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

Claire E L Smith

Showing results (1-10 of 26) with videos related to

Pageof 3
Sort By:
Frontiers in Cell and Developmental Biology|January 4, 2021
Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin PleaseClaire E L Smith, Alice V R Lake, Colin A Johnson
Plos One|September 29, 2017
A tissue-specific promoter derived from a SINE retrotransposon drives biallelic expression of PLAGL1 in human lymphocytesClaire E L Smith, Alexia Alexandraki, Sarah F Cordery, et al.
Frontiers in Physiology|July 12, 2017
Amelogenesis Imperfecta; Genes, Proteins, and PathwaysClaire E L Smith, James A Poulter, Agne Antanaviciute, et al.
Human Molecular Genetics|July 15, 2016
Deletion of amelotin exons 3-6 is associated with amelogenesis imperfectaClaire E L Smith, Gina Murillo, Steven J Brookes, et al.
Human Molecular Genetics|December 10, 2013
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfectaJames A Poulter, Steven J Brookes, Roger C Shore, et al.
Human Molecular Genetics|May 27, 2014
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfectaJames A Poulter, Gina Murillo, Steven J Brookes, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategiesBenjamin McClinton, Laura A Crinnion, Martin McKibbin, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Frontiers in Cell and Developmental Biology|January 4, 2021
Primary Cilia, Ciliogenesis and the Actin Cytoskeleton: A Little Less Resorption, A Little More Actin PleaseClaire E L Smith, Alice V R Lake, Colin A Johnson
Plos One|September 29, 2017
A tissue-specific promoter derived from a SINE retrotransposon drives biallelic expression of PLAGL1 in human lymphocytesClaire E L Smith, Alexia Alexandraki, Sarah F Cordery, et al.
Frontiers in Physiology|July 12, 2017
Amelogenesis Imperfecta; Genes, Proteins, and PathwaysClaire E L Smith, James A Poulter, Agne Antanaviciute, et al.
Human Molecular Genetics|July 15, 2016
Deletion of amelotin exons 3-6 is associated with amelogenesis imperfectaClaire E L Smith, Gina Murillo, Steven J Brookes, et al.
Human Molecular Genetics|December 10, 2013
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfectaJames A Poulter, Steven J Brookes, Roger C Shore, et al.
Human Molecular Genetics|May 27, 2014
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfectaJames A Poulter, Gina Murillo, Steven J Brookes, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Targeted nanopore sequencing enables complete characterisation of structural deletions initially identified using exon-based short-read sequencing strategiesBenjamin McClinton, Laura A Crinnion, Martin McKibbin, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.
Ophthalmology|November 18, 2022
ReplyChris F Inglehearn, Samar Yahya, Claire E L Smith, et al.
Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.
Pageof 3