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

Hans Matsson

Showing results (11-20 of 34) with videos related to

Pageof 4
Sort By:
Molecular and Cellular Biology|April 15, 2004
Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantationHans Matsson, Edward J Davey, Natalia Draptchinskaia, et al.
American Journal of Medical Genetics. Part A|February 11, 2026
Genome Sequencing in 19 Families With Bladder Exstrophy and Epispadias Complex Indicates Involvement of the ADGR-Gene FamilyAgneta Nordenskjöld, Samara Alm, Jesper Eisfeldt, et al.
Human Genome Variation|April 6, 2018
Evaluation of the <i>ISL1</i> gene in the pathogenesis of bladder exstrophy in a Swedish cohortSamara Arkani, Jia Cao, Johanna Lundin, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2011
Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's diseaseLouisa Goumidi, Karin Dahlman-Wright, Isabel Tapia-Paez, et al.
Human Genetics|September 25, 2015
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish familyElisabet Einarsdottir, Idor Svensson, Fahimeh Darki, et al.
Clinical Chemistry|September 18, 2015
Variant Profiling of Candidate Genes in Pancreatic Ductal AdenocarcinomaJiaqi Huang, Johannes-Matthias Löhr, Magnus Nilsson, et al.
Human Molecular Genetics|May 9, 2009
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexiaSatu Massinen, Kristiina Tammimies, Isabel Tapia-Páez, et al.
Biological Psychiatry|October 6, 2012
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteinsKristiina Tammimies, Morana Vitezic, Hans Matsson, et al.
BMC Medical Genetics|May 3, 2020
Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case reportAndrea Bieder, Elisabet Einarsdottir, Hans Matsson, et al.
Blood|January 1, 2005
Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemiaJohan Flygare, Thomas Kiefer, Koichi Miyake, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Molecular and Cellular Biology|April 15, 2004
Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantationHans Matsson, Edward J Davey, Natalia Draptchinskaia, et al.
American Journal of Medical Genetics. Part A|February 11, 2026
Genome Sequencing in 19 Families With Bladder Exstrophy and Epispadias Complex Indicates Involvement of the ADGR-Gene FamilyAgneta Nordenskjöld, Samara Alm, Jesper Eisfeldt, et al.
Human Genome Variation|April 6, 2018
Evaluation of the <i>ISL1</i> gene in the pathogenesis of bladder exstrophy in a Swedish cohortSamara Arkani, Jia Cao, Johanna Lundin, et al.
Journal of Alzheimer'S Disease : JAD|June 16, 2011
Study of estrogen receptor-α and receptor-β gene polymorphisms on Alzheimer's diseaseLouisa Goumidi, Karin Dahlman-Wright, Isabel Tapia-Paez, et al.
Human Genetics|September 25, 2015
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish familyElisabet Einarsdottir, Idor Svensson, Fahimeh Darki, et al.
Clinical Chemistry|September 18, 2015
Variant Profiling of Candidate Genes in Pancreatic Ductal AdenocarcinomaJiaqi Huang, Johannes-Matthias Löhr, Magnus Nilsson, et al.
Human Molecular Genetics|May 9, 2009
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexiaSatu Massinen, Kristiina Tammimies, Isabel Tapia-Páez, et al.
Biological Psychiatry|October 6, 2012
Molecular networks of DYX1C1 gene show connection to neuronal migration genes and cytoskeletal proteinsKristiina Tammimies, Morana Vitezic, Hans Matsson, et al.
BMC Medical Genetics|May 3, 2020
Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case reportAndrea Bieder, Elisabet Einarsdottir, Hans Matsson, et al.
Blood|January 1, 2005
Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemiaJohan Flygare, Thomas Kiefer, Koichi Miyake, et al.
Pageof 4