Pages that link to "Q57838448"
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The following pages link to Progranulin genetic variability contributes to amyotrophic lateral sclerosis (Q57838448):
Displaying 50 items.
- The genetics and neuropathology of frontotemporal lobar degeneration (Q24615201) (← links)
- Mechanisms of granulin deficiency: lessons from cellular and animal models (Q26824221) (← links)
- Therapeutic and diagnostic challenges for frontotemporal dementia (Q26998919) (← links)
- Potential roles of microglial cell progranulin in HIV-associated CNS pathologies and neurocognitive impairment (Q27011876) (← links)
- Progranulin: at the interface of neurodegenerative and metabolic diseases (Q27024421) (← links)
- A shift to organismal stress resistance in programmed cell death mutants (Q27320732) (← links)
- TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia (Q28294001) (← links)
- Mechanisms of loss of functions of human angiogenin variants implicated in amyotrophic lateral sclerosis (Q28481295) (← links)
- Granulin knock out zebrafish lack frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis pathology (Q28544656) (← links)
- Progranulin modulates zebrafish motoneuron development in vivoand rescues truncation defects associated with knockdown of Survival motor neuron 1 (Q30497278) (← links)
- A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells (Q30498840) (← links)
- Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis (Q30541723) (← links)
- Diagnostic and prognostic significance of neurofilament light chain NF-L, but not progranulin and S100B, in the course of amyotrophic lateral sclerosis: Data from the German MND-net (Q31141202) (← links)
- Progranulin is expressed within motor neurons and promotes neuronal cell survival (Q33513028) (← links)
- Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease (Q33742148) (← links)
- Recent insights into the molecular genetics of dementia (Q33830518) (← links)
- Survival profiles of patients with frontotemporal dementia and motor neuron disease (Q33896030) (← links)
- Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse. (Q33899853) (← links)
- Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma (Q34381669) (← links)
- Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research (Q34401653) (← links)
- rs5848 polymorphism and serum progranulin level (Q34891810) (← links)
- Progranulin expression is upregulated after spinal contusion in mice. (Q34916082) (← links)
- Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies (Q35092787) (← links)
- Low plasma progranulin levels in children with autism (Q35240854) (← links)
- No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort (Q36438687) (← links)
- The molecular basis of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum (Q36485513) (← links)
- Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival (Q36527176) (← links)
- Progranulin promotes neurite outgrowth and neuronal differentiation by regulating GSK-3β. (Q36922853) (← links)
- TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander (Q37204062) (← links)
- Update on recent molecular and genetic advances in frontotemporal lobar degeneration (Q37205729) (← links)
- Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration (Q37235164) (← links)
- FTD and ALS: A Tale of Two Diseases (Q37241079) (← links)
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia (Q37260852) (← links)
- Rare Variants in Neurodegeneration Associated Genes Revealed by Targeted Panel Sequencing in a German ALS Cohort (Q37334870) (← links)
- Roles of progranulin in sexual differentiation of the developing brain and adult neurogenesis (Q37335964) (← links)
- Clinical and pathological continuum of multisystem TDP-43 proteinopathies (Q37388933) (← links)
- Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases (Q37409270) (← links)
- EphA2 is a functional receptor for the growth factor progranulin. (Q37488302) (← links)
- Lack of estrogen receptor α in astrocytes of progranulin-deficient mice (Q37526276) (← links)
- RNA processing pathways in amyotrophic lateral sclerosis (Q37720436) (← links)
- Progranulin axis and recent developments in frontotemporal lobar degeneration (Q37978700) (← links)
- Primary phagocytosis of neurons by inflamed microglia: potential roles in neurodegeneration (Q37992053) (← links)
- CSF markers in amyotrophic lateral sclerosis (Q38007362) (← links)
- RNA metabolism in ALS: when normal processes become pathological. (Q38189807) (← links)
- Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges (Q38260359) (← links)
- TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells. (Q38326803) (← links)
- Circulating progranulin as a biomarker for neurodegenerative diseases (Q39472371) (← links)
- Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis (Q41595939) (← links)
- Unraveling gene expression profiles in peripheral motor nerve from amyotrophic lateral sclerosis patients: insights into pathogenesis (Q42096382) (← links)
- Increased progranulin in the skin of amyotrophic lateral sclerosis: An immunohistochemical study (Q44577010) (← links)