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M Pirastu

Showing results (11-20 of 101) with videos related to

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Science (New York, N.Y.)|March 2, 1984
Multiple mutations produce delta beta 0 thalassemia in SardiniaM Pirastu, Y W Kan, R Galanello, et al.
British Journal of Haematology|July 1, 1986
Molecular pathology of haemoglobin H disease in SardiniansE Paglietti, R Galanello, P Moi, et al.
Lancet (London, England)|February 1, 1986
Prenatal diagnosis of most common Mediterranean beta-thalassaemia mutantsA Loi, M Pirastu, A Cao, et al.
Nucleic Acids Research|August 26, 1986
Three RFLPs for the insulin receptor gene INSR: EcoRI, Pst I, Hind IIIM A Sanna, G I Bell, A Cao, et al.
Pediatric Research|February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2R Galanello, M A Melis, L Maccioni, et al.
Genomics|May 1, 1990
Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia AS Murru, L Casula, M Pecorara, et al.
Blood|May 1, 1991
Molecular basis of the delta thalassemia in cis to hemoglobin Knossos variantG Loudianos, A Cao, M Pirastu, et al.
Brain Research. Molecular Brain Research|May 1, 1997
Rat tyrosine hydroxylase gene polymorphismsS Murru, L Pani, D Poddie, et al.
The Journal of Biological Chemistry|October 25, 1984
Initiation codon mutation as a cause of alpha thalassemiaM Pirastu, G Saglio, J C Chang, et al.
The Journal of Clinical Investigation|November 1, 1987
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotypeP Moi, F E Cash, S A Liebhaber, et al.
Pageof 11

Showing results (11-20 of 101) with videos related to

Sort By:
Pageof 11
Science (New York, N.Y.)|March 2, 1984
Multiple mutations produce delta beta 0 thalassemia in SardiniaM Pirastu, Y W Kan, R Galanello, et al.
British Journal of Haematology|July 1, 1986
Molecular pathology of haemoglobin H disease in SardiniansE Paglietti, R Galanello, P Moi, et al.
Lancet (London, England)|February 1, 1986
Prenatal diagnosis of most common Mediterranean beta-thalassaemia mutantsA Loi, M Pirastu, A Cao, et al.
Nucleic Acids Research|August 26, 1986
Three RFLPs for the insulin receptor gene INSR: EcoRI, Pst I, Hind IIIM A Sanna, G I Bell, A Cao, et al.
Pediatric Research|February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2R Galanello, M A Melis, L Maccioni, et al.
Genomics|May 1, 1990
Illegitimate recombination produced a duplication within the FVIII gene in a patient with mild hemophilia AS Murru, L Casula, M Pecorara, et al.
Blood|May 1, 1991
Molecular basis of the delta thalassemia in cis to hemoglobin Knossos variantG Loudianos, A Cao, M Pirastu, et al.
Brain Research. Molecular Brain Research|May 1, 1997
Rat tyrosine hydroxylase gene polymorphismsS Murru, L Pani, D Poddie, et al.
The Journal of Biological Chemistry|October 25, 1984
Initiation codon mutation as a cause of alpha thalassemiaM Pirastu, G Saglio, J C Chang, et al.
The Journal of Clinical Investigation|November 1, 1987
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotypeP Moi, F E Cash, S A Liebhaber, et al.
Pageof 11