Kurnit DM - Search Results

1

Assignment of the human slow twitch skeletal muscle/cardiac troponin C gene (TNNC1) to human chromosome 3p21.3-->3p14.3 using somatic cell hybrids.

Song WJ, Van Keuren ML, Drabkin HA, Cypser JR, Gemmill RM, Kurnit DM. Song WJ, et al. Among authors: kurnit dm. Cytogenet Cell Genet. 1996;75(1):36-7. doi: 10.1159/000134453. Cytogenet Cell Genet. 1996. PMID: 8995486 No abstract available.

2

DNA sequences surrounding the centromere of chromosome 21.

Stewart GD, McCann DP, Van Keuren ML, Kurnit DM. Stewart GD, et al. Among authors: kurnit dm. Cytogenet Cell Genet. 1991;57(1):23-5. doi: 10.1159/000133106. Cytogenet Cell Genet. 1991. PMID: 1855388

3

Construction of human embryonic cDNA libraries: HD, PKD1 and BRCA1 are transcribed widely during embryogenesis.

Buraczynska MJ, Van Keuren ML, Buraczynska KM, Chang YS, Crombez E, Kurnit DM. Buraczynska MJ, et al. Among authors: kurnit dm. Cytogenet Cell Genet. 1995;71(2):197-202. doi: 10.1159/000134106. Cytogenet Cell Genet. 1995. PMID: 7656596

4

Transcription patterns of sequences on human chromosome 21.

Kurnit DM, Cheng J, Zhu Y, Van Keuren ML, Jiang Y, Pan Y, Whitley K, Crombez E. Kurnit DM, et al. Cytogenet Cell Genet. 1995;71(2):203-6. doi: 10.1159/000134107. Cytogenet Cell Genet. 1995. PMID: 7656597

5

Characterization of an unusual and complex chromosome 21 rearrangement using somatic cell genetics and cloned DNA probes.

Van Keuren ML, Stewart GD, Bradley CM, Kurnit DM, Neve RL, Watkins PC, Tanzi RE, Gusella JF, Patterson D. Van Keuren ML, et al. Among authors: kurnit dm. Am J Med Genet. 1989 Jul;33(3):369-75. doi: 10.1002/ajmg.1320330316. Am J Med Genet. 1989. PMID: 2529766 Free article.

6

Molecular structure of human chromosome 21.

Stewart GD, Van Keuren ML, Galt J, Kurachi S, Buraczynska MJ, Kurnit DM. Stewart GD, et al. Among authors: kurnit dm. Annu Rev Genet. 1989;23:409-23. doi: 10.1146/annurev.ge.23.120189.002205. Annu Rev Genet. 1989. PMID: 2694939 Review. No abstract available.

7

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: kurnit dm. Cytogenet Cell Genet. 1987;44(2-3):142-7. doi: 10.1159/000132358. Cytogenet Cell Genet. 1987. PMID: 3568763

8

Expressed sequence tags from the long arm of human chromosome 21.

Chiang PW, Dzida G, Grumet J, Cheng JF, Song WJ, Crombez E, Van Keuren ML, Kurnit DM. Chiang PW, et al. Among authors: kurnit dm. Genomics. 1995 Sep 20;29(2):383-9. doi: 10.1006/geno.1995.9991. Genomics. 1995. PMID: 8666385

9

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h.

Chiang PW, Wang S, Smithivas P, Song WJ, Ramamoorthy S, Hillman J, Puett S, Van Keuren ML, Crombez E, Kumar A, Glover TW, Miller DE, Tsai CH, Blackburn CC, Chen XN, Sun Z, Cheng JF, Korenberg JR, Kurnit DM. Chiang PW, et al. Among authors: kurnit dm. Genomics. 1996 Jun 15;34(3):328-33. doi: 10.1006/geno.1996.0294. Genomics. 1996. PMID: 8786132

10

Isolation and characterization of the human and mouse homologues (SUPT4H and Supt4h) of the yeast SPT4 gene.

Chiang PW, Wang SQ, Smithivas P, Song WJ, Crombez E, Akhtar A, Im R, Greenfield J, Ramamoorthy S, Van Keuren M, Blackburn CC, Tsai CH, Kurnit DM. Chiang PW, et al. Among authors: kurnit dm. Genomics. 1996 Jun 15;34(3):368-75. doi: 10.1006/geno.1996.0299. Genomics. 1996. PMID: 8786137

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