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T Martinsson

Showing results (131-140 of 146) with videos related to

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American Journal of Medical Genetics|March 15, 1994
Progress in a genome scan for linkage in schizophrenia in a large Swedish kindredC L Barr, J L Kennedy, A J Pakstis, et al.
Medical and Pediatric Oncology|July 24, 2001
Absence of somatostatin receptor expression in vivo is correlated to di- or tetraploid 1p36-deleted neuroblastomasF H Schilling, P F Ambros, H Bihl, et al.
British Journal of Cancer|January 22, 2004
SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinomaD Astuti, N F Da Silva, A Dallol, et al.
Oncogene|January 31, 2012
Anaplastic Lymphoma Kinase (ALK) regulates initiation of transcription of MYCN in neuroblastoma cellsC Schönherr, K Ruuth, S Kamaraj, et al.
Human Mutation|November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)G Matthijs, E Schollen, C Bjursell, et al.
Oncogene|June 30, 2015
Comparative genetic study of intratumoral heterogenous MYCN amplified neuroblastoma versus aggressive genetic profile neuroblastic tumorsA P Berbegall, E Villamón, M Piqueras, et al.
Tissue Antigens|December 1, 2000
The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disordersA T Naluai, S Nilsson, L Samuelsson, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11A T Naluai, S Nilsson, A H Gudjónsdóttir, et al.
Pageof 15

Showing results (131-140 of 146) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics|March 15, 1994
Progress in a genome scan for linkage in schizophrenia in a large Swedish kindredC L Barr, J L Kennedy, A J Pakstis, et al.
Medical and Pediatric Oncology|July 24, 2001
Absence of somatostatin receptor expression in vivo is correlated to di- or tetraploid 1p36-deleted neuroblastomasF H Schilling, P F Ambros, H Bihl, et al.
British Journal of Cancer|January 22, 2004
SLIT2 promoter methylation analysis in neuroblastoma, Wilms' tumour and renal cell carcinomaD Astuti, N F Da Silva, A Dallol, et al.
Oncogene|January 31, 2012
Anaplastic Lymphoma Kinase (ALK) regulates initiation of transcription of MYCN in neuroblastoma cellsC Schönherr, K Ruuth, S Kamaraj, et al.
Human Mutation|November 3, 2000
Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)G Matthijs, E Schollen, C Bjursell, et al.
Oncogene|June 30, 2015
Comparative genetic study of intratumoral heterogenous MYCN amplified neuroblastoma versus aggressive genetic profile neuroblastic tumorsA P Berbegall, E Villamón, M Piqueras, et al.
Tissue Antigens|December 1, 2000
The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disordersA T Naluai, S Nilsson, L Samuelsson, et al.
Oncogene|December 26, 2001
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumoursD Astuti, A Agathanggelou, S Honorio, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
European Journal of Human Genetics : EJHG|February 13, 2002
Genome-wide linkage analysis of Scandinavian affected sib-pairs supports presence of susceptibility loci for celiac disease on chromosomes 5 and 11A T Naluai, S Nilsson, A H Gudjónsdóttir, et al.
Pageof 15