Search Results - Chai Teng Chear

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  1. 1
    Deciphering the structural and functional impact of Q657L mutation in NLRC4 using computational methods

    Deciphering the structural and functional impact of Q657L mutation in NLRC4 using computational methods by Chear, Chai Teng, Mat Ripen, Adiratna, Mohamad, Saharuddin Bin

    Published in Molecular simulation
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  2. 2
    A single‐center pilot study in Malaysia on the clinical utility of whole‐exome sequencing for inborn errors of immunity

    A single‐center pilot study in Malaysia on the clinical utility of whole‐exome sequencing for inborn errors of immunity by Ripen, Adiratna Mat, Chear, Chai Teng, Baharin, Mohd Farid, Nallusamy, Revathy, Chan, Kwai Cheng, Kassim, Asiah, Choo, Chong Ming, Wong, Ke Juin, Fong, Siew Moy, Tan, Kah Kee, Nachiappan, Jeyaseelan P., Teo, Kai Ru, Chiow, Mei Yee, Hishamshah, Munirah, Ghani, Hamidah, Muralitharan, Rikeish R., Mohamad, Saharuddin Bin

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  3. 3
    Transcriptome profiling of monocytes from XLA patients revealed the innate immune function dysregulation due to the BTK gene expression deficiency

    Transcriptome profiling of monocytes from XLA patients revealed the innate immune function dysregulation due to the BTK gene expression deficiency by Mirsafian, Hoda, Ripen, Adiratna Mat, Leong, Wai-Mun, Chear, Chai Teng, Bin Mohamad, Saharuddin, Merican, Amir Feisal

    Published in Scientific reports
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  4. 4
    Atypical Presentation of Severe Fungal Necrotizing Fasciitis in a Patient with X-Linked Agammaglobulinemia

    Atypical Presentation of Severe Fungal Necrotizing Fasciitis in a Patient with X-Linked Agammaglobulinemia by Chear, Chai Teng, Nallusamy, Revathy, Chan, Kwai Cheng, Mohd Tap, Ratna, Baharin, Mohd Farid, Syed Yahya, Sharifah Nurul Husna, Krishnan, Prasobhan Bala, Mohamad, Saharuddin Bin, Ripen, Adiratna Mat

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  5. 5
    Clinical features and mutational analysis of X-linked agammaglobulinemia patients in Malaysia

    Clinical features and mutational analysis of X-linked agammaglobulinemia patients in Malaysia by Chear, Chai Teng, Ismail, Intan Hakimah, Chan, Kwai Cheng, Noh, Lokman Mohd, Kassim, Asiah, Latiff, Amir Hamzah Abdul, Gill, Sandeep Singh, Ramly, Nazatul Haslina, Tan, Kah Kee, Sundaraj, Charlotte, Choo, Chong Ming, Mohamed, Sharifah Adlena Syed, Baharin, Mohd Farid, Zamri, Amelia Suhana, Yahya, Sharifah Nurul Husna Syed, Mohamad, Saharuddin Bin, Ripen, Adiratna Mat

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  6. 6
    A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia

    A Novel De Novo NFKBIA Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia by Chear, Chai Teng, El Farran, Bader Abdul Kader, Sham, Marina, Ramalingam, Kavetha, Noh, Lokman Mohd, Ismail, Intan Hakimah, Chiow, Mei Yee, Baharin, Mohd Farid, Ripen, Adiratna Mat, Mohamad, Saharuddin Bin

    Published in Genes
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  7. 7
    Whole exome sequencing identifies compound heterozygous variants of CR2 gene in monozygotic twin patients with common variable immunodeficiency

    Whole exome sequencing identifies compound heterozygous variants of CR2 gene in monozygotic twin patients with common variable immunodeficiency by Mat Ripen, Adiratna, Ghani, Hamidah, Chear, Chai Teng, Chiow, Mei Yee, Syed Yahya, Sharifah Nurul Husna, Kassim, Asiah, Mohamad, Saharuddin Bin

    Published in SAGE open medicine
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  8. 8
    A novel de novo NLRC4 mutation reinforces the likely pathogenicity of specific LRR domain mutation

    A novel de novo NLRC4 mutation reinforces the likely pathogenicity of specific LRR domain mutation by Chear, Chai Teng, Nallusamy, Revathy, Canna, Scott W., Chan, Kwai Cheng, Baharin, Mohd Farid, Hishamshah, Munirah, Ghani, Hamidah, Ripen, Adiratna Mat, Mohamad, Saharuddin Bin

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  9. 9
    A novel BTK gene mutation creates a de-novo splice site in an X-linked agammaglobulinemia patient

    A novel BTK gene mutation creates a de-novo splice site in an X-linked agammaglobulinemia patient by Chear, Chai Teng, Ripen, Adiratna Mat, Mohamed, Sharifah Adlena Syed, Dhaliwal, Jasbir Singh

    Published in Gene
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  10. 10
    A Novel De Novo INFKBIA/I Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia

    A Novel De Novo INFKBIA/I Missense Mutation Associated to Ectodermal Dysplasia with Dysgammaglobulinemia by Chear, Chai Teng, El Farran, Bader Abdul Kader, Sham, Marina, Ramalingam, Kavetha, Noh, Lokman Mohd, Ismail, Intan Hakimah, Chiow, Mei Yee, Baharin, Mohd Farid, Ripen, Adiratna Mat, Mohamad, Saharuddin Bin

    Published in Genes
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  11. 11
    Whole exome sequencing identifies compound heterozygous variants of gene in monozygotic twin patients with common variable immunodeficiency

    Whole exome sequencing identifies compound heterozygous variants of gene in monozygotic twin patients with common variable immunodeficiency by Adiratna Mat Ripen, Hamidah Ghani, Chai Teng Chear, Mei Yee Chiow, Sharifah Nurul Husna Syed Yahya, Asiah Kassim, Saharuddin Bin Mohamad

    Published in SAGE open medicine
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