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S Cornelis

Showing results (31-40 of 47) with videos related to

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Nature Genetics|February 1, 1994
Instability of short tandem repeats (microsatellites) in human cancersR Wooster, A M Cleton-Jansen, N Collins, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2T Peelen, R S Cornelis, M van Vliet, et al.
American Journal of Human Genetics|February 5, 2022
Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severityStéphanie S Cornelis, Esmee H Runhart, Miriam Bauwens, et al.
Human Genetics|May 1, 1995
Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancerR S Cornelis, H F Vasen, H Meijers-Heijboer, et al.
Cell Death & Disease|March 3, 2011
Caspase-mediated cleavage of Beclin-1 inactivates Beclin-1-induced autophagy and enhances apoptosis by promoting the release of proapoptotic factors from mitochondriaE Wirawan, L Vande Walle, K Kersse, et al.
British Journal of Pharmacology|August 22, 2013
Reversible inhibition of the glycine transporter GlyT2 circumvents acute toxicity while preserving efficacy in the treatment of painA Mingorance-Le Meur, P Ghisdal, B Mullier, et al.
Genome Research|November 23, 2017
<i>ABCA4</i> midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt diseaseRiccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, et al.
Cancer Research|August 1, 1994
Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutationsR S Cornelis, M van Vliet, C B Vos, et al.
JAMA Ophthalmology|August 21, 2020
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt DiseaseEsmee H Runhart, Mubeen Khan, Stéphanie S Cornelis, et al.
HGG Advances|September 14, 2023
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritabilityZelia Corradi, Mubeen Khan, Rebekkah Hitti-Malin, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Nature Genetics|February 1, 1994
Instability of short tandem repeats (microsatellites) in human cancersR Wooster, A M Cleton-Jansen, N Collins, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
The majority of 22 Dutch high-risk breast cancer families are due to either BRCA1 or BRCA2T Peelen, R S Cornelis, M van Vliet, et al.
American Journal of Human Genetics|February 5, 2022
Personalized genetic counseling for Stargardt disease: Offspring risk estimates based on variant severityStéphanie S Cornelis, Esmee H Runhart, Miriam Bauwens, et al.
Human Genetics|May 1, 1995
Age at diagnosis as an indicator of eligibility for BRCA1 DNA testing in familial breast cancerR S Cornelis, H F Vasen, H Meijers-Heijboer, et al.
Cell Death & Disease|March 3, 2011
Caspase-mediated cleavage of Beclin-1 inactivates Beclin-1-induced autophagy and enhances apoptosis by promoting the release of proapoptotic factors from mitochondriaE Wirawan, L Vande Walle, K Kersse, et al.
British Journal of Pharmacology|August 22, 2013
Reversible inhibition of the glycine transporter GlyT2 circumvents acute toxicity while preserving efficacy in the treatment of painA Mingorance-Le Meur, P Ghisdal, B Mullier, et al.
Genome Research|November 23, 2017
<i>ABCA4</i> midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt diseaseRiccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, et al.
Cancer Research|August 1, 1994
Evidence for a gene on 17p13.3, distal to TP53, as a target for allele loss in breast tumors without p53 mutationsR S Cornelis, M van Vliet, C B Vos, et al.
JAMA Ophthalmology|August 21, 2020
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt DiseaseEsmee H Runhart, Mubeen Khan, Stéphanie S Cornelis, et al.
HGG Advances|September 14, 2023
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritabilityZelia Corradi, Mubeen Khan, Rebekkah Hitti-Malin, et al.
Pageof 5