Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Hiromi OHTSUBO"'
Autor:
Chika SHIRAKATA, Ryota HANAUE, Hiromi OHTSUBO, Akira SHIOZAKI, Kazue OHISHI, Soichiro ISHISAKA, Dai OHTSU
Publikováno v:
Journal of Veterinary Medical Science; 2024, Vol. 86 Issue 6, p665-669, 5p
Autor:
Shingo Abe, Hiromi Ohtsubo
Publikováno v:
Arerugi: Japanese Journal of Allergology; 2024, Vol. 73 Issue 2, p201-205, 5p
Autor:
Hiromi Ohtsubo, Dai Ohtsu
Publikováno v:
Japanese Journal of Zoo and Wildlife Medicine. 24:141-145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::484002aa1c2053a48ae2cc15751fb400
https://doi.org/10.5686/jjzwm.24.141
https://doi.org/10.5686/jjzwm.24.141
Autor:
Hiroshi Kaito, Akemi Shono, Kazumoto Iijima, Taro Okada, Yutaka Takaoka, Lifang Zhang, Kandai Nozu, Shun-ichi Nakamura, Katsuhiko Asanuma, Mariko Taniguchi-Ikeda, Koichi Nakanishi, Hiromi Ohtsubo
Publikováno v:
Pediatric Nephrology. 31:1459-1467
Glomerulopathy with fibronectin deposits (GFND) is a rare autosomal dominant disease characterized by massive fibronectin deposits, leading to end-stage renal failure. Although mutations within the heparin-binding domains of the fibronectin 1 gene (F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc08c190e21b93842bcafa06a17e032
https://doi.org/10.1007/s00467-016-3368-7
https://doi.org/10.1007/s00467-016-3368-7
Autor:
Akemi Shono, Kazumoto Iijima, Hiroshi Kaito, Koichi Nakanishi, Natsuki Matsunoshita, Hiromi Ohtsubo, Shogo Minamikawa, Yuko Shima, Yoshimi Nozu, Tomohiko Yamamura, Naoya Morisada, Norishige Yoshikawa, Naohiro Kamiyoshi, Kandai Nozu, Takeshi Ninchoji, Xue Jun Fu
Publikováno v:
Genetics in Medicine. 18:180-188
Phenotypic overlap exists among type III Bartter syndrome (BS), Gitelman syndrome (GS), and pseudo-BS/GS (p-BS/GS), which are clinically difficult to distinguish. We aimed to clarify the differences between these diseases, allowing accurate diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82735836d4f8ff2c9088737e787c6418
https://doi.org/10.1038/gim.2015.56
https://doi.org/10.1038/gim.2015.56
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 29:137-141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7adab49fe7fc63a65901df285186be6
https://doi.org/10.3165/jjpn.rv.2016.0095
https://doi.org/10.3165/jjpn.rv.2016.0095
Autor:
Fusako Hashimoto, Natsuki Matsunoshita, Masafumi Oka, Kazumoto Iijima, Koichi Nakanishi, Hiroshi Kaito, Shingo Ishimori, Hiromi Ohtsubo, Norishige Yoshikawa, Takeshi Ninchoji, Yuya Hashimura, Xue Jun Fu, Naohiro Kamiyoshi, Kandai Nozu, Naoya Morisada
Publikováno v:
Kidney International. 85:1208-1213
X-linked Alport syndrome is caused by mutations in the COL4A5 gene encoding the type IV collagen α5 chain (α5(IV)). Complete absence of α5(IV) in the renal basal membrane is considered a pathological characteristic in male patients; however, posit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::582d9e6922ad7475f7ebefa5821273e6
https://doi.org/10.1038/ki.2013.479
https://doi.org/10.1038/ki.2013.479
Autor:
Hiroshi Kaito, Naoya Morisada, Koichi Nakanishi, Hiromi Ohtsubo, Kazumoto Iijima, Koji Nagatani
Publikováno v:
Pediatric Nephrology. 27:1189-1192
Autosomal dominant mutations in paired box gene 2 (PAX2), on chromosome 10q24, are responsible for renal coloboma syndrome (RCS). The role of PAX2 in glomerular basement membrane (GBM) formation and maintenance remains unknown. We report a case of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59cf893c5b18fe7e2f04ed523f821afa
https://doi.org/10.1007/s00467-012-2125-9
https://doi.org/10.1007/s00467-012-2125-9
Autor:
Kandai Nozu, Eihiko Takahashi, Xue J Fu, Yuya Hashimura, Naoya Morisada, Koichi Nakanishi, Hiromi Ohtsubo, Mariko Taniguchi-Ikeda, Hiroshi Kaito, Takeshi Ninchoji, Kazumoto Iijima, Fusako Hashimoto, Hiroki Kurahashi
Publikováno v:
Human Genome Variation
We report the case of a 22-year-old male with autosomal recessive Alport syndrome. Molecular analysis showed that this patient has a homozygous missense (NM_000091.4:c.3266G>A) Gly1089Asp mutation in the COL4A3 gene. The proband inherited the mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abd86af34abeb3180f94c446ba693c36
https://pubmed.ncbi.nlm.nih.gov/27081500
https://pubmed.ncbi.nlm.nih.gov/27081500
Autor:
Hiromi Ohtsubo, Fusako Hashimoto, Naoya Morisada, Shingo Ishimori, Yuya Hashimura, Hitomi Takeichi, Kazumoto Iijima, Masaru Yoshida, Takeshi Ninchoji, Shin Nishiumi, Ichiro Morioka, Hideoki Fukuoka, Mari Chitose, Osamu Miyake, Hiroshi Kaito
Publikováno v:
Early human development. 89(5)
Background A metabolomic approach using umbilical cord blood from infants at birth has not been studied widely yet. Aim We examined changes in metabolite levels in umbilical cord blood at birth via gas chromatography/mass spectrometry (GC/MS)-based m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6751d7097f680ecaf5e35a7d2f6d0b4
https://pubmed.ncbi.nlm.nih.gov/23178109
https://pubmed.ncbi.nlm.nih.gov/23178109