Ikegawa S - Search Results

1

SIK3 is essential for chondrocyte hypertrophy during skeletal development in mice.

Sasagawa S, Takemori H, Uebi T, Ikegami D, Hiramatsu K, Ikegawa S, Yoshikawa H, Tsumaki N. Sasagawa S, et al. Among authors: ikegawa s. Development. 2012 Mar;139(6):1153-63. doi: 10.1242/dev.072652. Epub 2012 Feb 8. Development. 2012. PMID: 22318228

2

Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.

Kano H, Kurosawa K, Horii E, Ikegawa S, Yoshikawa H, Kurahashi H, Toda T. Kano H, et al. Among authors: ikegawa s. Hum Genet. 2005 Dec;118(3-4):477-83. doi: 10.1007/s00439-005-0074-0. Epub 2005 Oct 19. Hum Genet. 2005. PMID: 16235095

3

Cartilage intermediate layer protein promotes lumbar disc degeneration.

Seki S, Tsumaki N, Motomura H, Nogami M, Kawaguchi Y, Hori T, Suzuki K, Yahara Y, Higashimoto M, Oya T, Ikegawa S, Kimura T. Seki S, et al. Among authors: ikegawa s. Biochem Biophys Res Commun. 2014 Apr 18;446(4):876-81. doi: 10.1016/j.bbrc.2014.03.025. Epub 2014 Mar 14. Biochem Biophys Res Commun. 2014. PMID: 24631904

4

Modeling type II collagenopathy skeletal dysplasia by directed conversion and induced pluripotent stem cells.

Okada M, Ikegawa S, Morioka M, Yamashita A, Saito A, Sawai H, Murotsuki J, Ohashi H, Okamoto T, Nishimura G, Imaizumi K, Tsumaki N. Okada M, et al. Among authors: ikegawa s. Hum Mol Genet. 2015 Jan 15;24(2):299-313. doi: 10.1093/hmg/ddu444. Epub 2014 Sep 3. Hum Mol Genet. 2015. PMID: 25187577

5

Statin treatment rescues FGFR3 skeletal dysplasia phenotypes.

Yamashita A, Morioka M, Kishi H, Kimura T, Yahara Y, Okada M, Fujita K, Sawai H, Ikegawa S, Tsumaki N. Yamashita A, et al. Among authors: ikegawa s. Nature. 2014 Sep 25;513(7519):507-11. doi: 10.1038/nature13775. Epub 2014 Sep 17. Nature. 2014. PMID: 25231866

6

Carminerin contributes to chondrocyte calcification during endochondral ossification.

Yamada T, Kawano H, Koshizuka Y, Fukuda T, Yoshimura K, Kamekura S, Saito T, Ikeda T, Kawasaki Y, Azuma Y, Ikegawa S, Hoshi K, Chung UI, Nakamura K, Kato S, Kawaguchi H. Yamada T, et al. Among authors: ikegawa s. Nat Med. 2006 Jun;12(6):665-70. doi: 10.1038/nm1409. Epub 2006 May 7. Nat Med. 2006. PMID: 16680148

7

CANT1 deficiency in a mouse model of Desbuquois dysplasia impairs glycosaminoglycan synthesis and chondrocyte differentiation in growth plate cartilage.

Kodama K, Takahashi H, Oiji N, Nakano K, Okamura T, Niimi K, Takahashi E, Guo L, Ikegawa S, Furuichi T. Kodama K, et al. Among authors: ikegawa s. FEBS Open Bio. 2020 Jun;10(6):1096-1103. doi: 10.1002/2211-5463.12859. Epub 2020 Apr 23. FEBS Open Bio. 2020. PMID: 32277574 Free PMC article.

8

Differentiation of Hypertrophic Chondrocytes from Human iPSCs for the In Vitro Modeling of Chondrodysplasias.

Pretemer Y, Kawai S, Nagata S, Nishio M, Watanabe M, Tamaki S, Alev C, Yamanaka Y, Xue JY, Wang Z, Fukiage K, Tsukanaka M, Futami T, Ikegawa S, Toguchida J. Pretemer Y, et al. Among authors: ikegawa s. Stem Cell Reports. 2021 Mar 9;16(3):610-625. doi: 10.1016/j.stemcr.2021.01.014. Epub 2021 Feb 25. Stem Cell Reports. 2021. PMID: 33636111 Free PMC article.

9

CDC5L promotes early chondrocyte differentiation and proliferation by modulating pre-mRNA splicing of SOX9, COL2A1, and WEE1.

Jokoji G, Maeda S, Oishi K, Ijuin T, Nakajima M, Tawaratsumida H, Kawamura I, Tominaga H, Taketomi E, Ikegawa S, Taniguchi N. Jokoji G, et al. Among authors: ikegawa s. J Biol Chem. 2021 Aug;297(2):100994. doi: 10.1016/j.jbc.2021.100994. Epub 2021 Jul 21. J Biol Chem. 2021. PMID: 34298017 Free PMC article.

10

Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses.

Seki H, Kubota T, Ikegawa S, Haga N, Fujioka F, Ohzeki S, Wakui K, Yoshikawa H, Takaoka K, Fukushima Y. Seki H, et al. Among authors: ikegawa s. Am J Med Genet. 2001 Feb 15;99(1):59-62. doi: 10.1002/1096-8628(20010215)99:1<59::aid-ajmg1115>3.0.co;2-z. Am J Med Genet. 2001. PMID: 11170095

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