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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 1 |
1994 | 1 |
1995 | 1 |
1996 | 2 |
1997 | 1 |
1998 | 1 |
2024 | 0 |
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7 results
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Page 1
A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region.
Genomics. 1998 Mar 1;48(2):163-70. doi: 10.1006/geno.1997.5182.
Genomics. 1998.
PMID: 9521869
Free article.
Molecular cloning, mapping to human chromosome 1 q21-q23, and cell binding characteristics of Spalpha, a new member of the scavenger receptor cysteine-rich (SRCR) family of proteins.
Gebe JA, Kiener PA, Ring HZ, Li X, Francke U, Aruffo A.
Gebe JA, et al.
J Biol Chem. 1997 Mar 7;272(10):6151-8. doi: 10.1074/jbc.272.10.6151.
J Biol Chem. 1997.
PMID: 9045627
Free article.
Item in Clipboard
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.
Pérez Jurado LA, Peoples R, Kaplan P, Hamel BC, Francke U.
Pérez Jurado LA, et al.
Am J Hum Genet. 1996 Oct;59(4):781-92.
Am J Hum Genet. 1996.
PMID: 8808592
Free PMC article.
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The three genes of the human FCGR1 gene family encoding Fc gamma RI flank the centromere of chromosome 1 at 1p12 and 1q21.
Maresco DL, Chang E, Theil KS, Francke U, Anderson CL.
Maresco DL, et al.
Cytogenet Cell Genet. 1996;73(3):157-63. doi: 10.1159/000134330.
Cytogenet Cell Genet. 1996.
PMID: 8697799
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Cloning and regional assignment of the human myosin heavy chain 12 (MYH12) gene to chromosome band 15q21.
Moore KJ, Testa JR, Francke U, Milatovich A, Copeland NG, Jenkins NA.
Moore KJ, et al.
Cytogenet Cell Genet. 1995;69(1-2):53-8. doi: 10.1159/000133937.
Cytogenet Cell Genet. 1995.
PMID: 7835087
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Chromosome localizations of genes for five cAMP-specific phosphodiesterases in man and mouse.
Milatovich A, Bolger G, Michaeli T, Francke U.
Milatovich A, et al.
Somat Cell Mol Genet. 1994 Mar;20(2):75-86. doi: 10.1007/BF02290677.
Somat Cell Mol Genet. 1994.
PMID: 8009369
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The CD40 ligand, gp39, is defective in activated T cells from patients with X-linked hyper-IgM syndrome.
Aruffo A, Farrington M, Hollenbaugh D, Li X, Milatovich A, Nonoyama S, Bajorath J, Grosmaire LS, Stenkamp R, Neubauer M, et al.
Aruffo A, et al.
Cell. 1993 Jan 29;72(2):291-300. doi: 10.1016/0092-8674(93)90668-g.
Cell. 1993.
PMID: 7678782
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