Kazuhiko Nakabayashi
Kazuhiko Nakabayashi
National Research Institute for Child Health and Development
Verified email at ncchd.go.jp
Cited by
Cited by
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly
LA Lettice, T Horikoshi, SJH Heaney, MJ van Baren, HC van der Linde, ...
Proceedings of the national academy of sciences 99 (11), 7548-7553, 2002
Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks
H Kobayashi, T Sakurai, M Imai, N Takahashi, A Fukuda, O Yayoi, S Sato, ...
PLoS genetics 8 (1), e1002440, 2012
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line
ROS Center, FANTOM Consortium
Nature genetics 41 (5), 553, 2009
Targeted DNA demethylation in vivo using dCas9–peptide repeat and scFv–TET1 catalytic domain fusions
S Morita, H Noguchi, T Horii, K Nakabayashi, M Kimura, K Okamura, ...
Nature biotechnology 34 (10), 1060-1065, 2016
Human chromosome 7: DNA sequence and biology
SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ...
Science 300 (5620), 767-772, 2003
Human chromosome 7: DNA sequence and biology
SW Scherer, J Cheung, JR MacDonald, LR Osborne, K Nakabayashi, ...
Science 300 (5620), 767-772, 2003
Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia
L Feuk, A Kalervo, M Lipsanen-Nyman, J Skaug, K Nakabayashi, ...
The American Journal of Human Genetics 79 (5), 965-972, 2006
Human genetic variation database, a reference database of genetic variations in the Japanese population
K Higasa, N Miyake, J Yoshimura, K Okamura, T Niihori, H Saitsu, K Doi, ...
Journal of human genetics 61 (6), 547-553, 2016
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment
C Tayama, V Romanelli, A Martin-Trujillo, I Iglesias-Platas, K Okamura, ...
Genome research 24 (4), 554-569, 2014
5-Bromodeoxyuridine induces senescence-like phenomena in mammalian cells regardless of cell type or species
M Eriko, K Nakabayashi, T Suzuki, SC Kaul, H Ogino, M Fujii, Y Mitsui, ...
The Journal of Biochemistry 126 (6), 1052-1059, 1999
Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals
A Henckel, K Nakabayashi, LA Sanz, R Feil, K Hata, P Arnaud
Human molecular genetics 18 (18), 3375-3383, 2009
Post-transcriptional regulation of endothelial nitric-oxide synthase by an overlapping antisense mRNA transcript
GB Robb, AR Carson, SC Tai, JE Fish, S Singh, T Yamada, SW Scherer, ...
Journal of Biological Chemistry 279 (36), 37982-37996, 2004
Endothelial nitric-oxide synthase antisense (NOS3AS) gene encodes an autophagy-related protein (APG9-like2) highly expressed in trophoblast
T Yamada, AR Carson, I Caniggia, K Umebayashi, T Yoshimori, ...
Journal of Biological Chemistry 280 (18), 18283-18290, 2005
Offspring production with sperm grown in vitro from cryopreserved testis tissues
T Yokonishi, T Sato, M Komeya, K Katagiri, Y Kubota, K Nakabayashi, ...
Nature communications 5 (1), 1-6, 2014
Release of telomeric DNA from chromosomes in immortal human cells lacking telomerase activity
H Ogino, K Nakabayashi, M Suzuki, E Takahashi, M Fujii, T Suzuki, ...
Biochemical and biophysical research communications 248 (2), 223-227, 1998
ZNF384-related fusion genes define a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with a characteristic immunotype
S Hirabayashi, K Ohki, K Nakabayashi, H Ichikawa, Y Momozawa, ...
Haematologica 102 (1), 118, 2017
Chromosomal regions containing high-density and ambiguously mapped putative single nucleotide polymorphisms (SNPs) correlate with segmental duplications in the human genome
X Estivill, J Cheung, M Angel Pujana, K Nakabayashi, SW Scherer, ...
Human molecular genetics 11 (17), 1987-1995, 2002
Identification of the Imprinted KLF14 Transcription Factor Undergoing Human-Specific Accelerated Evolution
L Parker-Katiraee, AR Carson, T Yamada, P Arnaud, R Feil, ...
PLoS genetics 3 (5), e65, 2007
Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis
A Kubo, A Shiohama, T Sasaki, K Nakabayashi, H Kawasaki, T Atsugi, ...
The American Journal of Human Genetics 93 (5), 945-956, 2013
Genetic analysis of patients with the Saethre‐Chotzen phenotype
K Chun, AS Teebi, JH Jung, S Kennedy, R Laframboise, WS Meschino, ...
American journal of medical genetics 110 (2), 136-143, 2002
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