OGINO Toshihiko | Department of Orthopedic Surgery, Yamagata University School of Medicine

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概要

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著作論文

A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet
Ultrasonographic Assessment of the Ulnar Collateral Ligament and Medial Elbow Laxity in College Baseball Players
Hyaluronate Inhibits the Interleukin-1β-Induced Expression of Matrix Metalloproteinase (MMP)-1 and MMP-3 in Human Synovial Cells
TITANIUM PARTICLES MODULATE MMPs-TIMPs mRNA PRODUCTION IN MG-63 CELL : QUANTITATIVE ANALYSIS BY REAL TIME PCR
HISTOMORPHOMETRIC ANALYSIS OF CONNECTIVE TISSUE REMODELING IN BONE-ARTIFICIAL HIP PROSTHESIS INTERFACE
Spatio-temporal expression of activating transcription factor 5 in the skeletal development of mouse limb
Investigation of DNA Synthesis and Cell Condensation in the Developing Rat Hand Plate by the BrdU/anti-BrdU Technique
Busulfan-induced central polydactyly, syndactyly and cleft hand or foot : A common mechanism of disruption leads to divergent phenotypes
Radiological features of long bones in synovitis, acne, pustulosis, hyperostosis, osteitis syndrome and their correlation with pathological findings
Mid-term results of joint-preserving procedures by a modified Mann method for big toe deformities in rheumatoid patients undergoing forefoot surgeries
Antibiotics-impregnated cement spacers in the first step of two-stage revision for infected totally replaced hip joints : report of ten trial cases
Clinical Features of Congenital Contractural Arachnodactyly
Effects of bone morphogenetic protein-2 on human tumor cell growth and differentiation : a preliminary report
A Clinical and Experimental Study on Longitudinal Deficiencies in Lower Limbs in Relation to Pathogenesis of Cleft Foot
Clinical Features and Operative Findings of Congenital Flexion Deformity of Multiple Digits
Lumbosacral Plexus in Hoxa9 Knockout Mice with Special Reference to their Nerve Variations Identified According to whether they Were Interphenotypic or Intergenotypic Differences
Trichorhinophalangeal syndrome type II without the chromosome 8 deletion that resembled metachondromatosis
Dendritic cell and effector cell infiltration in soft tissue sarcomas with reactive lymphoid hyperplasia
Malignant intramuscular forearm tumor with overwhelming squamous element
FGFR2 mutation in a patient with Apert syndrome associated with humeroradial synostosis
Classification and treatment of congenital hand differences
Lipoblastoma with aberration in the long arm of chromosome 8
Aberrant muscle syndrome : Hypertrophy of the hand and arm due to aberrant muscles with or without hypertrophy of the muscles

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