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Junichiro Machida

Showing results (1-10 of 21) with videos related to

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Human Genome Variation|April 2, 2026
MSX1 variant causes nonsyndromic tooth agenesis in a Japanese patientYasuto Sano, Michiyo Ando, Reiko Tokuyama-Toda, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|November 21, 2017
Identification of nuclear localization signals in the human homeoprotein MSX1Akio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|January 15, 2009
Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleationNorio Kuroyanagi, Hidenori Sakuma, Satoru Miyabe, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|September 9, 2016
p53 and ki67 as biomarkers in determining response to chemoprevention for oral leukoplakiaToru Nagao, Saman Warnakulasuriya, Hidenori Sakuma, et al.
Human Genome Variation|January 26, 2018
WNT10A variants isolated from Japanese patients with congenital tooth agenesisJunichiro Machida, Hiroaki Goto, Tadashi Tatematsu, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontiaMunefumi Kamamoto, Junichiro Machida, Seishi Yamaguchi, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|October 9, 2004
Two missense mutations in the IRF6 gene in two Japanese families with Van der Woude syndromeNoriko Matsuzawa, Koh-Ichiro Yoshiura, Junichiro Machida, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 26, 2009
Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12)Junichiro Machida, Têmis M Félix, Jeffrey C Murray, et al.
European Journal of Oral Sciences|December 17, 2013
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4Masashi Kimura, Junichiro Machida, Seishi Yamaguchi, et al.
Plos One|August 8, 2014
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesisSeishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Human Genome Variation|April 2, 2026
MSX1 variant causes nonsyndromic tooth agenesis in a Japanese patientYasuto Sano, Michiyo Ando, Reiko Tokuyama-Toda, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|November 21, 2017
Identification of nuclear localization signals in the human homeoprotein MSX1Akio Shibata, Junichiro Machida, Seishi Yamaguchi, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|January 15, 2009
Prognostic factors for keratocystic odontogenic tumor (odontogenic keratocyst): analysis of clinico-pathologic and immunohistochemical findings in cysts treated by enucleationNorio Kuroyanagi, Hidenori Sakuma, Satoru Miyabe, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|September 9, 2016
p53 and ki67 as biomarkers in determining response to chemoprevention for oral leukoplakiaToru Nagao, Saman Warnakulasuriya, Hidenori Sakuma, et al.
Human Genome Variation|January 26, 2018
WNT10A variants isolated from Japanese patients with congenital tooth agenesisJunichiro Machida, Hiroaki Goto, Tadashi Tatematsu, et al.
European Journal of Human Genetics : EJHG|March 31, 2011
Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontiaMunefumi Kamamoto, Junichiro Machida, Seishi Yamaguchi, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|October 9, 2004
Two missense mutations in the IRF6 gene in two Japanese families with Van der Woude syndromeNoriko Matsuzawa, Koh-Ichiro Yoshiura, Junichiro Machida, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|November 26, 2009
Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12)Junichiro Machida, Têmis M Félix, Jeffrey C Murray, et al.
European Journal of Oral Sciences|December 17, 2013
Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4Masashi Kimura, Junichiro Machida, Seishi Yamaguchi, et al.
Plos One|August 8, 2014
Characterization of novel MSX1 mutations identified in Japanese patients with nonsyndromic tooth agenesisSeishi Yamaguchi, Junichiro Machida, Munefumi Kamamoto, et al.
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