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Clinical Heterogeneity and Phenotypic Expansion of NaPi-IIa–Associated Disease
The journal of clinical endocrinology and metabolism, 2017-12, Vol.102 (12), p.4604-4614
2017
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A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report
Frontiers in immunology, 2021-06, Vol.12
2021
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Endoplasmic reticulum-translocation is essential for APOL1 cellular toxicity
iScience, 2022-01, Vol.25 (1), p.103717, Article 103717
2022
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Candida albicans Cyclin Clb4 Carries S-Phase Cyclin Activity
Eukaryotic Cell, 2010-09, Vol.9 (9), p.1311-1319
2010
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Alternative pathways of disulfide bond formation yield secretion-competent, stable and functional immunoglobulins
Molecular immunology, 2008-11, Vol.46 (1), p.97-105
2008
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APOL1-Mediated Cell Injury Involves Disruption of Conserved Trafficking Processes
Journal of the American Society of Nephrology, 2017-04, Vol.28 (4), p.1117-1130
2017
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A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity
Rheumatology (Oxford, England), 2021-10, Vol.60 (10), p.4888-4898
2021
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Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney Disease
American journal of kidney diseases, 2024-02, Vol.83 (2), p.183
2024
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Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
Human genetics, 2015-03, Vol.134 (3), p.305-314
2015
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Role of a Candida albicans Nrm1/Whi5 homologue in cell cycle gene expression and DNA replication stress response
Molecular microbiology, 2012-05, Vol.84 (4), p.778-794
2012
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Erratum to: Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5
Human genetics, 2015-03, Vol.134 (3), p.315-315
2015
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Role of a Candida albicans Nrm1/Whi5 homolog in cell cycle gene expression and DNA replication stress response
Molecular microbiology, 2012-04, Vol.84 (4), p.778-794
2012
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A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report
Frontiers in immunology, 2021, Vol.12, p.608604-608604
2021
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Endocannabinoid levels in peripheral blood mononuclear cells of multiple sclerosis patients treated with dimethyl fumarate
Scientific reports, 2022-11, Vol.12 (1), p.20300-20300, Article 20300
2022
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Familial vs sporadic ovarian tumors: characteristic genomic alterations analyzed by CGH
Gynecologic oncology, 2003-09, Vol.90 (3), p.629-636
2003
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Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinoma
Cancer genetics and cytogenetics, 2009-04, Vol.190 (2), p.66-70
2009
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Original article: Genetic alterations detected by comparative genomic hybridization and recurrence rate in epithelial ovarian carcinoma
Cancer genetics and cytogenetics, 2009-04, Vol.190 (2), p.66-70
2009
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In silico chromosomal clustering of genes displaying altered expression patterns in ovarian cancer
Cancer genetics and cytogenetics, 2005-07, Vol.160 (1), p.35-42
2005
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Genomic analyses of primary and metastatic serous epithelial ovarian cancer
Cancer genetics and cytogenetics, 2004-10, Vol.154 (1), p.16-21
2004
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Comparative genomic hybridization analysis of radiation-associated and sporadic meningiomas
Cancer genetics and cytogenetics, 2001-12, Vol.131 (2), p.135-140
2001
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