Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Say Hean Lye"'
Autor:
Say-Hean Lye, Jagdish Kaur Chahil, Pramod Bagali, Livy Alex, Jamunarani Vadivelu, Wan Azman Wan Ahmad, Siew-Pheng Chan, Meow-Keong Thong, Shamsul Mohd Zain, Rosmawati Mohamed
Publikováno v:
PLoS ONE, Vol 8, Iss 4, p e60729 (2013)
Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by elevations in total cholesterol (TC) and low density lipoprotein cholesterol (LDLc). Development of FH can result in the increase of risk for premature cardiovascul
Externí odkaz:
https://doaj.org/article/d7e75060a16e44f8b9c38df9637f649a
Autor:
Khamsigan Munretnam, Ler Lian Wee, Nurul Hanis Ramzi, Nikman Adli Nor Hashim, Livy Alex, Jagdish Kaur Chahil, Sharmila Velapasamy, Nurulhafizah Samsudin, Say Hean Lye
Publikováno v:
Indian Journal of Clinical Biochemistry. 30:134-139
Genome-wide association studies have discovered multiple single nucleotide polymorphisms (SNPs) associated with the risk of common diseases. The objective of this study was to demonstrate the replication of previously published SNPs that showed stati
Autor:
Nurul Hanis Ramzi, Jagdish Kaur Chahil, Say Hean Lye, Khamsigan Munretnam, Kavitha Itagi Sahadevappa, Sharmila Velapasamy, Nikman Adli Nor Hashim, Soon Keat Cheah, GerardChin Chye Lim, Heselynn Hussein, Mohd Roslan Haron, Livy Alex, Lian Wee Ler
Publikováno v:
The Indian Journal of Medical Research
Indian Journal of Medical Research, Vol 139, Iss 6, Pp 873-882 (2014)
Indian Journal of Medical Research, Vol 139, Iss 6, Pp 873-882 (2014)
Background & objectives: Colorectal cancer (CRC) is second only to breast cancer as the leading cause of cancer-related deaths in Malaysia. In the Asia-Pacific area, it is the highest emerging gastrointestinal cancer. The aim of this study was to ide
Autor:
Nurul Hanis Ramzi, Say Hean Lye, Jagdish Kaur Chahil, Livy Alex, Sharmila Velapasamy, Khamsigan Munretnam, Lian Wee Ler, Vicknesh Visvalingam, Noraihan Mohd Nordin, Nikman Adli Nor Hashim
Publikováno v:
Genetic Testing and Molecular Biomarkers. 17:62-68
The identification of high-risk individuals can help to improve early cancer detection and patient survival. Risk assessment, however, can only be accomplished if the risk factors are known. To date, the genetic risk factors for ovarian cancer, other
Publikováno v:
Journal of Human Genetics. 57:358-362
Hypercholesterolemia is caused by different interactions of lifestyle and genetic determinants. At the genetic level, it can be attributed to the interactions of multiple polymorphisms, or as in the example of familial hypercholesterolemia (FH), it c
Autor:
Nurul Hanis, Ramzi, Jagdish Kaur, Chahil, Say Hean, Lye, Khamsigan, Munretnam, Kavitha Itagi, Sahadevappa, Sharmila, Velapasamy, Nikman Adli Nor, Hashim, Soon Keat, Cheah, Gerard Chin Chye, Lim, Heselynn, Hussein, Mohd Roslan, Haron, Livy, Alex, Lian Wee, Ler
Publikováno v:
The Indian Journal of Medical Research
Colorectal cancer (CRC) is second only to breast cancer as the leading cause of cancer-related deaths in Malaysia. In the Asia-Pacific area, it is the highest emerging gastrointestinal cancer. The aim of this study was to identify single nucleotide p
Autor:
Ramzi, Nurul Hanis, Chahil, Jagdish Kaur, Say Hean Lye, Khamsigan Munretnam, Itagi Kavitha, Sahadevappa, Velapasamy, Sharmila, Nikman Adli, Nor Hashim, Cheah, Soon Keat, Chin, Gerard, Chye Lim, Heselynn Hussein, Roslan Haron, Livy Alex, Lian, Wee Ler
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f648d03e4cf040524e155f12e748117
Autor:
Lian Wee Ler, Nurul Hanis Ramzi, Jagdish Kaur Chahil, Livy Alex, Sharmila Velapasamy, Nikman Adli Nor Hashim, Khamsigan Munretnam, I. S. Kavitha, Say Hean Lye
Publikováno v:
Molecular biology reports. 41(4)
There is growing global interest to stratify men into different levels of risk to developing prostate cancer, thus it is important to identify common genetic variants that confer the risk. Although many studies have identified more than a dozen commo
Autor:
Pramod Bagali, Wan Azman Wan Ahmad, Jamunarani Vadivelu, Jagdish Kaur Chahil, Siew-Pheng Chan, Shamsul Mohd Zain, Rosmawati Mohamed, Meow-Keong Thong, Livy Alex, Say-Hean Lye
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 4, p e60729 (2013)
PLoS ONE, Vol 8, Iss 4, p e60729 (2013)
Familial hypercholesterolemia (FH) is an autosomal dominant disorder characterized by elevations in total cholesterol (TC) and low density lipoprotein cholesterol (LDLc). Development of FH can result in the increase of risk for premature cardiovascul
Publikováno v:
Molecular biology reports. 39(7)
Familial hypercholesterolemia (FH) is a disease implicated with defects in either, Low density lipoprotein receptor gene (LDLR), Apolipoprotein B-100 gene (APOB), the Proprotein convertase subtilisin/kexin type 9 gene (PCSK9) or other related genes o