Focal segmental glomerulosclerosis: molecular genetics and targeted therapies - Wikidata - awgldk - TriplyDB

Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

http://www.wikidata.org/entity/Q35686453

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Pathology of Podocytopathies Causing Nephrotic Syndrome in Children Pathogenesis of Focal Segmental Glomerulosclerosis A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis Genetics of hereditary nephrotic syndrome: a clinical review.Focal Segmental Glomerulosclerosis.Disease modeling in genetic kidney diseases: mice.A Case of Transforming Growth Factor-β-Induced Gene-Related Oculorenal Syndrome: Granular Corneal Dystrophy Type II with a Unique Nephropathy.Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2.Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS.The mechanical challenges and cytoskeletal impairments in focal segmental glomerulosclerosis.Inverted formins: A subfamily of atypical formins.Both CLIC4 and CLIC5A activate ERM proteins in glomerular endothelium.Prospects for Precision Medicine in Glomerulonephritis Treatment.Proteinuric Kidney Diseases: A Podocyte's Slit Diaphragm and Cytoskeleton Approach A case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis

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P2860

Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

http://www.wikidata.org/entity/Q35686453

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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

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2015年論文

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2015年論文

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2015年论文

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2015年论文

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2015年论文

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name

Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

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Helen Liapis

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Ying Maggie Chen

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Creative Commons Attribution

P2860

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Mutations in PAX2 associate with adult-onset FSGS

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

The APOL1 gene and allograft survival after kidney transplantation

Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice

New insights into the pathology of podocyte loss: mitotic catastrophe

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focal segmental glomerulosclerosis

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