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

D Amaral

Showing results (271-280 of 288) with videos related to

Pageof 29
Sort By:
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Biochemical methods to assess CFTR expression and membrane localizationCarlos M Farinha, Deborah Penque, Mónica Roxo-Rosa, et al.
STAR Protocols|October 28, 2020
Protocol for Application, Standardization and Validation of the Forskolin-Induced Swelling Assay in Cystic Fibrosis Human Colon OrganoidsAnnelotte M Vonk, Peter van Mourik, Anabela S Ramalho, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 15, 2024
Repeatability and reproducibility of the Forskolin-induced swelling (FIS) assay on intestinal organoids from people with Cystic FibrosisMarlou C Bierlaagh, Anabela S Ramalho, Iris A L Silva, et al.
International Journal of Molecular Sciences|October 27, 2022
Drug Repurposing for Cystic Fibrosis: Identification of Drugs That Induce CFTR-Independent Fluid Secretion in Nasal OrganoidsLisa W Rodenburg, Livia Delpiano, Violeta Railean, et al.
Nature Genetics|August 27, 2013
Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator genePatrick R Sosnay, Karen R Siklosi, Fredrick Van Goor, et al.
Molecular Psychiatry|February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDB W M van Bon, B P Coe, R Bernier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 24, 2018
Genomic sequencing identifies secondary findings in a cohort of parent study participantsMichelle L Thompson, Candice R Finnila, Kevin M Bowling, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory allelesJ Nicholas Cochran, Emily C McKinley, Meagan Cochran, et al.
Clinical Genetics|April 14, 2018
Systematic reanalysis of genomic data improves quality of variant interpretationS M Hiatt, M D Amaral, K M Bowling, et al.
Life Science Alliance|August 3, 2022
Measuring cystic fibrosis drug responses in organoids derived from 2D differentiated nasal epitheliaGimano D Amatngalim, Lisa W Rodenburg, Bente L Aalbers, et al.
Pageof 29

Showing results (271-280 of 288) with videos related to

Sort By:
Pageof 29
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 7, 2004
Biochemical methods to assess CFTR expression and membrane localizationCarlos M Farinha, Deborah Penque, Mónica Roxo-Rosa, et al.
STAR Protocols|October 28, 2020
Protocol for Application, Standardization and Validation of the Forskolin-Induced Swelling Assay in Cystic Fibrosis Human Colon OrganoidsAnnelotte M Vonk, Peter van Mourik, Anabela S Ramalho, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 15, 2024
Repeatability and reproducibility of the Forskolin-induced swelling (FIS) assay on intestinal organoids from people with Cystic FibrosisMarlou C Bierlaagh, Anabela S Ramalho, Iris A L Silva, et al.
International Journal of Molecular Sciences|October 27, 2022
Drug Repurposing for Cystic Fibrosis: Identification of Drugs That Induce CFTR-Independent Fluid Secretion in Nasal OrganoidsLisa W Rodenburg, Livia Delpiano, Violeta Railean, et al.
Nature Genetics|August 27, 2013
Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator genePatrick R Sosnay, Karen R Siklosi, Fredrick Van Goor, et al.
Molecular Psychiatry|February 25, 2015
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDB W M van Bon, B P Coe, R Bernier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 24, 2018
Genomic sequencing identifies secondary findings in a cohort of parent study participantsMichelle L Thompson, Candice R Finnila, Kevin M Bowling, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory allelesJ Nicholas Cochran, Emily C McKinley, Meagan Cochran, et al.
Clinical Genetics|April 14, 2018
Systematic reanalysis of genomic data improves quality of variant interpretationS M Hiatt, M D Amaral, K M Bowling, et al.
Life Science Alliance|August 3, 2022
Measuring cystic fibrosis drug responses in organoids derived from 2D differentiated nasal epitheliaGimano D Amatngalim, Lisa W Rodenburg, Bente L Aalbers, et al.
Pageof 29