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Hiroshi Kitoh

Showing results (91-100 of 133) with videos related to

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Molecular Syndromology|April 9, 2015
A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial DysplasiaMasaki Mastushita, Hiroshi Kitoh, Asli Subasioglu, et al.
Orthopedics|October 22, 2015
Prediction of Clinically Significant Leg-Length Discrepancy in Congenital DisordersKenichi Mishima, Hiroshi Kitoh, Izumi Kadono, et al.
Plos One|December 11, 2013
Meclozine facilitates proliferation and differentiation of chondrocytes by attenuating abnormally activated FGFR3 signaling in achondroplasiaMasaki Matsushita, Hiroshi Kitoh, Bisei Ohkawara, et al.
BMC Musculoskeletal Disorders|March 17, 2023
Activated FGFR3 suppresses bone regeneration and bone mineralization in an ovariectomized mouse modelItaru Kawashima, Masaki Matsushita, Kenichi Mishima, et al.
Molecular Genetics & Genomic Medicine|January 25, 2020
Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case reportTadashi Nagata, Masaki Matsushita, Kenichi Mishima, et al.
Pediatric Radiology|August 6, 2016
Characteristic calcaneal ossification: an additional early radiographic finding in infants with fibrodysplasia ossificans progressivaSachi Hasegawa, Teresa Victoria, Hülya Kayserili, et al.
Clinical Orthopaedics and Related Research|May 16, 2002
Distraction osteogenesis enhanced by osteoblastlike cells and collagen gelYuji Takamine, Hiroki Tsuchiya, Takahiko Kitakoji, et al.
Human Genetics|May 20, 2011
Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8Hiroshi Kaneko, Hiroshi Kitoh, Tohru Matsuura, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
Novel COL9A3 mutation in a family with multiple epiphyseal dysplasiaEiji Nakashima, Hiroshi Kitoh, Koichi Maeda, et al.
Intractable & Rare Diseases Research|October 25, 2014
Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressivaKenichi Mishima, Hiroshi Kitoh, Nobuhiko Haga, et al.
Pageof 14

Showing results (91-100 of 133) with videos related to

Sort By:
Pageof 14
Molecular Syndromology|April 9, 2015
A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial DysplasiaMasaki Mastushita, Hiroshi Kitoh, Asli Subasioglu, et al.
Orthopedics|October 22, 2015
Prediction of Clinically Significant Leg-Length Discrepancy in Congenital DisordersKenichi Mishima, Hiroshi Kitoh, Izumi Kadono, et al.
Plos One|December 11, 2013
Meclozine facilitates proliferation and differentiation of chondrocytes by attenuating abnormally activated FGFR3 signaling in achondroplasiaMasaki Matsushita, Hiroshi Kitoh, Bisei Ohkawara, et al.
BMC Musculoskeletal Disorders|March 17, 2023
Activated FGFR3 suppresses bone regeneration and bone mineralization in an ovariectomized mouse modelItaru Kawashima, Masaki Matsushita, Kenichi Mishima, et al.
Molecular Genetics & Genomic Medicine|January 25, 2020
Severe achondroplasia due to two de novo variants in the transmembrane domain of FGFR3 on the same allele: A case reportTadashi Nagata, Masaki Matsushita, Kenichi Mishima, et al.
Pediatric Radiology|August 6, 2016
Characteristic calcaneal ossification: an additional early radiographic finding in infants with fibrodysplasia ossificans progressivaSachi Hasegawa, Teresa Victoria, Hülya Kayserili, et al.
Clinical Orthopaedics and Related Research|May 16, 2002
Distraction osteogenesis enhanced by osteoblastlike cells and collagen gelYuji Takamine, Hiroki Tsuchiya, Takahiko Kitakoji, et al.
Human Genetics|May 20, 2011
Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8Hiroshi Kaneko, Hiroshi Kitoh, Tohru Matsuura, et al.
American Journal of Medical Genetics. Part A|November 20, 2004
Novel COL9A3 mutation in a family with multiple epiphyseal dysplasiaEiji Nakashima, Hiroshi Kitoh, Koichi Maeda, et al.
Intractable & Rare Diseases Research|October 25, 2014
Radiographic characteristics of the hand and cervical spine in fibrodysplasia ossificans progressivaKenichi Mishima, Hiroshi Kitoh, Nobuhiko Haga, et al.
Pageof 14