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Experimental Cell Research
|
August 25, 1997
The alpha7beta1 integrin mediates adhesion and migration of skeletal myoblasts on laminin
S Crawley, E M Farrell, W Wang, et al.
Human Genetics
|
August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus
P Jedlicka, S Greer, D S Millar, et al.
Nucleic Acids Research
|
June 25, 1987
Precursor-product relationship between vitellogenin and the yolk proteins as derived from the complete sequence of a Xenopus vitellogenin gene
S Gerber-Huber, D Nardelli, J A Haefliger, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
October 1, 1995
Functional analysis of an unusual length polymorphism in the human antithrombin III (AT3) gene promoter
P C Winter, D A Scopes, L P Berg, et al.
Journal of Medical Genetics
|
June 15, 2010
Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions
V-F Mautner, L Kluwe, R E Friedrich, et al.
Thrombosis and Haemostasis
|
August 2, 1993
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
D A Lane, R J Olds, M Boisclair, et al.
Genomics
|
August 1, 1992
De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysis
L P Berg, C B Grundy, F Thomas, et al.
Cell
|
February 25, 1994
Galectins: a family of animal beta-galactoside-binding lectins
S H Barondes, V Castronovo, D N Cooper, et al.
Nucleic Acids Research
|
September 25, 1991
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene
E G Tuddenham, D N Cooper, J Gitschier, et al.
Human Genetics
|
August 15, 2000
Molecular genetic analysis of severe protein C deficiency
D S Millar, B Johansen, E Berntorp, et al.
Page
of 21
Search research articles
Search
Showing results (181-190 of 205) with videos related to
Sort By:
Page
of 21
Experimental Cell Research
|
August 25, 1997
The alpha7beta1 integrin mediates adhesion and migration of skeletal myoblasts on laminin
S Crawley, E M Farrell, W Wang, et al.
Human Genetics
|
August 1, 1990
Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus
P Jedlicka, S Greer, D S Millar, et al.
Nucleic Acids Research
|
June 25, 1987
Precursor-product relationship between vitellogenin and the yolk proteins as derived from the complete sequence of a Xenopus vitellogenin gene
S Gerber-Huber, D Nardelli, J A Haefliger, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis
|
October 1, 1995
Functional analysis of an unusual length polymorphism in the human antithrombin III (AT3) gene promoter
P C Winter, D A Scopes, L P Berg, et al.
Journal of Medical Genetics
|
June 15, 2010
Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions
V-F Mautner, L Kluwe, R E Friedrich, et al.
Thrombosis and Haemostasis
|
August 2, 1993
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
D A Lane, R J Olds, M Boisclair, et al.
Genomics
|
August 1, 1992
De novo splice site mutation in the antithrombin III (AT3) gene causing recurrent venous thrombosis: demonstration of exon skipping by ectopic transcript analysis
L P Berg, C B Grundy, F Thomas, et al.
Cell
|
February 25, 1994
Galectins: a family of animal beta-galactoside-binding lectins
S H Barondes, V Castronovo, D N Cooper, et al.
Nucleic Acids Research
|
September 25, 1991
Haemophilia A: database of nucleotide substitutions, deletions, insertions and rearrangements of the factor VIII gene
E G Tuddenham, D N Cooper, J Gitschier, et al.
Human Genetics
|
August 15, 2000
Molecular genetic analysis of severe protein C deficiency
D S Millar, B Johansen, E Berntorp, et al.
Page
of 21