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Biochemistry International
|
March 1, 1983
Hydroxyurea inhibits also the syntheses of thymine nucleotides and methionine in the cells of Escherichia coli
J 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 trachomatis
L Pulkkinen, E Vuorio, T Hyypia, et al.
International Journal of Dermatology
|
April 12, 2000
The gene gun: current applications in cutaneous gene therapy
M 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 atresia
L 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 styles
K 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 dystrophy
J 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 cluster
L 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 bullosa
A 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 bullosa
L 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.
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of 14
Search research articles
Search
Showing results (31-40 of 138) with videos related to
Sort By:
Page
of 14
Biochemistry International
|
March 1, 1983
Hydroxyurea inhibits also the syntheses of thymine nucleotides and methionine in the cells of Escherichia coli
J 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 trachomatis
L Pulkkinen, E Vuorio, T Hyypia, et al.
International Journal of Dermatology
|
April 12, 2000
The gene gun: current applications in cutaneous gene therapy
M 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 atresia
L 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 styles
K 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 dystrophy
J 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 cluster
L 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 bullosa
A 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 bullosa
L 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.
Page
of 14