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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

Nature genetics, 2004-04, Vol.36 (4), p.377-381

2004

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VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease

PloS one, 2010-10, Vol.5 (10), p.e13183

2010

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Mutant valosin-containing protein causes a novel type of frontotemporal dementia

Annals of neurology, 2005-03, Vol.57 (3), p.457-461

2005

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Novel Ubiquitin Neuropathology in Frontotemporal Dementia With Valosin-Containing Protein Gene Mutations

Journal of neuropathology and experimental neurology, 2006-06, Vol.65 (6), p.571-581

2006

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Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia

American journal of medical genetics. Part A, 2008-03, Vol.146A (6), p.745-757

2008

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The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis

Journal of molecular neuroscience, 2011-11, Vol.45 (3), p.522-531

2011

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Mutations in SEPT9 cause hereditary neuralgic amyotrophy

Nature genetics, 2005-10, Vol.37 (10), p.1044-1046

2005

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The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology

PloS one, 2012, Vol.7 (9), p.e46308-e46308

2012

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A case of late-onset proximal and distal muscle weakness

Neurology, 2009-11, Vol.73 (19), p.1592-1597

2009

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Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

Neuromuscular disorders : NMD, 2009-11, Vol.19 (11), p.766-772

2009

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Autosomal dominant inclusion body myopathy, paget disease of bone, and frontotemporal dementia

Alzheimer disease and associated disorders, 2005-10, Vol.19 (Supplement 1), p.S44-S47

2005

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Primate Genome Gain and Loss: A Bone Dysplasia, Muscular Dystrophy, and Bone Cancer Syndrome Resulting from Mutated Retroviral-Derived MTAP Transcripts

American journal of human genetics, 2012-04, Vol.90 (4), p.614-627

2012

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APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

Genetics in medicine, 2007-01, Vol.9 (1), p.9-13

2007

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Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis

Muscle & nerve, 2007-10, Vol.36 (4), p.447-454

2007

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Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22 : a novel locus for a musculoskeletal syndrome

Human genetics, 2005-12, Vol.118 (3-4), p.508-514

2005

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Field-based detection of biological samples for forensic analysis: Established techniques, novel tools, and future innovations

Forensic science international, 2018-04, Vol.285, p.147-160

2018

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The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology

PloS one, 2012-09, Vol.7 (9), p.e46308

2012

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Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone

Bone (New York, N.Y.), 2006-02, Vol.38 (2), p.280-285

2006

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Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

Human genetics, 2002-02, Vol.110 (2), p.166-172

2002

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Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes

Neuromuscular disorders : NMD, 2003-09, Vol.13 (7), p.559-567

2003

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VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder

Biochimica et biophysica acta, 2008-12, Vol.1782 (12), p.744-748

2008

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Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

Neurology, 2001-12, Vol.57 (11), p.1963-1968

2001

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Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy

American journal of medical genetics. Part A, 2006-02, Vol.140A (4), p.322-330

2006

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Assessing the performance of quantity and quality metrics using the QIAGEN Investigator® Quantiplex® pro RGQ kit

Science & justice, 2020-07, Vol.60 (4), p.388-397

2020

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Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

Clinical genetics, 2013-05, Vol.83 (5), p.422-431

2013

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

VCP associated inclusion body myopathy and paget disease of bone knock-in mouse model exhibits tissue pathology typical of human disease

Mutant valosin-containing protein causes a novel type of frontotemporal dementia

Novel Ubiquitin Neuropathology in Frontotemporal Dementia With Valosin-Containing Protein Gene Mutations

Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia

The Multiple Faces of Valosin-Containing Protein-Associated Diseases: Inclusion Body Myopathy with Paget’s Disease of Bone, Frontotemporal Dementia, and Amyotrophic Lateral Sclerosis

Mutations in SEPT9 cause hereditary neuralgic amyotrophy

The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology

A case of late-onset proximal and distal muscle weakness

Valosin containing protein associated inclusion body myopathy: abnormal vacuolization, autophagy and cell fusion in myoblasts

Autosomal dominant inclusion body myopathy, paget disease of bone, and frontotemporal dementia

Primate Genome Gain and Loss: A Bone Dysplasia, Muscular Dystrophy, and Bone Cancer Syndrome Resulting from Mutated Retroviral-Derived MTAP Transcripts

APOE is a potential modifier gene in an autosomal dominant form of frontotemporal dementia (IBMPFD)

Nuclear localization of valosin-containing protein in normal muscle and muscle affected by inclusion-body myositis

Mapping autosomal dominant progressive limb-girdle myopathy with bone fragility to chromosome 9p21-p22 : a novel locus for a musculoskeletal syndrome

Field-based detection of biological samples for forensic analysis: Established techniques, novel tools, and future innovations

The Homozygote VCPR155H/R155H Mouse Model Exhibits Accelerated Human VCP-Associated Disease Pathology

Evaluation of the role of Valosin-containing protein in the pathogenesis of familial and sporadic Paget's disease of bone

Evidence of a founder effect and refinement of the hereditary neuralgic amyotrophy (HNA) locus on 17q25 in American families

Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: Review of a unique disorder

Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

Manifestations in a family with autosomal dominant bone fragility and limb-girdle myopathy

Assessing the performance of quantity and quality metrics using the QIAGEN Investigator® Quantiplex® pro RGQ kit

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

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