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

F Baas

Showing results (131-140 of 245) with videos related to

Pageof 25
Sort By:
Neuromuscular Disorders : NMD|January 1, 1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
British Journal of Cancer|January 1, 1995
Reduced topoisomerase II activity in multidrug-resistant human non-small cell lung cancer cell linesE W Eijdems, M de Haas, A J Timmerman, et al.
Journal of Medical Genetics|October 9, 2010
Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomasI Christiaans, S B Kenter, H C Brink, et al.
British Journal of Cancer|December 19, 2007
Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndromeA C J Ammerlaan, A Ararou, M P W A Houben, et al.
ESC Heart Failure|July 17, 2022
Blood-based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta-analysisMark Jansen, Sila Algül, Laurens P Bosman, et al.
Gut|December 14, 2005
Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposisM Jansen, W W J de Leng, A F Baas, et al.
Biochemical and Biophysical Research Communications|August 21, 2001
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytomaD A Vandeputte, C B Meije, M van Dartel, et al.
Nature Genetics|December 1, 1992
Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1AL J Valentijn, F Baas, R A Wolterman, et al.
Annals of Neurology|October 1, 1994
Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsiesE C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Frontiers in Cardiovascular Medicine|May 2, 2022
Automatic Identification of Patients With Unexplained Left Ventricular Hypertrophy in Electronic Health Record Data to Improve Targeted Treatment and Family ScreeningArjan Sammani, Mark Jansen, Nynke M de Vries, et al.
Pageof 25

Showing results (131-140 of 245) with videos related to

Sort By:
Pageof 25
Neuromuscular Disorders : NMD|January 1, 1991
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a). The HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
British Journal of Cancer|January 1, 1995
Reduced topoisomerase II activity in multidrug-resistant human non-small cell lung cancer cell linesE W Eijdems, M de Haas, A J Timmerman, et al.
Journal of Medical Genetics|October 9, 2010
Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomasI Christiaans, S B Kenter, H C Brink, et al.
British Journal of Cancer|December 19, 2007
Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndromeA C J Ammerlaan, A Ararou, M P W A Houben, et al.
ESC Heart Failure|July 17, 2022
Blood-based biomarkers for the prediction of hypertrophic cardiomyopathy prognosis: a systematic review and meta-analysisMark Jansen, Sila Algül, Laurens P Bosman, et al.
Gut|December 14, 2005
Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposisM Jansen, W W J de Leng, A F Baas, et al.
Biochemical and Biophysical Research Communications|August 21, 2001
GOA, a novel gene encoding a ring finger B-box coiled-coil protein, is overexpressed in astrocytomaD A Vandeputte, C B Meije, M van Dartel, et al.
Nature Genetics|December 1, 1992
Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1AL J Valentijn, F Baas, R A Wolterman, et al.
Annals of Neurology|October 1, 1994
Prevalence of the 1.5-Mb 17p deletion in families with hereditary neuropathy with liability to pressure palsiesE C Mariman, A A Gabreëls-Festen, S E van Beersum, et al.
Frontiers in Cardiovascular Medicine|May 2, 2022
Automatic Identification of Patients With Unexplained Left Ventricular Hypertrophy in Electronic Health Record Data to Improve Targeted Treatment and Family ScreeningArjan Sammani, Mark Jansen, Nynke M de Vries, et al.
Pageof 25