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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.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
A <i>Drosophila</i> model to screen Alport syndrome <i>COL4A5</i> variants for their functional pathogenicity
Jianli Duan, Pei Wen, Yunpo Zhao, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
The landscape of allele-specific expression in human kidneys
Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas, et al.
Frontiers in Pediatrics
|
December 1, 2016
Renal and Cardiovascular Morbidities Associated with <i>APOL1</i> Status among African-American and Non-African-American Children with Focal Segmental Glomerulosclerosis
Robert P Woroniecki, Derek K Ng, Sophie Limou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 25, 2022
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit
Cristian V Riella, Michelle McNulty, Guilherme T Ribas, et al.
American Journal of Human Genetics
|
July 31, 2018
An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome
Christopher E Gillies, Rosemary Putler, Rajasree Menon, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2018
<i>UBD</i> modifies <i>APOL1</i>-induced kidney disease risk
Jia-Yue Zhang, Minxian Wang, Lei Tian, et al.
The Journal of Clinical Investigation
|
March 2, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis
Haiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
Nature Communications
|
April 19, 2023
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle T McNulty, Christopher J Benway, et al.
Kidney International
|
December 24, 2023
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population
Precil D Neves, Andreia Watanabe, Elieser H Watanabe, et al.
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of 10
Search research articles
Search
Showing results (41-50 of 94) with videos related to
Sort By:
Page
of 10
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.
Biorxiv : the Preprint Server for Biology
|
April 1, 2024
A <i>Drosophila</i> model to screen Alport syndrome <i>COL4A5</i> variants for their functional pathogenicity
Jianli Duan, Pei Wen, Yunpo Zhao, et al.
Biorxiv : the Preprint Server for Biology
|
December 22, 2025
The landscape of allele-specific expression in human kidneys
Ana C Onuchic-Whitford, Junmo Sung, Eric D Sakkas, et al.
Frontiers in Pediatrics
|
December 1, 2016
Renal and Cardiovascular Morbidities Associated with <i>APOL1</i> Status among African-American and Non-African-American Children with Focal Segmental Glomerulosclerosis
Robert P Woroniecki, Derek K Ng, Sophie Limou, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 25, 2022
ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit
Cristian V Riella, Michelle McNulty, Guilherme T Ribas, et al.
American Journal of Human Genetics
|
July 31, 2018
An eQTL Landscape of Kidney Tissue in Human Nephrotic Syndrome
Christopher E Gillies, Rosemary Putler, Rajasree Menon, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 14, 2018
<i>UBD</i> modifies <i>APOL1</i>-induced kidney disease risk
Jia-Yue Zhang, Minxian Wang, Lei Tian, et al.
The Journal of Clinical Investigation
|
March 2, 2016
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis
Haiyang Yu, Mykyta Artomov, Sebastian Brähler, et al.
Nature Communications
|
April 19, 2023
Mapping genomic regulation of kidney disease and traits through high-resolution and interpretable eQTLs
Seong Kyu Han, Michelle T McNulty, Christopher J Benway, et al.
Kidney International
|
December 24, 2023
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population
Precil D Neves, Andreia Watanabe, Elieser H Watanabe, et al.
Page
of 10