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

Matthew M Hims

Showing results (1-10 of 12) with videos related to

Pageof 2
Sort By:
Human Mutation|September 12, 2006
Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomiaEl Chérif Ibrahim, Matthew M Hims, Noam Shomron, et al.
Bioinformatics (Oxford, England)|February 10, 2015
NxTrim: optimized trimming of Illumina mate pair readsJared O'Connell, Ole Schulz-Trieglaff, Emma Carlson, et al.
Molecular and Cellular Biology|November 19, 2008
Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAPYei-Tsung Chen, Matthew M Hims, Ranjit S Shetty, et al.
Genomics|July 24, 2007
A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defectMatthew M Hims, Ranjit S Shetty, James Pickel, et al.
Human Molecular Genetics|August 9, 2011
Specific correction of a splice defect in brain by nutritional supplementationRanjit S Shetty, Cary S Gallagher, Yei-Tsung Chen, et al.
Human Molecular Genetics|January 8, 2004
Rescue of a human mRNA splicing defect by the plant cytokinin kinetinSusan A Slaugenhaupt, James Mull, Maire Leyne, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 9, 2007
Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomiaMatthew M Hims, El Chérif Ibrahim, Maire Leyne, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosaT Jeffrey Keen, Matthew M Hims, Arthur B McKie, et al.
Human Molecular Genetics|January 5, 2002
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaChristina F Chakarova, Matthew M Hims, Hanno Bolz, et al.
Nature Medicine|April 8, 2015
Studying clonal dynamics in response to cancer therapy using high-complexity barcodingHyo-eun C Bhang, David A Ruddy, Viveksagar Krishnamurthy Radhakrishna, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Human Mutation|September 12, 2006
Weak definition of IKBKAP exon 20 leads to aberrant splicing in familial dysautonomiaEl Chérif Ibrahim, Matthew M Hims, Noam Shomron, et al.
Bioinformatics (Oxford, England)|February 10, 2015
NxTrim: optimized trimming of Illumina mate pair readsJared O'Connell, Ole Schulz-Trieglaff, Emma Carlson, et al.
Molecular and Cellular Biology|November 19, 2008
Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAPYei-Tsung Chen, Matthew M Hims, Ranjit S Shetty, et al.
Genomics|July 24, 2007
A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defectMatthew M Hims, Ranjit S Shetty, James Pickel, et al.
Human Molecular Genetics|August 9, 2011
Specific correction of a splice defect in brain by nutritional supplementationRanjit S Shetty, Cary S Gallagher, Yei-Tsung Chen, et al.
Human Molecular Genetics|January 8, 2004
Rescue of a human mRNA splicing defect by the plant cytokinin kinetinSusan A Slaugenhaupt, James Mull, Maire Leyne, et al.
Journal of Molecular Medicine (Berlin, Germany)|January 9, 2007
Therapeutic potential and mechanism of kinetin as a treatment for the human splicing disease familial dysautonomiaMatthew M Hims, El Chérif Ibrahim, Maire Leyne, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
Mutations in a protein target of the Pim-1 kinase associated with the RP9 form of autosomal dominant retinitis pigmentosaT Jeffrey Keen, Matthew M Hims, Arthur B McKie, et al.
Human Molecular Genetics|January 5, 2002
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosaChristina F Chakarova, Matthew M Hims, Hanno Bolz, et al.
Nature Medicine|April 8, 2015
Studying clonal dynamics in response to cancer therapy using high-complexity barcodingHyo-eun C Bhang, David A Ruddy, Viveksagar Krishnamurthy Radhakrishna, et al.
Pageof 2