Collapsing Focal Segmental Glomerulosclerosis in Siblings With Compound Heterozygous Variants in NUP93 Expand the Spectrum of Kidney Phenotypes Associated With Nucleoporin Gene Mutations

Incidence and Relapse of Idiopathic Nephrotic Syndrome: Meta-analysis

(2021) Floor Veltkamp et al.   PEDIATRICS

Longitudinal Outcomes of COVID-19–Associated Collapsing Glomerulopathy and Other Podocytopathies

(2021) Satoru Kudose et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis

(2021) Brandon M. Lane et al.   JCI Insight

The spectrum of kidney biopsy findings in HIV-infected patients in the modern era

(2020) Satoru Kudose et al.   KIDNEY INTERNATIONAL

Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital Ataxia

(2019) Ginevra Zanni et al.   CEREBELLUM

Genetic diagnosis of steroid-resistant nephrotic syndrome in a longitudinal collection of Czech and Slovak patients: a high proportion of causative variants in NUP93

(2018) Martin Bezdíčka et al.   PEDIATRIC NEPHROLOGY

Treatment of steroid-resistant nephrotic syndrome in the genomic era

(2018) Adam R. Bensimhon et al.   PEDIATRIC NEPHROLOGY

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management

(2017) Agnieszka Bierzynska et al.   KIDNEY INTERNATIONAL

Collapsing glomerulopathy is common in the setting of thrombotic microangiopathy of the native kidney

(2016) David Buob et al.   KIDNEY INTERNATIONAL

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome

(2016) Daniela A Braun et al.   NATURE GENETICS

Functional Validation of an Alpha-Actinin-4 Mutation as a Potential Cause of an Aggressive Presentation of Adolescent Focal Segmental Glomerulosclerosis: Implications for Genetic Testing

(2016) Di Feng et al.   PLoS One

DNA damage-induced nuclear translocation of Apaf-1 is mediated by nucleoporin Nup107

(2015) Léonard Jagot-Lacoussiere et al.   CELL CYCLE

Clinical Features and Histology of Apolipoprotein L1-Associated Nephropathy in the FSGS Clinical Trial

(2015) J. B. Kopp et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

APOL1 Risk Variants Are Strongly Associated with HIV-Associated Nephropathy in Black South Africans

(2015) A. N. Kasembeli et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Apolipoprotein L1 Risk Variants Associate with Systemic Lupus Erythematosus-Associated Collapsing Glomerulopathy

(2013) C. P. Larsen et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

TRPC6 Mutations in Children with Steroid-Resistant Nephrotic Syndrome and Atypical Phenotype

(2011) M. Gigante et al.   Clinical Journal of the American Society of Nephrology

The C-terminal domain of Nup93 is essential for assembly of the structural backbone of nuclear pore complexes

(2011) Ruchika Sachdev et al.   MOLECULAR BIOLOGY OF THE CELL

Focal Segmental Glomerulosclerosis

(2011) Vivette D. D'Agati et al.   NEW ENGLAND JOURNAL OF MEDICINE

Treatment with IFN- , - , or -  Is Associated with Collapsing Focal Segmental Glomerulosclerosis

(2010) G. S. Markowitz et al.   Clinical Journal of the American Society of Nephrology

Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans

(2010) G. Genovese et al.   SCIENCE

Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis

(2008) Samuel F. Berkovic et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Collapsing glomerulopathy associated with inherited mitochondrial injury

(2008) Laura Barisoni et al.   KIDNEY INTERNATIONAL