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M L Tenchini Selected Research

Factor V Deficiency

6/2003Severe factor V deficiency: exon skipping in the factor V gene causing a partial deletion of the C1 domain.
9/2001Coexistence of a novel homozygous nonsense mutation in exon 13 of the factor V gene with the homozygous Leiden mutation in two unrelated patients with severe factor V deficiency.
12/2000A novel two base pair deletion in the factor V gene associated with severe factor V deficiency.
12/2000Concerns about the mutations identified in a case of familial coagulation factor V deficiency: factor V Stanford.

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M L Tenchini Research Topics

Disease

7Afibrinogenemia (Fibrinogen Deficiency)
04/2007 - 02/2000
4Factor V Deficiency
06/2003 - 12/2000
3Hemorrhage
01/2006 - 02/2000
1Inflammatory Bowel Diseases (Inflammatory Bowel Disease)
05/2007
1Uniparental Disomy
10/2006
1Thrombosis (Thrombus)
01/2006
1Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders)
04/2005
1Cardiovascular Diseases (Cardiovascular Disease)
08/2001
1Autosomal Dominant Nocturnal Frontal Lobe Epilepsy
07/2000

Drug/Important Bio-Agent (IBA)

7Fibrinogen (Factor I)FDA Link
04/2007 - 02/2000
4Factor V (Coagulation Factor V)IBA
06/2003 - 12/2000
3Nonsense Codon (Nonsense Mutation)IBA
10/2006 - 09/2001
1Member 1 Subfamily B ATP Binding Cassette TransporterIBA
05/2007
1Peptides (Polypeptides)IBA
10/2006
1Factor VIII (Coagulation Factor VIII)IBA
01/2006
1AnticoagulantsIBA
01/2006
1DNA (Deoxyribonucleic Acid)IBA
11/2005
1AntigensIBA
04/2005
1Proteins (Proteins, Gene)FDA Link
08/2001
1Messenger RNA (mRNA)IBA
12/2000
1fibrinopeptides gammaIBA
10/2000
1Nicotinic Receptors (Nicotinic Acetylcholine Receptor)IBA
07/2000
1fibrinogen AalphaIBA
02/2000
1BBeta fibrinogenIBA
02/2000