Furuichi Tatsuya 古市達哉

… Alternative Names

古市達哉フルイチタツヤ

FURUICHI Tatsuya 古市達哉

Less

Researcher Number	30392103
Other IDs	https://orcid.org/0000-0001-5656-1235
Affiliation (Current)	2024: 岩手大学, 農学部, 教授
Affiliation (based on the past Project Information) *help	2024: 岩手大学, 農学部, 教授 2021 – 2022: 岩手大学, 農学部, 教授 2015 – 2018: 岩手大学, 農学部, 教授 2011: 独立行政法人理化学研究所, 骨関節疾患研究チーム, 上級研究員 2010: The Institute of Physical and Chemical Research, 医学部, 講師 … More 2008 – 2009: The Institute of Physical and Chemical Research, 骨関節疾患研究チーム, 上級研究員 2008: 独立行政法人理化学研究所, 骨関節疾患研究チーム, 上級研究員 2007: 独立行政法人理化学研究所, 変形性関節症関連遺伝子研究チーム, 上級研究員 Less
Review Section/Research Field	Principal Investigator Basic Section 42020:Veterinary medical science-related / Laboratory animal science / Orthopaedic surgery Except Principal Investigator Orthopaedic surgery / Veterinary medical science
Keywords	Principal Investigator 遺伝子欠損マウス / 骨系統疾患 / ゲノム編集 / 軟骨 / 糖ヌクレオチド輸送体 / クリコサミニグリカン / ノックアウトマウス / 運動器 / 等ヌクレオチド / CANT1 … More / SLC35D1 / 運動器疾患 / 糖ヌクレオチド / 疾患モデルマウス / コンジェニックマウス / GDF5 / モデル動物 / 変形性関節症 / 小児運動器学 / 遺伝子診断 … More Except Principal Investigator 遺伝子 / 相関解析 / 腰椎椎間板ヘルニア / 脊椎脊髄病学 / 椎間板ヘルニア / 診断・検査 / 低酸素応答 / 小胞体ストレス / 分化 / 増殖 / 肥満細胞 / 検査 / 診断 / 病態 / 肥満細胞腫 / SNP / 分子病態 / アジア / アスポリン / COLIIA1 / 相関解析分子病態 / 疾患感受性遺伝子 / 椎間板変性症 / 骨・関節疾患 Less

糖ヌクレオチド輸送体が司る骨格形成メカニズムの解明Principal Investigator
- Principal Investigator
  
  古市達哉
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 42020:Veterinary medical science-related
- Research Institution
  Iwate University
運動器疾患の克服に向けた糖ヌクレオチド代謝の基礎研究Principal Investigator
- Principal Investigator
  
  古市達哉
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 42020:Veterinary medical science-related
- Research Institution
  Iwate University
Development of mouse models of osteoarthritis targeting the Gfd5 genePrincipal Investigator
- Principal Investigator
  
  Furuichi Tatsuya
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Laboratory animal science
- Research Institution
  Iwate University
Companion diagnostics and risk management on mast cell tumors in dogs
- Principal Investigator
  
  Tanaka Akane
- Project Period (FY)
  2015 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Veterinary medical science
- Research Institution
  Tokyo University of Agriculture and Technology
Identification of susceptibility gene for lumbar disc disease and clarification of its molecular pathogenesis
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Identification of the causative genes and investigation of the molecular pathogenesis for skeletal dysplasiasPrincipal Investigator
- Principal Investigator
  
  FURUICHI Tatsuya
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research
Identification of susceptibility gene for lumbar disc herniation and clarification of its molecular pathogenesis
- Principal Investigator
  
  IKEGAWA Shiro
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (A)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  The Institute of Physical and Chemical Research

All 2023 2022 2021 2018 2017 2016 2015 2011 2010 2009 2008

All Journal Article Presentation Book

[Book] 第20回日本整形外科学会骨系統疾患研究会記録集(蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定)2009
- Author(s)
  古市達哉、池川志郎
- Data Source
  KAKENHI-PROJECT-20390408
[Book] 実験医学(26)(糖ヌクレオチド輸送体SLC35D1は骨格形成に必須である)2008
- Author(s)
  池川志郎、古市達哉
- Data Source
  KAKENHI-PROJECT-20390408
[Book] 最新医学(63)(骨系統疾患と遺伝子異常-蝸牛様骨盤異形成症の原因遺伝子SLC35D1の発見-)2008
- Author(s)
  池川志郎、古市達哉、西村玄
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Mice lacking nucleotide sugar transporter SLC35A3 exhibit lethal chondrodysplasia with vertebral anomalies and impaired glycosaminoglycan biosynthesis2023
- Author(s)
  Saito S, Mizumoto S, Yonekura T, Yamashita R, Nakano K, Okubo T, Yamada S, Okamura T, Furuichi T.
- Journal Title
  
  PLoS One
  
  Volume: 18 Issue: 4 Pages: e0284292-e0284292
- DOI
  10.1371/journal.pone.0284292
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K05932
[Journal Article] Disruption of the mouse Slc39a14 gene encoding zinc transporter ZIP14 is associated with decreased bone mass, likely caused by enhanced bone resorption.2018
- Author(s)
  Sasaki S, Tsukamoto M, Saito M, Hojyo S, Fukada T, Takami M, Furuichi T.
- Journal Title
  
  FEBS Open Bio
  
  Volume: 8 Issue: 4 Pages: 655-663
- DOI
  10.1002/2211-5463.12399
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06797, KAKENHI-PROJECT-17H04011
[Journal Article] An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes2017
- Author(s)
  Ichimura S, Sasaki S, Murata T, Fukumura R, Gondo Y, Ikegawa S, Furuichi T.
- Journal Title
  
  Exp Amin
  
  Volume: 62 Pages: 138-144
- NAID
  130005635560
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06797
[Journal Article] Overexpression of BCLXL in Osteoblasts Inhibits Osteoblast Apoptosis and Increases Bone Volume and Strength2016
- Author(s)
  Moriishi T, Fukuyama R, Miyazaki T, Furuichi T, Ito M, Komori T.
- Journal Title
  
  J Bone Miner Res
  
  Volume: 印刷中 Issue: 7 Pages: 1366-1380
- DOI
  10.1002/jbmr.2808
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K06797, KAKENHI-PROJECT-15K10482, KAKENHI-PROJECT-26221310, KAKENHI-PROJECT-15K11015, KAKENHI-PROJECT-16K15781
[Journal Article] Endoplasmic reticulum stress-mediated apoptosis contributes to a skeletal dysplasia resembling platyspondylic lethal skeletal dysplasia, Torrance type, in a novel Col2a1 mutant mouse line.2015
- Author(s)
  Kimura M, Ichimura S, Sasaki K, Masuya H, Suzuki T, Wakana S, Ikegawa S, Furuichi T.
- Journal Title
  
  Biochem Biophys Res Commun
  
  Volume: 468 Issue: 1-2 Pages: 86-91
- DOI
  10.1016/j.bbrc.2015.10.160
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K06797
[Journal Article] CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant2011
- Author(s)
  Furuichi T
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 48 Pages: 32-37
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] CANT1 mutation is also responsible for Desbuquois dysplasia, type 2 and Kim variant.2011
- Author(s)
  Furuichi T
- Journal Title
  
  J Med Genet. 48
  
  Pages: 32-37
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] SMOC1 is essential for ocular and limb development in humans and mice.2011
- Author(s)
  Okada I, Furuichi T
- Journal Title
  
  Am J Hum Genet. 88
  
  Pages: 30-41
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome.2010
- Author(s)
  Miyake N, Furuichi T
- Journal Title
  
  Hum Mutat. 31
  
  Pages: 966-974
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Chondroitin sulfate N-acetylgalactosaminyl transferase-1 is required for normal cartilage development.2010
- Author(s)
  Watanabe Y, Furuichi T
- Journal Title
  
  Biochem J. 432
  
  Pages: 47-55
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family.2010
- Author(s)
  Dai J, Furuichi T
- Journal Title
  
  J Med Genet. 47
  
  Pages: 704-709
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Association of the tag SNPs in the human SKT Gene (KIAA1217) with lumbar disc herniation2009
- Author(s)
  Karasugi T, Semba K, Hirose Y, Kelempisioti A, Nakajima M, Miyake A, Furuichi T, Kawaguchi Y, Mikami Y, Chiba K, Kamata M, Ozaki K, Takahashi A, Makela P, Karppinen J, Kimura T, Kubo T, Toyama Y, Yamamura KI, Mannikko M, Mizuta H, Ikegawa S
- Journal Title
  
  J Bone Miner Res (Epub ahead of print)
  
  Pages: 0-0
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] Signaling mediated by the endoplasmic reticulum stress transducer OASISS is involved in bone formation.2009
- Author(s)
  Murakami T, Furuichi T
- Journal Title
  
  Nat Cell Biol. 11
  
  Pages: 1205-1211
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Association of the tag SNPs in the human SKT Gene(KIAA1217) with lumbar disc herniation2009
- Author(s)
  Karasugi T. Semba K, Hirose Y, Kelempisioti A, Nakajima M, Miyake A, Furuichi T, Kawaguchi Y, Mikami Y, Chiba K, Kamata M, Ozaki K, Takahashi A, Makela P, Karppinen J, Kimura T, Kubo T, Toyama Y, Yamamura K, Mannikko M, Mizuta H, Ikegawa S
- Journal Title
  
  J Bone Miner Res
  
  Volume: 24(9) Pages: 1537-1543
- Data Source
  KAKENHI-PROJECT-21249080
[Journal Article] Regulation of endoplasmic reticulum stress response by a BBF2H7-mediated Sec23a pathway is essential for chondrogenesis.2009
- Author(s)
  Saito A, Furuichi T
- Journal Title
  
  Nat Cell Biol 11
  
  Pages: 1197-1204
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases2009
- Author(s)
  古市達哉
- Journal Title
  
  Journal of Medical Genetics 46
  
  Pages: 562-568
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases.2009
- Author(s)
  Furuichi T
- Journal Title
  
  J Med Genet. 46
  
  Pages: 562-568
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] 蝸牛様骨盤異形成症の責任遺伝子SLC35Dの同定2009
- Author(s)
  古市達哉
- Journal Title
  
  第20回日本整形外科学会骨系統疾患研究会記録集
  
  Pages: 31-34
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] A compound heterozygote of novel and recurrent DTDST mutations results in a novel intermediate phenotype of Desbuquosis dysplasia, diastrophic dysplasia and recessive form of multiple epiphyseal dysplasia.2008
- Author(s)
  Miyake A, Furuichi T
- Journal Title
  
  J Hum Genet. 53
  
  Pages: 764-768
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] The Zinc transporter SLC39A13/ZIP13 is required for connective tissue development ; Its involvement in BMP/TGF-β signaling pathways.2008
- Author(s)
  Fukada T, Civic N, Furuichi T
- Journal Title
  
  PLoS One. 3
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Journal Article] A functional polymorphism in THBS2 that affects alternative splicing and MMP binding is associated with lumbar-disc herniation2008
- Author(s)
  Hirose Y, Chiba K, Karasugi T, Nakajima M, Kawaguchi Y, Mikami Y, Furuichi T, Mio F, Miyake A, Miyamoto T, Ozaki K, Takahashi A, Mizuta H, Kubo T, Kimura T, Tanaka T, Toyama Y, Ikegawa S
- Journal Title
  
  Am J Hum Genet 82(5)
  
  Pages: 1122-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19209049
[Journal Article] Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.2008
- Author(s)
  Furuichi T
- Journal Title
  
  J Hum Genet. 53
  
  Pages: 419-424
- NAID
  10021248849
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] Slc35a3欠損マウスの作製およびウシ複合脊椎形成不全症モデル動物としての評価2022
- Author(s)
  古市達哉、齋藤宗一郎、米倉司、中野堅太、岡村匡史.
- Organizer
  第69回日本実験動物学会総会
- Data Source
  KAKENHI-PROJECT-21K05932
[Presentation] 糖ヌクレオチド輸送体SLC35A3はグリコサミノグリカン合成に関与し、脊椎及び軟骨形成に必須である2022
- Author(s)
  米倉司、齋藤宗一郎、水本秀二、山田修平、大久保直、中野堅太、岡村匡史、古市達哉.
- Organizer
  第164回日本獣医学会
- Data Source
  KAKENHI-PROJECT-21K05932
[Presentation] Slc35a3欠損マウスの作製およびウシ複合脊椎形成不全症モデル動物としての評価2021
- Author(s)
  齋藤宗一郎、米倉司、中野堅太、岡村匡史、古市達哉
- Organizer
  第163回日本獣医学会
- Data Source
  KAKENHI-PROJECT-21K05932
[Presentation] CRIM1は軟骨細胞の増殖とアポトーシスを調節することで、骨格成長を制御する2021
- Author(s)
  生地伸康、矢神和広、齋藤宗一郎、新美君枝、高橋英機、古市達哉
- Organizer
  第163回日本獣医学会
- Data Source
  KAKENHI-PROJECT-21K05932
[Presentation] 「四肢異常を伴う小眼球症」の新規モデルマウスの樹立と原因遺伝子の同定2016
- Author(s)
  塚本愛美、佐藤有里子、福村龍太郎、権藤洋一、古市達哉
- Organizer
  第159回日本獣医学会
- Place of Presentation
  日本大学生物資源科学部 (神奈川県藤沢市）
- Year and Date
  2016-09-06
- Data Source
  KAKENHI-PROJECT-15K06797
[Presentation] 新規Col2a1変異マウスを用いたトーランス型扁平椎異形成症の病態機序の検討2016
- Author(s)
  木村允、市村鋭、桝谷啓志、鈴木智広、若菜茂晴、古市達哉
- Organizer
  第63回日本実験動物学会
- Place of Presentation
  ミューザ川崎シンフォニーホール (神奈川県川崎市）
- Year and Date
  2016-05-18
- Data Source
  KAKENHI-PROJECT-15K06797
[Presentation] 遺伝子改変動物を用いて骨格形成メカニズムに迫る2016
- Author(s)
  古市達哉
- Organizer
  第27回東北動物実験研究会
- Place of Presentation
  秋田温泉プラザ (秋田県秋田市）
- Invited
- Data Source
  KAKENHI-PROJECT-15K06797
[Presentation] 破骨細胞機能における亜鉛トランスポーターZIP14の役割2015
- Author(s)
  古市達哉、佐々木俊、北條慎太郎、深田俊幸
- Organizer
  第62回日本実験動物学会
- Place of Presentation
  京都テルサ (京都府）
- Year and Date
  2015-05-28
- Data Source
  KAKENHI-PROJECT-15K06797
[Presentation] モデルマウスを用いたトーランス型扁平椎異形成症の病態機序の検討2015
- Author(s)
  木村允、市村鋭、桝谷啓志、鈴木智広、若菜茂晴、古市達哉
- Organizer
  第158回日本獣医学会
- Place of Presentation
  北里大学（青森県十和田市）
- Year and Date
  2015-09-09
- Data Source
  KAKENHI-PROJECT-15K06797
[Presentation] ENUミュータジェネシスによる新規II 型コラーゲン遺伝子(Col2a1)変異マウスの同定2010
- Author(s)
  古市達哉
- Organizer
  第150回日本獣医学会
- Place of Presentation
  帯広
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 遺伝子改変マウスから見いだされた骨格異常を伴う新規トランスポーター病とその分子病態解析2010
- Author(s)
  古市達哉
- Organizer
  第38回北陸実験動物研究会
- Place of Presentation
  富山
- Year and Date
  2010-10-02
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 遺伝子改変マウスから見いだされた骨格異常を伴う新規トランスポーター病とその分子病態解析2010
- Author(s)
  古市達哉
- Organizer
  第38回北陸実験動物研究会
- Place of Presentation
  富山(招待講演)
- Year and Date
  2010-10-02
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] ENUミュータジェネシスによる新規II型コラーゲン遺伝子(Col2a1)変異マウスの同定2010
- Author(s)
  古市達哉
- Organizer
  第150回日本獣医学会
- Place of Presentation
  帯広
- Year and Date
  2010-09-17
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 大規模関連解析による変形性関節症感受性遺伝子の同定2009
- Author(s)
  古市達哉、池川志郎
- Organizer
  第82回日本生化学会シンポジウム : 「運動器」形成・再生のための分子基盤.
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 糖ヌクレオチド輸送体SLC35D1は軟骨組織におけるコンドロイチン硫酸合成に必須であり、その機能欠損は重度な骨格形成不全を引き起こす2009
- Author(s)
  古市達哉、池川志郎
- Organizer
  第1回新潟プロテオグリカン研究会
- Place of Presentation
  新潟
- Year and Date
  2009-03-06
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 亜鉛トランスポーター遺伝子ZIP13/SLC39A13の機能消失型変異はEhlers-Danlos症候群を引き起こす2009
- Author(s)
  古市達哉
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] マウスとヒトの融合遺伝アプローチによる新規のトランスポーター病の同定とその分子病態の解明2009
- Author(s)
  池川志郎、古市達哉
- Organizer
  日本薬学会129年会シンポジウム : 遺伝子改変マウスから見いだされたトランスポーター・チャンネルの新規機能
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 亜鉛トランスポーター遺伝子ZIP13/SLC39A13の機能消失型変異は Ehlers-Danlos 症候群を引き起こす2009
- Author(s)
  古市達哉
- Organizer
  第54回日本人類遺伝学会
- Place of Presentation
  東京
- Year and Date
  2009-09-24
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] Nucleotide-Sugar transporter SLC35D1 is critical to chondroitin sulfate synthesis in cartilage and skeletal development in mouse and human.2009
- Author(s)
  古市達哉
- Organizer
  The 26th Naito Conference : OSTEO BIOLOGY
- Place of Presentation
  Awaji-shima, Japan
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] Novel and recurrent mutations in TRPV4 cause SMD, Kozlowski type and Metaropic dysplasia in Asians.2009
- Author(s)
  Dai J, 古市達哉
- Organizer
  第54回日本人類遺伝学会.
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定2008
- Author(s)
  古市達哉
- Organizer
  第53回日本人類遺伝学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20390408
[Presentation] 蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定2008
- Author(s)
  古市達哉
- Organizer
  第20回日本整形外科学会骨系統疾患研究会
- Place of Presentation
  東京
- Year and Date
  2008-12-12
- Data Source
  KAKENHI-PROJECT-20390408

1. IKEGAWA Shiro (30272496)

# of Collaborated Projects: 3 results

# of Collaborated Products: 9 results
2. INABA Ikuyo (60415081)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
3. Tanaka Akane (80418673)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 永岡謙太郎 (60376564)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 種田久美子 (40750469)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. 岡村匡史 (00333790)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. 水本秀二 (40443973)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

Furuichi Tatsuya 古市 達哉

古市 達哉 フルイチ タツヤ

FURUICHI Tatsuya 古市 達哉

Research Projects

Research Products

Co-Researchers

糖ヌクレオチド輸送体が司る骨格形成メカニズムの解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

運動器疾患の克服に向けた糖ヌクレオチド代謝の基礎研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of mouse models of osteoarthritis targeting the Gfd5 genePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Companion diagnostics and risk management on mast cell tumors in dogs

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of susceptibility gene for lumbar disc disease and clarification of its molecular pathogenesis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of the causative genes and investigation of the molecular pathogenesis for skeletal dysplasiasPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification of susceptibility gene for lumbar disc herniation and clarification of its molecular pathogenesis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 第20回日本整形外科学会 骨系統疾患研究会記録集(蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定)2009

Author(s)

Data Source

[Book] 実験医学(26)(糖ヌクレオチド輸送体SLC35D1は骨格形成に必須である)2008

Author(s)

Data Source

[Book] 最新医学(63)(骨系統疾患と遺伝子異常-蝸牛様骨盤異形成症の原因遺伝子SLC35D1の発見-)2008

Author(s)

Data Source

[Journal Article] Mice lacking nucleotide sugar transporter SLC35A3 exhibit lethal chondrodysplasia with vertebral anomalies and impaired glycosaminoglycan biosynthesis2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Disruption of the mouse Slc39a14 gene encoding zinc transporter ZIP14 is associated with decreased bone mass, likely caused by enhanced bone resorption.2018

Author(s)

Journal Title

DOI

Data Source

[Journal Article] An ENU-induced p.C225S missense mutation in the mouse Tgfb1 gene does not cause Camurati-Engelmann disease-like skeletal phenotypes2017

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Overexpression of BCLXL in Osteoblasts Inhibits Osteoblast Apoptosis and Increases Bone Volume and Strength2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Endoplasmic reticulum stress-mediated apoptosis contributes to a skeletal dysplasia resembling platyspondylic lethal skeletal dysplasia, Torrance type, in a novel Col2a1 mutant mouse line.2015

Author(s)

Journal Title

Furuichi Tatsuya 古市達哉

古市達哉フルイチタツヤ

FURUICHI Tatsuya 古市達哉

[Book] 第20回日本整形外科学会骨系統疾患研究会記録集(蝸牛様骨盤異形成症の責任遺伝子SLC35D1の同定)2009