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Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.
Prawitt D, Enklaar T, Klemm G, Gärtner B, Spangenberg C, Winterpacht A, Higgins M, Pelletier J, Zabel B. Prawitt D, et al. Among authors: pelletier j. Hum Mol Genet. 2000 Jan 22;9(2):203-16. doi: 10.1093/hmg/9.2.203. Hum Mol Genet. 2000. PMID: 10607831
Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.
Prawitt D, Enklaar T, Gärtner-Rupprecht B, Spangenberg C, Oswald M, Lausch E, Schmidtke P, Reutzel D, Fees S, Lucito R, Korzon M, Brozek I, Limon J, Housman DE, Pelletier J, Zabel B. Prawitt D, et al. Among authors: pelletier j. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4085-90. doi: 10.1073/pnas.0500037102. Epub 2005 Mar 2. Proc Natl Acad Sci U S A. 2005. PMID: 15743916 Free PMC article.
Functional characterization of human nucleosome assembly protein-2 (NAP1L4) suggests a role as a histone chaperone.
Rodriguez P, Munroe D, Prawitt D, Chu LL, Bric E, Kim J, Reid LH, Davies C, Nakagama H, Loebbert R, Winterpacht A, Petruzzi MJ, Higgins MJ, Nowak N, Evans G, Shows T, Weissman BE, Zabel B, Housman DE, Pelletier J. Rodriguez P, et al. Among authors: pelletier j. Genomics. 1997 Sep 15;44(3):253-65. doi: 10.1006/geno.1997.4868. Genomics. 1997. PMID: 9325046
Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation.
Bohne F, Langer D, Martiné U, Eider CS, Cencic R, Begemann M, Elbracht M, Bülow L, Eggermann T, Zechner U, Pelletier J, Zabel BU, Enklaar T, Prawitt D. Bohne F, et al. Among authors: pelletier j. Clin Epigenetics. 2016 May 4;8:47. doi: 10.1186/s13148-016-0215-4. eCollection 2016. Clin Epigenetics. 2016. PMID: 27152123 Free PMC article.
1,997 results