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Nature Genetics
|
December 30, 1999
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I
P Momeni, G Glöckner, O Schmidt, et al.
Human Mutation
|
May 6, 2008
Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster
Karin Buiting, Deniz Kanber, José I Martín-Subero, et al.
The Journal of Biological Chemistry
|
September 13, 2014
Mouse macrophages completely lacking Rho subfamily GTPases (RhoA, RhoB, and RhoC) have severe lamellipodial retraction defects, but robust chemotactic navigation and altered motility
Volker Königs, Richard Jennings, Thomas Vogl, et al.
Cancer Research
|
May 17, 2003
Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities
Frank Tschentscher, Johannes Hüsing, Tanja Hölter, et al.
European Journal of Medical Genetics
|
October 12, 2010
Parental origin and functional relevance of a de novo UBE3A variant
Bernhard Horsthemke, Michaela Wawrzik, Stephanie Gross, et al.
Plos One
|
September 15, 2011
Altered development of NKT cells, γδ T cells, CD8 T cells and NK cells in a PLZF deficient patient
Maggie Eidson, Justin Wahlstrom, Aimee M Beaulieu, et al.
Clinical Epigenetics
|
August 22, 2021
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes
Sara Di Persio, Elsa Leitão, Marius Wöste, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
July 10, 2010
Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort
Sonali Pechlivanis, André Scherag, Thomas W Mühleisen, et al.
Nature Genetics
|
March 10, 2001
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
O El-Maarri, K Buiting, E G Peery, et al.
Human Molecular Genetics
|
February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
J Wirth, E Back, A Hüttenhofer, et al.
Page
of 37
Search research articles
Search
Showing results (321-330 of 368) with videos related to
Sort By:
Page
of 37
Nature Genetics
|
December 30, 1999
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type I
P Momeni, G Glöckner, O Schmidt, et al.
Human Mutation
|
May 6, 2008
Clinical features of maternal uniparental disomy 14 in patients with an epimutation and a deletion of the imprinted DLK1/GTL2 gene cluster
Karin Buiting, Deniz Kanber, José I Martín-Subero, et al.
The Journal of Biological Chemistry
|
September 13, 2014
Mouse macrophages completely lacking Rho subfamily GTPases (RhoA, RhoB, and RhoC) have severe lamellipodial retraction defects, but robust chemotactic navigation and altered motility
Volker Königs, Richard Jennings, Thomas Vogl, et al.
Cancer Research
|
May 17, 2003
Tumor classification based on gene expression profiling shows that uveal melanomas with and without monosomy 3 represent two distinct entities
Frank Tschentscher, Johannes Hüsing, Tanja Hölter, et al.
European Journal of Medical Genetics
|
October 12, 2010
Parental origin and functional relevance of a de novo UBE3A variant
Bernhard Horsthemke, Michaela Wawrzik, Stephanie Gross, et al.
Plos One
|
September 15, 2011
Altered development of NKT cells, γδ T cells, CD8 T cells and NK cells in a PLZF deficient patient
Maggie Eidson, Justin Wahlstrom, Aimee M Beaulieu, et al.
Clinical Epigenetics
|
August 22, 2021
Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes
Sara Di Persio, Elsa Leitão, Marius Wöste, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
July 10, 2010
Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the Heinz Nixdorf recall cohort
Sonali Pechlivanis, André Scherag, Thomas W Mühleisen, et al.
Nature Genetics
|
March 10, 2001
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
O El-Maarri, K Buiting, E G Peery, et al.
Human Molecular Genetics
|
February 13, 2001
A translocation breakpoint cluster disrupts the newly defined 3' end of the SNURF-SNRPN transcription unit on chromosome 15
J Wirth, E Back, A Hüttenhofer, et al.
Page
of 37