Pages that link to "Q28212105"
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The following pages link to Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia (Q28212105):
Displaying 50 items.
- How citation distortions create unfounded authority: analysis of a citation network (Q24260685) (← links)
- The genetics and neuropathology of frontotemporal lobar degeneration (Q24615201) (← links)
- Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia (Q26782984) (← links)
- Mouse models of frontotemporal dementia (Q26829009) (← links)
- The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology (Q27316347) (← links)
- Mutations in the Human AAA+ Chaperone p97 and Related Diseases (Q28080241) (← links)
- (Q28179557) (redirect page) (← links)
- Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737) (Q28212538) (← links)
- Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein (Q29619232) (← links)
- Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery (Q30444138) (← links)
- VCP mutations causing frontotemporal lobar degeneration disrupt localization of TDP-43 and induce cell death (Q30487226) (← links)
- Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease (Q33255969) (← links)
- Involvement of peripheral and central nervous systems in a valosin-containing protein mutation (Q33594785) (← links)
- Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum (Q33653996) (← links)
- VCP Associated Inclusion Body Myopathy and Paget Disease of Bone Knock-In Mouse Model Exhibits Tissue Pathology Typical of Human Disease (Q33721995) (← links)
- A Brazilian family with hereditary inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (Q33849069) (← links)
- The VCP/p97 system at a glance: connecting cellular function to disease pathogenesis. (Q34178673) (← links)
- A novel autosomal dominant inclusion body myopathy linked to 7q22.1-31.1. (Q34314374) (← links)
- Mouse large can modify complex N- and mucin O-glycans on alpha-dystroglycan to induce laminin binding (Q34405965) (← links)
- Giant cell tumor in a case of Paget's disease of bone: an aggressive benign tumor exhibiting a quick response to an innovative therapeutic agent. (Q34417248) (← links)
- Cognitive impairment in amyotrophic lateral sclerosis (Q34583928) (← links)
- Emerging strategies and therapies for treatment of Paget’s disease of bone (Q34987305) (← links)
- Genetic and environmental risk factors for idiopathic inflammatory myopathies (Q35036200) (← links)
- Global gene expression profiling in R155H knock-in murine model of VCP disease (Q35085137) (← links)
- Targeted excision of VCP R155H mutation by Cre-LoxP technology as a promising therapeutic strategy for valosin-containing protein disease (Q35110776) (← links)
- A network of RNA and protein interactions in Fronto Temporal Dementia (Q35194634) (← links)
- Rapamycin and chloroquine: the in vitro and in vivo effects of autophagy-modifying drugs show promising results in valosin containing protein multisystem proteinopathy (Q35462835) (← links)
- Young onset dementia (Q35518978) (← links)
- Familial Frontotemporal Dementia: From Gene Discovery to Clinical Molecular Diagnostics (Q35538685) (← links)
- Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies (Q35607253) (← links)
- Valosin containing protein associated fronto-temporal lobar degeneration: clinical presentation, pathologic features and pathogenesis (Q35635102) (← links)
- Global gene profiling of VCP-associated inclusion body myopathy (Q36034366) (← links)
- A progressive translational mouse model of human valosin-containing protein disease: the VCP(R155H/+) mouse (Q36565507) (← links)
- Mechanisms of disease: genetics of Paget's disease of bone and related disorders (Q36577488) (← links)
- Novel mutation in VCP gene causes atypical amyotrophic lateral sclerosis (Q36605617) (← links)
- Structural and functional deviations in disease-associated p97 mutants (Q36677811) (← links)
- Contribution of genetic factors to the pathogenesis of Paget's disease of bone and related disorders (Q36710160) (← links)
- Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia (Q36745555) (← links)
- Update on frontotemporal dementia (Q36784381) (← links)
- Frontotemporal lobar degeneration: current concepts in the light of recent advances (Q36817228) (← links)
- The genetics of frontotemporal lobar degeneration (Q36926070) (← links)
- The molecular genetics and neuropathology of frontotemporal lobar degeneration: recent developments (Q36931728) (← links)
- Neuronal-specific overexpression of a mutant valosin-containing protein associated with IBMPFD promotes aberrant ubiquitin and TDP-43 accumulation and cognitive dysfunction in transgenic mice. (Q37062875) (← links)
- Phenotypic variability in three families with valosin-containing protein mutation. (Q37072776) (← links)
- A review on primary progressive aphasia. (Q37129799) (← links)
- Epidemiological aspects of frontotemporal dementia. (Q37217962) (← links)
- Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia (Q37452177) (← links)
- Active Paget's disease of bone with normal biomarkers of bone metabolism: a case report and review of the literature. (Q37795638) (← links)
- Genetic Causes of Frontotemporal Degeneration (Q37799472) (← links)
- The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis. (Q37926529) (← links)