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

David Valle

Showing results (51-60 of 146) with videos related to

Pageof 15
Sort By:
The Journal of Investigative Dermatology|January 29, 2014
Decreased expression of the chromatin remodeler ATRX associates with melanoma progressionZulekha A Qadeer, Sara Harcharik, David Valle-Garcia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian GenomicsJulie Jurgens, Hua Ling, Kurt Hetrick, et al.
Molecular and Cellular Biology|November 6, 2002
PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferationXiaoling Li, Eveline Baumgart, Gao-Xiang Dong, et al.
Human Mutation|February 16, 2022
The impact of GeneMatcher on international data sharing and collaborationAda Hamosh, Elizabeth Wohler, Renan Martin, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
miRNA mutations are not a common cause of deafnessMichael S Hildebrand, P Dane Witmer, Shunbin Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2007
Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B geneDimitrios Avramopoulos, Virginia K Lasseter, M Daniele Fallin, et al.
European Journal of Pediatrics|November 2, 2004
Delta1-pyrroline-5-carboxylate synthase deficiency: neurodegeneration, cataracts and connective tissue manifestations combined with hyperammonaemia and reduced ornithine, citrulline, arginine and prolineMatthias R Baumgartner, Daniel Rabier, Marie-Cécile Nassogne, et al.
Molecular and Cellular Biology|October 1, 2004
PHR1, a PH domain-containing protein expressed in primary sensory neuronsShunbin Xu, Yanshu Wang, Haiqing Zhao, et al.
American Journal of Human Genetics|June 23, 2004
Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish familiesM Daniele Fallin, Virginia K Lasseter, Paula S Wolyniec, et al.
Psychiatric Genetics|May 1, 2010
Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish womenYaping Liu, Pei-Lung Chen, John McGrath, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
The Journal of Investigative Dermatology|January 29, 2014
Decreased expression of the chromatin remodeler ATRX associates with melanoma progressionZulekha A Qadeer, Sara Harcharik, David Valle-Garcia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian GenomicsJulie Jurgens, Hua Ling, Kurt Hetrick, et al.
Molecular and Cellular Biology|November 6, 2002
PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferationXiaoling Li, Eveline Baumgart, Gao-Xiang Dong, et al.
Human Mutation|February 16, 2022
The impact of GeneMatcher on international data sharing and collaborationAda Hamosh, Elizabeth Wohler, Renan Martin, et al.
American Journal of Medical Genetics. Part A|February 27, 2010
miRNA mutations are not a common cause of deafnessMichael S Hildebrand, P Dane Witmer, Shunbin Xu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2007
Stage II follow-up on a linkage scan for bipolar disorder in the Ashkenazim provides suggestive evidence for chromosome 12p and the GRIN2B geneDimitrios Avramopoulos, Virginia K Lasseter, M Daniele Fallin, et al.
European Journal of Pediatrics|November 2, 2004
Delta1-pyrroline-5-carboxylate synthase deficiency: neurodegeneration, cataracts and connective tissue manifestations combined with hyperammonaemia and reduced ornithine, citrulline, arginine and prolineMatthias R Baumgartner, Daniel Rabier, Marie-Cécile Nassogne, et al.
Molecular and Cellular Biology|October 1, 2004
PHR1, a PH domain-containing protein expressed in primary sensory neuronsShunbin Xu, Yanshu Wang, Haiqing Zhao, et al.
American Journal of Human Genetics|June 23, 2004
Genomewide linkage scan for bipolar-disorder susceptibility loci among Ashkenazi Jewish familiesM Daniele Fallin, Virginia K Lasseter, Paula S Wolyniec, et al.
Psychiatric Genetics|May 1, 2010
Replication of an association of a common variant in the Reelin gene (RELN) with schizophrenia in Ashkenazi Jewish womenYaping Liu, Pei-Lung Chen, John McGrath, et al.
Pageof 15