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

C Murray

Showing results (1341-1350 of 1,465) with videos related to

Pageof 147
Sort By:
Human Genetics|January 6, 2017
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Frontiers in Cell and Developmental Biology|April 26, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel RegionsNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|April 18, 2024
Shared genetic risk between major orofacial cleft phenotypes in an African populationAzeez Alade, Tabitha Peter, Tamara Busch, et al.
Molecular Psychiatry|June 5, 2013
Childhood cognitive ability accounts for associations between cognitive ability and brain cortical thickness in old ageS Karama, M E Bastin, C Murray, et al.
Pediatrics|June 12, 2013
Individual and center-level factors affecting mortality among extremely low birth weight infantsBrandon W Alleman, Edward F Bell, Lei Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeRenata L L Ferreira de Lima, Sarah A Hoper, Michella Ghassibe, et al.
Genetic Epidemiology|February 22, 2022
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
The Journal of Clinical Investigation|July 20, 2023
The predominant PAR4 variant in individuals of African ancestry worsens murine and human stroke outcomesFrederik Denorme, Nicole D Armstrong, Michelle L Stoller, et al.
Bioorganic & Medicinal Chemistry Letters|February 4, 2006
Potent blockers of the monocarboxylate transporter MCT1: novel immunomodulatory compoundsS D Guile, J R Bantick, D R Cheshire, et al.
Pageof 147

Showing results (1341-1350 of 1,465) with videos related to

Sort By:
Pageof 147
Human Genetics|January 6, 2017
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palateElizabeth J Leslie, Jenna C Carlson, John R Shaffer, et al.
Frontiers in Cell and Developmental Biology|April 26, 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel RegionsNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|April 18, 2024
Shared genetic risk between major orofacial cleft phenotypes in an African populationAzeez Alade, Tabitha Peter, Tamara Busch, et al.
Molecular Psychiatry|June 5, 2013
Childhood cognitive ability accounts for associations between cognitive ability and brain cortical thickness in old ageS Karama, M E Bastin, C Murray, et al.
Pediatrics|June 12, 2013
Individual and center-level factors affecting mortality among extremely low birth weight infantsBrandon W Alleman, Edward F Bell, Lei Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeRenata L L Ferreira de Lima, Sarah A Hoper, Michella Ghassibe, et al.
Genetic Epidemiology|February 22, 2022
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypesNandita Mukhopadhyay, Eleanor Feingold, Lina Moreno-Uribe, et al.
Genetic Epidemiology|June 8, 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signalsJenna C Carlson, Deepti Anand, Azeez Butali, et al.
The Journal of Clinical Investigation|July 20, 2023
The predominant PAR4 variant in individuals of African ancestry worsens murine and human stroke outcomesFrederik Denorme, Nicole D Armstrong, Michelle L Stoller, et al.
Bioorganic & Medicinal Chemistry Letters|February 4, 2006
Potent blockers of the monocarboxylate transporter MCT1: novel immunomodulatory compoundsS D Guile, J R Bantick, D R Cheshire, et al.
Pageof 147