Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Taeko Hashimoto"'
Autor:
Yoko Shirai, Kenichiro Miura, Naoto Kaneko, Kiyonobu Ishizuka, Amane Endo, Taeko Hashimoto, Shoichiro Kanda, Yutaka Harita, Motoshi Hattori
Publikováno v:
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Heterozygous truncating variants in the Tripartite motif containing 8 (TRIM8) gene have been reported to cause epileptic encephalopathy, both with and without proteinuria. A recent study showed a lack of TRIM8 protein expression,
Externí odkaz:
https://doaj.org/article/8a4e8c58834f4dc68149135dd6fa1a85
Autor:
Kiyonobu Ishizuka, Kenichiro Miura, Taeko Hashimoto, Naoto Kaneko, Yutaka Harita, Tomoo Yabuuchi, Masataka Hisano, Shuichiro Fujinaga, Tae Omori, Yutaka Yamaguchi, Motoshi Hattori
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Abstract Determining the cause of focal segmental glomerulosclerosis (FSGS) has crucial implications for evaluating the risk of posttransplant recurrence. The degree of foot process effacement (FPE) on electron micrographs (EM) of native kidney biops
Externí odkaz:
https://doaj.org/article/b9e7060f78464a0dba6b0f0444f37379
Autor:
Taeko Hashimoto, Yutaka Harita, Keiichi Takizawa, Seiya Urae, Kiyonobu Ishizuka, Kenichiro Miura, Shigeru Horita, Daisuke Ogino, Gen Tamiya, Hideki Ishida, Tetsuo Mitsui, Kiyoshi Hayasaka, Motoshi Hattori
Publikováno v:
Kidney International Reports, Vol 4, Iss 9, Pp 1312-1322 (2019)
Introduction: Mutations in genes encoding nucleoporins (NUPs; components of nuclear pore complexes [NPCs]), such as NUP93, have been reported to cause steroid-resistant nephrotic syndrome (SRNS) or focal segmental glomerulosclerosis (FSGS), which oft
Externí odkaz:
https://doaj.org/article/41e6a07eedce4ec9a065f923faba22bd
Autor:
Yamato Kikkawa, Taeko Hashimoto, Keiichi Takizawa, Seiya Urae, Haruka Masuda, Masumi Matsunuma, Yuji Yamada, Keisuke Hamada, Motoyoshi Nomizu, Helen Liapis, Masataka Hisano, Yuko Akioka, Kenichiro Miura, Motoshi Hattori, Jeffrey H. Miner, Yutaka Harita
Publikováno v:
JCI Insight, Vol 6, Iss 6 (2021)
Mutations in LAMB2, encoding laminin β2, cause Pierson syndrome and occasionally milder nephropathy without extrarenal abnormalities. The most deleterious missense mutations that have been identified affect primarily the N-terminus of laminin β2. O
Externí odkaz:
https://doaj.org/article/04282997f5944b87a6b1ddb1678242ad
Autor:
Kenichiro Miura, Naoto Kaneko, Taeko Hashimoto, Kiyonobu Ishizuka, Yoko Shirai, Masataka Hisano, Hiroko Chikamoto, Yuko Akioka, Shoichiro Kanda, Yutaka Harita, Toshiyuki Yamamoto, Motoshi Hattori
Publikováno v:
Pediatric Nephrology. 38:417-429
Establishing a molecular genetic diagnosis of focal segmental glomerulosclerosis (FSGS)/steroid-resistant nephrotic syndrome (SRNS) can be useful for predicting post-transplant recurrence. Monogenic causes are reportedly present in approximately 20-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94ebc6310ed43272464a047bf85d78c0
https://doi.org/10.1007/s00467-022-05604-3
https://doi.org/10.1007/s00467-022-05604-3
Autor:
Taro Ando, Kenichiro Miura, Riku Hamada, Kei Nishiyama, Hiroshi Hataya, Yoshimitsu Gotoh, Kiyonobu Ishizuka, Taeko Hashimoto, Seiichiro Shishido, Naoya Fujita, Motoshi Hattori, Yuko Hamasaki, Kiyohiko Hotta, Naoto Kaneko, Shoichiro Kanda
Publikováno v:
Pediatric transplantationREFERENCES. 26(8)
Background Recurrence of SRNS is a major challenge in KT. Several clinical factors, including initial steroid sensitivity, have been associated with increased post-transplant SRNS recurrence risk. However, conflicting data have been reported, possibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d573fe241eb6ceb0c41e073ae7c88246
https://pubmed.ncbi.nlm.nih.gov/34309142
https://pubmed.ncbi.nlm.nih.gov/34309142
Autor:
Yutaka Harita, Taeko Hashimoto, Naoto Kaneko, Tae Omori, Shuichiro Fujinaga, Kiyonobu Ishizuka, Masataka Hisano, Motoshi Hattori, Kenichiro Miura, Tomoo Yabuuchi, Yutaka Yamaguchi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-10 (2021)
Scientific Reports
Scientific Reports
Determining the cause of focal segmental glomerulosclerosis (FSGS) has crucial implications for evaluating the risk of posttransplant recurrence. The degree of foot process effacement (FPE) on electron micrographs (EM) of native kidney biopsies can r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253b13a5c42fe011b6e30cfca0f09528
https://doi.org/10.1038/s41598-021-91520-9
https://doi.org/10.1038/s41598-021-91520-9
Autor:
Kiyoshi Hayasaka, Hideki Ishida, Keiichi Takizawa, Seiya Urae, Motoshi Hattori, Daisuke Ogino, Tetsuo Mitsui, Yutaka Harita, Shigeru Horita, Taeko Hashimoto, Kiyonobu Ishizuka, Kenichiro Miura, Gen Tamiya
Publikováno v:
Kidney International Reports
Kidney International Reports, Vol 4, Iss 9, Pp 1312-1322 (2019)
Kidney International Reports, Vol 4, Iss 9, Pp 1312-1322 (2019)
Introduction: Mutations in genes encoding nucleoporins (NUPs; components of nuclear pore complexes [NPCs]), such as NUP93, have been reported to cause steroid-resistant nephrotic syndrome (SRNS) or focal segmental glomerulosclerosis (FSGS), which oft
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75a6b3ab09954cdcbff92e946d6d99e9
https://doi.org/10.1016/j.ekir.2019.05.1157
https://doi.org/10.1016/j.ekir.2019.05.1157
Autor:
Yoko Shirai, Kenichiro Miura, Naoto Kaneko, Kiyonobu Ishizuka, Amane Endo, Taeko Hashimoto, Shoichiro Kanda, Yutaka Harita, Motoshi Hattori
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
BMC Nephrology, Vol 22, Iss 1, Pp 1-8 (2021)
Background Heterozygous truncating variants in the Tripartite motif containing 8 (TRIM8) gene have been reported to cause epileptic encephalopathy, both with and without proteinuria. A recent study showed a lack of TRIM8 protein expression, with supp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7649262c8ec78855bbe1716f99e921e3
https://pubmed.ncbi.nlm.nih.gov/34930159
https://pubmed.ncbi.nlm.nih.gov/34930159
Autor:
Sayuri Shirai, Akira Matsunaga, Hiroshi Sato, Kiyoshi Hayasaka, Minoru Ito, Daisuke Ogino, Takao Saito, Taeko Hashimoto, Ikuto Masakane, Gen Tamiya, Kentaro Toyota, Kazuo Umetsu, Noriyuki Degawa
Publikováno v:
Journal of Human Genetics. 58:254-258
Lipoprotein glomerulopathy (LPG) is a hereditary disease characterized by lipoprotein thrombi in the glomerulus, hyperlipoproteinemia, and a marked increase in serum apolipoprotein E (APOE). More than 12 APOE mutations have been identified as causes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::703b00e8a7f368e6914c2bb590738464
https://doi.org/10.1038/jhg.2013.8
https://doi.org/10.1038/jhg.2013.8