Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Sung-Joo Kim Yoon"'
Publikováno v:
Protein & Peptide Letters. 17:485-491
Rho GTPase controls multiple signal-transduction pathways involving the actin cytoskeleton and the microtubule cytoskeleton in processes such as the cell cycle, morphogenesis, and cell migration. The activity of Rho GTPases, such as Rac1, Cdc42, and
Autor:
Kyu Hyuk Cho, Yang Seok Oh, Sung Joo Kim Yoon, Sang Seop Han, Seok Joo Yoon, Chang-Woo Song, Jong Bok Yoon, Dal Sun Cha, YoonYi Nam, Jun-Gyo Suh, Jeong Ki Kim, Jae-Woo Cho
Publikováno v:
Genomics. 87(4):520-526
A novel autosomal recessive mutant was produced using N-ethyl-N-nitrosourea mutagenesis. The characteristics of the mutant mice included progressive irreversible hair loss within a month of birth, wrinkled skin, and long curved nails. Linkage analysi
Autor:
Young Mo Seong, Seongman Kang, Hyangshuk Rhim, Hyo Jin Park, Ju Youn Choi, Chul Han, Sung Joo Kim Yoon
Publikováno v:
Biotechnology Letters. 25:1597-1603
HtrA2/Omi, a mitochondrial serine protease, is pivotal in regulating apoptotic cell death. To determine the location of antigenic determinants in HtrA2/Omi, we expressed a series of the N-terminally truncated HtrA2/Omi as GST fusion proteins in E. co
Autor:
Silke Sperling, Adrian J. L. Clark, Steffen Hennig, Katrin Handschug, Sung-Joo Kim Yoon, Angela Huebner
Publikováno v:
Human Molecular Genetics. 10:283-290
The triple A syndrome (MIM 231550) is a rare autosomal recessive disorder characterized by adrenal insufficiency, achalasia and alacrima. The frequent association with a variety of neurological features may result in a severely disabling disease. We
Autor:
Sung-Joo Kim Yoon, Choun-Ki Joo, Eunice Lee, Stephanie Lau, Angela Huebner, Hyoungnam Lee, Raju Kucherlapati, Young Seomun, Eunkyung Choi, Kate Montgomery
Publikováno v:
Genome Research. 10:1561-1567
The chromosome 12q13 (ch12q13) region of the human chromosome has been implicated in many diseases as well as various chromosomal anomalies. The region is linked to numerous inherited genetic diseases including keratin-associated diseases, triple A s
Publikováno v:
The American Journal of Human Genetics. 64(6):1775-1778
Autor:
Jacqueline T. Hecht, Sung Joo Kim Yoon, Jose L. Dieguez, David Hewett-Emmett, Michelle Deere, Albert de la Chapelle
Publikováno v:
Genome Research. 9:449-456
DSPG3, the human homolog to chick PG-Lb, is a member of the small leucine-rich repeat proteoglycan (SLRP) family, including decorin, biglycan, fibromodulin, and lumican. In contrast to the tissue distribution of the other SLRPs, DSPG3 is predominantl
Autor:
Raju Kucherlapati, Sung-Joo Kim Yoon, David C. Ward, Janine M. LeBlanc-Straceski, Kenneth Krauter
Publikováno v:
Genomics. 24:502-508
Keratin proteins constitute intermediate filaments and are the major differentiation products of mammalian epithelial cells. The epithelial keratins are classified into two groups, type I and type II, and one member of each group is expressed in a gi
Autor:
Jae-Woo Cho, Min Ji Kang, Sung Joo Kim Yoon, Eun Min Kim, Jeong Ki Kim, Kyu Hyuk Cho, Jae-Young Kim, Chang-Woo Song
Publikováno v:
BMB reports. 41(9)
A mouse with cataract, Kec, was generated from N-ethyl-N-nitrosourea (ENU) mutagenesis. Cataract in the Kec mouse was observable at about 5 weeks after birth and this gradually progressed to become completely opaque by 12 weeks. Dissection microscopy
Autor:
Yangsoo Jang, Sungha Park, Kuchan Kimm, Min Young Song, Ha Jung Ryu, Hyun Young Park, Seung Hun Cha, Jong-Keuk Lee, Jae-Jung Kim, Sung Joo Kim Yoon, Jin Hyoung Park, Bermseok Oh, Hung Tae Kim
Publikováno v:
Journal of hypertension. 25(12)
Objective Coronary artery disease is caused by multiple genetic and environmental factors. The disease is also closely associated with cardiovascular conditions such as hypertension. In order to investigate any possible role of hypertension candidate