Carbon nanocapsules and single‐layered nanotubes produced with platinum‐group metals (Ru, Rh, Pd, Os, Ir, Pt) by arc discharge
…, K Nishikubo, K Kawabata, T Matsumoto - Journal of applied …, 1996 - pubs.aip.org
Encapsulation of platinum‐group metals (Ru, Rh, Pd, Os, Ir, Pt) within carbon nanocapsules
and synthesis of single‐layered (SL) carbon nanotubes by arc evaporation of metal/carbon …
and synthesis of single‐layered (SL) carbon nanotubes by arc evaporation of metal/carbon …
Extra-chromosomal telomere repeat DNA in telomerase-negative immortalized cell lines
Y Tokutake, T Matsumoto, T Watanabe, S Maeda… - Biochemical and …, 1998 - Elsevier
We found novel extra-chromosomal telomere repeat (ECTR) DNAs in telomerase-negative
immortalized KMST-6 cells, by staining these cells with a (TTAGGG) n probe using both …
immortalized KMST-6 cells, by staining these cells with a (TTAGGG) n probe using both …
[HTML][HTML] Crystal structure of the human BRD2 bromodomain: insights into dimerization and recognition of acetylated histone H4
…, H Hamana, T Terada, N Adachi, T Matsumoto… - Journal of biological …, 2007 - ASBMB
The BET (bromodomains and extra terminal domain) family proteins recognize acetylated
chromatin through their bromodomain and act as transcriptional activators. One of the BET …
chromatin through their bromodomain and act as transcriptional activators. One of the BET …
Severe growth defect in mouse cells lacking the telomerase RNA component
H Niida, T Matsumoto, H Satoh, M Shiwa, Y Tokutake… - Nature …, 1998 - nature.com
The ribonucleoprotein enzyme telomerase synthesizes telomeric DNA onto chromosome
ends 1. Telomere length is maintained, by the presence of telomerase activity, in the vast …
ends 1. Telomere length is maintained, by the presence of telomerase activity, in the vast …
Differential regulation of human RecQ family helicases in cell transformation and cell cycle
…, K Nishikawa, A Shimamoto, M Shiratori, T Matsumoto… - Oncogene, 2000 - nature.com
Three human RecQ DNA helicases, WRN, BLM and RTS, are involved in the genetic disorders
associated with genomic instability and a high incidence of cancer. RecQL1 and RecQL5 …
associated with genomic instability and a high incidence of cancer. RecQL1 and RecQL5 …
Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNA
…, Y Shinkai, MP Hande, T Matsumoto… - … and cellular biology, 2000 - Taylor & Francis
Telomere dynamics, chromosomal instability, and cellular viability were studied in serial
passages of mouse embryonic stem (ES) cells in which the telomerase RNA (mTER) gene was …
passages of mouse embryonic stem (ES) cells in which the telomerase RNA (mTER) gene was …
Unusual features of thyroid carcinomas in Japanese patients with Werner syndrome and possible genotype–phenotype relations to cell type and race
Y Ishikawa, H Sugano, T Matsumoto, Y Furuichi… - Cancer, 1999 - Wiley Online Library
BACKGROUND Werner syndrome (WS), an autosomal recessive disease characterized by
premature aging, has a high frequency of association with six rare neoplasms in Japanese …
premature aging, has a high frequency of association with six rare neoplasms in Japanese …
Encapsulation of carbides of chromium, molybdenum and tungsten in carbon nanocapsules by arc discharge
Y Saito, T Matsumoto, K Nishikubo - Journal of crystal growth, 1997 - Elsevier
Encapsulation of Cr, Mo and W in multilayered graphitic cages by arc evaporation of metal/carbon
composites under different pressures of helium gas (100, 600 and 1500 Torr) has …
composites under different pressures of helium gas (100, 600 and 1500 Torr) has …
WRN helicase accelerates the transcription of ribosomal RNA as a component of an RNA polymerase I-associated complex
…, T Suzuki, C Itoh, M Goto, Y Furuichi, T Matsumoto - Oncogene, 2002 - nature.com
Werner syndrome (WS) is a rare autosmomal recessive genetic disorder causing premature
aging. The gene (WRN) responsible for WS encodes a protein homologous to the RecQ-…
aging. The gene (WRN) responsible for WS encodes a protein homologous to the RecQ-…
Mutation and haplotype analyses of the Werner's syndrome gene based on its genomic structure: genetic epidemiology in the Japanese population
T Matsumoto, O Imamura, Y Yamabe, J Kuromitsu… - Human genetics, 1997 - Springer
The correlation between mutations in the Werner’s syndrome (WRN) gene and the
haplotypes of surrounding markers was studied in Japanese patients. We have elucidated the …
haplotypes of surrounding markers was studied in Japanese patients. We have elucidated the …