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

S Kenwrick

Showing results (41-50 of 57) with videos related to

Pageof 6
Sort By:
Brain : a Journal of Neurology|November 10, 2001
Abnormal corticospinal function but normal axonal guidance in human L1CAM mutationsC B Dobson, F Villagra, G J Clowry, et al.
The EMBO Journal|September 2, 1999
Pathological missense mutations of neural cell adhesion molecule L1 affect homophilic and heterophilic binding activitiesE De Angelis, J MacFarlane, J S Du, et al.
Gene|March 28, 1998
The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish FuguO Coutelle, G Nyakatura, S Taudien, et al.
Genomics|September 15, 1994
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patientS Murru, L Casula, L Casarino, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
Nature Genetics|July 1, 1994
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 geneM Jouet, A Rosenthal, G Armstrong, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Cancer Research|April 16, 1998
Chinese hamster ovary cells resistant to the topoisomerase II catalytic inhibitor ICRF-159: a Tyr49Phe mutation confers high-level resistance to bisdioxopiperazinesM Sehested, I Wessel, L H Jensen, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Linkage analysis in 16 families with incontinentia pigmentiM Jouet, H Stewart, S Landy, et al.
Human Molecular Genetics|November 16, 2001
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genesS Aradhya, T Bardaro, P Galgóczy, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Brain : a Journal of Neurology|November 10, 2001
Abnormal corticospinal function but normal axonal guidance in human L1CAM mutationsC B Dobson, F Villagra, G J Clowry, et al.
The EMBO Journal|September 2, 1999
Pathological missense mutations of neural cell adhesion molecule L1 affect homophilic and heterophilic binding activitiesE De Angelis, J MacFarlane, J S Du, et al.
Gene|March 28, 1998
The neural cell adhesion molecule L1: genomic organisation and differential splicing is conserved between man and the pufferfish FuguO Coutelle, G Nyakatura, S Taudien, et al.
Genomics|September 15, 1994
A DNA fragment from Xq21 replaces a deleted region containing the entire FVIII gene in a severe hemophilia A patientS Murru, L Casula, L Casarino, et al.
Clinical Genetics|March 5, 1999
X-inactivation and marker studies in three families with incontinentia pigmenti: implications for counselling and gene localisationH Woffendin, T Jakins, M Jouet, et al.
Nature Genetics|July 1, 1994
X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 geneM Jouet, A Rosenthal, G Armstrong, et al.
Human Molecular Genetics|April 1, 1994
Identification of a 5' splice site mutation in intron 4 of the L1CAM gene in an X-linked hydrocephalus familyP Coucke, L Vits, G Van Camp, et al.
Cancer Research|April 16, 1998
Chinese hamster ovary cells resistant to the topoisomerase II catalytic inhibitor ICRF-159: a Tyr49Phe mutation confers high-level resistance to bisdioxopiperazinesM Sehested, I Wessel, L H Jensen, et al.
European Journal of Human Genetics : EJHG|May 1, 1997
Linkage analysis in 16 families with incontinentia pigmentiM Jouet, H Stewart, S Landy, et al.
Human Molecular Genetics|November 16, 2001
Multiple pathogenic and benign genomic rearrangements occur at a 35 kb duplication involving the NEMO and LAGE2 genesS Aradhya, T Bardaro, P Galgóczy, et al.
Pageof 6