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

P Mustajoki

Showing results (101-110 of 109) with videos related to

Pageof 11
Sort By:
You have reached the last page of results.This site can display upto 109 results.
Human Mutation|January 1, 1997
Diagnostic strategy, genetic diagnosis and identification of new mutations in intermittent porphyria by denaturing gradient gel electrophoresisH Nissen, N E Petersen, S Mustajoki, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24M Ohman, L Oksanen, J Kaprio, et al.
Clinical Science (London, England : 1979)|November 1, 1992
Weight loss normalizes the inhibitory effect of N6-(phenylisopropyl)adenosine on lipolysis in fat cells of massively obese human subjectsJ J Ohisalo, J M Kaartinen, S Ranta, et al.
The Journal of Investigative Dermatology|April 5, 2001
Homozygous variegate porphyria: 20 y follow-up and characterization of molecular defectR Kauppinen, K Timonen, M von und zu Fraunberg, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairsM Ohman, L Oksanen, K Kainulainen, et al.
European Journal of Clinical Investigation|October 1, 1989
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminaseB Grandchamp, C Picat, R Kauppinen, et al.
Diabetologia|August 1, 1984
Remissions in newly diagnosed type 1 (insulin-dependent) diabetes: influence of interferon as an adjunct to insulin therapyV A Koivisto, A Aro, K Cantell, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 18, 2003
Melanocortin-3-receptor gene variants in morbid obesityC Schalin-Jäntti, K Valli-Jaakola, L Oksanen, et al.
Human Genetics|May 1, 1997
Markers for the gene ob and serum leptin levels in human morbid obesityL Oksanen, M Ohman, M Heiman, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
Human Mutation|January 1, 1997
Diagnostic strategy, genetic diagnosis and identification of new mutations in intermittent porphyria by denaturing gradient gel electrophoresisH Nissen, N E Petersen, S Mustajoki, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24M Ohman, L Oksanen, J Kaprio, et al.
Clinical Science (London, England : 1979)|November 1, 1992
Weight loss normalizes the inhibitory effect of N6-(phenylisopropyl)adenosine on lipolysis in fat cells of massively obese human subjectsJ J Ohisalo, J M Kaartinen, S Ranta, et al.
The Journal of Investigative Dermatology|April 5, 2001
Homozygous variegate porphyria: 20 y follow-up and characterization of molecular defectR Kauppinen, K Timonen, M von und zu Fraunberg, et al.
European Journal of Human Genetics : EJHG|April 10, 1999
Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairsM Ohman, L Oksanen, K Kainulainen, et al.
European Journal of Clinical Investigation|October 1, 1989
Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminaseB Grandchamp, C Picat, R Kauppinen, et al.
Diabetologia|August 1, 1984
Remissions in newly diagnosed type 1 (insulin-dependent) diabetes: influence of interferon as an adjunct to insulin therapyV A Koivisto, A Aro, K Cantell, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|January 18, 2003
Melanocortin-3-receptor gene variants in morbid obesityC Schalin-Jäntti, K Valli-Jaakola, L Oksanen, et al.
Human Genetics|May 1, 1997
Markers for the gene ob and serum leptin levels in human morbid obesityL Oksanen, M Ohman, M Heiman, et al.
Pageof 11