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

R J Scott

Showing results (161-170 of 226) with videos related to

Pageof 23
Sort By:
Human Mutation|January 4, 2001
Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genesA Jakubowska, B Górski, G Kurzawski, et al.
Molecular Psychiatry|June 27, 2012
Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophreniaM J Green, M J Cairns, J Wu, et al.
Human Genetics|December 1, 1996
Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coliR B van der Luijt, P Meera Khan, H F Vasen, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 17, 2013
Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosisM C Graves, M Benton, R A Lea, et al.
Veterinary and Comparative Orthopaedics and Traumatology : V.C.O.T|June 12, 2008
Biomechanical characteristics of allogeneic cortical bone pins designed for fracture fixationJ M Liptak, M R Edwards, S P James, et al.
The American Journal of Pathology|November 14, 2000
Potential biological role of transforming growth factor-beta1 in human congenital kidney malformationsS P Yang, A S Woolf, H T Yuan, et al.
Clinical Genetics|July 20, 2010
Can a familial gastrointestinal tumour syndrome be allelic with Waardenburg syndrome?R E Vilain, T Dudding, S G Braye, et al.
Neuroscience|January 22, 2013
Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiationB Acikyol, R M Graham, D Trinder, et al.
Molecular Biology and Evolution|November 28, 2014
The evolution and adaptive potential of transcriptional variation in sticklebacks--signatures of selection and widespread heritabilityErica H Leder, R J Scott McCairns, Tuomas Leinonen, et al.
Journal of Medical Genetics|April 1, 1996
Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC geneZ Dobbie, M Spycher, J L Mary, et al.
Pageof 23

Showing results (161-170 of 226) with videos related to

Sort By:
Pageof 23
Human Mutation|January 4, 2001
Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genesA Jakubowska, B Górski, G Kurzawski, et al.
Molecular Psychiatry|June 27, 2012
Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophreniaM J Green, M J Cairns, J Wu, et al.
Human Genetics|December 1, 1996
Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coliR B van der Luijt, P Meera Khan, H F Vasen, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 17, 2013
Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosisM C Graves, M Benton, R A Lea, et al.
Veterinary and Comparative Orthopaedics and Traumatology : V.C.O.T|June 12, 2008
Biomechanical characteristics of allogeneic cortical bone pins designed for fracture fixationJ M Liptak, M R Edwards, S P James, et al.
The American Journal of Pathology|November 14, 2000
Potential biological role of transforming growth factor-beta1 in human congenital kidney malformationsS P Yang, A S Woolf, H T Yuan, et al.
Clinical Genetics|July 20, 2010
Can a familial gastrointestinal tumour syndrome be allelic with Waardenburg syndrome?R E Vilain, T Dudding, S G Braye, et al.
Neuroscience|January 22, 2013
Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiationB Acikyol, R M Graham, D Trinder, et al.
Molecular Biology and Evolution|November 28, 2014
The evolution and adaptive potential of transcriptional variation in sticklebacks--signatures of selection and widespread heritabilityErica H Leder, R J Scott McCairns, Tuomas Leinonen, et al.
Journal of Medical Genetics|April 1, 1996
Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC geneZ Dobbie, M Spycher, J L Mary, et al.
Pageof 23