Below are the most recent publications written about "Chromosome Inversion" by people in Profiles.
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Beck CR, Carvalho CM, Banser L, Gambin T, Stubbolo D, Yuan B, Sperle K, McCahan SM, Henneke M, Seeman P, Garbern JY, Hobson GM, Lupski JR. Complex genomic rearrangements at the PLP1 locus include triplication and quadruplication. PLoS Genet. 2015 Mar; 11(3):e1005050.
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Tan Y, Timakhov RA, Rao M, Altomare DA, Xu J, Liu Z, Gao Q, Jhanwar SC, Di Cristofano A, Wiest DL, Knepper JE, Testa JR. A novel recurrent chromosomal inversion implicates the homeobox gene Dlx5 in T-cell lymphomas from Lck-Akt2 transgenic mice. Cancer Res. 2008 Mar 01; 68(5):1296-302.
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McClarren J, Donnenfeld AE, Ravnan JB. Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing truncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion. Prenat Diagn. 2006 Dec; 26(13):1212-5.
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de Chadar?vian JP, Dunn S, Malatack JJ, Ganguly A, Blecker U, Punnett HH. Chromosome rearrangement with no apparent gene mutation in familial adenomatous polyposis and hepatocellular neoplasia. Pediatr Dev Pathol. 2002 Jan-Feb; 5(1):69-75.
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Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, Feldman GJ, Volta M, Andolfi G, Gilgenkrantz S, Marion RW, Hennekam RC, Opitz JM, Muenke M, Ropers HH, Ballabio A. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet. 1997 Nov; 17(3):285-91.
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Hustad CM, Perry WL, Siracusa LD, Rasberry C, Cobb L, Cattanach BM, Kovatch R, Copeland NG, Jenkins NA. Molecular genetic characterization of six recessive viable alleles of the mouse agouti locus. Genetics. 1995 May; 140(1):255-65.
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Kupershmidt S, Rall GF, Lu ZQ, Ben-Porat T. Cleavage of concatemeric DNA at the internal junction of "translocation" mutants of pseudorabies virus and inversion of their L component appear to be linked. Virology. 1992 Mar; 187(1):223-32.
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Rall GF, Kupershmidt S, Lu XQ, Mettenleiter TC, Ben-Porat T. Low-level inversion of the L component of pseudorabies virus is not dependent on sequence homology. J Virol. 1991 Dec; 65(12):7016-9.
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Schauer GM, Dunn LK, Godmilow L, Eagle RC, Knisely AS. Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks. Am J Med Genet. 1990 Dec; 37(4):583-91.
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Pologe LG, de Bruin D, Ravetch JV. A and T homopolymeric stretches mediate a DNA inversion in Plasmodium falciparum which results in loss of gene expression. Mol Cell Biol. 1990 Jun; 10(6):3243-6.