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Publications by Sheela Kumari Raghavan

Progranulin Mutation Analysis: Identification of One Novel Mutation in Exon 12 Associated With Frontotemporal Dementia

Neurobiology of Aging

Aging

Gerontology

Developmental Biology

English

Related publications

Frontotemporal Dementia-Associated N279K Tau Mutation Localizes at the Nuclear Compartment

Frontiers in Cellular Neuroscience

Molecular Neuroscience

Cellular

2018

English

Molecular Analysis of Wilson Disease in Taiwan: Identification of One Novel Mutation and Evidence of Haplotype-Mutation Association

Journal of Human Genetics

Genetics

2000

English

IL2RG Hypomorphic Mutation: Identification of a Novel Pathogenic Mutation in Exon 8 and a Review of the Literature

Allergy, Asthma and Clinical Immunology

English

A Presenilin 1 Mutation Associated With Familial Frontotemporal Dementia Inhibits Γ-Secretase Cleavage of APP and Notch

Neurobiology of Disease

Neurology

2002

English

Progranulin Deficiency Induces Overactivation of WNT5A Expression via TNF-α/NF-κB Pathway in Peripheral Cells From Frontotemporal Dementia-Linked Granulin Mutation Carriers

Journal of Psychiatry and Neuroscience

Medicine

Psychiatry

Biological Psychiatry

Mental Health

Pharmacology

2016

English

Frontotemporal Dementia: Impact of P301L Tau Mutation on a Healthy Carrier

Journal of Neurology, Neurosurgery and Psychiatry

English

Pathology of Frontotemporal Dementia With Limb Girdle Muscular Dystrophy Caused by a DNAJB6 Mutation

Clinical Neurology and Neurosurgery

English

Presence of Reactive Microglia and Neuroinflammatory Mediators in a Case of Frontotemporal Dementia With P301S Mutation

Neurodegenerative Diseases

Neurology

2011

English

JAK2 Exon 12 Mutation in Myelodysplastic/Myeloproliferative Neoplasm With Ring Sideroblasts and Thrombocytosis: Not an Exclusive Mutation to Polycythaemia Vera

British Journal of Haematology

Hematology

2019

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Sheela Kumari Raghavan

Progranulin Mutation Analysis: Identification of One Novel Mutation in Exon 12 Associated With Frontotemporal Dementia

Related publications

Frontotemporal Dementia-Associated N279K Tau Mutation Localizes at the Nuclear Compartment

Molecular Analysis of Wilson Disease in Taiwan: Identification of One Novel Mutation and Evidence of Haplotype-Mutation Association

IL2RG Hypomorphic Mutation: Identification of a Novel Pathogenic Mutation in Exon 8 and a Review of the Literature

A Presenilin 1 Mutation Associated With Familial Frontotemporal Dementia Inhibits Γ-Secretase Cleavage of APP and Notch

Progranulin Deficiency Induces Overactivation of WNT5A Expression via TNF-α/NF-κB Pathway in Peripheral Cells From Frontotemporal Dementia-Linked Granulin Mutation Carriers

Frontotemporal Dementia: Impact of P301L Tau Mutation on a Healthy Carrier

Pathology of Frontotemporal Dementia With Limb Girdle Muscular Dystrophy Caused by a DNAJB6 Mutation

Presence of Reactive Microglia and Neuroinflammatory Mediators in a Case of Frontotemporal Dementia With P301S Mutation

JAK2 Exon 12 Mutation in Myelodysplastic/Myeloproliferative Neoplasm With Ring Sideroblasts and Thrombocytosis: Not an Exclusive Mutation to Polycythaemia Vera