The epsilon-sarcoglycan gene (SGCE), mutated in myoclonus-dystonia syndrome, is maternally imprinted
暂无分享,去创建一个
T. Meitinger | T. Strom | F. Asmus | T. Gasser | V. Kalscheuer | A. Zimprich | B. Lorenz-Depiereux | M. Grabowski
[1] V. Rakyan,et al. Metastable epialleles in mammals. , 2002, Trends in genetics : TIG.
[2] Jun Kawai,et al. Asb4, Ata3, and Dcn are novel imprinted genes identified by high-throughput screening using RIKEN cDNA microarray. , 2002, Biochemical and biophysical research communications.
[3] T. Meitinger,et al. Mutations in the gene encoding ɛ-sarcoglycan cause myoclonus–dystonia syndrome , 2001, Nature Genetics.
[4] Christoph Grunau,et al. Bisulfite genomic sequencing: systematic investigation of critical experimental parameters , 2001, Nucleic Acids Res..
[5] T. Kohda,et al. A retrotransposon-derived gene, PEG10, is a novel imprinted gene located on human chromosome 7q21. , 2001, Genomics.
[6] M. Dichgans,et al. Inherited myoclonus‐dystonia syndrome: Narrowing the 7q21‐q31 locus in German families , 2001, Annals of neurology.
[7] C. Beechey. Peg1/Mest locates distal to the currently defined imprinting region on mouse proximal chromosome 6 and identifies a new imprinting region affecting growth , 2000, Cytogenetic and Genome Research.
[8] K. Scheidtmann,et al. Familiäres Myoklonus-Dystonie-Syndrom assoziiert mit Panikattacken , 2000, Der Nervenarzt.
[9] T. Ogata,et al. Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome. , 2000, American journal of human genetics.
[10] H. Ropers,et al. Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. , 2000, Human molecular genetics.
[11] N. Copeland,et al. Zac1 (Lot1), a Potential Tumor Suppressor Gene, and the Gene for ɛ-Sarcoglycan Are Maternally Imprinted Genes: Identification by a Subtractive Screen of Novel Uniparental Fibroblast Lines , 2000, Molecular and Cellular Biology.
[12] Y. Hahn,et al. Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest , 2000, FEBS letters.
[13] H. Ropers,et al. gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome. , 1999, Human molecular genetics.
[14] S. Clark,et al. Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA. , 1997, Nucleic acids research.
[15] J. Kere,et al. Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. , 1997, Genomics.
[16] O. Tsutsumi,et al. Human PEG1/MEST, an imprinted gene on chromosome 7. , 1997, Human molecular genetics.
[17] G. Deuschl,et al. Linkage studies in alcohol‐responsive myoclonic dystonia , 1996, Movement disorders : official journal of the Movement Disorder Society.
[18] L. E. McDonald,et al. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[19] Heidemarie Neitzel,et al. A routine method for the establishment of permanent growing lymphoblastoid cell lines , 1986, Human Genetics.
[20] M. Surani,et al. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis , 1984, Nature.
[21] T. Meitinger,et al. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. , 2001, Nature genetics.
[22] J. Kere,et al. A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region. , 2001, American journal of human genetics.
[23] E. Koenig,et al. [Familial myoclonus-dystonia syndrome associated with panic attacks]. , 2000, Der Nervenarzt.