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    Das, Satrupa (15)
    Munshi, Anjana (15)Jyothy, Akka (9)Kaul, Subhash (6)Roy, Sitara (6)Khetarpal, Preeti (3)Kumar, Roshan (2)Rao, Venkateshwar (2)Valecha, Monica (2)Amirisetty, Ramesh (1)... View MoreSubjectFemale (3)Genotype (3)Human (3)Adult Brain Hemorrhage (2)Apert syndrome (2)Brain Ischemia (2)Controlled Study (2)Craniosynostosis (2)Exome sequencing (2)FGFR2 gene (2)... View MoreDate Issued2014 (3)2015 (3)2016 (3)2017 (3)2018 (3)Has File(s)Yes (13)No (2)

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    Role of TLR4 (C1196T) and CD14 (C-260T) Polymorphisms in Development of Ischemic Stroke, Its Subtypes and Hemorrhagic Stroke 

    Das, Satrupa; Kaul, & Subhash; Jyothy, Akka; Munshi, Anjana (Springer New York LLC, 2017)
    In the present study, we evaluated the association of TLR4 and CD14 polymorphisms, i.e. C1196T and C-260T, respectively, with ischemic stroke (n?=?700), its subtypes and hemorrhagic stroke (n?=?300) in a South Indian ...
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    GSTM1 and GSTT1 null polymorphism and antioxidant levels in oral submucous fibrosis, leukoplakia and oral cancer patients among a South Indian Population 

    Madhulatha, G.; Das, Satrupa; Venkateswarlu, N.; Pujar, , Akhilesh; Jyothy, Akka; Munshi, Anjana (Elsevier Ltd, 2018)
    Objective: We investigated the null polymorphism in GSTM1 and GSTT1 genes and the antioxidant levels in oral submucous fibrosis (OSMF), leukoplakia and oral cancer patients along with healthy controls in a South Indian ...
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    Interleukin 1ß (+3954, -511 and -31) polymorphism in chronic periodontitis patients from North India 

    Amirisetty, Ramesh; Patel, Ritu Prabha; Das, Satrupa; Saraf, Jitendra; Jyothy, Akka; Munshi, Anjana (Informa Healthcare, 2015)
    Objective. Several studies have implicated the role of interleukin-1 in various chronic diseases including periodontitis. The present study was carried out with an aim to evaluate the role of interleukin 1? polymorphisms, ...
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    Research advances in Apert syndrome 

    Das, Satrupa; Munshi, Anjana (Elsevier B.V., 2018)
    Apert syndrome is one of the several genetic syndromes associated with craniosynostosis, a condition that includes premature fusion of one or multiple cranial sutures. There has been significant clinical variation among ...
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    Apert's syndrome: Study by whole exome sequencing 

    Munshi, Anjana; Khetarpal, Preeti; Das, Satrupa; Rao, Venkateshwar; Valecha, Monica; Bansal, Manita; Kumar, Roshan (Chongqing yi ke da xue, di 2 lin chuang xue yuan Bing du xing gan yan yan jiu suo, 2018)
    In the present study we attempted a parent-child trio, whole exome sequencing (WES) approach to study Apert's syndrome. Clinical characteristics of the child were noted down and WES was carried out using Ion Torrent System ...
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    Apert’s syndrome: study by whole exome sequencing 

    Munshi, Anjana; Khetarpal, Preeti; Das, Satrupa; Rao, Venkateshwar; Valecha, Monica; Bansal, Vanita; Kumar, Roshan (Elsevier, 2017)
    In the present study we attempted a parent-child trio, whole exome sequencing (WES) approach to study Apert’s syndrome. Clinical characteristics of the child were noted down and WES was carried out using Ion Torrent System ...
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    Primordial dwarfism: overview of clinical and genetic aspects 

    Khetarpal, Preeti; Das, Satrupa; Panigrahi, Inusha; Munshi, Anjana (Springer Verlag, 2016)
    Primordial dwarfism is a group of genetic disorders which include Seckel Syndrome, Silver?Russell Syndrome, Microcephalic Osteodysplastic Primordial Dwarfism types I/III, II and Meier?Gorlin Syndrome. This genetic disorder ...
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    MTHFR Gene (C677T) Polymorphism in Ischemic Stroke, its Subtypes and Hemorrhagic Stroke in a South Indian Population 

    Das, Satrupa; Roy, Sitara; Kaul, Subhash; Jyothy, Akka; Munshi, Anjana (2015)
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    Association of APOE (E2, E3 and E4) gene variants and lipid levels in ischemic stroke, its subtypes and hemorrhagic stroke in a South Indian population 

    Das, Satrupa; Kaul, Subhash; Jyothy, Akka; Munshi, Anjana (Elsevier Ireland Ltd, 2016)
    In the present study we evaluated the association of APOE (E2/E3/E4) polymorphism with ischemic stroke (n = 620), its subtypes and hemorrhagic stroke (n = 250) in a South Indian population from Telangana. The genotypes ...
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    Association between PDE4D gene and ischemic stroke: recent advancements 

    Das, Satrupa; Roy, Sitara; Munshi, Anjana (Taylor and Francis Ltd, 2016)
    Stroke is a severe complication and a leading cause of death worldwide and genetic studies among different ethnicities has provided the basis for involvement of phosphodiesterase 4D (PDE4D) gene in cerebrovascular diseases. ...
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    Initiatives by University Library 
    Central University of Punjab