Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Changsoo Kang"'
Autor:
Stephen F. Pastore, Tahir Muhammad, Ricardo Harripaul, Rebecca Lau, Muhammad Tariq Masood Khan, Muhammad Ismail Khan, Omar Islam, Changsoo Kang, Muhammad Ayub, Musharraf Jelani, John B. Vincent
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract In a multi-branch family from Pakistan, individuals presenting with palmoplantar keratoderma segregate in autosomal dominant fashion, and individuals with intellectual disability (ID) segregate in apparent autosomal recessive fashion. Initia
Externí odkaz:
https://doaj.org/article/2ba8a4534d8c463e94a9689d1d8a2244
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0145220 (2015)
The thoracic-to-hip circumference ratio (THR) is an anthropometric marker recently described as a predictor of type 2 diabetes. In this study, we performed a genome-wide association study (GWAS) followed by confirmatory analyses to identify genetic m
Externí odkaz:
https://doaj.org/article/93a98a70d01f487ebe3b07fe7c167835
Autor:
Changsoo Kang
Publikováno v:
Journal of Genetic Medicine. 18:75-82
Publikováno v:
Genes & Genomics. 43:471-478
Amyloidosis cutis dyschromica (ACD) is a rare variant of cutaneous amyloidosis. This disorder often clusters in families, and it has been suggested that genetic factors might be involved in its development. To identify the genetic causes of ACD, we r
Autor:
Changsoo Kang, Muhammad Ayub, Musharraf Jelani, Tahir Muhammad, Omar Islam, Ricardo Harripaul, Muhammad Ismail Khan, Muhammad Tariq Masood Khan, John B. Vincent, Rebecca Lau, Stephen Pastore
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
In a multi-branch family from Pakistan, individuals presenting with palmoplantar keratoderma segregate in autosomal dominant fashion, and individuals with intellectual disability (ID) segregate in apparent autosomal recessive fashion. Initial attempt
Autor:
Changsoo Kang, Wu Rui
Publikováno v:
Korean Review of Corporation Management. 10:377-401
Autor:
Asifullah Khan, Jamal Nasir, Musharraf Jelani, Hannah C. Dooley, Jumana Y. Al-Aama, Nirmal Vadgama, Hussein Sheikh Ali Mohamoud, Amin Jan, Andrea Gubas, Sharon A. Tooze, Fazal Rahim, Muhammad Ismail Khan, Muhammad Tariq Masood Khan, Changsoo Kang, Zahir Ali
Publikováno v:
Brain
Defects in autophagy are implicated in a growing number of diseases. Jelani et al. identify a mutation in WIPI2, a major autophagy gene, associated with a multisystemic global developmental disorder. Functional studies in cell lines derived from pati
Autor:
Roshan Ali, Muhammad Zahid, Soyeon Choi, Changsoo Kang, Musharraf Jelani, Muhammad Ismail Khan, Habib Ahmad
Publikováno v:
Genes & Genomics. 40:789-795
Palmoplantar keratoderma (PPK) is a rare group of excessive skin disorder characterized by thickness over the palms and soles. The striate palmoplantar keratoderma (PPKS) is a form in which hyperkeratotic lesions are restricted to the pressure region
Autor:
Changsoo Kang
Publikováno v:
Korean Review of Corporation Management. 8:125-140
Autor:
Changsoo Kang
Publikováno v:
Korea International Accounting Review. :383-415