Matthijs G - Search Results

1

Regional assignment of seven loci to 12p13.2-pter by PCR analysis of somatic cell hybrids containing the der(12) or the der(X) chromosome from a mesothelioma showing t(X;12)(q22;p13).

Aerssens J, Chaffanet M, Baens M, Matthijs G, Van den Berghe H, Cassiman JJ, Marynen P. Aerssens J, et al. Among authors: matthijs g. Genomics. 1994 Mar 1;20(1):119-21. doi: 10.1006/geno.1994.1136. Genomics. 1994. PMID: 8020938

2

PMM (PMM1), the human homologue of SEC53 or yeast phosphomannomutase, is localized on chromosome 22q13.

Matthijs G, Schollen E, Pirard M, Budarf ML, Van Schaftingen E, Cassiman JJ. Matthijs G, et al. Genomics. 1997 Feb 15;40(1):41-7. doi: 10.1006/geno.1996.4536. Genomics. 1997. PMID: 9070917 Free article.

3

Structure of the human alpha-2 macroglobulin gene and its promotor.

Matthijs G, Devriendt K, Cassiman JJ, Van den Berghe H, Marynen P. Matthijs G, et al. Biochem Biophys Res Commun. 1992 Apr 30;184(2):596-603. doi: 10.1016/0006-291x(92)90631-t. Biochem Biophys Res Commun. 1992. PMID: 1374237

4

A deletion polymorphism in the human alpha-2-macroglobulin (A2M) gene.

Matthijs G, Marynen P. Matthijs G, et al. Nucleic Acids Res. 1991 Sep 25;19(18):5102. doi: 10.1093/nar/19.18.5102. Nucleic Acids Res. 1991. PMID: 1717945 Free PMC article.

5

Characterization of the human alpha 2-macroglobulin gene promoter: identification of a novel, triple TRE/RARE/ERE response element.

Matthijs G, Cassiman JJ, Van den Berghe H, Marynen P. Matthijs G, et al. Biochem Biophys Res Commun. 1994 Jul 15;202(1):65-72. doi: 10.1006/bbrc.1994.1894. Biochem Biophys Res Commun. 1994. PMID: 7518682

6

Evidence for genetic heterogeneity in the carbohydrate-deficient glycoprotein syndrome type I (CDG1).

Matthijs G, Legius E, Schollen E, Vandenberk P, Jaeken J, Barone R, Fiumara A, Visser G, Lambert M, Cassiman JJ. Matthijs G, et al. Genomics. 1996 Aug 1;35(3):597-9. doi: 10.1006/geno.1996.0404. Genomics. 1996. PMID: 8812498

7

Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.

Devriendt K, Petit P, Matthijs G, Vermeesch JR, Holvoet M, De Muelenaere A, Marynen P, Cassiman JJ, Fryns JP. Devriendt K, et al. Among authors: matthijs g. J Med Genet. 1997 May;34(5):395-9. doi: 10.1136/jmg.34.5.395. J Med Genet. 1997. PMID: 9152837 Free PMC article.

8

The promoter of the human alpha 2-macroglobulin gene binds HNF-4 or a related nuclear factor for its expression in hepatocytes and lung fibroblasts.

Matthijs G, Marynen P. Matthijs G, et al. Ann N Y Acad Sci. 1994 Sep 10;737:472-5. doi: 10.1111/j.1749-6632.1994.tb44343.x. Ann N Y Acad Sci. 1994. PMID: 7524424 No abstract available.

9

Cloning and characterization of the promoter region of the murine alpha-4 integrin subunit.

De Meirsman C, Schollen E, Jaspers M, Ongena K, Matthijs G, Marynen P, Cassiman JJ. De Meirsman C, et al. Among authors: matthijs g. DNA Cell Biol. 1994 Jul;13(7):743-54. doi: 10.1089/dna.1994.13.743. DNA Cell Biol. 1994. PMID: 7772255

10

A regulatory element in the 5'UTR directs cell-specific expression of the mouse alpha 4 gene.

Schollen E, De Meirsman C, Matthijs G, Cassiman JJ. Schollen E, et al. Among authors: matthijs g. Biochem Biophys Res Commun. 1995 Jun 6;211(1):115-22. doi: 10.1006/bbrc.1995.1785. Biochem Biophys Res Commun. 1995. PMID: 7779075

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