- Home
- Publications
- Publication Search
- Publication Details
Title
Glomerular diseases: genetic causes and future therapeutics
Authors
Keywords
-
Journal
Nature Reviews Nephrology
Volume 6, Issue 9, Pages 539-554
Publisher
Springer Nature
Online
2010-07-20
DOI
10.1038/nrneph.2010.103
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Endoplasmic reticulum stress as a progression factor for kidney injury
- (2010) Reiko Inagi CURRENT OPINION IN PHARMACOLOGY
- “Treasure your exceptions”: recent advances in molecular genetics of glomerular disease
- (2010) Andrzej Ciechanowicz et al. JOURNAL OF APPLIED GENETICS
- Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations
- (2010) Jutta Gellermann et al. PEDIATRIC NEPHROLOGY
- von Willebrand factor-cleaving protease ADAMTS13 reduces ischemic brain injury in experimental stroke
- (2009) B.-Q. Zhao et al. BLOOD
- ADAMTS13 gene deletion aggravates ischemic brain damage: a possible neuroprotective role of ADAMTS13 by ameliorating postischemic hypoperfusion
- (2009) M. Fujioka et al. BLOOD
- Lipoprotein glomerulopathy induced by ApoE-Sendai is different from glomerular lesions in aged apoE-deficient mice
- (2009) Atsunori Ishimura et al. Clinical and Experimental Nephrology
- Confirmation of Genetic Associations at ELMO1 in the GoKinD Collection Supports Its Role as a Susceptibility Gene in Diabetic Nephropathy
- (2009) M. G. Pezzolesi et al. DIABETES
- Genome-Wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes
- (2009) M. G. Pezzolesi et al. DIABETES
- Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish
- (2009) Weibin Zhou et al. GENE EXPRESSION PATTERNS
- Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier
- (2009) Martin Zenker et al. JOURNAL OF MOLECULAR MEDICINE-JMM
- Guidelines to Diagnosis and Monitoring of Fabry Disease and Review of Treatment Experiences
- (2009) Ana Maria Martins et al. JOURNAL OF PEDIATRICS
- Stem Cell Therapies Benefit Alport Syndrome
- (2009) V. LeBleu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Cell Therapy for Alport Syndrome
- (2009) C. J. Wong et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- The Mesangial Cell Revisited: No Cell Is an Island
- (2009) D. Schlondorff et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Slit Diaphragms Contain Tight Junction Proteins
- (2009) H. Fukasawa et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- The Renal Lesions of Alport Syndrome
- (2009) L. Heidet et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- The enigmatic parietal epithelial cell is finally getting noticed: a review
- (2009) Takamoto Ohse et al. KIDNEY INTERNATIONAL
- Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data
- (2009) A Mehta et al. LANCET
- Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
- (2009) Elizabeth J Brown et al. NATURE GENETICS
- Sugars and immune complex formation in IgA nephropathy
- (2009) Jonathan Barratt et al. Nature Reviews Nephrology
- The role of transient receptor potential channels in kidney disease
- (2009) Titia E. Woudenberg-Vrenken et al. Nature Reviews Nephrology
- New insights into the role of podocytes in proteinuria
- (2009) Jaakko Patrakka et al. Nature Reviews Nephrology
- Glomerular filtration is normal in the absence of both agrin and perlecan–heparan sulfate from the glomerular basement membrane
- (2009) Seth Goldberg et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
- (2009) M. Gigante et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Thrombomodulin Mutations in Atypical Hemolytic–Uremic Syndrome
- (2009) Mieke Delvaeye et al. NEW ENGLAND JOURNAL OF MEDICINE
- Atypical Hemolytic–Uremic Syndrome
- (2009) Marina Noris et al. NEW ENGLAND JOURNAL OF MEDICINE
- Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation
- (2009) Michal Malina et al. PEDIATRIC NEPHROLOGY
- 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
- The Role of Aminoacyl-tRNA Synthetases in Genetic Diseases
- (2008) Anthony Antonellis et al. Annual Review of Genomics and Human Genetics
- Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome
- (2008) V. Fremeaux-Bacchi et al. BLOOD
- Therapeutic targets in focal and segmental glomerulosclerosis
- (2008) Peter J Lavin et al. CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
- A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome
- (2008) A. Balreira et al. HUMAN MOLECULAR GENETICS
- Endoplasmic reticulum stress—A double edged sword for Z alpha-1 antitrypsin deficiency hepatoxicity
- (2008) Matthew W. Lawless et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- Irradiation Prolongs Survival of Alport Mice
- (2008) K. Katayama et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- Stem Cell-Based Therapy for Glomerular Diseases: An Evolving Concept
- (2008) V. S. LeBleu et al. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
- MYH9 is associated with nondiabetic end-stage renal disease in African Americans
- (2008) W H Linda Kao et al. NATURE GENETICS
- MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis
- (2008) Jeffrey B Kopp et al. NATURE GENETICS
- Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis
- (2008) M. Lowik et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Stem cell therapy for Alport syndrome: the hope beyond the hype
- (2008) O. Gross et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Genetic variation at the SLC12A3 locus is unlikely to explain risk for advanced diabetic nephropathy in Caucasians with type 2 diabetes
- (2008) D. P. K. Ng et al. NEPHROLOGY DIALYSIS TRANSPLANTATION
- Primary Coenzyme Q Deficiency in Pdss2 Mutant Mice Causes Isolated Renal Disease
- (2008) Min Peng et al. PLoS Genetics
- Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia
- (2007) W.H. Yiu et al. KIDNEY INTERNATIONAL
- Inherited diseases of the glomerular basement membrane
- (2007) Marie Claire Gubler Nature clinical practice. Nephrology
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreFind the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
Search