Francke U - Search Results

1

Molecular cloning, chromosomal mapping, and characterization of the mouse UDP-galactose:ceramide galactosyltransferase gene.

Coetzee T, Li X, Fujita N, Marcus J, Suzuki K, Francke U, Popko B. Coetzee T, et al. Among authors: francke u. Genomics. 1996 Jul 1;35(1):215-22. doi: 10.1006/geno.1996.0341. Genomics. 1996. PMID: 8661123

2

DNA sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: identification of polymorphic alleles.

You KH, Hsieh CL, Hayes C, Stahl N, Francke U, Popko B. You KH, et al. Among authors: francke u. Genomics. 1991 Apr;9(4):751-7. doi: 10.1016/0888-7543(91)90370-t. Genomics. 1991. PMID: 1709914

3

Molecular cloning of the human homolog of a striatum-enriched phosphatase (STEP) gene and chromosomal mapping of the human and murine loci.

Li X, Luna J, Lombroso PJ, Francke U. Li X, et al. Among authors: francke u. Genomics. 1995 Aug 10;28(3):442-9. doi: 10.1006/geno.1995.1173. Genomics. 1995. PMID: 7490079 Free article.

4

cDNA cloning of the human monocarboxylate transporter 1 and chromosomal localization of the SLC16A1 locus to 1p13.2-p12.

Garcia CK, Li X, Luna J, Francke U. Garcia CK, et al. Among authors: francke u. Genomics. 1994 Sep 15;23(2):500-3. doi: 10.1006/geno.1994.1532. Genomics. 1994. PMID: 7835905 Free article.

5

Backfoot, a novel homeobox gene, maps to human chromosome 5 (BFT) and mouse chromosome 13 (Bft).

Shang J, Li X, Ring HZ, Clayton DA, Francke U. Shang J, et al. Among authors: francke u. Genomics. 1997 Feb 15;40(1):108-13. doi: 10.1006/geno.1996.4558. Genomics. 1997. PMID: 9070926 Free article.

6

Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18.

Li X, Pereira L, Zhang H, Sanguineti C, Ramirez F, Bonadio J, Francke U. Li X, et al. Among authors: francke u. Genomics. 1993 Dec;18(3):667-72. doi: 10.1016/s0888-7543(05)80371-4. Genomics. 1993. PMID: 8307578 Free article.

7

High-density radiation hybrid map of human chromosome 18 and contig of 18p.

Giacalone J, Li X, Lehrach H, Francke U. Giacalone J, et al. Among authors: francke u. Genomics. 1996 Oct 1;37(1):9-18. doi: 10.1006/geno.1996.0514. Genomics. 1996. PMID: 8921364 Free article.

8

Autosomal recessive neuromuscular disorder in a transgenic line of mice.

Kelly D, Chancellor K, Milatovich A, Francke U, Suzuki K, Popko B. Kelly D, et al. Among authors: francke u. J Neurosci. 1994 Jan;14(1):198-207. doi: 10.1523/JNEUROSCI.14-01-00198.1994. J Neurosci. 1994. PMID: 7506762 Free PMC article.

9

Assignment of the gene SLC1A2 coding for the human glutamate transporter EAAT2 to human chromosome 11 bands p13-p12.

Li X, Francke U. Li X, et al. Among authors: francke u. Cytogenet Cell Genet. 1995;71(3):212-3. doi: 10.1159/000134111. Cytogenet Cell Genet. 1995. PMID: 7587378 No abstract available.

10

The human calcitonin receptor gene (CALCR) at 7q21.3 is outside the deletion associated with the Williams syndrome.

Pérez Jurado LA, Li X, Francke U. Pérez Jurado LA, et al. Among authors: francke u. Cytogenet Cell Genet. 1995;70(3-4):246-9. doi: 10.1159/000134044. Cytogenet Cell Genet. 1995. PMID: 7789182

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