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

Helga Westers

Showing results (21-30 of 45) with videos related to

Pageof 5
Sort By:
International Journal of Molecular Sciences|October 26, 2024
Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Michiel R Fokkens, et al.
Gene|October 21, 2022
SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnosticsMohamed Z Alimohamed, Ludolf G Boven, Krista K van Dijk, et al.
Scientific Reports|April 21, 2022
Evaluation of a seven gene mutational profile as a prognostic factor in a population-based study of clear cell renal cell carcinomaJeroen A A van de Pol, Paranita Ferronika, Helga Westers, et al.
Genes, Chromosomes & Cancer|April 18, 2009
Do microsatellite instability profiles really differ between colorectal and endometrial tumors?Ana M Ferreira, Helga Westers, Ying Wu, et al.
Neurology. Genetics|December 7, 2023
Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Marloes Benjamins-Stok, et al.
Microbiology and Molecular Biology Reviews : MMBR|June 10, 2004
Proteomics of protein secretion by Bacillus subtilis: separating the "secrets" of the secretomeHarold Tjalsma, Haike Antelmann, Jan D H Jongbloed, et al.
Human Mutation|September 9, 2014
High frequency of RPL22 mutations in microsatellite-unstable colorectal and endometrial tumorsAna M Ferreira, Iina Tuominen, Krista van Dijk-Bos, et al.
Genes, Chromosomes & Cancer|January 22, 2009
Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndromeJianghua Ou, Merete Rasmussen, Helga Westers, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
The Journal of Pathology|June 13, 2009
Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patientsAna M Ferreira, Helga Westers, Sónia Sousa, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
International Journal of Molecular Sciences|October 26, 2024
Identification and Copy Number Variant Analysis of Enhancer Regions of Genes Causing Spinocerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Michiel R Fokkens, et al.
Gene|October 21, 2022
SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnosticsMohamed Z Alimohamed, Ludolf G Boven, Krista K van Dijk, et al.
Scientific Reports|April 21, 2022
Evaluation of a seven gene mutational profile as a prognostic factor in a population-based study of clear cell renal cell carcinomaJeroen A A van de Pol, Paranita Ferronika, Helga Westers, et al.
Genes, Chromosomes & Cancer|April 18, 2009
Do microsatellite instability profiles really differ between colorectal and endometrial tumors?Ana M Ferreira, Helga Westers, Ying Wu, et al.
Neurology. Genetics|December 7, 2023
Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar AtaxiaFatemeh Ghorbani, Eddy N de Boer, Marloes Benjamins-Stok, et al.
Microbiology and Molecular Biology Reviews : MMBR|June 10, 2004
Proteomics of protein secretion by Bacillus subtilis: separating the "secrets" of the secretomeHarold Tjalsma, Haike Antelmann, Jan D H Jongbloed, et al.
Human Mutation|September 9, 2014
High frequency of RPL22 mutations in microsatellite-unstable colorectal and endometrial tumorsAna M Ferreira, Iina Tuominen, Krista van Dijk-Bos, et al.
Genes, Chromosomes & Cancer|January 22, 2009
Biochemical characterization of MLH3 missense mutations does not reveal an apparent role of MLH3 in Lynch syndromeJianghua Ou, Merete Rasmussen, Helga Westers, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
The Journal of Pathology|June 13, 2009
Mononucleotide precedes dinucleotide repeat instability during colorectal tumour development in Lynch syndrome patientsAna M Ferreira, Helga Westers, Sónia Sousa, et al.
Pageof 5