Perou CM - Search Results

1

Identification of the murine beige gene by YAC complementation and positional cloning.

Perou CM, Moore KJ, Nagle DL, Misumi DJ, Woolf EA, McGrail SH, Holmgren L, Brody TH, Dussault BJ Jr, Monroe CA, Duyk GM, Pryor RJ, Li L, Justice MJ, Kaplan J. Perou CM, et al. Nat Genet. 1996 Jul;13(3):303-8. doi: 10.1038/ng0796-303. Nat Genet. 1996. PMID: 8673129

2

"Synchronized" endocytosis and intracellular sorting in alveolar macrophages: the early sorting endosome is a transient organelle.

Ward DM, Perou CM, Lloyd M, Kaplan J. Ward DM, et al. Among authors: perou cm. J Cell Biol. 1995 Jun;129(5):1229-40. doi: 10.1083/jcb.129.5.1229. J Cell Biol. 1995. PMID: 7775570 Free PMC article.

3

Chediak-Higashi syndrome is not due to a defect in microtubule-based lysosomal mobility.

Perou CM, Kaplan J. Perou CM, et al. J Cell Sci. 1993 Sep;106 ( Pt 1):99-107. doi: 10.1242/jcs.106.1.99. J Cell Sci. 1993. PMID: 8270647

4

Complementation analysis of Chediak-Higashi syndrome: the same gene may be responsible for the defect in all patients and species.

Perou CM, Kaplan J. Perou CM, et al. Somat Cell Mol Genet. 1993 Sep;19(5):459-68. doi: 10.1007/BF01233251. Somat Cell Mol Genet. 1993. PMID: 8291023

5

Complementation of the beige mutation in cultured cells by episomally replicating murine yeast artificial chromosomes.

Perou CM, Justice MJ, Pryor RJ, Kaplan J. Perou CM, et al. Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5905-9. doi: 10.1073/pnas.93.12.5905. Proc Natl Acad Sci U S A. 1996. PMID: 8650191 Free PMC article.

6

Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome.

Nagle DL, Karim MA, Woolf EA, Holmgren L, Bork P, Misumi DJ, McGrail SH, Dussault BJ Jr, Perou CM, Boissy RE, Duyk GM, Spritz RA, Moore KJ. Nagle DL, et al. Among authors: perou cm. Nat Genet. 1996 Nov;14(3):307-11. doi: 10.1038/ng1196-307. Nat Genet. 1996. PMID: 8896560

7

Comparative mapping in the beige-satin region of mouse chromosome 13.

Perou CM, Perchellet A, Jago T, Pryor R, Kaplan J, Justice MJ. Perou CM, et al. Genomics. 1997 Jan 15;39(2):136-46. doi: 10.1006/geno.1996.4478. Genomics. 1997. PMID: 9027500

8

The bg allele mutation is due to a LINE1 element retrotransposition.

Perou CM, Pryor RJ, Naas TP, Kaplan J. Perou CM, et al. Genomics. 1997 Jun 1;42(2):366-8. doi: 10.1006/geno.1997.4740. Genomics. 1997. PMID: 9192864 Free article. No abstract available.

9

The Beige/Chediak-Higashi syndrome gene encodes a widely expressed cytosolic protein.

Perou CM, Leslie JD, Green W, Li L, Ward DM, Kaplan J. Perou CM, et al. J Biol Chem. 1997 Nov 21;272(47):29790-4. doi: 10.1074/jbc.272.47.29790. J Biol Chem. 1997. PMID: 9368050 Free article.

10

Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition.

Rodriguez-Martin B, Alvarez EG, Baez-Ortega A, Zamora J, Supek F, Demeulemeester J, Santamarina M, Ju YS, Temes J, Garcia-Souto D, Detering H, Li Y, Rodriguez-Castro J, Dueso-Barroso A, Bruzos AL, Dentro SC, Blanco MG, Contino G, Ardeljan D, Tojo M, Roberts ND, Zumalave S, Edwards PA, Weischenfeldt J, Puiggròs M, Chong Z, Chen K, Lee EA, Wala JA, Raine KM, Butler A, Waszak SM, Navarro FCP, Schumacher SE, Monlong J, Maura F, Bolli N, Bourque G, Gerstein M, Park PJ, Wedge DC, Beroukhim R, Torrents D, Korbel JO, Martincorena I, Fitzgerald RC, Van Loo P, Kazazian HH, Burns KH; PCAWG Structural Variation Working Group; Campbell PJ, Tubio JMC; PCAWG Consortium. Rodriguez-Martin B, et al. Nat Genet. 2020 Mar;52(3):306-319. doi: 10.1038/s41588-019-0562-0. Epub 2020 Feb 5. Nat Genet. 2020. PMID: 32024998 Free PMC article.

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