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조태준 교수

Tae-Joon Cho

서울대학교 · 의학

연구실 소개

조태준 교수의 연구실은 뼈 형성과 골수 손상 치유 메커니즘을 중심으로, 성장 인자인 BMP, TGF-β, CNP 등 신호전달 경로의 분자적 역할을 규명하고 있습니다. 특히 골형성 조절 단백질과 그 유전자 발현의 시계열적 변화, 뼈와 연골의 발달 및 성장에 영향을 미치는 분자 기전에 초점을 맞추고 있으며, 골수세포의 분화 능력과 골다공로증, 골이형성 등 뼈 질환의 분자 기전 연구도 진행 중입니다. 또한 나노소재 기반의 신약 전달체 개발과 골 형성 촉진을 위한 나노입자 설계 등 응용 연구도 병행하고 있습니다.

골형성성장 인자BMPCNP 신호전달나노소재 기반 치료

연구 현황

논문 수
451
총 인용 수
10,414
최근 5년 논문
31
주요 분야
의학

연구 성과 추이

표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.

5개년 연도별 논문 게재 수
31총합
2022
2023
2024
2025
2026
5개년 연도별 피인용 수
100총합
20222023202420252026

주요 논문

15
1
논문|인용수 738·2002
Differential Temporal Expression of Members of the Transforming Growth Factor β Superfamily During Murine Fracture Healing
Tae‐Joon Cho, Louis C. Gerstenfeld, Thomas A. Einhorn
SJR Q1FWCI 11.2Journal of Bone and Mineral Research

Fracture healing is a unique postnatal repair process in which the events of endochondral and intramembranous bone formation follow a definable temporal sequence. The temporal patterns of messenger RNA (mRNA) expression for members of the transforming growth factor beta (TGF-beta) superfamily were examined over a 28-day period of fracture healing in mouse tibias. Bone morphogenetic protein 2 (BMP-2) and growth and differentiation factor 8 (GDF8) showed maximal expression on day 1 after fracture,

EpidemiologyMedicine
2
논문|인용수 260·2012
A Single Recurrent Mutation in the 5′-UTR of IFITM5 Causes Osteogenesis Imperfecta Type V
Tae‐Joon Cho, Kyung-Eun Lee, Sook-Kyung Lee, Su Jeong Song, Kyung Jin Kim, Daehyun Jeon, Gene Lee, Ha-Neui Kim, Hyeran Lee, Hye-Hyun Eom, Zhuang Min Lee, Ok-Hwa Kim
SJR Q1FWCI 20.3The American Journal of Human GeneticsOA
GeneticsBiochemistry, Genetics and Molecular Biology
3
논문|인용수 148·2008
Mobilization of endothelial progenitor cells in fracture healing and distraction osteogenesis
Dong Yeon Lee, Tae‐Joon Cho, Jin A Kim, Hyeran Lee, Won Joon Yoo, Chin Youb Chung, In Ho Choi
SJR Q1FWCI 10.4Bone
SurgeryMedicine
4
논문|인용수 89·2013
Overgrowth syndrome associated with a gain‐of‐function mutation of the natriuretic peptide receptor 2 (<i>NPR2</i>) gene
Kohji Miura, Ok‐Hwa Kim, Hey Ran Lee, Noriyuki Namba, Toshimi Michigami, Won Joon Yoo, In Ho Choi, Keiichi Ozono, Tae‐Joon Cho
SJR Q2FWCI 2.8American Journal of Medical Genetics Part AOA

The signal pathway of the C-type natriuretic (CNP) and its receptor, natriuretic peptide receptor 2 (NPR2) is involved in the longitudinal growth of long bones. Loss of function mutations at NPR2 cause acromesomelic dysplasia, type Maroteaux, while overproduction of CNP by chromosomal translocation and a gain-of-function mutation at NPR2 have been reported to be responsible for an overgrowth syndrome in three cases and one family, respectively. We identified a four-generation family with an over

OncologyMedicine
5
논문|인용수 88·2008
Biologic Characteristics of Fibrous Hamartoma from Congenital Pseudarthrosis of the Tibia Associated with Neurofibromatosis Type 1
Tae‐Joon Cho, Joong-Bae Seo, Hyeran Lee, Won Joon Yoo, Chin Youb Chung, In Ho Choi
SJR Q1FWCI 1.9Journal of Bone and Joint Surgery

Fibrous hamartoma cells maintain some of the mesenchymal lineage cell phenotypes, but do not undergo osteoblastic differentiation in response to BMP. They are more osteoclastogenic than are tibial periosteal cells.

RheumatologyMedicine
6
논문|인용수 86·2005
Calcaneal Lengthening for the Planovalgus Foot Deformity in Children With Cerebral Palsy
Won Joon Yoo, Chin Youb Chung, In Ho Choi, Tae‐Joon Cho, Donghan Kim
SJR Q2FWCI 1.5Journal of Pediatric Orthopaedics

The authors studied the outcomes of calcaneal lengthening for the treatment of planovalgus foot deformity in ambulatory children with cerebral palsy (92 feet in 56 children, mean age 9.2 years), attempting to define the surgical indication in terms of the severity of the foot deformity. Sixty-nine cases (75%) showed satisfactory clinical outcomes at an average follow-up of 5.2 years (range 4.0-17.2 years). Gait parameters such as foot progression angle, ankle motion in sagittal plane, and its po

Orthopedics and Sports MedicineMedicine
7
논문|인용수 85·2007
Prediction of cyclic freeze–thaw damage in concrete structures based on response surface method
Tae‐Joon Cho
SJR Q1FWCI 2.6Construction and Building Materials
PollutionEnvironmental Science
8
논문|인용수 83·2007
Interlocking Telescopic Rod for Patients with Osteogenesis Imperfecta
Tae‐Joon Cho, In Ho Choi, Chin Youb Chung, Won Joon Yoo, Ki Seok Lee, Dong Yeon Lee
SJR Q1FWCI 2.0Journal of Bone and Joint Surgery

Both insertion and removal of an interlocking telescopic rod are much less invasive than insertion and removal of a conventional telescopic rod with a T-piece anchor. The interlocking pin at the distal epiphysis provides effective anchorage for telescoping. Our interim results showed survival of the device to be comparable with, or better than, that of the conventional telescopic rod.

GeneticsBiochemistry, Genetics and Molecular Biology
9
논문|인용수 82·2014
Managing knowledge performance: testing the components of a knowledge management system on organizational performance
Taejun Cho, Russell Korte
SJR Q1FWCI 14.1Asia Pacific Education Review
CommunicationSocial Sciences
10
논문|인용수 70·2019
The structural relationship between organizational justice and organizational citizenship behavior in university faculty in China: the mediating effect of organizational commitment
Zhao Donglong, Taejun Cho, Ahn Julie, Sang-Hun Lee
SJR Q1FWCI 4.3Asia Pacific Education Review
Organizational Behavior and Human Resource ManagementBusiness, Management and Accounting
11
논문|인용수 70·2007
Expression and Role of Interleukin-6 in Distraction Osteogenesis
Tae‐Joon Cho, J. A. Kim, Chin Youb Chung, Won Joon Yoo, L. C. Gerstenfeld, Thomas A. Einhorn, In Ho Choi
SJR Q1FWCI 1.0Calcified Tissue International
EpidemiologyMedicine
12
논문|인용수 69·2011
“4-in-1 Osteosynthesis” for Atrophic-type Congenital Pseudarthrosis of the Tibia
In Ho Choi, Soong Joon Lee, Hyuk Ju Moon, Tae‐Joon Cho, Won Joon Yoo, Chin Youb Chung, Moon Seok Park
SJR Q2FWCI 1.4Journal of Pediatric Orthopaedics

Level III, Retrospective comparative study.

GeneticsBiochemistry, Genetics and Molecular Biology
13
논문|인용수 65·2000
The Sprengel deformity
Tae‐Joon Cho, In Ho Choi, Chin Youb Chung, Jae Kwang Hwang
FWCI 3.1Journal of Bone and Joint Surgery - British VolumeOA

We evaluated scapular dysplasia and malposition in 15 patients with the Sprengel deformity using three-dimensional CT (3D-CT). The shape, height-to-width ratio, the areas of both scapulae, the anterior curvature of the supraspinous portion and glenoid version were assessed on scapular posterior, medial and inferior views. The degree of rotation and superior displacement were measured on the trunk posterior view. The omovertebral connection was also assessed and correlated with the operative find

Mechanical EngineeringEngineering
14
논문|인용수 63·2005
Surgical Treatment of the Severe Sequelae of Infantile Septic Arthritis of the Hip
In Ho Choi, Yong‐Woon Shin, Chin Youb Chung, Tae‐Joon Cho, Won Joon Yoo, Duk Yong Lee
SJR Q1FWCI 2.0Clinical Orthopaedics and Related Research

We retrospectively reviewed 45 hips in 43 patients with severe sequelae of infantile septic arthritis of the hip to compare the efficacy of various hip reconstructive and salvage surgeries, and to propose an algorithmic treatment protocol for the different types. Ten hips were classified as Choi Type IIIA, three as Type IIIB, 14 as Type IVA, and 18 as Type IVB sequelae. A total of 78 hip surgeries and 18 limb-length equalizations (three contralateral femoral epiphysiodesis and 15 ipsilateral fem

SurgeryMedicine
15
논문|인용수 63·2012
TRPV4‐pathy manifesting both skeletal dysplasia and peripheral neuropathy: A report of three patients
Tae‐Joon Cho, Kazu Matsumoto, Virginia Fano, Jin Dai, Ok‐Hwa Kim, Jong‐Hee Chae, Won Joon Yoo, Yuji Tanaka, Yoshito Matsui, Iori Takigami, Soledad Monges, Bernhard Zabel
SJR Q2FWCI 3.6American Journal of Medical Genetics Part A

Heterozygous missense mutations of transient receptor potential vanilloid 4 channel (TRPV4) cause a spectrum of skeletal disorders, including brachyolmia, spondylometaphyseal dysplasia Kozlowski type, metatropic dysplasia, parastremmatic dysplasia, and spondyloepimetaphyseal dysplasia Maroteaux type. Similarly, heterozygous missense mutations of TRPV4 cause a spectrum of peripheral neuropathy, including hereditary motor and sensory neuropathy type IIC, congenital spinal muscular atrophy, and sca

Sensory SystemsNeuroscience

대표 연구 분야

GeneticsSurgeryEpidemiologyPsychiatry and Mental healthRheumatologyCivil and Structural Engineering

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