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L Pulkkinen

Showing results (131-140 of 138) with videos related to

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Diabetologia|May 26, 2006
Association of sequence variations in the gene encoding adiponectin receptor 1 (ADIPOR1) with body size and insulin levels. The Finnish Diabetes Prevention StudyN Siitonen, L Pulkkinen, U Mager, et al.
Scientific Reports|March 13, 2021
Ketone body 3-hydroxybutyrate as a biomarker of aggressionA M Whipp, E Vuoksimaa, T Korhonen, et al.
International Journal of Obesity (2005)|September 13, 2007
Weight reduction modulates expression of genes involved in extracellular matrix and cell death: the GENOBIN studyM Kolehmainen, T Salopuro, U S Schwab, et al.
The Journal of Investigative Dermatology|June 26, 1999
Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: positional effects of premature termination codon mutations on clinical severity. Japanese Collaborative Study Group on Epidermolysis BullosaK Tamai, T Murai, M Mayama, et al.
Archives of Dermatological Research|February 1, 1997
Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosaH Shimizu, Y Takizawa, J A McGrath, et al.
American Journal of Human Genetics|November 1, 1996
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16G Tromp, H Kuivaniemi, S Raphael, et al.
Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.
Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
Pageof 14

Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Diabetologia|May 26, 2006
Association of sequence variations in the gene encoding adiponectin receptor 1 (ADIPOR1) with body size and insulin levels. The Finnish Diabetes Prevention StudyN Siitonen, L Pulkkinen, U Mager, et al.
Scientific Reports|March 13, 2021
Ketone body 3-hydroxybutyrate as a biomarker of aggressionA M Whipp, E Vuoksimaa, T Korhonen, et al.
International Journal of Obesity (2005)|September 13, 2007
Weight reduction modulates expression of genes involved in extracellular matrix and cell death: the GENOBIN studyM Kolehmainen, T Salopuro, U S Schwab, et al.
The Journal of Investigative Dermatology|June 26, 1999
Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: positional effects of premature termination codon mutations on clinical severity. Japanese Collaborative Study Group on Epidermolysis BullosaK Tamai, T Murai, M Mayama, et al.
Archives of Dermatological Research|February 1, 1997
Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosaH Shimizu, Y Takizawa, J A McGrath, et al.
American Journal of Human Genetics|November 1, 1996
Genetic linkage of familial granulomatous inflammatory arthritis, skin rash, and uveitis to chromosome 16G Tromp, H Kuivaniemi, S Raphael, et al.
Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.
Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.
Pageof 14