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M E Chamberlin

Showing results (21-30 of 31) with videos related to

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Nucleic Acids Research|June 1, 1978
Studies on nucleic acid reassociation kinetics: V. Effects of disparity in tracer and driver fragment lengthsM E Chamberlin, G A Galau, R J Britten, et al.
Biochimica Et Biophysica Acta|July 31, 2001
Distinct patterns of protein binding to the MAT2A promoter in normal and leukemic T cellsA B Halim, H L LeGros, M E Chamberlin, et al.
Archives of Biochemistry and Biophysics|January 6, 2000
Structural requirements for catalysis and dimerization of human methionine adenosyltransferase I/IIIM E Chamberlin, T Ubagai, V Y Pao, et al.
Developmental Biology|June 1, 1988
Molecular analysis of cDNA coding for ZP3, a sperm binding protein of the mouse zona pellucidaM J Ringuette, M E Chamberlin, A W Baur, et al.
American Journal of Human Genetics|March 1, 1997
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A geneM E Chamberlin, T Ubagai, S H Mudd, et al.
Biochemistry|June 14, 1994
Pregnancy-specific glycoprotein gene expression and the induction by 5-bromo-2'-deoxyuridineC J Pan, M E Chamberlin, S M Wu, et al.
The Journal of Clinical Investigation|August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiencyM E Chamberlin, T Ubagai, S H Mudd, et al.
The Journal of Biological Chemistry|August 15, 1993
Characterization of two allelic variants of a human pregnancy-specific glycoprotein geneK J Lei, C Wang, M E Chamberlin, et al.
The Journal of Biological Chemistry|March 30, 2001
Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activityI Pérez Mato, M M Sanchez del Pino, M E Chamberlin, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Nucleic Acids Research|June 1, 1978
Studies on nucleic acid reassociation kinetics: V. Effects of disparity in tracer and driver fragment lengthsM E Chamberlin, G A Galau, R J Britten, et al.
Biochimica Et Biophysica Acta|July 31, 2001
Distinct patterns of protein binding to the MAT2A promoter in normal and leukemic T cellsA B Halim, H L LeGros, M E Chamberlin, et al.
Archives of Biochemistry and Biophysics|January 6, 2000
Structural requirements for catalysis and dimerization of human methionine adenosyltransferase I/IIIM E Chamberlin, T Ubagai, V Y Pao, et al.
Developmental Biology|June 1, 1988
Molecular analysis of cDNA coding for ZP3, a sperm binding protein of the mouse zona pellucidaM J Ringuette, M E Chamberlin, A W Baur, et al.
American Journal of Human Genetics|March 1, 1997
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A geneM E Chamberlin, T Ubagai, S H Mudd, et al.
Biochemistry|June 14, 1994
Pregnancy-specific glycoprotein gene expression and the induction by 5-bromo-2'-deoxyuridineC J Pan, M E Chamberlin, S M Wu, et al.
The Journal of Clinical Investigation|August 15, 1996
Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiencyM E Chamberlin, T Ubagai, S H Mudd, et al.
The Journal of Biological Chemistry|August 15, 1993
Characterization of two allelic variants of a human pregnancy-specific glycoprotein geneK J Lei, C Wang, M E Chamberlin, et al.
The Journal of Biological Chemistry|March 30, 2001
Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activityI Pérez Mato, M M Sanchez del Pino, M E Chamberlin, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
Pageof 4