Hart IM - Search Results

1

A somatic cell hybrid with a single human chromosome 22 corrects the defect in the CHO mutant (Ade-I) lacking adenylosuccinase activity.

Van Keuren ML, Hart IM, Kao FT, Neve RL, Bruns GA, Kurnit DM, Patterson D. Van Keuren ML, et al. Among authors: hart im. Cytogenet Cell Genet. 1987;44(2-3):142-7. doi: 10.1159/000132358. Cytogenet Cell Genet. 1987. PMID: 3568763

2

Mapping of a locus correcting lack of phosphoribosylaminoimidazole carboxylase activity in Chinese hamster ovary cell Ade-D mutants to human chromosome 4.

Barton JW, Hart IM, Patterson D. Barton JW, et al. Among authors: hart im. Genomics. 1991 Feb;9(2):314-21. doi: 10.1016/0888-7543(91)90259-h. Genomics. 1991. PMID: 2004782

3

A gene correcting the defect in the CHO mutant Ade -H, deficient in a branch point enzyme (adenylosuccinate synthetase) of de novo purine biosynthesis, is located on the long arm of chromosome 1.

Lai LW, Hart IM, Patterson D. Lai LW, et al. Among authors: hart im. Genomics. 1991 Feb;9(2):322-8. doi: 10.1016/0888-7543(91)90260-l. Genomics. 1991. PMID: 2004783

4

Regional assignment of human liver-type 6-phosphofructokinase to chromosome 21q22.3 by using somatic cell hybrids and a monoclonal anti-L antibody.

Van Keuren M, Drabkin H, Hart I, Harker D, Patterson D, Vora S. Van Keuren M, et al. Hum Genet. 1986 Sep;74(1):34-40. doi: 10.1007/BF00278782. Hum Genet. 1986. PMID: 2944814

5

Chromosomal location of human genes encoding major heat-shock protein HSP70.

Harrison GS, Drabkin HA, Kao FT, Hartz J, Hart IM, Chu EH, Wu BJ, Morimoto RI. Harrison GS, et al. Among authors: hart im. Somat Cell Mol Genet. 1987 Mar;13(2):119-30. doi: 10.1007/BF01534692. Somat Cell Mol Genet. 1987. PMID: 3470951 Free article.

6

Molecular analysis and breakpoint definition of a set of human chromosome 21 somatic cell hybrids.

Graw SL, Gardiner K, Hall-Johnson K, Hart I, Joetham A, Walton K, Donaldson D, Patterson D. Graw SL, et al. Somat Cell Mol Genet. 1995 Nov;21(6):415-28. doi: 10.1007/BF02310208. Somat Cell Mol Genet. 1995. PMID: 8600569

7

Molecular and cytogenetic characterization of a Chinese hamster/human hybrid cell line containing a der (21)t(Ypter-->cenY::cen21-->21qter) chromosome.

Patterson D, Hart I, Lai LW, Brahe C, Moscetti A, Tassone F, Raimondi E, Jones C. Patterson D, et al. Genomics. 1993 Jan;15(1):177-9. doi: 10.1006/geno.1993.1026. Genomics. 1993. PMID: 8432530

8

Identification of class-mu glutathione transferase genes GSTM1-GSTM5 on human chromosome 1p13.

Pearson WR, Vorachek WR, Xu SJ, Berger R, Hart I, Vannais D, Patterson D. Pearson WR, et al. Am J Hum Genet. 1993 Jul;53(1):220-33. Am J Hum Genet. 1993. PMID: 8317488 Free PMC article.

9

Localization of human ERBA2 to the 3p22----3p24.1 region of chromosome 3 and variable deletion in small cell lung cancer.

Drabkin H, Kao FT, Hartz J, Hart I, Gazdar A, Weinberger C, Evans R, Gerber M. Drabkin H, et al. Proc Natl Acad Sci U S A. 1988 Dec;85(23):9258-62. doi: 10.1073/pnas.85.23.9258. Proc Natl Acad Sci U S A. 1988. PMID: 2848257 Free PMC article.

10

Translocation of c-myc in the hereditary renal cell carcinoma associated with a t(3;8)(p14.2;q24.13) chromosomal translocation.

Drabkin HA, Bradley C, Hart I, Bleskan J, Li FP, Patterson D. Drabkin HA, et al. Proc Natl Acad Sci U S A. 1985 Oct;82(20):6980-4. doi: 10.1073/pnas.82.20.6980. Proc Natl Acad Sci U S A. 1985. PMID: 2995998 Free PMC article.

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