KASHIMADA Kenichi

J-GLOBAL         Last updated: Oct 16, 2019 at 02:45
 
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Name
KASHIMADA Kenichi
E-mail
kkashimada.pedtmd.ac.jp
URL
http://www.tmd.ac.jp/med/ped/home.html
Affiliation
Tokyo Medical and Dental University
Section
Medical Hospital Hospital Departments Department of Pediatrics, Maternal and Woman's Medicine Pediatrics
Job title
Junior Associate Professor
Degree
PhD(Tokyo Medical and Dental University)
Research funding number
80451938

Research Areas

 
 

Academic & Professional Experience

 
Apr 2007
 - 
Mar 2009
Assistant Professor, Graduate School of Medical and Dental Sciences Medical and Dental Sciences Bio-Environmental Response Pediatrics and Developmental Biology Department of Pediacrics and Developmental Biology, Tokyo Medical and Dental University
 
Apr 2011
 - 
Jun 2013
Assistant Professor, Graduate School of Medical and Dental Sciences Medical and Dental Sciences Bio-Environmental Response Pediatrics and Developmental Biology Department of Pediatrics and developmental biology, Tokyo Medical and Dental University
 
Jul 2013
 - 
Today
Junior Associate Professor, Medical Hospital Hospital Departments Department of Pediatrics, Maternal and Woman's Medicine Pediatrics, Tokyo Medical and Dental University
 
Apr 2008
 - 
Mar 2011
Post doctral fellow, Institute for Molecular Bioscience (IMB), The university of Queensland
 
Mar 2004
 - 
Mar 2007
Director, Department of pediatrics, Tokyo-kita Medical Centor
 

Education

 
Apr 1997
 - 
Mar 2002
Pediatrics, Graduate School, Division of Medical Sciences, Tokyo Medical and Dental University
 
Apr 1988
 - 
Mar 1994
Faculty of Medicine, Tokyo Medical and Dental University
 

Published Papers

 
Takeru Yamauchi, Kei Takasawa, Takahiro Kamiya, Shizuka Kirino, Maki Gau, Kento Inoue, Akihiro Hoshino, Kenichi Kashimada, Hirokazu Kanegane, Tomohiro Morio
Pediatr Diabetes   20(7) 1035-1040   Nov 2019   [Refereed]
Immune dysregulation, polyendocrinopathy, enteropathy, and X-linked (IPEX) syndrome is an autoimmune disorder caused by the dysfunction of FOXP3, which leads to regulatory T (Treg) cell dysfunction and subsequently autoimmunity including type 1 di...
Hasegawa S, Kumada S, Tanuma N, Tsuji-Hosokawa A, Kashimada A, Mizuno T, Moriyama K, Sugawara Y, Shirai I, Miyata Y, Nishida H, Mashimo H, Hasegawa T, Hosokawa T, Hisakawa H, Uematsu M, Fujine A, Miyata R, Sakuma H, Kashimada K, Imai K, Morio T, Hayashi M, Mizutani S, Takagi M.
Pediatr Neurol      May 2019   [Refereed]
Ataxia telangiectasia is an autosomal recessive disorder characterized by cerebellar ataxia, telangiectases, immune defects, and a predisposition to malignancy. Quality of life is severely impaired by neurological symptoms. However, curative optio...
Risa Nomura, Kenichi Kashimada, Hitomi Suzuki, Liang Zhao, Atusmi Hosokawa-Tsuji, Hideo Yagita, Masatoshi Takagi, Yoshiakira Kanai, Josephine Bowles, Peter Koopman, Masami Kanai-Azuma, Tomohiro Morio
J. Cell. Sci.   132(8)    Apr 2019   [Refereed]
during the fetal period optimizes ovarian development by fine-tuning of Notch signaling.
Yuichi Miyakawa, Kei Takasawa, Yohei Matsubara, Kenji Ihara, Yoshiaki Ohtsu, Hotaka Kamasaki, Kazuteru Kitsuda, Hironori Kobayashi, Mari Satoh, Sinichiro Sano, Sumito Dateki, Hiroshi Mochizuki, Ichiro Yokota, Yukihiro Hasegawa, Kenichi Kashimada
Endocr. J.   66(3) 215-221   Mar 2019
Pseudohypoparathyroidism type 1A (PHP1A) is characterized by resistance to multiple hormones, the Albright Hereditary Osteodystrophy phenotype, obesity, and developmental delay. Developmental delay usually appears prior to hypocalcemia due to para...
Misako Nagatsuma, Kei Takasawa, Takeru Yamauchi, Ryuichi Nakagawa, Tomoko Mizuno, Eriko Tanaka, Kouhei Yamamoto, Noriko Uemura, Kenichi Kashimada, Tomohiro Morio
J. Hum. Genet.   64(2) 177-181   Feb 2019
Schimmelpenning syndrome is a rare neurocutaneous disorder categorized as a mosaic RASopathy due to postzygotic HRAS or KRAS mutations. We report a 6-year-old girl diagnosed with Schimmelpenning syndrome due to a postzygotic KRAS G12D mutation. Th...

Misc

 
Kenichi Kashimada, Peter Koopman
Development   137(23) 3921-3930   Dec 2010   [Refereed][Invited]
SRY, the mammalian Y-chromosomal testis-determining gene, induces male sex determination. Recent studies in mice reveal that the major role of SRY is to achieve sufficient expression of the related gene Sox9, in order to induce Sertoli cell differ...

Conference Activities & Talks

 
A case of homozygous familial hypobetalipoproteinemia associated with chronic liver dysfunction
Takeru Yamauchi, Kei Takasawa, Yoshichika Maeda, Manabu Takahashi, Tomohiro Morio, Shun Isibashi, Kenichi Kashimada
第53回日本小児内分泌学会学術集会   27 Sep 2019   日本小児内分泌学会
Diagnosis and clinical management of DSD in past and present [Invited]
Kenichi Kashimada
Pediatric Academic Societies Meeting   28 Apr 2019   
Prematurity of 23 or less weeks' gestation is a risk for transient late-onset hyperglycemia in neonates
Yamauchi T, Sugie M, Takasawa K, Imamura M, Kashimada K
ESPE 2018   28 Sep 2018   ESPE
A case of central diabetes insipidus developed 4 years after the non-CNS-risk unifocal bone lesion of Langerhans cell histiocytosis
Nakatani H, Miyai K, Takasawa K, Kashimada K, Morimorto A, nagasawa M, Oshiba A
ESPE2018   28 Sep 2018   ESPE
Enforced expression of Nr5a1/Ad4bp/Sf1 in mouse fetal ovaries causes premature ovarian insufficiency by dysregulating Notch signaling
Kashimada K, Nomura R, Suzuki H, Zhao L, Tsuji-Hosokawa A, Kanai Y, Yagita H, Bowles J, Koopman P, kanai-Azuma M, Morio T
8th International Symposium on the Biology of Vertebrate Sex determination   16 Apr 2018   8th International Symposium on the Biology of Vertebrate Sex determination