Toshihiko Shiroishi
Title
Cited by
Cited by
Year
Behavioral phenotypes of Disc1 missense mutations in mice
SJ Clapcote, TV Lipina, JK Millar, S Mackie, S Christie, F Ogawa, ...
Neuron 54 (3), 387-402, 2007
5522007
Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning
N Kondrashov, A Pusic, CR Stumpf, K Shimizu, AC Hsieh, S Xue, ...
Cell 145 (3), 383-397, 2011
4372011
Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q
N Miyoshi, H Wagatsuma, S Wakana, T Shiroishi, M Nomura, K Aisaka, ...
Genes to Cells 5 (3), 211-220, 2000
3702000
Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb
T Sagai, M Hosoya, Y Mizushina, M Tamura, T Shiroishi
Development 132 (4), 797-803, 2005
3652005
Abnormal skeletal patterning in embryos lacking a single Cbp allele: a partial similarity with Rubinstein–Taybi syndrome
Y Tanaka, I Naruse, T Maekawa, H Masuya, T Shiroishi, S Ishii
Proceedings of the National Academy of Sciences 94 (19), 10215-10220, 1997
3381997
Male-to-female sex reversal in M33 mutant mice
Y Katoh-Fukui, R Tsuchiya, T Shiroishi, Y Nakahara, N Hashimoto, ...
Nature 393 (6686), 688-692, 1998
3041998
Chromosomal dynamics at the Shh locus: limb bud-specific differential regulation of competence and active transcription
T Amano, T Sagai, H Tanabe, Y Mizushina, H Nakazawa, T Shiroishi
Developmental cell 16 (1), 47-57, 2009
2762009
Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
Y Kuroiwa, T Kaneko-Ishino, F Kagitani, T Kohda, LL Li, M Tada, R Suzuki, ...
Nature genetics 12 (2), 186-190, 1996
2681996
Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method
Y Hayashizaki, H Shibata, S Hirotsune, H Sugino, Y Okazaki, N Sasaki, ...
Nature genetics 6 (1), 33-40, 1994
2601994
Unique functions of Sonic hedgehog signaling during external genitalia development
R Haraguchi, R Mo, C Hui, J Motoyama, S Makino, T Shiroishi, W Gaffield, ...
Development 128 (21), 4241-4250, 2001
2262001
Identification of two Sox17 messenger RNA isoforms, with and without the high mobility group box region, and their differential expression in mouse spermatogenesis.
Y Kanai, M Kanai-Azuma, T Noce, TC Saido, T Shiroishi, Y Hayashi, ...
The Journal of cell biology 133 (3), 667-681, 1996
2211996
A duplicated zone of polarizing activity in polydactylous mouse mutants.
H Masuya, T Sagai, S Wakana, K Moriwaki, T Shiroishi
Genes & development 9 (13), 1645-1653, 1995
2111995
Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
Y Obata, T Kaneko-Ishino, T Koide, Y Takai, T Ueda, I Domeki, T Shiroishi, ...
Development 125 (8), 1553-1560, 1998
2081998
Autoimmune disorders associated with gain of function of the intracellular sensor MDA5
M Funabiki, H Kato, Y Miyachi, H Toki, H Motegi, M Inoue, O Minowa, ...
Immunity 40 (2), 199-212, 2014
1852014
Expression of the Elm1 Gene, a Novel Gene of the CCN (Connective Tissue Growth Factor, Cyr61/Cef10, and Neuroblastoma Overexpressed Gene) Family …
Y Hashimoto, N Shindo-Okada, M Tani, Y Nagamachi, K Takeuchi, ...
The Journal of experimental medicine 187 (3), 289-296, 1998
1541998
Phylogenetic conservation of a limb-specific, cis-acting regulator of Sonic hedgehog (Shh)
T Sagai, H Masuya, M Tamura, K Shimizu, Y Yada, S Wakana, Y Gondo, ...
Mammalian Genome 15 (1), 23-34, 2004
1472004
Members of a novel gene family, Gsdm, are expressed exclusively in the epithelium of the skin and gastrointestinal tract in a highly tissue-specific manner
M Tamura, S Tanaka, T Fujii, A Aoki, H Komiyama, K Ezawa, K Sumiyama, ...
Genomics 89 (5), 618-629, 2007
1382007
Functional annotation of mouse genome sequences
JH Nadeau, R Balling, G Barsh, D Beier, SDM Brown, M Bucan, ...
Science 291 (5507), 1251-1255, 2001
1342001
The autocrine motility factor receptor gene encodes a novel type of seven transmembrane protein 1
K Shimizu, M Tani, H Watanabe, Y Nagamachi, Y Niinaka, T Shiroishi, ...
FEBS letters 456 (2), 295-300, 1999
1321999
Hybrid breakdown caused by substitution of the X chromosome between two mouse subspecies
A Oka, A Mita, N Sakurai-Yamatani, H Yamamoto, N Takagi, ...
Genetics 166 (2), 913-924, 2004
1272004
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