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

K Forsman

Showing results (51-60 of 69) with videos related to

Pageof 7
Sort By:
The Journal of Biological Chemistry|March 5, 1987
Fibronectin's cell-adhesive domain and an amino-terminal matrix assembly domain participate in its assembly into fibroblast pericellular matrixJ A McDonald, B J Quade, T J Broekelmann, et al.
Journal of Dental Research|May 31, 2001
Cloning and characterization of the mouse and human enamelin genesJ C Hu, C H Zhang, Y Yang, et al.
Neurology|December 11, 2002
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1A Carlsson, L Forsgren, P-O Nylander, et al.
The European Respiratory Journal|October 4, 2011
Total desmosines in plasma and urine correlate with lung functionC A Lindberg, G Engström, M Gerhardsson de Verdier, et al.
European Journal of Oral Sciences|May 2, 2001
Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patientsC K Mårdh, B Bäckman, D Simmons, et al.
Social Psychiatry and Psychiatric Epidemiology|December 1, 2018
Determinants of multidimensional mental wellbeing in the oldest old: a rapid reviewJohanna Cresswell-Smith, Francesco Amaddeo, Valeria Donisi, et al.
Clinical Genetics|September 1, 1992
The gene for Best's macular dystrophy is located at 11q13 in a Swedish familyK Forsman, C Graff, S Nordström, et al.
European Heart Journal|February 1, 1993
Non-invasive magnetocardiographic localization of ventricular pre-excitation in the Wolff-Parkinson-White syndrome using a realistic torso modelJ Nenonen, M Mäkijärvi, L Toivonen, et al.
Genomics|April 1, 1997
Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21M MacDougall, B R DuPont, D Simmons, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Pageof 7

Showing results (51-60 of 69) with videos related to

Sort By:
Pageof 7
The Journal of Biological Chemistry|March 5, 1987
Fibronectin's cell-adhesive domain and an amino-terminal matrix assembly domain participate in its assembly into fibroblast pericellular matrixJ A McDonald, B J Quade, T J Broekelmann, et al.
Journal of Dental Research|May 31, 2001
Cloning and characterization of the mouse and human enamelin genesJ C Hu, C H Zhang, Y Yang, et al.
Neurology|December 11, 2002
Identification of a susceptibility locus for migraine with and without aura on 6p12.2-p21.1A Carlsson, L Forsgren, P-O Nylander, et al.
The European Respiratory Journal|October 4, 2011
Total desmosines in plasma and urine correlate with lung functionC A Lindberg, G Engström, M Gerhardsson de Verdier, et al.
European Journal of Oral Sciences|May 2, 2001
Human ameloblastin gene: genomic organization and mutation analysis in amelogenesis imperfecta patientsC K Mårdh, B Bäckman, D Simmons, et al.
Social Psychiatry and Psychiatric Epidemiology|December 1, 2018
Determinants of multidimensional mental wellbeing in the oldest old: a rapid reviewJohanna Cresswell-Smith, Francesco Amaddeo, Valeria Donisi, et al.
Clinical Genetics|September 1, 1992
The gene for Best's macular dystrophy is located at 11q13 in a Swedish familyK Forsman, C Graff, S Nordström, et al.
European Heart Journal|February 1, 1993
Non-invasive magnetocardiographic localization of ventricular pre-excitation in the Wolff-Parkinson-White syndrome using a realistic torso modelJ Nenonen, M Mäkijärvi, L Toivonen, et al.
Genomics|April 1, 1997
Ameloblastin gene (AMBN) maps within the critical region for autosomal dominant amelogenesis imperfecta at chromosome 4q21M MacDougall, B R DuPont, D Simmons, et al.
Ophthalmic Genetics|January 3, 2001
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the familyM Van Ghelue, H L Eriksen, V Ponjavic, et al.
Pageof 7