Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Norunaluwar Jalil"'
Autor:
Bin Hashim Halim-Fikri, Carsten W. Lederer, Atif Amin Baig, Siti Nor Assyuhada Mat-Ghani, Sharifah-Nany Rahayu-Karmilla Syed-Hassan, Wardah Yusof, Diana Abdul Rashid, Nurul Fatihah Azman, Suthat Fucharoen, Ramdan Panigoro, Catherine Lynn T. Silao, Vip Viprakasit, Norunaluwar Jalil, Norafiza Mohd Yasin, Rosnah Bahar, Veena Selvaratnam, Norsarwany Mohamad, Nik Norliza Nik Hassan, Ezalia Esa, Amanda Krause, Helen Robinson, Julia Hasler, Coralea Stephanou, Raja-Zahratul-Azma Raja-Sabudin, Jacques Elion, Ghada El-Kamah, Domenico Coviello, Narazah Yusoff, Zarina Abdul Latiff, Chris Arnold, John Burn, Petros Kountouris, Marina Kleanthous, Raj Ramesar, Bin Alwi Zilfalil, on behalf of the Global Globin Network (GGN)
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 4, p 552 (2022)
The Global Globin Network (GGN) is a project-wide initiative of the Human Variome/Global Variome Project (HVP) focusing on haemoglobinopathies to build the capacity for genomic diagnosis, clinical services, and research in low- and middle-income coun
Externí odkaz:
https://doaj.org/article/4c55a38af8f849dfb97fd7efe216a305
Autor:
S. Sobri, Norunaluwar Jalil, N. Ab Aziz, Noor Suhana Sulaiman, Nafisah Khalid, Farah Saleena Taip
Publikováno v:
Food Research. 5:188-192
The limited budget allocation and storage chemicals space are the main reasons food SMEs manufacturers took cleaning and sanitation for granted. A portable Electrolyzed Water Cleaning Rig which can generate sanitation solution and at the same time ge
Autor:
Norunaluwar Jalil, Raja Zahratul Azma Raja Sabudin, Sy Wee, Malisa My, Azlin Ithnin, Ainoon O, Hafiza Alauddin, Qistina Wn
Publikováno v:
Medicine & Health. 15:106-118
Haemoglobin S (HbS, α2β26GluVal) is a variant haemoglobin resulted from GAGGTG mutation on codon 6 of HBB gene. HbS haemoglobinopathy is uncommon in Malaysia and mainly seen in immigrants. However, Malaysian Indians and Malays are rarely affe
Autor:
Bin Hashim, Halim-Fikri, Carsten W, Lederer, Atif Amin, Baig, Siti Nor Assyuhada, Mat-Ghani, Sharifah-Nany Rahayu-Karmilla, Syed-Hassan, Wardah, Yusof, Diana, Abdul Rashid, Nurul Fatihah, Azman, Suthat, Fucharoen, Ramdan, Panigoro, Catherine Lynn T, Silao, Vip, Viprakasit, Norunaluwar, Jalil, Norafiza, Mohd Yasin, Rosnah, Bahar, Veena, Selvaratnam, Norsarwany, Mohamad, Nik Norliza, Nik Hassan, Ezalia, Esa, Amanda, Krause, Helen, Robinson, Julia, Hasler, Coralea, Stephanou, Raja-Zahratul-Azma, Raja-Sabudin, Jacques, Elion, Ghada, El-Kamah, Domenico, Coviello, Narazah, Yusoff, Zarina, Abdul Latiff, Chris, Arnold, John, Burn, Petros, Kountouris, Marina, Kleanthous, Raj, Ramesar, Bin Alwi, Zilfalil, On Behalf Of The Global Globin Network Ggn
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 4; Pages: 552
The Global Globin Network (GGN) is a project-wide initiative of the Human Variome/Global Variome Project (HVP) focusing on haemoglobinopathies to build the capacity for genomic diagnosis, clinical services, and research in low- and middle-income coun
Autor:
Khairina Kamarudin, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Loh C-Khai, Norunaluwar Jalil, Danny Koh-Xuan-Rong, Azlin Ithnin, Tang Yee Loong, Endom Ismail, Ainoon Othman, Hamidah Alias, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 42:247-251
Nondeletional α-globin mutations are known to cause more serious clinical effects than deletional ones. A rare IVS-I-1 (G>A) (HBA2: c.95+1G>A) donor splice site mutation interferes with normal splicing of pre mRNA and results in activation of a cryp
Autor:
Nurasyikin Yusof, Raja Zahratul Azma Raja Sabudin, Nor Rafeah Tumian, Qhasmira Abu Hazir, Norunaluwar Jalil, Hafiza Alauddin
Publikováno v:
Hemoglobin. 43:358-358
Fast-moving hemoglobins (Hbs) are a group of rare Hb variants that have a higher anodal electrophoretic mobility than Hb A on alkaline gel electrophoresis. Hb J-Bangkok (HBB: c.170G>A), a member of...
Autor:
Loh C-Khai, Hafiza Alauddin, Norunaluwar Jalil, Azma Rz, Nur Zainura Mohamad, Zarina Abdul Latiff
Publikováno v:
Hemoglobin. 43:357-357
IVS-I-2 (T>C) (HBB: c.92 ± 2T>C) is a point mutation that affect the splice junction between the exon and intron of the HBB gene. The aberrant splicing site generates an abnormal mRNA. It is a rare...
Autor:
Hafiza Alauddin, Lailatul Hadziyah Mohd Pauzy, Norunaluwar Jalil, Raja Zahratul Azma Raja Sabudin
Publikováno v:
Hemoglobin. 43:356-356
Autor:
Norunaluwar, Jalil1,2 (AUTHOR) norunaluwar@ppukm.ukm.edu.my, Azma, Raja Zahratul2 (AUTHOR), Alauddin, Hafiza2 (AUTHOR), Ithnin, Azlin2 (AUTHOR), Latiff, Zarina Abdul3 (AUTHOR), Alias, Hamidah3 (AUTHOR), Tumian, Nor Rafeah4 (AUTHOR), Yusoff, Malisa Mohd1 (AUTHOR), Hassan, Syahzuwan5 (AUTHOR), Othman, Ainoon6 (AUTHOR)
Publikováno v:
Hemoglobin. Nov2019, Vol. 43 Issue 6, p351-351. 1p.
Autor:
Norunaluwar, Jalil1,2 (AUTHOR), Raja Sabudin, Raja Zahratul Azma1 (AUTHOR) zahratul@ppukm.ukm.edu.my, Hafiza, Alauddin1 (AUTHOR), Azlin, Ithnin1 (AUTHOR), Badrulzaman, Hussin2 (AUTHOR), Kah-Mei, Carmene3 (AUTHOR), Sanada, Abu Bakar4 (AUTHOR), Ainoon, Othman5 (AUTHOR)
Publikováno v:
Hemoglobin. Nov2019, Vol. 43 Issue 6, p355-355. 1p.