Papers - HAYASHI, Yoshitaka
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Aberrant promoter methylation in overexpression of CITED1 in papillary thyroid cancer. Reviewed
M. Sassa, Y. Hayashi, R. Watanabe, T. Kikumori, T. Imai, J. Kurebayashi, T. Kiuchi, Y. Murata
Thyroid Vol. 21 ( 5 ) page： 511-517 2011.5
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A novel Caspr mutation causes the shambling mouse phenotype by disrupting axo-glial interactions of myelinated nerves. Reviewed
X.Y. Sun, Y. Takagishi, E. Okabe, Y. Chishima, Y. Kanou, S. Murase, K. Mizumura, M. Inaba, Y. Komatsu, Y. Hayashi, E. Peles, S. Oda, Y. Murata
J Neuropathol Exp Neurol Vol. 68 ( 11 ) page： 1207-1218 2009.11
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Possible involvement of BRAFV600E in altered gene expression in papillary thyroid cancer. Invited Reviewed
R. Watanabe, Y. Hayashi, M. Sassa, T. Kikumori, T. Imai, T. Kiuchih, Y. Murata
Endocr J Vol. 56 page： 407-414 2009.6
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Prevention of neural tube defects by loss of function of inducible nitric oxide synthase in fetuses of a mouse model of streptozotocin-induced diabetes. Reviewed
Y. Sugimura, T. Murase, K. Oyama, A. Uchida, N. Sato, S. Hayasaka, Y. Kano, Y. Takagishi, Y. Hayashi, Y. Oiso, Y. Murata
Diabetologia Vol. 56 page： 962-971 2009.5
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Oculocutaneous Albinism in Suncus murinus: Establishment of a Strain and Identification of its Responsible Gene. Reviewed
K. Tsuboi, Y. Hayashi, T. Jogahara, G. Ogura, Y. Murata,S. Oda
Exp Anim Vol. 58 ( 1 ) page： 31-40 2009.1
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Laminin isoforms containing the gamma3 chain are unable to bind to integrins due to the absence of the glutamic acid residue conserved in the C-terminal regions of the gamma1 and gamma2 chains. Reviewed
Ido H, Ito S, Taniguchi Y, Hayashi M, Sato-Nishiuchi R, Sanzen N, Hayashi Y, Futaki S, Sekiguchi K
J Biol Chem Vol. 283 ( 42 ) page： 28149-28157 2008.10
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Identification of genes differentially expressed in mouse fetuses from streptozotocin-induced diabetic pregnancy by cDNA subtraction. Reviewed
Sato N, Sugimura Y, Hayashi Y, Murase T, Kanou Y, Kikkawa F, Murata Y
Endocr J Vol. 55 ( 2 ) page： 317-323 2008.5
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Insertion of an intracisternal A particle retrotransposon element in plasma membrane calcium ATPase 2 gene attenuates its expression and produces an ataxic phenotype in joggle mutant mice. Reviewed
Sun XY, Chen ZY, Hayashi Y, Kanou Y, Takagishi Y, Oda S, Murata Y
Gene Vol. 411 ( 1-2 ) page： 94-102 2008.3
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Long-term amiodarone treatment causes cardioselective hypothyroid-like alteration in gene expression profile. Reviewed
R.Q. Shi, J. K. Lee, Y. Hayashi, Y. Takeuchi, F. Kambe, S. Futaki, H. Seo, Y. Murata, I. Kodama
Eur J Parmacol Vol. 578 page： 270-278 2008
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Mapping of jog locus to the region between D6Mit104 and D6Mit336 on mouse chromosome 6. Reviewed
Sun XY, Chen ZY, Kanou Y, Hayashi Y, Ohno T, Murata Y, Oda S
Vol. 56 ( 5 ) page： 389-392 2007.10
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A case with isolated growth hormone deficiency caused by compound heterozygous mutations in GH-1: a novel missense mutation in the initiation codon and a 7.6kb deletion Reviewed
Hayashi Y, Kamijo T, Yamamoto M, Murata Y, Phillips JA 3rd, Ogawa M, Seo H.
Growth Horm IGF Res Vol. 17 ( 36 ) page： 249-253 2007.6
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Molecular cloning of prostaglandin EP3 receptors from canine sensory ganglia and their facilitatory action on bradykinin-induced mobilization of intracellular calcium Reviewed
Kozaki Y, Kambe F, Hayashi Y, Ohmori S, Seo H, Kumazawa T, Mizumura K
J Neurochem Vol. 100 ( 6 ) page： 1636-1647 2007.3
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Regulation of mesodermal differentiation of mouse embryonic stem cells by basement membranes. Reviewed
Fujiwara H, Hayashi Y, Sanzen N, Kobayashi R, Weber CN, Emoto T, Futaki S, Niwa H, Murray P, Edgar D, Sekiguchi K.
J Biol Chem Vol. 282 page： 29701-29711 2007
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The Sp family of transcription factors regulates the human laminin alpha1 gene in JAR choriocarcinoma cells. Reviewed
Niimi T, Hayashi Y, Sekiguchi K, Kitagawa Y.
Biochim Biophys Acta Vol. 2006 ( 11-12 ) page： 573-579 2006.11
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A novel large-scale production system for modified basement membrane matrices using gene-swapped parietal endoderm cells. Reviewed
Hayashi Y, Weber CN, Emoto T, Fujiwara H, Sanzen N, Futaki S, Sekiguchi K.
Matrix Biol Vol. 25 ( 2 ) page： 85-88 2006.3
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Activation of the RhoB signaling pathway by thyroid hormone receptor ß in thyroid cancer cells. Reviewed
S. Ichijo, F. Furuya, H. Shimura, Y. Hayashi, K. Takahashi, K. Ohta, T. Kobayashi, K. Kitamura.
PLoS ONE Vol. 9 ( 12 ) page： e116252 2005.12
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Growth hormone releasing hormone receptor (GHRH-r) gene mutation in Indian children with familial isolated growth hormone deficiency: a study from western India Reviewed
Desai MP, Upadhye PS, Kamijo T, Yamamoto M, Ogawa M, Hayashi Y, Seo H, Nair SR.
J Pediatr Endocrinol Metab Vol. 18 ( 10 ) page： 1955-973 2005.10
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The transcriptional landscape of the mammalian genome. Reviewed
Carninci P et al FANTOM Consortium; RIKEN Genome Exploration Research Group and Genome Science Group (Genome Network Project Core Group).
Science Vol. 309 page： 1559-1563 2005.9
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Sox7 Plays Crucial Roles in Parietal Endoderm Differentiation in F9 Embryonal Carcinoma Cells through Regulating Gata-4 and Gata-6 Expression. Reviewed
S. Futaki, Y. Hayashi, T. Emoto, C.N. Weber, K. SekiguchiS. Futaki, Y. Hayashi, T. Emoto, C.N. Weber, K. Sekiguchi
Mol Cell Biol Vol. 24 ( 12 ) page： 10495-10503 2004.12
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A nonsense mutation (E72X) in growth hormone releasing hormone receptor (GHRHR) gene is the major cause of familial isolated growth hormone deficiency in Western region of India: founder effect suggested by analysis of dinucleotide repeat polymorphism close to GHRHR gene Reviewed
Kamijo, T. Hayashi, Y. Seo, H. Yamamoto, M. Ogawa, M. Choski, C. S. Sawant, N. J. Colaco, M. P. Desai, M. P.
Growth Horm IGF Res Vol. 14 ( 5 ) page： 394-401 2004.10