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

Peter Gustavsson

Showing results (11-20 of 33) with videos related to

Pageof 4
Sort By:
British Journal of Haematology|October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) genePeter Gustavsson, Joakim Klar, Hans Matsson, et al.
Molecular and Cellular Biochemistry|March 14, 2013
Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brainKit-Yi Leung, Sandra C P De Castro, Filipe Cabreiro, et al.
European Journal of Human Genetics : EJHG|May 26, 2005
Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardationMahmoud Reza Mansouri, Lena Marklund, Peter Gustavsson, et al.
Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Plos One|January 8, 2019
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirthEllika Sahlin, Anna Gréen, Peter Gustavsson, et al.
European Journal of Radiology|July 12, 2025
Performance of MRI-based surveillance for high-risk individuals for pancreatic cancerRaffaella M Pozzi Mucelli, Miroslav Vujasinovic, Ana Farah-Mwais, et al.
European Journal of Medical Genetics|February 6, 2015
No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformationsJohanna Winberg, Håkan Berggren, Torsten Malm, et al.
Plos Genetics|November 21, 2012
Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in miceSandra C P De Castro, Ashraf Malhas, Kit-Yi Leung, et al.
Plos One|January 14, 2014
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL associationJohanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
Partial tetrasomy 14 associated with multiple malformationsJohanna Winberg, Kristina Lagerstedt Robinson, Karin Naess, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|October 3, 2002
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) genePeter Gustavsson, Joakim Klar, Hans Matsson, et al.
Molecular and Cellular Biochemistry|March 14, 2013
Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brainKit-Yi Leung, Sandra C P De Castro, Filipe Cabreiro, et al.
European Journal of Human Genetics : EJHG|May 26, 2005
Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardationMahmoud Reza Mansouri, Lena Marklund, Peter Gustavsson, et al.
Human Molecular Genetics|August 28, 2007
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse modelPeter Gustavsson, Nicholas D E Greene, Dina Lad, et al.
Plos One|January 8, 2019
Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirthEllika Sahlin, Anna Gréen, Peter Gustavsson, et al.
European Journal of Radiology|July 12, 2025
Performance of MRI-based surveillance for high-risk individuals for pancreatic cancerRaffaella M Pozzi Mucelli, Miroslav Vujasinovic, Ana Farah-Mwais, et al.
European Journal of Medical Genetics|February 6, 2015
No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformationsJohanna Winberg, Håkan Berggren, Torsten Malm, et al.
Plos Genetics|November 21, 2012
Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in miceSandra C P De Castro, Ashraf Malhas, Kit-Yi Leung, et al.
Plos One|January 14, 2014
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL associationJohanna Winberg, Peter Gustavsson, Nikos Papadogiannakis, et al.
American Journal of Medical Genetics. Part A|April 25, 2013
Partial tetrasomy 14 associated with multiple malformationsJohanna Winberg, Kristina Lagerstedt Robinson, Karin Naess, et al.
Pageof 4