Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Otto

Showing results (661-670 of 750) with videos related to

Pageof 75
Sort By:
Signal Transduction and Targeted Therapy|April 20, 2026
Hypoxia inducible factor network reflects kidney disease progression in diabetes and sodium-glucose co-transporters inhibitionViji Nair, Akihiro Minakawa, Cathy Smith, et al.
Journal of Medical Genetics|October 23, 2015
MKS1 regulates ciliary INPP5E levels in Joubert syndromeGisela G Slaats, Christine R Isabella, Hester Y Kroes, et al.
Nature Genetics|February 22, 2005
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulinEdgar A Otto, Bart Loeys, Hemant Khanna, et al.
American Journal of Human Genetics|January 6, 2015
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingMarkus Schueler, Daniela A Braun, Gayathri Chandrasekar, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Defining the molecular correlate of arteriolar hyalinosis in kidney disease progression by integration of single cell transcriptomic analysis and pathology scoringRajasree Menon, Edgar A Otto, Laura Barisoni, et al.
Nature Genetics|May 23, 2017
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseHao Lu, Maria C Rondón Galeano, Elisabeth Ott, et al.
Journal of Medicinal Chemistry|October 18, 2016
The Discovery, Preclinical, and Early Clinical Development of Potent and Selective GPR40 Agonists for the Treatment of Type 2 Diabetes Mellitus (LY2881835, LY2922083, and LY2922470)Chafiq Hamdouchi, Steven D Kahl, Anjana Patel Lewis, et al.
The Journal of Molecular Diagnostics : JMD|June 25, 2018
Analytical Validation of a Hybrid Capture-Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNATravis A Clark, Jon H Chung, Mark Kennedy, et al.
Kidney International|October 10, 2020
SARS-CoV-2 receptor networks in diabetic and COVID-19-associated kidney diseaseRajasree Menon, Edgar A Otto, Rachel Sealfon, et al.
Pageof 75

Showing results (661-670 of 750) with videos related to

Sort By:
Pageof 75
Signal Transduction and Targeted Therapy|April 20, 2026
Hypoxia inducible factor network reflects kidney disease progression in diabetes and sodium-glucose co-transporters inhibitionViji Nair, Akihiro Minakawa, Cathy Smith, et al.
Journal of Medical Genetics|October 23, 2015
MKS1 regulates ciliary INPP5E levels in Joubert syndromeGisela G Slaats, Christine R Isabella, Hester Y Kroes, et al.
Nature Genetics|February 22, 2005
Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulinEdgar A Otto, Bart Loeys, Hemant Khanna, et al.
American Journal of Human Genetics|January 6, 2015
DCDC2 mutations cause a renal-hepatic ciliopathy by disrupting Wnt signalingMarkus Schueler, Daniela A Braun, Gayathri Chandrasekar, et al.
The Journal of Clinical Investigation|July 23, 2013
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signalingHeon Yung Gee, Pawaree Saisawat, Shazia Ashraf, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Defining the molecular correlate of arteriolar hyalinosis in kidney disease progression by integration of single cell transcriptomic analysis and pathology scoringRajasree Menon, Edgar A Otto, Laura Barisoni, et al.
Nature Genetics|May 23, 2017
Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney diseaseHao Lu, Maria C Rondón Galeano, Elisabeth Ott, et al.
Journal of Medicinal Chemistry|October 18, 2016
The Discovery, Preclinical, and Early Clinical Development of Potent and Selective GPR40 Agonists for the Treatment of Type 2 Diabetes Mellitus (LY2881835, LY2922083, and LY2922470)Chafiq Hamdouchi, Steven D Kahl, Anjana Patel Lewis, et al.
The Journal of Molecular Diagnostics : JMD|June 25, 2018
Analytical Validation of a Hybrid Capture-Based Next-Generation Sequencing Clinical Assay for Genomic Profiling of Cell-Free Circulating Tumor DNATravis A Clark, Jon H Chung, Mark Kennedy, et al.
Kidney International|October 10, 2020
SARS-CoV-2 receptor networks in diabetic and COVID-19-associated kidney diseaseRajasree Menon, Edgar A Otto, Rachel Sealfon, et al.
Pageof 75