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Development (Cambridge, England)|October 1, 1996
Msx1 controls inductive signaling in mammalian tooth morphogenesisY Chen, M Bei, I Woo, et al.Nature Genetics|April 1, 1994
Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth developmentI Satokata, R MaasNature|March 30, 1995
Sexually dimorphic sterility phenotypes in Hoxa10-deficient miceI Satokata, G Benson, R MaasNature Genetics|March 31, 2000
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formationI Satokata, L Ma, H Ohshima, et al.Critical Reviews in Oral Biology and Medicine : an Official Publication of the American Association of Oral Biologists|January 1, 1997
The genetic control of early tooth developmentR Maas, M BeiDevelopment (Cambridge, England)|October 1, 1998
FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth developmentM Bei, R MaasJournal of Human Hypertension|February 1, 1993
Erythrocyte Na/K flux ratio in relation to sodium intake and a family history of essential hypertension in normotensive childrenM Uchiyama, I SatokataCellular and Molecular Biology (Noisy-Le-Grand, France)|October 8, 1999
Middle ear defects associated with the double knock out mutation of murine goosecoid and Msx1 genesS Kuratani, I Satokata, M Blum, et al.Human Genetics|March 1, 1992
Molecular basis of group A xeroderma pigmentosum: a missense mutation and two deletions located in a zinc finger consensus sequence of the XPAC geneI Satokata, K Tanaka, Y OkadaMutation Research|March 1, 1992
Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosumI Satokata, K Tanaka, S Yuba, et al.Pageof 1,654