Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Toshikatsu Mitsui"'
Autor:
Yosuke Yasui, Toshikatsu Mitsui, Fujiyo Arima, Keiko Uchida, Mikako Inokuchi, Mitsuaki Tokumura, Tetsuo Nakayama
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 17, Iss 8, Pp 2494-2500 (2021)
A national immunization program using two doses of live attenuated varicella vaccine was introduced for children aged one to two years in Japan in October 2014. Varicella cases declined after 2014, and immunological status against varicella among vac
Externí odkaz:
https://doaj.org/article/f9639df7a50a4e85a41c92fd6d0da363
Autor:
Toshikatsu Mitsui, Yosuke Yasui, Tetsuo Nakayama, Fujiyo Arima, Mitsuaki Tokumura, Keiko Uchida, Mikako Inokuchi
Publikováno v:
Hum Vaccin Immunother
A national immunization program using two doses of live attenuated varicella vaccine was introduced for children aged one to two years in Japan in October 2014. Varicella cases declined after 2014, and immunological status against varicella among vac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b51e649dfc2fdcdd770113a07ffe016
https://europepmc.org/articles/PMC8475580/
https://europepmc.org/articles/PMC8475580/
Autor:
Toshikatsu Mitsui, Masaaki Mori, Mikako Inokuchi, Tomoyasu Nishimura, Yosuke Yasui, Keiko Uchida, Tetsuo Nakayama, Mitsuaki Tokumura
Publikováno v:
Vaccine. 36(20)
Many countries including Japan have adapted acellular pertussis vaccines combined with diphtheria and tetanus toxoids (DTaP). DTaP vaccine coverage is approximately >90%, but pertussis re-emergence has been observed since 2000 in Japan. In the presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a9febeb3e12f35e9d7f1eca96c036ae
https://pubmed.ncbi.nlm.nih.gov/29609967
https://pubmed.ncbi.nlm.nih.gov/29609967
Autor:
Masanori Adachi, Tomonobu Hasegawa, Kenji Ihara, Tomohiro Ishii, Ryuji Fukuzawa, Koji Muroya, Yukihiro Hasegawa, Toshikatsu Mitsui, Takeshi Sato, Seiji Sato, Junko Igaki
Publikováno v:
European journal of endocrinology. 175(2)
Objective Congenital lipoid adrenal hyperplasia (lipoid CAH) results in impairment of adrenal and gonadal steroidogenesis caused by STAR mutations. Our previous study revealed upregulation of genes associated with inflammatory or immune response and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0de8294ef11016e739dd48f8053721c2
https://pubmed.ncbi.nlm.nih.gov/27190208
https://pubmed.ncbi.nlm.nih.gov/27190208
Publikováno v:
Endocrinology. 153:2714-2723
Steroidogenic acute regulatory protein (StAR) facilitates cholesterol transfer into the inner mitochondrial membrane in the acute phase of steroidogenesis. Mice lacking StAR (Star−/−) share phenotypes with human individuals having congenital lipo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::452a1e060cfc0c940364af85b3b57ea8
https://doi.org/10.1210/en.2011-1627
https://doi.org/10.1210/en.2011-1627
Autor:
Keisuke Nagasaki, Satoshi Narumi, Tomohiro Ishii, Tomonobu Hasegawa, Toshikatsu Mitsui, Masaki Takagi
Publikováno v:
American Journal of Medical Genetics Part A. :261-264
A Family of Pseudohypoparathyroidism Type Ia With an 850-kb Submicroscopic Deletion Encompassing the Whole GNAS Locus Toshikatsu Mitsui, Keisuke Nagasaki, Masaki Takagi, Satoshi Narumi, Tomohiro Ishii, and Tomonobu Hasegawa* Department of Pediatrics,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bab5e2909c764d19929fb096a37f239f
https://doi.org/10.1002/ajmg.a.34393
https://doi.org/10.1002/ajmg.a.34393
Autor:
Satoshi Narumi, Mie Nakazawa, Mikako Inokuchi, Toshikatsu Mitsui, Keisuke Nagasaki, Goro Sasaki, Tomonobu Hasegawa
Publikováno v:
The Journal of clinical endocrinology and metabolism. 99(11)
In most patients with hypoparathyroidism (HP), the etiology is not defined clinically. Eight genes (AIRE, CASR, CLDN16, GATA3, GCM2, PTH, TBCE, and TRPM6) are known to be responsible genes associated with HP; however, no previous study has screened t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319dddf085b87d9863bf10afc8aa51a4
https://pubmed.ncbi.nlm.nih.gov/25137426
https://pubmed.ncbi.nlm.nih.gov/25137426
Autor:
Mohamad Zubair, Tomonobu Hasegawa, Richard J. Auchus, Tomohiro Ishii, Goro Sasaki, Toshikatsu Mitsui
Publikováno v:
Molecular endocrinology (Baltimore, Md.). 28(7)
The steroidogenic acute regulatory protein (StAR) facilitates the delivery of cholesterol to the inner mitochondrial membrane, where the cholesterol side-chain cleavage enzyme catalyzes the initial step of steroid hormone biosynthesis. StAR was initi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b82546280b070bfe00b5760e3826089d
https://pubmed.ncbi.nlm.nih.gov/24850413
https://pubmed.ncbi.nlm.nih.gov/24850413
Autor:
Dong Kyu Jin, Ok Hwa Kim, Teck-Hock Toh, Gen Nishimura, Tomonobu Hasegawa, Dai Keino, Tomohiro Ishii, Shohei Matsubayashi, Amaka C. Offiah, Diana Johnson, Shun Soneda, Toshikatsu Mitsui, Christine Hall
Publikováno v:
American journal of medical genetics. Part A. (10)
Acroscyphodysplasia (OMIM250215) is a distinctive form of metaphyseal dysplasia characterized by the distal femoral and proximal tibial epiphyses embedded in cup-shaped, large metaphyses known as metaphyseal scypho ("scypho" = cup) deformity. It is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b972fef9af7e26710341a0a6ffd8625
https://pubmed.ncbi.nlm.nih.gov/25044890
https://pubmed.ncbi.nlm.nih.gov/25044890
Publikováno v:
European journal of medical genetics. 56(9)
We identified 2.0 Mb of a novel deletion on chromosome 14q12, involving 8 genes and putative regulatory elements of FOXG1 by array CGH in a patient with severe growth and psychomotor retardation, hypotonia, microcephaly, dysmorphic face, and hypoplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::253e23d1ee75aadb37ccad59bfbc7e2c
https://pubmed.ncbi.nlm.nih.gov/23895774
https://pubmed.ncbi.nlm.nih.gov/23895774