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L A Passmore

Showing results (1-10 of 7) with videos related to

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Biochemical Society Transactions|October 21, 2004
The anaphase-promoting complex (APC): the sum of its parts?L A Passmore
Methods in Enzymology|August 31, 2016
Specimen Preparation for High-Resolution Cryo-EML A Passmore, C J Russo
Human Genetics|September 15, 2000
Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino populationL A Passmore, B Kaesmann-Kellner, B H Weber
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|January 1, 1991
Social support networks among families of children with craniofacial anomaliesB A Benson, A M Gross, S C Messer, et al.
Human Molecular Genetics|August 13, 1998
Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)A Marquardt, H Stöhr, L A Passmore, et al.
Biochemistry|August 20, 1996
Inhibitor-induced changes in the intrinsic fluorescence of human cyclooxygenase-2V Houtzager, M Ouellet, J P Falgueyret, et al.
Molecular and Cellular Biology|November 20, 1998
Regulation of RasGRP via a phorbol ester-responsive C1 domainC E Tognon, H E Kirk, L A Passmore, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biochemical Society Transactions|October 21, 2004
The anaphase-promoting complex (APC): the sum of its parts?L A Passmore
Methods in Enzymology|August 31, 2016
Specimen Preparation for High-Resolution Cryo-EML A Passmore, C J Russo
Human Genetics|September 15, 2000
Novel and recurrent mutations in the tyrosinase gene and the P gene in the German albino populationL A Passmore, B Kaesmann-Kellner, B H Weber
Health Psychology : Official Journal of the Division of Health Psychology, American Psychological Association|January 1, 1991
Social support networks among families of children with craniofacial anomaliesB A Benson, A M Gross, S C Messer, et al.
Human Molecular Genetics|August 13, 1998
Mutations in a novel gene, VMD2, encoding a protein of unknown properties cause juvenile-onset vitelliform macular dystrophy (Best's disease)A Marquardt, H Stöhr, L A Passmore, et al.
Biochemistry|August 20, 1996
Inhibitor-induced changes in the intrinsic fluorescence of human cyclooxygenase-2V Houtzager, M Ouellet, J P Falgueyret, et al.
Molecular and Cellular Biology|November 20, 1998
Regulation of RasGRP via a phorbol ester-responsive C1 domainC E Tognon, H E Kirk, L A Passmore, et al.
Pageof 1