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

J P Faber

Showing results (1-10 of 14) with videos related to

Pageof 2
Sort By:
Medizinische Klinik (Munich, Germany : 1983)|April 15, 1993
[Molecular analysis of pulmonary risk genes. Relevance for clinical research, diagnosis and therapy]W C Poller, J P Faber
Nucleic Acids Research|January 11, 1991
Sequence polymorphism in the human alpha-2-macroglobulin (A2M) geneW Poller, J P Faber, K Olek
American Journal of Human Genetics|June 1, 1990
Sequence data of the rare deficient alpha 1-antitrypsin variant PI ZaugsburgJ P Faber, S Weidinger, K Olek
Klinische Wochenschrift|September 3, 1990
Highly variable clinical course in severe alpha 1-antitrypsin deficiency--use of polymerase chain reaction for the detection of rare deficiency allelesW Poller, J P Faber, K Olek
Human Genetics|January 1, 1992
Cloning of the human alpha 2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester siteW Poller, J P Faber, G Klobeck, et al.
Electrophoresis|September 1, 1992
Improved phenotyping of alpha 1-antichymotrypsin (ACT) by isoelectric focusing and immunoprinting: first demonstration of a deficient protein variant in the ACT systemS Weidinger, W Poller, J P Faber, et al.
Human Genetics|March 1, 1991
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg)W Poller, J P Faber, S Weidinger, et al.
American Journal of Human Genetics|July 1, 1989
The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the geneJ P Faber, S Weidinger, H W Goedde, et al.
Klinische Wochenschrift|September 16, 1991
Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical courseW Poller, J P Faber, S Scholz, et al.
American Journal of Human Genetics|December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M alleleJ P Faber, W Poller, S Weidinger, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Medizinische Klinik (Munich, Germany : 1983)|April 15, 1993
[Molecular analysis of pulmonary risk genes. Relevance for clinical research, diagnosis and therapy]W C Poller, J P Faber
Nucleic Acids Research|January 11, 1991
Sequence polymorphism in the human alpha-2-macroglobulin (A2M) geneW Poller, J P Faber, K Olek
American Journal of Human Genetics|June 1, 1990
Sequence data of the rare deficient alpha 1-antitrypsin variant PI ZaugsburgJ P Faber, S Weidinger, K Olek
Klinische Wochenschrift|September 3, 1990
Highly variable clinical course in severe alpha 1-antitrypsin deficiency--use of polymerase chain reaction for the detection of rare deficiency allelesW Poller, J P Faber, K Olek
Human Genetics|January 1, 1992
Cloning of the human alpha 2-macroglobulin gene and detection of mutations in two functional domains: the bait region and the thiolester siteW Poller, J P Faber, G Klobeck, et al.
Electrophoresis|September 1, 1992
Improved phenotyping of alpha 1-antichymotrypsin (ACT) by isoelectric focusing and immunoprinting: first demonstration of a deficient protein variant in the ACT systemS Weidinger, W Poller, J P Faber, et al.
Human Genetics|March 1, 1991
DNA polymorphisms associated with a new alpha 1-antitrypsin PIQ0 variant (PIQ0riedenburg)W Poller, J P Faber, S Weidinger, et al.
American Journal of Human Genetics|July 1, 1989
The deficient alpha-I-antitrypsin phenotype PI P is associated with an A-to-T transversion in exon III of the geneJ P Faber, S Weidinger, H W Goedde, et al.
Klinische Wochenschrift|September 16, 1991
Sequence analysis of the cystic fibrosis gene in patients with disseminated bronchiectatic lung disease. Application in the identification of a cystic fibrosis patient with atypical clinical courseW Poller, J P Faber, S Scholz, et al.
American Journal of Human Genetics|December 1, 1994
Identification and DNA sequence analysis of 15 new alpha 1-antitrypsin variants, including two PI*Q0 alleles and one deficient PI*M alleleJ P Faber, W Poller, S Weidinger, et al.
Pageof 2