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

Ellen Markljung

Showing results (1-10 of 16) with videos related to

Pageof 2
Sort By:
Journal of Pediatric Surgery|November 21, 2012
A rare microduplication in a familial case of annular pancreas and duodenal stenosisEllen Markljung, Tatjana Adamovic, Lisa Ortqvist, et al.
Journal of Human Genetics|February 18, 2011
Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndromeXufeng Zhang, Yougen Chen, Shentiang Zhao, et al.
Gene|July 24, 2012
Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotypeEllen Markljung, Tatjana Adamovic, Jia Cao, et al.
Journal of Pediatric Surgery|April 15, 2014
A novel stop mutation in the EDNRB gene in a family with Hirschsprung's disease associated with multiple sclerosisAnna Löf Granström, Ellen Markljung, Katharina Fink, et al.
Nature Reviews. Genetics|January 1, 2025
The effects of loss of Y chromosome on male healthBozena Bruhn-Olszewska, Ellen Markljung, Edyta Rychlicka-Buniowska, et al.
European Journal of Medical Genetics|March 30, 2010
Mutational study of the MAMLD1-gene in hypospadiasYougen Chen, Hanh T T Thai, Johanna Lundin, et al.
Transcription|February 18, 2011
ZBED6: The birth of a new transcription factor in the common ancestor of placental mammalsLeif Andersson, Göran Andersson, Göran Hjälm, et al.
Molecular Genetics & Genomic Medicine|May 3, 2019
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate geneJohanna Lundin, Ellen Markljung, Izabella Baranowska Körberg, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Physiological Genomics|March 21, 2013
Expression of carnitine palmitoyl-CoA transferase-1B is influenced by a cis-acting eQTL in two chicken lines selected for high and low body weightSojeong Ka, Ellen Markljung, Henrik Ring, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Pediatric Surgery|November 21, 2012
A rare microduplication in a familial case of annular pancreas and duodenal stenosisEllen Markljung, Tatjana Adamovic, Lisa Ortqvist, et al.
Journal of Human Genetics|February 18, 2011
Hypospadias associated with hypertelorism, the mildest phenotype of Opitz syndromeXufeng Zhang, Yougen Chen, Shentiang Zhao, et al.
Gene|July 24, 2012
Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotypeEllen Markljung, Tatjana Adamovic, Jia Cao, et al.
Journal of Pediatric Surgery|April 15, 2014
A novel stop mutation in the EDNRB gene in a family with Hirschsprung's disease associated with multiple sclerosisAnna Löf Granström, Ellen Markljung, Katharina Fink, et al.
Nature Reviews. Genetics|January 1, 2025
The effects of loss of Y chromosome on male healthBozena Bruhn-Olszewska, Ellen Markljung, Edyta Rychlicka-Buniowska, et al.
European Journal of Medical Genetics|March 30, 2010
Mutational study of the MAMLD1-gene in hypospadiasYougen Chen, Hanh T T Thai, Johanna Lundin, et al.
Transcription|February 18, 2011
ZBED6: The birth of a new transcription factor in the common ancestor of placental mammalsLeif Andersson, Göran Andersson, Göran Hjälm, et al.
Molecular Genetics & Genomic Medicine|May 3, 2019
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate geneJohanna Lundin, Ellen Markljung, Izabella Baranowska Körberg, et al.
Human Molecular Genetics|June 25, 2015
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafishIzabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung, et al.
Physiological Genomics|March 21, 2013
Expression of carnitine palmitoyl-CoA transferase-1B is influenced by a cis-acting eQTL in two chicken lines selected for high and low body weightSojeong Ka, Ellen Markljung, Henrik Ring, et al.
Pageof 2