Authors:
Mudd, SH
Cerone, R
Schiaffino, MC
Fantasia, AR
Minniti, G
Caruso, U
Lorini, R
Watkins, D
Matiaszuk, N
Rosenblatt, DS
Schwahn, B
Rozen, R
LeGros, L
Kotb, M
Capdevila, A
Luka, Z
Finkelstein, JD
Tangerman, A
Stabler, SP
Allen, RH
Wagner, C
Citation: Sh. Mudd et al., Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia, J INH MET D, 24(4), 2001, pp. 448-464
Authors:
LeGros, L
Halim, AB
Chamberlin, ME
Geller, A
Kotb, M
Citation: L. Legros et al., Regulation of the human MAT2B gene encoding the regulatory beta subunit ofmethionine adenosyltransferase, MAT II, J BIOL CHEM, 276(27), 2001, pp. 24918-24924
Authors:
Halim, AB
LeGros, L
Chamberlin, ME
Geller, A
Kotb, M
Citation: Ab. Halim et al., Regulation of the human MAT2A gene encoding the catalytic alpha 2 subunit of methionine adenosyltransferase, MAT II - Gene organization, promoter characterization, and identification of a site in the proximal promoter that is essential for its activity, J BIOL CHEM, 276(13), 2001, pp. 9784-9791
Citation: Ab. Halim et al., Expression and functional interaction of the catalytic and regulatory subunits of human methionine adenosyltransferase in mammalian cells, J BIOL CHEM, 274(42), 1999, pp. 29720-29725