Kucherlapati RS - Search Results

1

Assignment of the human myogenic factors 5 and 6 (MYF5, MYF6) gene cluster to 12q21 by in situ hybridization and physical mapping of the locus between D12S350 and D12S106.

Cupelli L, Renault B, Leblanc-Straceski J, Banks A, Ward D, Kucherlapati RS, Krauter K. Cupelli L, et al. Among authors: kucherlapati rs. Cytogenet Cell Genet. 1996;72(2-3):250-1. doi: 10.1159/000134201. Cytogenet Cell Genet. 1996. PMID: 8978788 No abstract available.

2

Mutations in the non-helical linker segment L1-2 of keratin 5 in patients with Weber-Cockayne epidermolysis bullosa simplex.

Chan YM, Yu QC, LeBlanc-Straceski J, Christiano A, Pulkkinen L, Kucherlapati RS, Uitto J, Fuchs E. Chan YM, et al. Among authors: kucherlapati rs. J Cell Sci. 1994 Apr;107 ( Pt 4):765-74. doi: 10.1242/jcs.107.4.765. J Cell Sci. 1994. PMID: 7520042

3

Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomas.

Schoenberg Fejzo M, Ashar HR, Krauter KS, Powell WL, Rein MS, Weremowicz S, Yoon SJ, Kucherlapati RS, Chada K, Morton CC. Schoenberg Fejzo M, et al. Among authors: kucherlapati rs. Genes Chromosomes Cancer. 1996 Sep;17(1):1-6. doi: 10.1002/(SICI)1098-2264(199609)17:1<1::AID-GCC1>3.0.CO;2-0. Genes Chromosomes Cancer. 1996. PMID: 8889500

4

Report and abstracts of the Second International Workshop on Human Chromosome 12 mapping 1994. New Haven, Connecticut, June 20-22, 1994.

Kucherlapati R, Craig I, Marynen P. Kucherlapati R, et al. Cytogenet Cell Genet. 1994;67(4):245-76. doi: 10.1159/000133868. Cytogenet Cell Genet. 1994. PMID: 7924453 No abstract available.

5

Report of the first international workshop on human chromosome 12 mapping.

Craig I, Gemmill R, Kucherlapati R. Craig I, et al. Cytogenet Cell Genet. 1992;61(4):243-51. doi: 10.1159/000133416. Cytogenet Cell Genet. 1992. PMID: 1362534 No abstract available.

6

Report of the Third International Workshop on Human Chromosome 12 Mapping 1995.

Marynen P, Kucherlapati R. Marynen P, et al. Cytogenet Cell Genet. 1996;73(1-2):1-24. doi: 10.1159/000134308. Cytogenet Cell Genet. 1996. PMID: 8646874 No abstract available.

7

Report of the fourth International Workshop in Human Chromosome 12 Mapping, 1997.

Kucherlapati R, Marynen P, Turc-Carel C. Kucherlapati R, et al. Cytogenet Cell Genet. 1997;78(2):82-95. Cytogenet Cell Genet. 1997. PMID: 9371396 No abstract available.

8

Report of the International Meeting on Chromosome 12 Genes in Cancer.

Van de Ven W, Hagemeijer A, Kucherlapati R, Marynen P. Van de Ven W, et al. Cytogenet Cell Genet. 1996;73(1-2):25-32. doi: 10.1159/000134309. Cytogenet Cell Genet. 1996. PMID: 8646887 No abstract available.

9

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases.

Kobayashi H, Montgomery KT, Bohlander SK, Adra CN, Lim BL, Kucherlapati RS, Donis-Keller H, Holt MS, Le Beau MM, Rowley JD. Kobayashi H, et al. Among authors: kucherlapati rs. Blood. 1994 Nov 15;84(10):3473-82. Blood. 1994. PMID: 7949101 Free article. Clinical Trial.

10

SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients.

Swanson KD, Winter JM, Reis M, Bentires-Alj M, Greulich H, Grewal R, Hruban RH, Yeo CJ, Yassin Y, Iartchouk O, Montgomery K, Whitman SP, Caligiuri MA, Loh ML, Gilliland DG, Look AT, Kucherlapati R, Kern SE, Meyerson M, Neel BG. Swanson KD, et al. Genes Chromosomes Cancer. 2008 Mar;47(3):253-9. doi: 10.1002/gcc.20527. Genes Chromosomes Cancer. 2008. PMID: 18064648

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