A new assay for the analysis of X-chromosome inactivation in carriers with an X-linked diseaseKUBOTA, Takeo.Brain & development (Tokyo. 1979). 2001, Vol 23, pp S177-S181, issn 0387-7604, SUP1Conference Paper

Epigenetics in congenital diseases and pervasive developmental disorders : Frontiers in Epigenetics MedicineKUBOTA, Takeo.Environmental health and preventive medicine. 2008, Vol 13, Num 1, pp 3-7, issn 1342-078X, 5 p.Article

Real time spectroscopic ellipsometry study on growth processes of ZrO₂ thin films in metallorganic chemical vapor depositionKUBOTA, Takeo; HARA, Nobuyoshi; SUGIMOTO, Katsuhisa et al.Journal of the Electrochemical Society. 2001, Vol 148, Num 9, pp C632-C639, issn 0013-4651Article

Molecular genetic study of japanese patients with X-linked α-thalassemia/mental retardation syndrome (ATR-X)WADA, Takahito; KUBOTA, Takeo; FUKUSHIMA, Yoshimitsu et al.American journal of medical genetics. 2000, Vol 94, Num 3, pp 242-248, issn 0148-7299Article

Myelination of a fetus with Pelizaeus-Merzbacher disease: Immunopathological studySHIRAISHI, Kazuhiro; ITOH, Masayski; SANO, Kenji et al.Annals of neurology. 2003, Vol 54, Num 2, pp 259-262, issn 0364-5134, 4 p.Article

Dilinoleoyl-phosphatidylethanolamine from Hericium erinaceum protects against ER stress-dependent Neuro2a cell death via protein kinase C pathwayNAGAI, Kaom; CHIBA, Akiko; NISHINO, Toru et al.Journal of nutritional biochemistry. 2006, Vol 17, Num 8, pp 525-530, issn 0955-2863, 6 p.Article

22q13 Microduplication in Two Patients With Common Clinical Manifestations : A Recognizable Syndrome?OKAMOTO, Nobuhiko; KUBOTA, Takeo; HOSOKAI, Noboru et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 23, pp 2804-2809, issn 1552-4825, 6 p.Article

Combined hypermethylation and chromosome loss associated with inactivation of SST-1/SOCS-1/JAB gene in human hepatocellular carcinomasNAGAI, Hisaki; YONG SUNG KIM; KONISHI, Noboru et al.Cancer letters. 2002, Vol 186, Num 1, pp 59-65, issn 0304-3835, 7 p.Article

Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostosesSEKI, Hiroshi; KUBOTA, Takeo; IKEGAWA, Shiro et al.American journal of medical genetics. 2001, Vol 99, Num 1, pp 59-62, issn 0148-7299Article

Analysis of Renal Cell Carcinoma as a First Step for Developing Mass Spectrometry-Based DiagnosticsYOSHIMURA, Kentaro; CHEN, Lee Chuin; KATOH, Ryohei et al.Journal of the American Society for Mass Spectrometry. 2012, Vol 23, Num 10, pp 1741-1749, issn 1044-0305, 9 p.Article

The Incidence of Hypoplasia of the Corpus Callosum in Patients With dup (X)[q28] Involving MECP2 Is Associated With the Location of Distal BreakpointsHONDA, Shozo; HAYASHI, Shin; NAKAGAWA, Eiji et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 6, pp 1292-1303, issn 1552-4825, 12 p.Article

Functional disomy for Xq22-q23 in a girl with complex rearrangements of chromosomes 3 and XIDA, Tomoko; MIHARU, Norio; HAYASHITANI, Michiko et al.American journal of medical genetics. 2003, Vol 120A, Num 4, pp 557-561, issn 0148-7299, 5 p.Article

Mutational analysis of the WASP gene in 2 Korean families with Wiskott-Aldrich syndromeJO, Eun-Kyeong; FUTATANI, Takeshi; KANEGANE, Hirokazu et al.International journal of hematology. 2003, Vol 78, Num 1, pp 40-44, issn 0925-5710, 5 p.Article

Duplication of 15q11.2-q14, including the P gene, in a woman with generalized skin hyperpigmentationAKAHOSHI, Keiko; FUKAI, Kazuyoshi; KATO, Atsushi et al.American journal of medical genetics. 2001, Vol 104, Num 4, pp 299-302, issn 0148-7299Article

Severe cervical kyphosis in osteopathia striata with cranial sclerosis : case reportKONDOH, Tatsuro; YOSHINAGA, Muneyoshi; MATSUMOTO, Tadashi et al.Pediatric radiology. 2001, Vol 31, Num 9, pp 659-662, issn 0301-0449Article

Total Performance of 32-nm-Node Ultralow-k/Cu Dual-Damascene Interconnects Featuring Short-TAT Silylated Porous Silica (k = 2.1)ODA, Noriaki; CHIKAKI, Shinichi; HAYASHI, Ryo et al.I.E.E.E. transactions on electron devices. 2010, Vol 57, Num 11, pp 2821-2830, issn 0018-9383, 10 p.Article

ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutationKUBOTA, Takeo; FURUUMI, Hiroyasu; KAMODA, Tomohiro et al.American journal of medical genetics. 2004, Vol 129A, Num 3, pp 290-293, issn 0148-7299, 4 p.Article

Prenatal interphase FISH diagnosis of PLP1 duplication associated with Pelizaeus-Merzbacher diseaseINOUE, Ken; KANAI, Makoto; TANABE, Yuzo et al.Prenatal diagnosis. 2001, Vol 21, Num 13, pp 1133-1136, issn 0197-3851Article

Role of Complement Factor H I62V and Age-Related Maculopathy Susceptibility 2 A69S Variants in the Clinical Expression of Polypoidal Choroidal VasculopathySAKURADA, Yoichi; KUBOTA, Takeo; IMASAWA, Mitsuhiro et al.Ophthalmology (Rochester, MN). 2011, Vol 118, Num 7, pp 1402-1407, issn 0161-6420, 6 p.Article

Methyl CpG-binding protein 2 (a mutation of which causes rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brainsITOH, Masayuki; IDE, Shuhei; TANABE, Yuzo et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 2, pp 117-123, issn 0022-3069, 7 p.Article

Methylation status of the p15 and p16 genes in paediatric myelodysplastic syndrome and juvenile myelomonocytic leukaemiaHASEGAWA, Daisuke; MANABE, Atsushi; SAKASHITA, Kuzuo et al.British journal of haematology. 2005, Vol 128, Num 6, pp 805-812, issn 0007-1048, 8 p.Article

Three novel DNMT3B mutations in japanese patients with ICF syndromeSHIROHZU, Hisao; KUBOTA, Takeo; HAYASHI, Masatoshi et al.American journal of medical genetics. 2002, Vol 112, Num 1, pp 31-37, issn 0148-7299Article

Ambient imaging mass spectrometry by electrospray ionization using solid needle as sampling probeLEE CHUIN CHEN; YOSHIMURA, Kentaro; HIRAOKA, Kenzo et al.Journal of mass spectrometry. 2009, Vol 44, Num 10, pp 1469-1477, issn 1076-5174, 9 p.Article

Association of LOC387715 A69S With Vitreous Hemorrhage in Polypoidal Choroidal VasculopathySAKURADA, Yoichi; KUBOTA, Takeo; MABUCHI, Fumihiko et al.American journal of ophthalmology. 2008, Vol 145, Num 6, pp 1058-1062, issn 0002-9394, 5 p.Article

Secreted protein-based reporter systems for monitoring inflammatory events : Critical interference by endoplasmic reticulum stressHIRAMATSU, Nobuhiko; KASAI, Ayumi; HAYAKAWA, Kunihiro et al.Journal of immunological methods. 2006, Vol 315, Num 1-2, pp 202-207, issn 0022-1759, 6 p.Article