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Matthew B Lanktree

Showing results (71-80 of 103) with videos related to

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Journal of the American Society of Nephrology : JASN|February 24, 2022
Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney DiseaseCaitlyn Vlasschaert, Amy J M McNaughton, Michael Chong, et al.
Blood|January 18, 2023
A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic data setsCaitlyn Vlasschaert, Taralynn Mack, J Brett Heimlich, et al.
Canadian Journal of Kidney Health and Disease|June 8, 2026
Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney DiseaseMatthew B Lanktree, Nick Ashawasega, Micheli Bevilacqua, et al.
Genetics in Medicine Open|September 22, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in OntarioAngela Du, Kaitlyn Lemay, Amit Bagga, et al.
Journal of Lipid Research|July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentrationMatthew B Lanktree, Clara C Elbers, Yun Li, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
American Journal of Human Genetics|December 7, 2010
Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signalingYun Li, Kathrin Laue, Samia Temtamy, et al.
JCI Insight|December 22, 2025
Inhibition of cell surface GRP78 and activated α2M interaction attenuates kidney fibrosisJackie Trink, Ifeanyi Kennedy Nmecha, Katrine Pilely, et al.
Renal Failure|September 7, 2019
Exome sequencing of Saudi Arabian patients with ADPKDFahad A Al-Muhanna, Abdullah M Al-Rubaish, Chittibabu Vatte, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Journal of the American Society of Nephrology : JASN|February 24, 2022
Association of Clonal Hematopoiesis of Indeterminate Potential with Worse Kidney Function and Anemia in Two Cohorts of Patients with Advanced Chronic Kidney DiseaseCaitlyn Vlasschaert, Amy J M McNaughton, Michael Chong, et al.
Blood|January 18, 2023
A practical approach to curate clonal hematopoiesis of indeterminate potential in human genetic data setsCaitlyn Vlasschaert, Taralynn Mack, J Brett Heimlich, et al.
Canadian Journal of Kidney Health and Disease|June 8, 2026
Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney DiseaseMatthew B Lanktree, Nick Ashawasega, Micheli Bevilacqua, et al.
Genetics in Medicine Open|September 22, 2025
Framework for standardized genetic testing recommendations for chronic kidney disease in OntarioAngela Du, Kaitlyn Lemay, Amit Bagga, et al.
Journal of Lipid Research|July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentrationMatthew B Lanktree, Clara C Elbers, Yun Li, et al.
Circulation. Cardiovascular Genetics|December 3, 2011
Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemiaChristopher T Johansen, Jian Wang, Adam D McIntyre, et al.
American Journal of Human Genetics|December 7, 2010
Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signalingYun Li, Kathrin Laue, Samia Temtamy, et al.
JCI Insight|December 22, 2025
Inhibition of cell surface GRP78 and activated α2M interaction attenuates kidney fibrosisJackie Trink, Ifeanyi Kennedy Nmecha, Katrine Pilely, et al.
Renal Failure|September 7, 2019
Exome sequencing of Saudi Arabian patients with ADPKDFahad A Al-Muhanna, Abdullah M Al-Rubaish, Chittibabu Vatte, et al.
Nature Genetics|July 27, 2010
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemiaChristopher T Johansen, Jian Wang, Matthew B Lanktree, et al.
Pageof 11