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P Fortina

Showing results (41-50 of 67) with videos related to

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European Journal of Human Genetics : EJHG|November 28, 2000
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISCP Forabosco, A Collins, A Latiano, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Simple two-color array-based approach for mutation detectionP Fortina, K Delgrosso, T Sakazume, et al.
Oncogene|October 15, 2013
The retinoblastoma tumor suppressor pathway modulates the invasiveness of ErbB2-positive breast cancerA K Witkiewicz, D W Cox, D Rivadeneira, et al.
British Heart Journal|December 1, 1995
Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarctionE Arbustini, M Grasso, R Fasani, et al.
Minerva Pediatrica|September 15, 1985
[Prenatal diagnosis of thalassemia: experience in Piedmont]V Gabutti, C Amione, C Bessè, et al.
Human Genetics|December 1, 1992
Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reactionP Fortina, R Conant, G Monokian, et al.
Gastroenterology|February 7, 2004
The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: an *IG-IBD studyA Andriulli, V Annese, A Latiano, et al.
Blood|June 1, 1994
Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemiaP Fortina, T Parrella, M Sartore, et al.
Analytical Biochemistry|March 26, 1998
Degenerate oligonucleotide primed-polymerase chain reaction and capillary electrophoretic analysis of human DNA on microchip-based devicesJ Cheng, L C Waters, P Fortina, et al.
The Journal of Clinical Investigation|January 1, 1994
Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIbM Poncz, S Rifat, B S Coller, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
European Journal of Human Genetics : EJHG|November 28, 2000
Combined segregation and linkage analysis of inflammatory bowel disease in the IBD1 region using severity to characterise Crohn's disease and ulcerative colitis. On behalf of the GISCP Forabosco, A Collins, A Latiano, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Simple two-color array-based approach for mutation detectionP Fortina, K Delgrosso, T Sakazume, et al.
Oncogene|October 15, 2013
The retinoblastoma tumor suppressor pathway modulates the invasiveness of ErbB2-positive breast cancerA K Witkiewicz, D W Cox, D Rivadeneira, et al.
British Heart Journal|December 1, 1995
Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarctionE Arbustini, M Grasso, R Fasani, et al.
Minerva Pediatrica|September 15, 1985
[Prenatal diagnosis of thalassemia: experience in Piedmont]V Gabutti, C Amione, C Bessè, et al.
Human Genetics|December 1, 1992
Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reactionP Fortina, R Conant, G Monokian, et al.
Gastroenterology|February 7, 2004
The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: an *IG-IBD studyA Andriulli, V Annese, A Latiano, et al.
Blood|June 1, 1994
Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemiaP Fortina, T Parrella, M Sartore, et al.
Analytical Biochemistry|March 26, 1998
Degenerate oligonucleotide primed-polymerase chain reaction and capillary electrophoretic analysis of human DNA on microchip-based devicesJ Cheng, L C Waters, P Fortina, et al.
The Journal of Clinical Investigation|January 1, 1994
Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIbM Poncz, S Rifat, B S Coller, et al.
Pageof 7