)

Journal Title

Data Source

[Journal Article] 溶血性尿毒症症候群発症8年後より高度蛋白尿を呈し、糸球体硬化および著明な間質の線維化を認めた1例2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009

Author(s)

Journal Title

Data Source

[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.2009

Author(s)

Journal Title

Data Source

[Journal Article] IPEX症候群と腎疾患2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene2009

Author(s)

Journal Title

Data Source

[Journal Article] Minimal change nephrotic syndrome associated with IPEX syndrome.2009

Author(s)

Journal Title

Data Source

[Journal Article] 偽性低アルドステロン症I型2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.2009

Author(s)

Journal Title

Data Source

[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2009

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[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008

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[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008

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[Presentation] Nutcracker症候群を合併した軽症IgA腎症の1例2011

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Year and Date

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[Presentation] レシピエント選定基準改定後に経験した小児献腎移植の5例2010

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HASHIMURA Yuya 橋村裕也