Zobrazeno 1 - 10
of 202
pro vyhledávání: '"Ramachandran Vasudevan"'
Autor:
Mohammed H. Albujja, Ramachandran Vasudevan, Saleh Alghamdi, Chong P. Pei, Khairul A. Bin Mohd Ghani, Yazan Ranneh, Patimah B. Ismail
Publikováno v:
Prostate International, Vol 8, Iss 4, Pp 135-145 (2020)
Prostate cancer (PCa) is a challenging polygenic disease because the genes that cause PCa remain largely elusive and are affected by several causal factors. Consequently, research continuously strives to identify a genetic marker which could be used
Externí odkaz:
https://doaj.org/article/701595330e4d457aaf40566e332235d2
Autor:
Nur Ilyana Jaafar, Ramachandran Vasudevan, Patimah Ismail, Ahmad Fazli Abdul Aziz, Nur Afiqah Mohamad, Geetha Kandavello, Raja Nurzatul Effah Raja Adnan, Vinod Balasubramaniam
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 5, Iss 3, p 48 (2018)
Genetic polymorphisms are variations in DNA sequences which can influence either disease susceptibility, severity, or prognosis. Pulmonary arterial hypertension (PAH) is one of the complications that occurs in certain patients who have atrial septal
Externí odkaz:
https://doaj.org/article/5f3a7d5da82844cba04de2513205c6ac
Publikováno v:
Cardiovascular Diabetology, Vol 8, Iss 1, p 11 (2009)
Abstract Background The renin-angiotensin aldosterone system (RAAS) plays an important role in regulating the blood pressure and the genetic polymorphisms of RAAS genes has been extensively studied in relation to the cardiovascular diseases in variou
Externí odkaz:
https://doaj.org/article/5c71e405644a4a80ae25d6f93da4b3d5
Autor:
Kouhi Fayegh, Asieh, Mat Din, Hazwan, Wan Sulaiman, Wan Aliaa, Ravanipour, Maryam, Basri, Hamidon, Bin Mohamed, Mohd Hazmi, Ramachandran, Vasudevan, Inche Mat, Liyana Najwa
Publikováno v:
Neuropsychiatrie; Dec2024, Vol. 38 Issue 4, p174-181, 8p
Autor:
Ching, Siew Mooi, Lee, Kai Wei, Yusof Khan, Abdul Hanif Khan, Devaraj, Navin Kumar, Cheong, Ai Theng, Yap, Sook Fan, Hoo, Fan Kee, Wan Sulaiman, Wan Aliaa, Loh, Wei Chao, Chong, Shen Horng, Patil, Mansi, Ramachandran, Vasudevan
Publikováno v:
PLoS ONE; 10/29/2024, Vol. 19 Issue 10, p1-13, 13p
Autor:
Lee, Kai Wei, Ching, Siew Mooi, Hoo, Fan Kee, Ramachandran, Vasudevan, Chong, Seng Choi, Tusimin, Maiza, Mohd Nordin, Noraihan, Devaraj, Navin Kumar, Cheong, Ai Theng, Chia, Yook Chin
Publikováno v:
In Midwifery February 2020 81
Autor:
Ansari, Neda1, Ramachandran, Vasudevan2,3 drvasu@ucmi.edu.my, Mohamad, Nur Afiqah4, Salim, Elnaz1, Ismail, Patimah1, Hazmi, Mohamad5, Mat, Liyana Najwa Inchee6,7 liyananajwa@upm.edu.my
Publikováno v:
Global Medical Genetics. Jan2023, Vol. 10 Issue 1, p12-18. 7p.
Autor:
Ching, Siew-Mooi, Cheong, Ai Theng, Yee, Anne, Thurasamy, Ramayah, Lim, Poh Ying, Zarina, Irmi Ismail, Lee, Kai Wei, Taher, Sri Wahyu, Ramachandran, Vasudevan
Publikováno v:
Irish Journal of Medical Science; Apr2024, Vol. 193 Issue 2, p851-863, 13p
Autor:
Md Bakri, Norshakimah, Ramachandran, Vasudevan, Hoo, Fan Kee, Subrayan, Visvaraja, Isa, Hazlita, Ngah, Nor Fariza, Mohamad, Nur Afiqah, Ching, Siew Mooi, Chan, Yoke Mun, Ismail, Patimah, Ismail, Fazliana, Sukiman, Erma Suryana, Wan Sulaiman, Wan Alia
Publikováno v:
In Egyptian Journal of Medical Human Genetics July 2018 19(3):207-213
Autor:
Mohamad, Nur Afiqah, Ramachandran, Vasudevan, Ismail, Patimah, Isa, Hazlita Mohd, Chan, Yoke Mun, Ngah, Nor Fariza, Bakri, Norshakimah Md, Ching, Siew Mooi, Hoo, Fan Kee, Sulaiman, Wan Aliaa Wan
Publikováno v:
In Egyptian Journal of Medical Human Genetics April 2018 19(2):77-81