AAAAAA

   
Results: 1-8 |
Results: 8
CONSENSUS NOMENCLATURE FOR THE MAMMALIAN METHIONINE ADENOSYLTRANSFERASE GENES AND GENE-PRODUCTS
Authors: KOTB M MUDD SH MATO JM GELLER AM KREDICH NM CHOU JY CANTONI GL
Citation: M. Kotb et al., CONSENSUS NOMENCLATURE FOR THE MAMMALIAN METHIONINE ADENOSYLTRANSFERASE GENES AND GENE-PRODUCTS, Trends in genetics, 13(2), 1997, pp. 51-52
NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA
Authors: CHAMBERLIN ME UBAGAI T MUDD SH PAO VY NGUYEN TK GREENE CL THOMAS JA FREEHAUF C CHOU JY
Citation: Me. Chamberlin et al., NOVEL MUTATIONS IN THE METHIONINE ADENOSYLTRANSFERASE 1A GENE THAT CAUSE ISOLATED PERSISTENT HYPERMETHIONINEMIA, American journal of human genetics, 61(4), 1997, pp. 1448-1448
DOMINANT INHERITANCE OF ISOLATED HYPERMETHIONINEMIA IS ASSOCIATED WITH A MUTATION IN THE HUMAN METHIONINE ADENOSYLTRANSFERASE 1A GENE
Authors: CHAMBERLIN ME UBAGAI T MUDD SH LEVY HL CHOU JY
Citation: Me. Chamberlin et al., DOMINANT INHERITANCE OF ISOLATED HYPERMETHIONINEMIA IS ASSOCIATED WITH A MUTATION IN THE HUMAN METHIONINE ADENOSYLTRANSFERASE 1A GENE, American journal of human genetics, 60(3), 1997, pp. 540-546
DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH DEFECTS IN THE HEPATIC FORM OF METHIONINE ADENOSYL TRANSFERASE
Authors: UBAGAI T CHAMBERLIN ME MUDD SH CHOU JY
Citation: T. Ubagai et al., DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH DEFECTS IN THE HEPATIC FORM OF METHIONINE ADENOSYL TRANSFERASE, The FASEB journal, 10(6), 1996, pp. 2147-2147
DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH METHIONINE ADENOSYLTRANSFERASE I II DEFICIENCY/
Authors: CHAMBERLIN ME UBAGAI T MUDD SH WILSON WG LEONARD JV CHOU JY
Citation: Me. Chamberlin et al., DEMYELINATION OF THE BRAIN IS ASSOCIATED WITH METHIONINE ADENOSYLTRANSFERASE I II DEFICIENCY/, The Journal of clinical investigation, 98(4), 1996, pp. 1021-1027
PLASMA HOMOCYST(E)INE OR HOMOCYSTEINE
Authors: MUDD SH LEW HL
Citation: Sh. Mudd et Hl. Lew, PLASMA HOMOCYST(E)INE OR HOMOCYSTEINE, The New England journal of medicine, 333(5), 1995, pp. 325-325
MOLECULAR MECHANISMS OF AN INBORN ERROR OF METHIONINE PATHWAY - METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
Authors: UBAGAI T LEI KJ HUANG S MUDD SH LEVY HL CHOU JY
Citation: T. Ubagai et al., MOLECULAR MECHANISMS OF AN INBORN ERROR OF METHIONINE PATHWAY - METHIONINE ADENOSYLTRANSFERASE DEFICIENCY, The Journal of clinical investigation, 96(4), 1995, pp. 1943-1947
ISOLATED PERSISTENT HYPERMETHIONINEMIA
Authors: MUDD SH LEVY HL TANGERMAN A BOUJET C BUIST N DAVIDSONMUNDT A HUDGINS L OYANAGI K NAGAO M WILSON WG
Citation: Sh. Mudd et al., ISOLATED PERSISTENT HYPERMETHIONINEMIA, American journal of human genetics, 57(4), 1995, pp. 882-892
Risultati: 1-8 |