Search Results - "Rani, Abdul Qawee"

Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel DMD gene splicing patterns by Mahyoob Rani, Abdul Qawee, Maeta, Kazuhiro, Kawaguchi, Tatsuya, Awano, Hiroyuki, Nagai, Masashi, Nishio, Hisahide, Matsuo, Masafumi

“…The DMD gene is one of the largest human genes, being composed of 79 exons. Dystrophin Dp116 expressed from the promoter in intron 55 is a Schwann…”
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Conditional Cell Reprogramming and Air-Liquid Interface Modeling Life Cycle of Oncogenic Viruses (HPV and EBV) in Epithelial Cells and Virus-Associated Human Carcinomas by Rani, Abdul Qawee, Nurmemet, Dilber, Liffick, Joseph, Khan, Anam, Mitchell, Darrion, Li, Jenny, Zhao, Bo, Liu, Xuefeng

“…Several oncogenic viruses are associated with approximately 20% of human cancers. Experimental models are crucial for studying the pathogenicity and biological…”
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Dystrophin Dp71ab is monoclonally expressed in human satellite cells and enhances proliferation of myoblast cells by Farea, Manal, Rani, Abdul Qawee Mahyoob, Maeta, Kazuhiro, Nishio, Hisahide, Matsuo, Masafumi

“…Dystrophin Dp71 is the smallest isoform of the DMD gene, mutations in which cause Duchenne muscular dystrophy (DMD). Dp71 has also been shown to have roles in…”
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Dual Fluorescence Splicing Reporter Minigene Identifies an Antisense Oligonucleotide to Skip Exon v8 of the CD44 Gene by Fukushima, Sachiyo, Farea, Manal, Maeta, Kazuhiro, Rani, Abdul Qawee Mahyoob, Fujioka, Kazumichi, Nishio, Hisahide, Matsuo, Masafumi

“…Splicing reporter minigenes are used in cell-based in vitro splicing studies. Exon skippable antisense oligonucleotide (ASO) has been identified using minigene…”
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Intronic Alternative Polyadenylation in the Middle of the DMD Gene Produces Half-Size N-Terminal Dystrophin with a Potential Implication of ECG Abnormalities of DMD Patients by Rani, Abdul Qawee Mahyoob, Yamamoto, Tetsushi, Kawaguchi, Tatsuya, Maeta, Kazuhiro, Awano, Hiroyuki, Nishio, Hisahide, Matsuo, Masafumi

“…The gene is one of the largest human genes, being composed of 79 exons, and encodes dystrophin Dp427m which is deficient in Duchenne muscular dystrophy (DMD)…”
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Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System by Kawaguchi, Tatsuya, Niba, Emma Tabe Eko, Rani, Abdul Qawee Mahyoob, Onishi, Yoshiyuki, Koizumi, Makoto, Awano, Hiroyuki, Matsumoto, Masaaki, Nagai, Masashi, Yoshida, Shinobu, Sakakibara, Sachiko, Maeda, Naoyuki, Sato, Osamu, Nishio, Hisahide, Matsuo, Masafumi

“…Dystrophin Dp71 is one of the isoforms produced by the gene which is mutated in patients with Duchenne muscular dystrophy (DMD). Although Dp71 is expressed…”
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Isolation and enhancement of a homogenous in vitro human Hertwig's epithelial root sheath cell population by Farea, Manal, Halim, Ahmad Sukari, Abdullah, Nurul Asma, Lim, Chin Keong, Mokhtar, Khairani Idah, Berahim, Zurairah, Mokhtar, Kasmawati, Rani, Abdul Qawee, Husein, Adam

“…Hertwig's epithelial root sheath (HERS) cells play a pivotal role during root formation of the tooth and are able to form cementum-like tissue. The aim of the…”
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DMD transcripts in CRL-2061 rhabdomyosarcoma cells show high levels of intron retention by intron-specific PCR amplification by Niba, Emma Tabe Eko, Yamanaka, Ryo, Rani, Abdul Qawee Mahyoob, Awano, Hiroyuki, Matsumoto, Masaaki, Nishio, Hisahide, Matsuo, Masafumi

“…The gene encoding dystrophin is mutated in Duchenne muscular dystrophy, a fatal progressive muscle wasting disease. has also been shown to act as a tumor…”
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Recent progress in homogeneous immunosensors based on fluorescence or bioluminescence using antibody engineering by Rani, Abdul Qawee, Zhu, Bo, Ueda, Hiroshi, Kitaguchi, Tetsuya

“…Homogeneous immunosensors integrate the advantages of both biosensors and immunoassays; they include speed, high sensitivity, and accuracy. They have been…”
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Identification of HPV oncogene and host cell differentiation associated cellular heterogeneity in cervical cancer via single‐cell transcriptomic analysis by Li, Yingjie, Wang, Cankun, Ma, Anjun, Rani, Abdul Qawee, Luo, Mingjue, Li, Jenny, Liu, Xuefeng, Ma, Qin

“…Human Papillomaviruses (HPVs) are associated with around 5%–10% of human cancer, notably nearly 99% of cervical cancer. The mechanisms HPV interacts with…”
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BRD4 as a potential target for human papillomaviruses associated cancer by Rani, Abdul Qawee, Bonam, Srinivasa Reddy, Zhou, Jia, Li, Jenny, Hu, Haitao, Liu, Xuefeng

“…Around 99% of cervical cancer and 5%–10% of human cancer are associated with human papillomaviruses (HPV). Notably, the life‐cycle of HPV begins by low‐level…”
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Identification of the shortest splice variant of Dp71, together with five known variants, in glioblastoma cells by Rani, Abdul Qawee Mahyoob, Farea, Manal, Maeta, Kazuhiro, Kawaguchi, Tatsuya, Awano, Hiroyuki, Nagai, Masashi, Nishio, Hisahide, Matsuo, Masafumi

“…Dystrophin Dp71 mRNA is produced from the most distal alternative promoter of the DMD gene, mutations in which cause Duchenne muscular dystrophy (DMD). Dp71 is…”
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Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1 / TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex by Dila Ismail, Nur Farrah, Rani, Abdul Qawee, Ariff Nik Abdul Malik, Nik Mohd, Hock, Chia Boon, Mohd Azlan, Siti Nabilahuda, Razak, Salmi Abdul, Keng, Wee Teik, Ngu, Lock Hock, Silawati, Abdul Rashid, AzniYahya, Nor, Yusoff, Narazah Mohd, Sasongko, Teguh Haryo, Mohd Hussin, Zabidi Azhar

“…Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder characterized by tumor growth in multiple organs and caused by mutations in…”
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Two closely spaced nonsense mutations in the DMD gene in a Malaysian family by Rani, Abdul Qawee, Malueka, Rusdy Ghazali, Sasongko, Teguh Haryo, Awano, Hiroyuki, Lee, Tomoko, Yagi, Mariko, Zilfalil, Bin Alwi, Salmi, A.B. Razak, Takeshima, Yasuhiro, Zabidi-Hussin, Z.A.M.H., Matsuo, Masafumi

“…In Duchenne muscular dystrophy (DMD), identification of one nonsense mutation in the DMD gene has been considered an endpoint of genetic diagnosis. Here, we…”
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Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy by Rani, Abdul Qawee, Sasongko, Teguh Haryo, Sulong, Sarina, Bunyan, David, Salmi, Abdul Razak, Zilfalil, Bin Alwi, Matsuo, Masafumi, Zabidi-Hussin, Z. A. M. H.

“…Abstract We undertook the clinical feature examination and dystrophin analysis using multiplex ligation-dependent probe amplification (MLPA) and direct DNA…”
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