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R Arruda

Showing results (91-100 of 185) with videos related to

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Open Veterinary Journal|October 2, 2025
Ancient origin of the furin sequence in the wolf F8 geneJoshua I Siner, Shannon Barber-Meyer, Benjamin J Samelson-Jones, et al.
Thrombosis and Haemostasis|May 1, 1996
Very low incidence of Arg506-->Gin mutation in the factor V gene among the Amazonian Indians and the Brazilian black populationV R Arruda, P M von Zuben, M C Soares, et al.
Clinical Genetics|October 27, 1998
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?V R Arruda, C E Grignolli, M S Gonçalves, et al.
Hemoglobin|May 1, 1994
Association of Hb Santa Ana [alpha 2 beta (2)88(F4)Leu- > Pro] and Hb Porto Alegre [alpha 2 beta (2)9(A6)Ser- > Cys] in a Brazilian femaleM S Gonçalves, M F Sonati, M Kimura, et al.
Journal of Virology|September 20, 2002
Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vectorFederico Mingozzi, Jörg Schüttrumpf, Valder R Arruda, et al.
Acta Haematologica|June 6, 2000
Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patientsE Nogueira, V R Arruda, J M Bizzacchi, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Loss of factor VIII in zebrafish rebalances antithrombin deficiency but has a limited bleeding diathesisCatherine E Richter, Azhwar Raghunath, Megan S Griffin, et al.
Cardiovascular Research|April 16, 1998
Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarctionV R Arruda, L H Siquiera, L C Chiaparini, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9P A Fields, V R Arruda, E Armstrong, et al.
European Journal of Haematology|September 21, 2000
beta0-thalassemia resulting from a novel mutation: beta66/u-->stop codonC R Grignoli, M H Carvalho, E M Kimura, et al.
Pageof 19

Showing results (91-100 of 185) with videos related to

Sort By:
Pageof 19
Open Veterinary Journal|October 2, 2025
Ancient origin of the furin sequence in the wolf F8 geneJoshua I Siner, Shannon Barber-Meyer, Benjamin J Samelson-Jones, et al.
Thrombosis and Haemostasis|May 1, 1996
Very low incidence of Arg506-->Gin mutation in the factor V gene among the Amazonian Indians and the Brazilian black populationV R Arruda, P M von Zuben, M C Soares, et al.
Clinical Genetics|October 27, 1998
Prevalence of homozygosity for the deleted alleles of glutathione S-transferase mu (GSTM1) and theta (GSTT1) among distinct ethnic groups from Brazil: relevance to environmental carcinogenesis?V R Arruda, C E Grignolli, M S Gonçalves, et al.
Hemoglobin|May 1, 1994
Association of Hb Santa Ana [alpha 2 beta (2)88(F4)Leu- > Pro] and Hb Porto Alegre [alpha 2 beta (2)9(A6)Ser- > Cys] in a Brazilian femaleM S Gonçalves, M F Sonati, M Kimura, et al.
Journal of Virology|September 20, 2002
Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vectorFederico Mingozzi, Jörg Schüttrumpf, Valder R Arruda, et al.
Acta Haematologica|June 6, 2000
Possible association between cytomegalovirus infection and gastrointestinal bleeding in hemophiliac patientsE Nogueira, V R Arruda, J M Bizzacchi, et al.
Biorxiv : the Preprint Server for Biology|February 3, 2025
Loss of factor VIII in zebrafish rebalances antithrombin deficiency but has a limited bleeding diathesisCatherine E Richter, Azhwar Raghunath, Megan S Griffin, et al.
Cardiovascular Research|April 16, 1998
Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarctionV R Arruda, L H Siquiera, L C Chiaparini, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 8, 2001
Risk and prevention of anti-factor IX formation in AAV-mediated gene transfer in the context of a large deletion of F9P A Fields, V R Arruda, E Armstrong, et al.
European Journal of Haematology|September 21, 2000
beta0-thalassemia resulting from a novel mutation: beta66/u-->stop codonC R Grignoli, M H Carvalho, E M Kimura, et al.
Pageof 19