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Journal of the American Society of Nephrology : JASN
|
February 11, 2014
Phenotypic expansion of DGKE-associated diseases
Rik Westland, Monica Bodria, Alba Carrea, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families
Dalia Pantel, Nils D Mertens, Ronen Schneider, et al.
Experimental Dermatology
|
June 7, 2019
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
Lynn Petukhova, Aakash V Patel, Rachel K Rigo, et al.
BMC Bioinformatics
|
June 12, 2016
tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine
Christopher E Gillies, Edgar A Otto, Virginia Vega-Warner, et al.
American Journal of Nephrology
|
February 20, 2007
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss
Simone Sanna-Cherchi, Maria Luisa Carnevali, Davide Martorana, et al.
Blood
|
March 18, 2024
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
Justine Ryu, Joel T Rämö, Sean J Jurgens, et al.
Journal of Thrombosis and Haemostasis : JTH
|
October 9, 2024
Loss of function in protein Z (PROZ) is associated with increased risk of ischemic stroke in the UK Biobank
Amelia K Haj, Justine Ryu, Sean J Jurgens, et al.
Gene Expression
|
April 1, 2006
Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome
Roberta Oleggini, Roberta Bertelli, Armando Di Donato, et al.
The Journal of Clinical Investigation
|
April 21, 2015
Genomic imbalances in pediatric patients with chronic kidney disease
Miguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, et al.
Kidney International
|
June 19, 2009
Renal outcome in patients with congenital anomalies of the kidney and urinary tract
Simone Sanna-Cherchi, Pietro Ravani, Valentina Corbani, et al.
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Search research articles
Search
Showing results (21-30 of 93) with videos related to
Sort By:
Page
of 10
Journal of the American Society of Nephrology : JASN
|
February 11, 2014
Phenotypic expansion of DGKE-associated diseases
Rik Westland, Monica Bodria, Alba Carrea, et al.
Pediatric Nephrology (Berlin, Germany)
|
September 5, 2023
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families
Dalia Pantel, Nils D Mertens, Ronen Schneider, et al.
Experimental Dermatology
|
June 7, 2019
Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
Lynn Petukhova, Aakash V Patel, Rachel K Rigo, et al.
BMC Bioinformatics
|
June 12, 2016
tarSVM: Improving the accuracy of variant calls derived from microfluidic PCR-based targeted next generation sequencing using a support vector machine
Christopher E Gillies, Edgar A Otto, Virginia Vega-Warner, et al.
American Journal of Nephrology
|
February 20, 2007
Alterations of type IV collagen alpha chains in patients with chronic acquired glomerulopathies: mRNA levels, protein expression and urinary loss
Simone Sanna-Cherchi, Maria Luisa Carnevali, Davide Martorana, et al.
Blood
|
March 18, 2024
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank
Justine Ryu, Joel T Rämö, Sean J Jurgens, et al.
Journal of Thrombosis and Haemostasis : JTH
|
October 9, 2024
Loss of function in protein Z (PROZ) is associated with increased risk of ischemic stroke in the UK Biobank
Amelia K Haj, Justine Ryu, Sean J Jurgens, et al.
Gene Expression
|
April 1, 2006
Rare functional variants of podocin (NPHS2) promoter in patients with nephrotic syndrome
Roberta Oleggini, Roberta Bertelli, Armando Di Donato, et al.
The Journal of Clinical Investigation
|
April 21, 2015
Genomic imbalances in pediatric patients with chronic kidney disease
Miguel Verbitsky, Simone Sanna-Cherchi, David A Fasel, et al.
Kidney International
|
June 19, 2009
Renal outcome in patients with congenital anomalies of the kidney and urinary tract
Simone Sanna-Cherchi, Pietro Ravani, Valentina Corbani, et al.
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of 10