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L Pulkkinen

Showing results (31-40 of 138) with videos related to

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Biochemistry International|March 1, 1983
Hydroxyurea inhibits also the syntheses of thymine nucleotides and methionine in the cells of Escherichia coliJ Heinonen, L Pulkkinen, M Karjalainen, et al.
The Journal of Rheumatology|August 1, 1986
Lack of DNA homology between arthritis triggering bacteria and plasmid of Yersinia enterocolitica or Chlamydia trachomatisL Pulkkinen, E Vuorio, T Hyypia, et al.
International Journal of Dermatology|April 12, 2000
The gene gun: current applications in cutaneous gene therapyM T Lin, L Pulkkinen, J Uitto, et al.
The American Journal of Pathology|April 18, 1998
Compound heterozygosity for missense (L156P) and nonsense (R554X) mutations in the beta4 integrin gene (ITGB4) underlies mild, nonlethal phenotype of epidermolysis bullosa with pyloric atresiaL Pulkkinen, L Bruckner-Tuderman, C August, et al.
Scandinavian Journal of Psychology|February 5, 2000
The role of parents' self-esteem, mastery-orientation and social background in their parenting stylesK Aunola, J E Nurmi, T Onatsu-Arvilommi, et al.
Experimental Dermatology|October 1, 1996
Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophyJ Uitto, L Pulkkinen, F J Smith, et al.
The Journal of Clinical Investigation|January 1, 1993
Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene clusterL Pulkkinen, A M Christiano, R G Knowlton, et al.
The Journal of Investigative Dermatology|April 1, 1996
Compound heterozygosity for nonsense and missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosaA M Christiano, L Pulkkinen, R A Eady, et al.
American Journal of Human Genetics|October 27, 1997
Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosaL Pulkkinen, F Bullrich, P Czarnecki, et al.
Human Mutation|January 1, 1995
Detection of sequence variants in the gene encoding the beta 3 chain of laminin 5 (LAMB3)L Pulkkinen, J A McGrath, A M Christiano, et al.
Pageof 14

Showing results (31-40 of 138) with videos related to

Sort By:
Pageof 14
Biochemistry International|March 1, 1983
Hydroxyurea inhibits also the syntheses of thymine nucleotides and methionine in the cells of Escherichia coliJ Heinonen, L Pulkkinen, M Karjalainen, et al.
The Journal of Rheumatology|August 1, 1986
Lack of DNA homology between arthritis triggering bacteria and plasmid of Yersinia enterocolitica or Chlamydia trachomatisL Pulkkinen, E Vuorio, T Hyypia, et al.
International Journal of Dermatology|April 12, 2000
The gene gun: current applications in cutaneous gene therapyM T Lin, L Pulkkinen, J Uitto, et al.
The American Journal of Pathology|April 18, 1998
Compound heterozygosity for missense (L156P) and nonsense (R554X) mutations in the beta4 integrin gene (ITGB4) underlies mild, nonlethal phenotype of epidermolysis bullosa with pyloric atresiaL Pulkkinen, L Bruckner-Tuderman, C August, et al.
Scandinavian Journal of Psychology|February 5, 2000
The role of parents' self-esteem, mastery-orientation and social background in their parenting stylesK Aunola, J E Nurmi, T Onatsu-Arvilommi, et al.
Experimental Dermatology|October 1, 1996
Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophyJ Uitto, L Pulkkinen, F J Smith, et al.
The Journal of Clinical Investigation|January 1, 1993
Epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma). Genetic linkage to chromosome 12q in the region of the type II keratin gene clusterL Pulkkinen, A M Christiano, R G Knowlton, et al.
The Journal of Investigative Dermatology|April 1, 1996
Compound heterozygosity for nonsense and missense mutations in the LAMB3 gene in nonlethal junctional epidermolysis bullosaA M Christiano, L Pulkkinen, R A Eady, et al.
American Journal of Human Genetics|October 27, 1997
Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosaL Pulkkinen, F Bullrich, P Czarnecki, et al.
Human Mutation|January 1, 1995
Detection of sequence variants in the gene encoding the beta 3 chain of laminin 5 (LAMB3)L Pulkkinen, J A McGrath, A M Christiano, et al.
Pageof 14