Chandrasekharappa SC - Search Results

1

The primacy of NF1 loss as the driver of tumorigenesis in neurofibromatosis type 1-associated plexiform neurofibromas.

Pemov A, Li H, Patidar R, Hansen NF, Sindiri S, Hartley SW, Wei JS, Elkahloun A, Chandrasekharappa SC; NISC Comparative Sequencing Program; Boland JF, Bass S; NCI DCEG Cancer Genomics Research Laboratory; Mullikin JC, Khan J, Widemann BC, Wallace MR, Stewart DR. Pemov A, et al. Among authors: chandrasekharappa sc. Oncogene. 2017 Jun 1;36(22):3168-3177. doi: 10.1038/onc.2016.464. Epub 2017 Jan 9. Oncogene. 2017. PMID: 28068329 Free PMC article.

2

Mutations in the human Jagged1 gene are responsible for Alagille syndrome.

Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoli DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC. Oda T, et al. Among authors: chandrasekharappa sc. Nat Genet. 1997 Jul;16(3):235-42. doi: 10.1038/ng0797-235. Nat Genet. 1997. PMID: 9207787

3

Identification and cloning of the human homolog (JAG1) of the rat Jagged1 gene from the Alagille syndrome critical region at 20p12.

Oda T, Elkahloun AG, Meltzer PS, Chandrasekharappa SC. Oda T, et al. Among authors: chandrasekharappa sc. Genomics. 1997 Aug 1;43(3):376-9. doi: 10.1006/geno.1997.4820. Genomics. 1997. PMID: 9268641

4

Stable overexpression of MEN1 suppresses tumorigenicity of RAS.

Kim YS, Burns AL, Goldsmith PK, Heppner C, Park SY, Chandrasekharappa SC, Collins FS, Spiegel AM, Marx SJ. Kim YS, et al. Among authors: chandrasekharappa sc. Oncogene. 1999 Oct 21;18(43):5936-42. doi: 10.1038/sj.onc.1203005. Oncogene. 1999. PMID: 10557080

5

Identification of a larger than 3 Mb deletion including JAG1 in an Alagille syndrome patient with a translocation t(3;20)(q13.3;p12.2).

Oda T, Elkahloun AG, Meltzer PS, Okajima K, Sugiyama K, Wada Y, Chandrasekharappa SC. Oda T, et al. Among authors: chandrasekharappa sc. Hum Mutat. 2000 Jul;16(1):92. doi: 10.1002/1098-1004(200007)16:1<92::AID-HUMU23>3.0.CO;2-4. Hum Mutat. 2000. PMID: 10874319

6

Methods for reverse genetic screening in zebrafish by resequencing and TILLING.

Sood R, English MA, Jones M, Mullikin J, Wang DM, Anderson M, Wu D, Chandrasekharappa SC, Yu J, Zhang J, Paul Liu P. Sood R, et al. Among authors: chandrasekharappa sc. Methods. 2006 Jul;39(3):220-7. doi: 10.1016/j.ymeth.2006.04.012. Methods. 2006. PMID: 16828311

7

Chromosome 8 BAC array comparative genomic hybridization and expression analysis identify amplification and overexpression of TRMT12 in breast cancer.

Rodriguez V, Chen Y, Elkahloun A, Dutra A, Pak E, Chandrasekharappa S. Rodriguez V, et al. Genes Chromosomes Cancer. 2007 Jul;46(7):694-707. doi: 10.1002/gcc.20454. Genes Chromosomes Cancer. 2007. PMID: 17440925

8

Mouse embryo fibroblasts lacking the tumor suppressor menin show altered expression of extracellular matrix protein genes.

Ji Y, Prasad NB, Novotny EA, Kaur S, Elkahloun A, Chen Y, Zhang RZ, Chu ML, Agarwal SK, Marx SJ, Collins FS, Chandrasekharappa SC. Ji Y, et al. Among authors: chandrasekharappa sc. Mol Cancer Res. 2007 Oct;5(10):1041-51. doi: 10.1158/1541-7786.MCR-06-0379. Mol Cancer Res. 2007. PMID: 17951404

9

Personalized genomic medicine: lessons from the exome.

Solomon BD, Pineda-Alvarez DE, Hadley DW, NISC Comparative Sequencing Program, Teer JK, Cherukuri PF, Hansen NF, Cruz P, Young AC, Blakesley RW, Lanpher B, Mayfield Gibson S, Sincan M, Chandrasekharappa SC, Mullikin JC. Solomon BD, et al. Among authors: chandrasekharappa sc. Mol Genet Metab. 2011 Sep-Oct;104(1-2):189-91. doi: 10.1016/j.ymgme.2011.06.022. Epub 2011 Jul 5. Mol Genet Metab. 2011. PMID: 21767969 Free PMC article.

10

Recombination mapping using Boolean logic and high-density SNP genotyping for exome sequence filtering.

Markello TC, Han T, Carlson-Donohoe H, Ahaghotu C, Harper U, Jones M, Chandrasekharappa S, Anikster Y, Adams DR; NISC Comparative Sequencing Program; Gahl WA, Boerkoel CF. Markello TC, et al. Mol Genet Metab. 2012 Mar;105(3):382-9. doi: 10.1016/j.ymgme.2011.12.014. Epub 2011 Dec 23. Mol Genet Metab. 2012. PMID: 22264778 Free PMC article.

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