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American Journal of Human Genetics
|
May 1, 2018
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease
Emilie Cornec-Le Gall, Rory J Olson, Whitney Besse, et al.
American Journal of Human Genetics
|
June 4, 2016
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
Binu Porath, Vladimir G Gainullin, Emilie Cornec-Le Gall, et al.
American Journal of Human Genetics
|
January 6, 2015
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling
Markus Schueler, Daniela A Braun, Gayathri Chandrasekar, et al.
Kidney Medicine
|
November 8, 2021
Genomics Integration Into Nephrology Practice
Filippo Pinto E Vairo, Carri Prochnow, Jennifer L Kemppainen, et al.
Nature Genetics
|
April 30, 2008
Progress and prospects in rat genetics: a community view
Timothy J Aitman, John K Critser, Edwin Cuppen, et al.
Gastroenterology
|
December 15, 2023
Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease
Ria Schönauer, Dana Sierks, Melissa Boerrigter, et al.
American Journal of Human Genetics
|
December 10, 2021
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype
Sarah R Senum, Ying Sabrina M Li, Katherine A Benson, et al.
Nature Genetics
|
January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Ursula M Smith, Mark Consugar, Louise J Tee, et al.
Kidney International
|
January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summary
Vicente E Torres, Curie Ahn, Thijs R M Barten, et al.
Nature Genetics
|
March 30, 2007
Analysis of published PKD1 gene sequence variants
Alexander M Gout, , David Ravine, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 314) with videos related to
Sort By:
Page
of 32
American Journal of Human Genetics
|
May 1, 2018
Monoallelic Mutations to DNAJB11 Cause Atypical Autosomal-Dominant Polycystic Kidney Disease
Emilie Cornec-Le Gall, Rory J Olson, Whitney Besse, et al.
American Journal of Human Genetics
|
June 4, 2016
Mutations in GANAB, Encoding the Glucosidase IIα Subunit, Cause Autosomal-Dominant Polycystic Kidney and Liver Disease
Binu Porath, Vladimir G Gainullin, Emilie Cornec-Le Gall, et al.
American Journal of Human Genetics
|
January 6, 2015
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signaling
Markus Schueler, Daniela A Braun, Gayathri Chandrasekar, et al.
Kidney Medicine
|
November 8, 2021
Genomics Integration Into Nephrology Practice
Filippo Pinto E Vairo, Carri Prochnow, Jennifer L Kemppainen, et al.
Nature Genetics
|
April 30, 2008
Progress and prospects in rat genetics: a community view
Timothy J Aitman, John K Critser, Edwin Cuppen, et al.
Gastroenterology
|
December 15, 2023
Sex, Genotype, and Liver Volume Progression as Risk of Hospitalization Determinants in Autosomal Dominant Polycystic Liver Disease
Ria Schönauer, Dana Sierks, Melissa Boerrigter, et al.
American Journal of Human Genetics
|
December 10, 2021
Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype
Sarah R Senum, Ying Sabrina M Li, Katherine A Benson, et al.
Nature Genetics
|
January 18, 2006
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
Ursula M Smith, Mark Consugar, Louise J Tee, et al.
Kidney International
|
January 23, 2025
KDIGO 2025 clinical practice guideline for the evaluation, management, and treatment of autosomal dominant polycystic kidney disease (ADPKD): executive summary
Vicente E Torres, Curie Ahn, Thijs R M Barten, et al.
Nature Genetics
|
March 30, 2007
Analysis of published PKD1 gene sequence variants
Alexander M Gout, , David Ravine, et al.
Page
of 32