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M Delpech

Showing results (51-60 of 96) with videos related to

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European Journal of Biochemistry|March 15, 1993
Characterization, purification and cDNA cloning of a rat perchloric-acid-soluble 23-kDa protein present only in liver and kidneyF Levy-Favatier, L Cuisset, B Nedelec, et al.
Antimicrobial Agents and Chemotherapy|January 30, 1999
Characterization and nucleotide sequence of CARB-6, a new carbenicillin-hydrolyzing beta-lactamase from Vibrio choleraeD Choury, G Aubert, M F Szajnert, et al.
Neurology|July 11, 2001
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)E Ellie, F Camou, A Vital, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|February 1, 1993
Complement component C4 deficiencies and gene alterations in patients with systemic lupus erythematosusQ Fan, B Uring-Lambert, B Weill, et al.
Antimicrobial Agents and Chemotherapy|March 18, 2000
Nucleotide sequence of the bla(RTG-2) (CARB-5) gene and phylogeny of a new group of carbenicillinasesD Choury, M F Szajnert, M L Joly-Guillou, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosisO Dupuy, O Blétry, A S Blanc, et al.
Annales De Genetique|January 1, 1997
Prevalence, male germ-line origin and new patterns of inversions in haemophilia AS Valleix, K Nafa, N Stieltjes, et al.
Rheumatology (Oxford, England)|September 7, 2007
Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndromeW Ammouri, L Cuisset, S Rouaghe, et al.
Kidney International|April 25, 2001
Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid CommunicationM Jadoul, C Dodé, J P Cosyns, et al.
Human Mutation|January 1, 1992
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia AK Nafa, M Baudis, N Deburgrave, et al.
Pageof 10

Showing results (51-60 of 96) with videos related to

Sort By:
Pageof 10
European Journal of Biochemistry|March 15, 1993
Characterization, purification and cDNA cloning of a rat perchloric-acid-soluble 23-kDa protein present only in liver and kidneyF Levy-Favatier, L Cuisset, B Nedelec, et al.
Antimicrobial Agents and Chemotherapy|January 30, 1999
Characterization and nucleotide sequence of CARB-6, a new carbenicillin-hydrolyzing beta-lactamase from Vibrio choleraeD Choury, G Aubert, M F Szajnert, et al.
Neurology|July 11, 2001
Recurrent subarachnoid hemorrhage associated with a new transthyretin variant (Gly53Glu)E Ellie, F Camou, A Vital, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|February 1, 1993
Complement component C4 deficiencies and gene alterations in patients with systemic lupus erythematosusQ Fan, B Uring-Lambert, B Weill, et al.
Antimicrobial Agents and Chemotherapy|March 18, 2000
Nucleotide sequence of the bla(RTG-2) (CARB-5) gene and phylogeny of a new group of carbenicillinasesD Choury, M F Szajnert, M L Joly-Guillou, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|February 26, 1999
A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosisO Dupuy, O Blétry, A S Blanc, et al.
Annales De Genetique|January 1, 1997
Prevalence, male germ-line origin and new patterns of inversions in haemophilia AS Valleix, K Nafa, N Stieltjes, et al.
Rheumatology (Oxford, England)|September 7, 2007
Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndromeW Ammouri, L Cuisset, S Rouaghe, et al.
Kidney International|April 25, 2001
Autosomal-dominant periodic fever with AA amyloidosis: Novel mutation in tumor necrosis factor receptor 1 gene Rapid CommunicationM Jadoul, C Dodé, J P Cosyns, et al.
Human Mutation|January 1, 1992
A novel mutation (Arg-->Leu in exon 18) in factor VIII gene responsible for moderate hemophilia AK Nafa, M Baudis, N Deburgrave, et al.
Pageof 10