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

N Hahn

Showing results (161-170 of 210) with videos related to

Pageof 21
Sort By:
Scientific Reports|July 10, 2015
Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and ProteomicsZhiqiang Hu, Hamish S Scott, Guangrong Qin, et al.
Haematologica|March 30, 2019
A novel germline <i>SAMD9L</i> mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemiaJesse J C Cheah, Anna L Brown, Andreas W Schreiber, et al.
Physiological Genomics|April 21, 2005
Expression profiling reveals functionally important genes and coordinately regulated signaling pathway genes during in vitro angiogenesisC N Hahn, Z J Su, C J Drogemuller, et al.
Genome Biology|October 6, 2009
Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profilingKing-Hwa Ling, Chelsee A Hewitt, Tim Beissbarth, et al.
Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
Frontiers in Cardiovascular Medicine|July 9, 2025
Case Report: A heterozygous loss-of-function variant of the <i>ERG</i> gene in a family with vascular pathologiesPhilipp Erhart, Nicola Dikow, Eva M C Schwaibold, et al.
Human Mutation|June 22, 2016
Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome SequencingChristopher P Barnett, Nathalie J Nataren, Manuela Klingler-Hoffmann, et al.
Plos One|October 12, 2016
Evaluating Soluble EMMPRIN as a Marker of Disease Activity in Multiple Sclerosis: Studies of Serum and Cerebrospinal FluidDeepak K Kaushik, Heather Y F Yong, Jennifer N Hahn, et al.
BMC Genomics|April 7, 2011
Deep sequencing analysis of the developing mouse brain reveals a novel microRNAKing-Hwa Ling, Peter J Brautigan, Christopher N Hahn, et al.
NPJ Genomic Medicine|November 23, 2019
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Alicia B Byrne, Peer Arts, Steven W Polyak, et al.
Pageof 21

Showing results (161-170 of 210) with videos related to

Sort By:
Pageof 21
Scientific Reports|July 10, 2015
Revealing Missing Human Protein Isoforms Based on Ab Initio Prediction, RNA-seq and ProteomicsZhiqiang Hu, Hamish S Scott, Guangrong Qin, et al.
Haematologica|March 30, 2019
A novel germline <i>SAMD9L</i> mutation in a family with ataxia-pancytopenia syndrome and pediatric acute lymphoblastic leukemiaJesse J C Cheah, Anna L Brown, Andreas W Schreiber, et al.
Physiological Genomics|April 21, 2005
Expression profiling reveals functionally important genes and coordinately regulated signaling pathway genes during in vitro angiogenesisC N Hahn, Z J Su, C J Drogemuller, et al.
Genome Biology|October 6, 2009
Molecular networks involved in mouse cerebral corticogenesis and spatio-temporal regulation of Sox4 and Sox11 novel antisense transcripts revealed by transcriptome profilingKing-Hwa Ling, Chelsee A Hewitt, Tim Beissbarth, et al.
Human Mutation|August 13, 2021
GATA2 deficiency syndrome: A decade of discoveryClaire C Homan, Parvathy Venugopal, Peer Arts, et al.
Frontiers in Cardiovascular Medicine|July 9, 2025
Case Report: A heterozygous loss-of-function variant of the <i>ERG</i> gene in a family with vascular pathologiesPhilipp Erhart, Nicola Dikow, Eva M C Schwaibold, et al.
Human Mutation|June 22, 2016
Ectrodactyly and Lethal Pulmonary Acinar Dysplasia Associated with Homozygous FGFR2 Mutations Identified by Exome SequencingChristopher P Barnett, Nathalie J Nataren, Manuela Klingler-Hoffmann, et al.
Plos One|October 12, 2016
Evaluating Soluble EMMPRIN as a Marker of Disease Activity in Multiple Sclerosis: Studies of Serum and Cerebrospinal FluidDeepak K Kaushik, Heather Y F Yong, Jennifer N Hahn, et al.
BMC Genomics|April 7, 2011
Deep sequencing analysis of the developing mouse brain reveals a novel microRNAKing-Hwa Ling, Peter J Brautigan, Christopher N Hahn, et al.
NPJ Genomic Medicine|November 23, 2019
Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6Alicia B Byrne, Peer Arts, Steven W Polyak, et al.
Pageof 21