Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
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Long-term Outcomes of Childhood Onset Nephrotic SyndromePlasma Levels of Risk-Variant APOL1 Do Not Associate with Renal Disease in a Population-Based CohorttarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine.Complete Remission in the Nephrotic Syndrome Study Network.Drug discovery in focal and segmental glomerulosclerosisLocal TNF causes NFATc1-dependent cholesterol-mediated podocyte injury.Assessment of kidney function in preterm infants: lifelong implications.Defining Glomerular Disease in Mechanistic Terms: Implementing an Integrative Biology Approach in Nephrology.APOL1 Renal-Risk Variants Induce Mitochondrial Dysfunction.APOL1-associated glomerular disease among African-American children: a collaboration of the Chronic Kidney Disease in Children (CKiD) and Nephrotic Syndrome Study Network (NEPTUNE) cohorts.Apolipoprotein L1 risk variants associate with prevalent atherosclerotic disease in African American systemic lupus erythematosus patients.Transgenic expression of human APOL1 risk variants in podocytes induces kidney disease in mice.The Cell Biology of APOL1.A Phase 2, Double-Blind, Placebo-Controlled, Randomized Study of Fresolimumab in Patients With Steroid-Resistant Primary Focal Segmental Glomerulosclerosis.HLA-DQA1 and APOL1 as Risk Loci for Childhood-Onset Steroid-Sensitive and Steroid-Resistant Nephrotic Syndrome.Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Differentiating Primary, Genetic, and Secondary FSGS in Adults: A Clinicopathologic Approach.AT2 R deficiency mediated podocyte loss via activation of ectopic hedgehog interacting protein (Hhip) gene expression.APOL1-G0 or APOL1-G2 Transgenic Models Develop Preeclampsia but Not Kidney Disease.Genetic risk of APOL1 and kidney disease in children and young adults of African ancestry.UBD modifies APOL1-induced kidney disease risk.Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults.Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic SyndromeIdentification of a two-SNP PLA2R1 Haplotype and HLA-DRB1 Alleles as Primary Risk Associations in Idiopathic Membranous NephropathyAPOL1 risk allele RNA contributes to renal toxicity by activating protein kinase R
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P2860
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE Subjects.
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2015 nî lūn-bûn
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
@zh-hk
2015年論文
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2015年論文
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2015年论文
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name
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@ast
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@en
type
label
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@ast
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@en
prefLabel
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@ast
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@en
P2093
P2860
P50
P356
P1476
Integrative Genomics Identifie ...... pes in Black NEPTUNE Subjects.
@en
P2093
Anne Randolph
Catherine C Robertson
Christopher E Gillies
Daniel C Cattran
Debbie S Gipson
Duncan B Johnstone
Felix Eichinger
Jeffrey B Kopp
John F O'Toole
John R Sedor
P2860
P304
P356
10.1681/ASN.2014111131
P577
2015-07-06T00:00:00Z