Search Results - "Ahmad, Rahimah"

Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research by Ahmad, Rahimah, Saleem, Mohamed, Aloysious, Nisha Sabrina, Yelumalai, Punithawathy, Mohamed, Nurul, Hassan, Syahzuwan

“…Alpha thalassaemia is highly prevalent in the plural society of Malaysia and is a public health problem. Haematological and molecular data from 5016 unrelated…”
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Molecular characterization of α- and β-thalassaemia among Malay patients by Yatim, Nur Fatihah Mohd, Rahim, Masitah Abd, Menon, Kavitha, Al-Hassan, Faisal Muti, Ahmad, Rahimah, Manocha, Anita Bhajan, Saleem, Mohamed, Yahaya, Badrul Hisham

“…Both α- and β-thalassaemia syndromes are public health problems in the multi-ethnic population of Malaysia. To molecularly characterise the α- and…”
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Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis by Osman, Hussam Ali, Hamid, Muzamil Mahdi Abdel, Ahmad, Rahimah Binti, Saleem, Mohamed, Abdallah, Sana Altahir

“…Alpha-thalassemia is a genetic disorder characterized by deletions of one or more α globin genes that result in deficient of α globin chains reducing…”
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A Novel Single Gene Deletion (−αMAL3.5) Giving Rise to Silent α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients with Hb H Disease: Case Report of Two Probands by Abdul Hamid, Faidatul Syazlin, Ahmad, Rahimah, Saleem, Mohamed, Aziz, Nur Aisyah, Omar, Syahira Lazira, Mohamad Arif, Siti Hida Hajira, Sathar, Jameela, Zakaria, Zubaidah

“…We report a novel deletion at the HBA2 presented with Hb H disease in two Malaysian- Chinese patients. The two unrelated probands were diagnosed with Hb H…”
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Educational development and reformation in Malaysia: past, present and future by Haji Ahmad, Rahimah

“…Discusses educational development, focussing on curriculum changes and issues affecting the change in Malaysia and perspectives for the future. Begins with an…”
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A nonsense mutation in exon 8 of the APC gene (Arg283Ter) causes clinically variable FAP in a Malaysian Chinese family by Mohamed, Zulqarnain, Ahmad, Rahimah, Yoke, Ng Sau, Zakaria, Zubaidah, Ahmad, Harun, Yew, Tong Hung

“…The present study was carried out to characterize the causative genetic mutation in a medium‐sized Malaysian Chinese pedigree of three generations affected…”
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Inhibition of ricin A-chain (RTA) catalytic activity by a viral genome-linked protein (VPg) by Aitbakieva, Valentina R., Ahmad, Rahimah, Singh, Shaneen, Domashevskiy, Artem V.

“…Ricin is a plant derived protein toxin produced by the castor bean plant (Ricinus communis). The Centers for Disease Control (CDC) classifies ricin as a…”
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Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review by Aziz, Aisyah, Baharin, Mohd Farid, Fauzi, Muhammad Yusri, Abdul Hamid, Faidatul Syazlin, Nadarajaw, Thiyagar, Ahmad, Rahimah, Hashim, Hafizah

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Abstract 476: A human scFv as a tool to understand the biogenesis of a subset of oncogenic microRNAs by Embrione, Valerio, Scarpati, Michael, Uzzel, Zachary D., Ahmad, Rahimah, Sury, Fortuna A. De, Sheetz, Tyler J., Coppola, Vincenzo, Singh, Shaneen M., Saxena, Anjana D., Croce, Carlo M., Palmieri, Dario

“…Abstract Trans-acting factors such as RNA-binding proteins (RBPs) and microRNAs (miRNA) have recently been recognized as prime regulators of gene expression…”
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Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia by Koh, Danny Xuan Rong, Raja Sabudin, Raja Zahratul Azma, Mohd Yusoff, Malisa, Hussin, Noor Hamidah, Ahmad, Rahimah, Othman, Ainoon, Ismail, Endom

“…Summary Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the…”
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Abstract 2609: Columbia University’s Center for Cancer Systems Therapeutics (CaST) 2017 Scholars Program: A synergistic partnership with students from Brooklyn College, CUNY by Ahmad, Rahimah, Azad, Tasnim, Barreto, Carlos, Begum, Kamrun, Butt, Mahlaqa, Gruffat, Daniel, Jerliu, Aulon, Kwiat, Jonathan, Murph, Mikaela, Gómez, Katherine A. Rivera, Honig, Barry, Califano, Andrea, Singh, Shaneen, Murray, Diana

“…Abstract The Cancer Systems Therapeutics (CaST) Outreach helps foster community building throughout the NCI Cancer Systems Biology Consortium (CSBC). The…”
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Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia by Koh, Danny Xuan Rong, Raja Sabudin, Raja Zahratul Azma, Mohd Yusoff, Malisa, Hussin, Noor Hamidah, Ahmad, Rahimah, Othman, Ainoon, Ismail, Endom

“…Summary Thalassaemia is a public health problem in Malaysia, with each ethnic group having their own common mutations. However, there is a lack on data on the…”
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Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction by Hassan, Syahzuwan, Ahmad, Rahimah, Zakaria, Zubaidah, Zulkafli, Zefarina, Abdullah, Wan Zaidah

“…β-thalassaemia is one of the most common single-gene disorders worldwide. Each ethnic population has its own common mutations, accounting for the majority of…”
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First Two Cases of Fungal Infections Associated with Multi-drug Resistant Yeast, Fereydounia khargensis by Tap, Ratna Mohd, Ramli, Nur Yasmin, Sabaratnam, Parameswari, Hashim, Rohaidah, Bakri, Ahmed Rafezzan Ahmed, Bee, Lim Bee, Ginsapu, Stephanie Jane, Ahmad, Rahimah, Razak, Mohd Fuat Abd, Ahmad, Norazah

“…The number of new fungal pathogens is increasing due to growing population of immunocompromised patients and advanced identification techniques. Fereydounia…”
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Molecular Characterization of [alpha]- and [beta]-Thalassaemia among Malay Patients by Yatim, Nur Fatihah Mohd, Rahim, Masitah Abd, Menon, Kavitha, Al-Hassan, Faisal Muti, Ahmad, Rahimah, Manocha, Anita Bhajan, Saleem, Mohamed, Yahaya, Badrul Hisham

“…Both [alpha]- and [beta]-thalassaemia syndromes are public health problems in the multi-ethnic population of Malaysia. To molecularly characterise the [alpha]-…”
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Reprogramming of peripheral blood from Malaysian beta thalassaemia patients to induced pluripotent stem cell by Thena, Mohan, Moon, Lim, Pooi, Mok, Rahimah, Ahmad, Jameela, Satar, Zubaidah, Zakaria

“…Abstract only…”
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Distribution of alpha thalassaemia in 16 year old Malaysian Students in Penang, Melaka and Sabah by Rahimah, A N, Nisha, S, Safiah, B, Roshida, H, Punithawathy, Y, Nurul, H, Syahzuwan, H, Zubaidah, Z

“…Alpha thalassaemia is wide spread in Malaysia and is a public health problem. This study aimed to describe the carrier frequencies of α‒thalassaemia and its…”
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Detection of [Beta]-globin Gene Mutations Among [Beta]-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction by Hassan, Syahzuwan, Ahmad, Rahimah, Zakaria, Zubaidah, Zulkafli, Zefarina, Abdullah, Wan Zaidah

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Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia by Hanafi, Sarifah, Hassan, Rosline, Bahar, Rosnah, Abdullah, Wan Zaidah, Johan, Muhammad Farid, Rashid, Noor Diana, Azman, Nurul Fatihah, Nasir, Ariffin, Hassan, Syahzuwan, Ahmad, Rahimah, Othman, Azizah, Ibrahim, Mohd Ismail, Sukeri, Surianti, Sulong, Sarina, Yusoff, Surini, Mohamad, Nor Sarwany, Hussein, Adil, Hassan, Rozita, Yusoff, Narazah, Yahaya, Badrul Hisyam, Ismail, Endom, Yussof, Nik Khairuddin Nik, Salleh, Sinari, Zilfalil, Bin Alwi

“…The aim of this study was to adapt MARMS with some modifications to detect beta mutation in our cohort of thalassemia patients. We focused only on…”
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Haemoglobin sickle d punjab: - a case report by Rahimah, A, Syahira Lazira, O, Siti Hida, H M A, Faidatul Syazlin, A H, Nur Aisyah, A, Nik Hafidzah, N M, Zubaidah, Z

“…Haemoglobin S D-Punjab is a rare compound heterozygous haemoglobinopathy characterised by the presence of two β globin gene variants: Β6(GAG→GTG) and…”
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