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L Pulkkinen

Showing results (121-130 of 138) with videos related to

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Pediatric Research|May 1, 2001
Epidermolysis bullosa with congenital pyloric atresia: novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlationsA Nakano, L Pulkkinen, D Murrell, et al.
The British Journal of Dermatology|June 1, 1997
Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutationJ R McMillan, J A McGrath, L Pulkkinen, et al.
The Journal of Cell Biology|June 2, 1997
Targeted disruption of the pemphigus vulgaris antigen (desmoglein 3) gene in mice causes loss of keratinocyte cell adhesion with a phenotype similar to pemphigus vulgarisP J Koch, M G Mahoney, H Ishikawa, et al.
Nature Genetics|March 1, 1994
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)D Aberdam, M F Galliano, J Vailly, et al.
Diabetologia|August 12, 2009
Link between plasma ceramides, inflammation and insulin resistance: association with serum IL-6 concentration in patients with coronary heart diseaseV D F de Mello, M Lankinen, U Schwab, et al.
The Journal of Investigative Dermatology|September 1, 1997
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skinN Hammami-Hauasli, D U Kalinke, H Schumann, et al.
International Journal of Obesity (2005)|July 6, 2005
Genetic variation in leptin receptor gene is associated with type 2 diabetes and body weight: The Finnish Diabetes Prevention StudyT Salopuro, L Pulkkinen, J Lindström, et al.
Diabetologia|September 2, 2008
Downregulation of genes involved in NFkappaB activation in peripheral blood mononuclear cells after weight loss is associated with the improvement of insulin sensitivity in individuals with the metabolic syndrome: the GENOBIN studyV D F de Mello, M Kolehmainen, L Pulkkinen, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 9, 2006
Association of the Leu72Met polymorphism of the ghrelin gene with the risk of Type 2 diabetes in subjects with impaired glucose tolerance in the Finnish Diabetes Prevention StudyU Mager, V Lindi, J Lindström, et al.
The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Pediatric Research|May 1, 2001
Epidermolysis bullosa with congenital pyloric atresia: novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlationsA Nakano, L Pulkkinen, D Murrell, et al.
The British Journal of Dermatology|June 1, 1997
Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutationJ R McMillan, J A McGrath, L Pulkkinen, et al.
The Journal of Cell Biology|June 2, 1997
Targeted disruption of the pemphigus vulgaris antigen (desmoglein 3) gene in mice causes loss of keratinocyte cell adhesion with a phenotype similar to pemphigus vulgarisP J Koch, M G Mahoney, H Ishikawa, et al.
Nature Genetics|March 1, 1994
Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the gamma 2 subunit of nicein/kalinin (LAMININ-5)D Aberdam, M F Galliano, J Vailly, et al.
Diabetologia|August 12, 2009
Link between plasma ceramides, inflammation and insulin resistance: association with serum IL-6 concentration in patients with coronary heart diseaseV D F de Mello, M Lankinen, U Schwab, et al.
The Journal of Investigative Dermatology|September 1, 1997
A combination of a common splice site mutation and a frameshift mutation in the COL7A1 gene: absence of functional collagen VII in keratinocytes and skinN Hammami-Hauasli, D U Kalinke, H Schumann, et al.
International Journal of Obesity (2005)|July 6, 2005
Genetic variation in leptin receptor gene is associated with type 2 diabetes and body weight: The Finnish Diabetes Prevention StudyT Salopuro, L Pulkkinen, J Lindström, et al.
Diabetologia|September 2, 2008
Downregulation of genes involved in NFkappaB activation in peripheral blood mononuclear cells after weight loss is associated with the improvement of insulin sensitivity in individuals with the metabolic syndrome: the GENOBIN studyV D F de Mello, M Kolehmainen, L Pulkkinen, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|June 9, 2006
Association of the Leu72Met polymorphism of the ghrelin gene with the risk of Type 2 diabetes in subjects with impaired glucose tolerance in the Finnish Diabetes Prevention StudyU Mager, V Lindi, J Lindström, et al.
The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.
Pageof 14