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Items: 1 to 20 of 426

1.

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, Chan M, Rozen R.

Mamm Genome. 1998 Aug;9(8):652-6. Erratum in: Mamm Genome 1999 Feb;10(2):204.

PMID:
9680386
2.

Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms.

Tran P, Leclerc D, Chan M, Pai A, Hiou-Tim F, Wu Q, Goyette P, Artigas C, Milos R, Rozen R.

Mamm Genome. 2002 Sep;13(9):483-92.

PMID:
12370778
3.
4.

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification.

Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R.

Nat Genet. 1994 Jun;7(2):195-200. Erratum in: Nat Genet. 1994 Aug;7(4):551.

PMID:
7920641
5.

Human retina-specific amine oxidase: genomic structure of the gene (AOC2), alternatively spliced variant, and mRNA expression in retina.

Imamura Y, Noda S, Mashima Y, Kudoh J, Oguchi Y, Shimizu N.

Genomics. 1998 Jul 15;51(2):293-8.

PMID:
9722954
6.

Genomic structure and transcript variants of the human methylenetetrahydrofolate reductase gene.

Homberger A, Linnebank M, Winter C, Willenbring H, Marquardt T, Harms E, Koch HG.

Eur J Hum Genet. 2000 Sep;8(9):725-9.

8.

Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.

Kluijtmans LA, Wendel U, Stevens EM, van den Heuvel LP, Trijbels FJ, Blom HJ.

Eur J Hum Genet. 1998 May-Jun;6(3):257-65.

9.

Functional characterization of human methylenetetrahydrofolate reductase in Saccharomyces cerevisiae.

Shan X, Wang L, Hoffmaster R, Kruger WD.

J Biol Chem. 1999 Nov 12;274(46):32613-8. Erratum in: J Biol Chem 1999 Dec 10;274(50):36030.

11.

Saccharomyces cerevisiae expresses two genes encoding isozymes of methylenetetrahydrofolate reductase.

Raymond RK, Kastanos EK, Appling DR.

Arch Biochem Biophys. 1999 Dec 15;372(2):300-8.

PMID:
10600168
12.

Molecular cloning of the mouse gene coding for carbonic anhydrase IV.

Tamai S, Cody LB, Sly WS.

Biochem Genet. 1996 Feb;34(1-2):31-43.

PMID:
8935991
13.

Isolation and molecular characterization of the porcine stearoyl-CoA desaturase gene.

Ren J, Knorr C, Huang L, Brenig B.

Gene. 2004 Sep 29;340(1):19-30.

PMID:
15556291
14.

Characterization and chromosomal mapping of a mouse ortholog of the late-infantile ceroid-lipofuscinosis gene CLN2.

Katz ML, Liu PC, Grob-Nunn SE, Shibuya H, Johnson GS.

Mamm Genome. 1999 Nov;10(11):1050-3.

PMID:
10556422
15.

Cathepsin K: isolation and characterization of the murine cDNA and genomic sequence, the homologue of the human pycnodysostosis gene.

Gelb BD, Moissoglu K, Zhang J, Martignetti JA, Brömme D, Desnick RJ.

Biochem Mol Med. 1996 Dec;59(2):200-6.

PMID:
8986645
16.

Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue.

Kvist AP, Latvanlehto A, Sund M, Horelli-Kuitunen N, Rehn M, Palotie A, Beier D, Pihlajaniemi T.

Matrix Biol. 1999 Jun;18(3):261-74.

PMID:
10429945
17.

The genomic structure of two protein kinase CK2alpha genes of Xenopus laevis and features of the putative promoter region.

Wilhelm V, Neckelman G, Allende JE, Allende CC.

Mol Cell Biochem. 2001 Nov;227(1-2):175-83.

PMID:
11827169
18.
19.

Genomic characterization of the human and mouse protein tyrosine phosphatase-1B genes.

Forsell PA, Boie Y, Montalibet J, Collins S, Kennedy BP.

Gene. 2000 Dec 30;260(1-2):145-53.

PMID:
11137300
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