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L B Andersen

Showing results (111-120 of 124) with videos related to

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Archives of Disease in Childhood|May 24, 2005
Infant feeding and components of the metabolic syndrome: findings from the European Youth Heart StudyD A Lawlor, C J Riddoch, A S Page, et al.
Pediatric Obesity|May 1, 2013
Association between sweet drink intake and adiposity in Danish children participating in a long-term intervention studyB W Jensen, B M Nielsen, I Husby, et al.
Nucleic Acids Research|January 11, 1991
A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]L B Andersen, M R Wallace, D A Marchuk, et al.
Molecular and Cellular Biology|January 1, 1993
A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activityL B Andersen, R Ballester, D A Marchuk, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Genes, Chromosomes & Cancer|November 1, 1990
A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis regionM R Wallace, L B Andersen, J W Fountain, et al.
Nature Genetics|February 1, 1993
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell linesL B Andersen, J W Fountain, D H Gutmann, et al.
Clinical Endocrinology|January 12, 2013
Parity and tanned white skin as novel predictors of vitamin D status in early pregnancy: a population-based cohort studyL B Andersen, B Abrahamsen, C Dalgård, et al.
Diabetologia|February 3, 2009
PPARGC1A sequence variation and cardiovascular risk-factor levels: a study of the main genetic effects and gene x environment interactions in children from the European Youth Heart StudyE C Brito, K S Vimaleswaran, S Brage, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
Pageof 13

Showing results (111-120 of 124) with videos related to

Sort By:
Pageof 13
Archives of Disease in Childhood|May 24, 2005
Infant feeding and components of the metabolic syndrome: findings from the European Youth Heart StudyD A Lawlor, C J Riddoch, A S Page, et al.
Pediatric Obesity|May 1, 2013
Association between sweet drink intake and adiposity in Danish children participating in a long-term intervention studyB W Jensen, B M Nielsen, I Husby, et al.
Nucleic Acids Research|January 11, 1991
A polymorphic cDNA probe on chromosome 17q11.2 located within the NF1 gene [D17S376]L B Andersen, M R Wallace, D A Marchuk, et al.
Molecular and Cellular Biology|January 1, 1993
A conserved alternative splice in the von Recklinghausen neurofibromatosis (NF1) gene produces two neurofibromin isoforms, both of which have GTPase-activating protein activityL B Andersen, R Ballester, D A Marchuk, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Genes, Chromosomes & Cancer|November 1, 1990
A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis regionM R Wallace, L B Andersen, J W Fountain, et al.
Nature Genetics|February 1, 1993
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell linesL B Andersen, J W Fountain, D H Gutmann, et al.
Clinical Endocrinology|January 12, 2013
Parity and tanned white skin as novel predictors of vitamin D status in early pregnancy: a population-based cohort studyL B Andersen, B Abrahamsen, C Dalgård, et al.
Diabetologia|February 3, 2009
PPARGC1A sequence variation and cardiovascular risk-factor levels: a study of the main genetic effects and gene x environment interactions in children from the European Youth Heart StudyE C Brito, K S Vimaleswaran, S Brage, et al.
Genomics|March 1, 1991
cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 geneR M Cawthon, L B Andersen, A M Buchberg, et al.
Pageof 13