Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kenji Nanao"'
Autor:
Takuma Ohnishi, Yoshinori Mishima, Tomomi Naito, Nozomi Matsuda, Shohei Ariji, Daisuke Umino, Kikuko Tamura, Hajime Nishimoto, Keiji Kinoshita, Naonori Maeda, Azusa Kawaguchi, Ryuta Yonezawa, Shigenao Mimura, Hiroyuki Fukushima, Kenji Nanao, Makoto Yoshida, Toshio Sekijima, Isamu Kamimaki
Publikováno v:
International Journal of Infectious Diseases, Vol 125, Iss , Pp 97-102 (2022)
Objectives: The incidence of infections caused by extended-spectrum beta-lactamase (ESBL)–producing bacteria has increased. This study aimed to clarify the risk factors and treatment strategies for febrile urinary tract infection (fUTI) caused by E
Externí odkaz:
https://doaj.org/article/2bb226e618314de7bf59e410aed27b91
Publikováno v:
European journal of pediatrics. 175(8)
It is known that tricyclic antidepressants induce long QT intervals associated with forms of life-threatening arrhythmia such as torsades de pointes (TdP), and these adverse effects may also occur in neonates whose mothers take tricyclic antidepressa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43753665a49655a5dbb64c859f10c16
https://pubmed.ncbi.nlm.nih.gov/27068648
https://pubmed.ncbi.nlm.nih.gov/27068648
Autor:
Michihiko Aramaki, Kenji Nanao, Yoshio Makita, Hiroshi Kawame, Shozo Oku, Nobuhiko Okamoto, Toru Udaka, Hiroshi Yoshihashi, Kenjiro Kosaki, Hirotaka Oki, Yoshimitsu Fukushima, Takao Takahashi, Tomonobu Hasegawa, Rika Kosaki, Nobuko Moriyama
Publikováno v:
The Journal of Pediatrics. 148:410-414
CHD7 gene mutations were identified in 17 (71%) of 24 children clinically diagnosed to have CHARGE syndrome (C, coloboma of the iris or retina; H, heart defects; A, atresia of the choanae; R, retardation of growth and/or development; G, genital anoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89c08af17fbc05be85915056d5fe8ae0
https://doi.org/10.1016/j.jpeds.2005.10.044
https://doi.org/10.1016/j.jpeds.2005.10.044
Publikováno v:
Japanese journal of human genetics. 37:303-306
We mapped PMP-22 gene, candidate gene for the Charcot-Marie-Tooth disease (CMT) 1A, by direct R-banding fluorescence in situ hybridization. The signals of PMP-22 probe were localized to chromosome band 17p11.2. The present result was within the map p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49a825e085437a6f59630bcbebc4603e
https://doi.org/10.1007/bf01883321
https://doi.org/10.1007/bf01883321
Autor:
Ei-ichi Takahashi, Keiichi Uyemura, Wataru Sato, Goro Takada, Kenji Nanao, Masato Himoro, Kiyoshi Hayasaka, Masayuki Miura
Publikováno v:
Biochemical and Biophysical Research Communications. 186:827-831
A full length cDNA of PMP-22 (PAS-II/SR13/Gas-3) of peripheral myelin has been isolated from a cDNA library of human fetus spinal cord. The clone is 1823 base pairs (bp) in length and contains a 480 bp open reading frame encoding a polypeptide or 160
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::905bc98b8cbabe4c059e59d3aa084a05
https://doi.org/10.1016/0006-291x(92)90820-b
https://doi.org/10.1016/0006-291x(92)90820-b
Autor:
Masayuki Miura, Keiichi Uyemura, Wataru Sato, Kenji Nanao, Kiyoshi Hayasaka, Marie Tahara, Goro Takada
Publikováno v:
Biochemical and Biophysical Research Communications. 181:204-207
A full length cDNA of P2 protein of peripheral myelin has been isolated from a cDNA library of human fetus spinal cord. The clone is 2150 base pairs (bp) in length and contains a 393 bp open reading frame encoding a polypeptide of 131 residues. The d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a812ff7db07f95784ccb05a2f41e7040
https://doi.org/10.1016/s0006-291x(05)81402-0
https://doi.org/10.1016/s0006-291x(05)81402-0
Autor:
Keiichi Uyemura, Goro Takada, Kiyoshi Hayasaka, Marie Tahara, Masayuki Miura, Wataru Sato, Kenji Nanao
Publikováno v:
Biochemical and Biophysical Research Communications. 180:515-518
Summary A full length cDNA of the major structural protein of peripheral myelin ( PO protein ) has been isolated from a cDNA library of human fetus spinal cord. The clone is 1948 base pairs ( bp ) in length and contains a 744 bp open reading frame en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ce01dff5dc80d2ffa8e36b69f405174
https://doi.org/10.1016/s0006-291x(05)81094-0
https://doi.org/10.1016/s0006-291x(05)81094-0
Publikováno v:
Endocrine journal. 51(3)
ACTH and 17-hydroxyprogesterone (17OHP) levels during clitoro- and labinoplasty for CYP21A2 deficiency have not been reported. In this study, we measured these levels during surgery. Intensive glucocorticoid supplement (IGS Tx; intravenous bolus inje
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1109644553f353e5303408dabc59dfc5
https://pubmed.ncbi.nlm.nih.gov/15256784
https://pubmed.ncbi.nlm.nih.gov/15256784
Autor:
Yukihiro Hasegawa, Jun Nakae, Ikuko Takahashi, Toshihiro Tajima, Nozomi Shinohara, Kenji Fujieda, Kenji Nanao, Kohei Sato
Publikováno v:
The Journal of clinical endocrinology and metabolism. 87(7)
Gain-of-function mutations of the calcium-sensing receptor (CaR) gene cause autosomal dominant and/or sporadic hypocalcemia with hypercalciuria. Because treatment of the hypocalcemia with vitamin D and/or calcium in patients with such mutations resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6807b54bc8381c4b6b1de30ff013f1d
https://pubmed.ncbi.nlm.nih.gov/12107202
https://pubmed.ncbi.nlm.nih.gov/12107202
Autor:
Hiroshi Terasaki, Yukihiro Hasegawa, Tsutomu Ogata, Mari Matsuo, Koji Muroya, Kenjiro Kosaki, Kenji Nanao
Publikováno v:
American journal of medical genetics. 91(4)
We report on a mother and daughter both with a 45,X/46,X,r(X)(p22. 3q28) karyotype and mental retardation. Fluorescence in situ hybridization (FISH) and microsatellite analyses for 14 loci/region at Xp22.3 and seven loci/region at Xq28 indicated that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::119d953011cd281f8483229b2e3bc55b
https://pubmed.ncbi.nlm.nih.gov/10766981
https://pubmed.ncbi.nlm.nih.gov/10766981