Pages that link to "Q37411590"
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The following pages link to Gene expression study on peripheral blood identifies progranulin mutations (Q37411590):
Displaying 50 items.
- Human-specific transcriptional regulation of CNS development genes by FOXP2 (Q24655742) (← links)
- Molecular Pathways Bridging Frontotemporal Lobar Degeneration and Psychiatric Disorders (Q26766487) (← links)
- Potential roles of microglial cell progranulin in HIV-associated CNS pathologies and neurocognitive impairment (Q27011876) (← links)
- Frontotemporal Dementia (Q30234793) (← links)
- Quantifying the white blood cell transcriptome as an accessible window to the multiorgan transcriptome (Q30505781) (← links)
- Using iPSC-derived neurons to uncover cellular phenotypes associated with Timothy syndrome (Q30529349) (← links)
- An epigenetic signature in peripheral blood associated with the haplotype on 17q21.31, a risk factor for neurodegenerative tauopathy (Q31153643) (← links)
- Deficits in bioenergetics and impaired immune response in granulocytes from children with autism (Q33551727) (← links)
- Sporadic corticobasal syndrome due to FTLD-TDP. (Q33703433) (← links)
- Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease (Q33742148) (← links)
- Blood-based biomarkers of Alzheimer's disease: challenging but feasible (Q33824444) (← links)
- The effects of globin on microarray-based gene expression analysis of mouse blood (Q33935713) (← links)
- Accelerated lipofuscinosis and ubiquitination in granulin knockout mice suggest a role for progranulin in successful aging (Q33947272) (← links)
- Chronic administration of cholesterol oximes in mice increases transcription of cytoprotective genes and improves transcriptome alterations induced by alpha-synuclein overexpression in nigrostriatal dopaminergic neurons (Q34056025) (← links)
- Regulation of progranulin expression in human microglia and proteolysis of progranulin by matrix metalloproteinase-12 (MMP-12). (Q34235574) (← links)
- Genetics of dementia (Q34248849) (← links)
- Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders (Q34506868) (← links)
- TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers. (Q34555400) (← links)
- rs5848 polymorphism and serum progranulin level (Q34891810) (← links)
- Brain progranulin expression in GRN-associated frontotemporal lobar degeneration (Q35014879) (← links)
- A network of RNA and protein interactions in Fronto Temporal Dementia (Q35194634) (← links)
- DNA methylation, insulin resistance and second-generation antipsychotics in bipolar disorder. (Q35848001) (← links)
- Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. (Q36096125) (← links)
- Amyloid in dementia associated with familial FTLD: not an innocent bystander (Q36327682) (← links)
- No major progranulin genetic variability contribution to disease etiopathogenesis in an ALS Italian cohort (Q36438687) (← links)
- Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defects (Q36495839) (← links)
- Secreted progranulin is a homodimer and is not a component of high density lipoproteins (HDL) (Q36708664) (← links)
- Functional genomic analyses identify pathways dysregulated by progranulin deficiency, implicating Wnt signaling (Q36787346) (← links)
- Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members (Q37148011) (← links)
- Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia (Q37260852) (← links)
- Genome-wide analysis of a Wnt1-regulated transcriptional network implicates neurodegenerative pathways (Q37377851) (← links)
- TDP-43 and frontotemporal dementia (Q37576086) (← links)
- Role of progranulin as a biomarker for Alzheimer's disease (Q37730008) (← links)
- Use of peripheral blood transcriptome biomarkers for epilepsy prediction (Q37855043) (← links)
- Behavioural Variant Frontotemporal Dementia—Defining Genetic and Pathological Subtypes (Q37874158) (← links)
- Cellular effects of progranulin in health and disease (Q37879596) (← links)
- Frontotemporal dementia: from Mendelian genetics towards genome wide association studies (Q37928504) (← links)
- Recent insights into the involvement of progranulin in frontotemporal dementia. (Q38015344) (← links)
- The Receptor-interacting Serine/Threonine Protein Kinase 1 (RIPK1) Regulates Progranulin Levels (Q38722210) (← links)
- Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation (Q38922949) (← links)
- Progranulin Deficiency Reduces CDK4/6/pRb Activation and Survival of Human Neuroblastoma SH-SY5Y Cells. (Q38942093) (← links)
- Opposing effects of progranulin deficiency on amyloid and tau pathologies via microglial TYROBP network (Q39030129) (← links)
- Molecular Genetics of Neurodegenerative Dementias (Q39035458) (← links)
- The Progranulin Cleavage Products, Granulins, Exacerbate TDP-43 Toxicity and Increase TDP-43 Levels. (Q42410235) (← links)
- Progranulin plasma levels in the diagnosis of frontotemporal dementia (Q42721059) (← links)
- An 8-week, open-label, dose-finding study of nimodipine for the treatment of progranulin insufficiency from GRN gene mutations (Q43557976) (← links)
- In silico identification of new genetic variations as potential risk factors for Alzheimer's disease in a microarray-oriented simulation (Q46401111) (← links)
- Searching for new genetic risk factors for neuropsychiatric disorders in expression databases (Q48234429) (← links)
- Profiling of Circulating Serum MicroRNAs in Children with Autism Spectrum Disorder using Stem-loop qRT-PCR Assay. (Q50345104) (← links)
- A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy. (Q52851529) (← links)