A telomerase component is defective in the human disease dyskeratosis congenita
暂无分享,去创建一个
[1] R. Reddel,et al. Telomere maintenance mechanisms and cellular immortalization. , 1999, Current opinion in genetics & development.
[2] Jeffrey B. Cheng,et al. A Box H/ACA Small Nucleolar RNA-Like Domain at the Human Telomerase RNA 3′ End , 1999, Molecular and Cellular Biology.
[3] M. Mann,et al. Cbf5p, a potential pseudouridine synthase, and Nhp2p, a putative RNA-binding protein, are present together with Gar1p in all H BOX/ACA-motif snoRNPs and constitute a common bipartite structure. , 1998, RNA.
[4] S. Klauck,et al. X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions , 1998, Nature Genetics.
[5] L. Luzzatto,et al. Dyskeratosis and ribosomal rebellion , 1998, Nature Genetics.
[6] V. Lundblad,et al. The telomerase reverse transcriptase: components and regulation. , 1998, Genes & development.
[7] D. Tollervey,et al. The box H + ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthase. , 1998, Genes & development.
[8] T. Ide,et al. Abnormal telomere dynamics of B-lymphoblastoid cell strains from Werner's syndrome patients transformed by Epstein – Barr virus , 1997, Oncogene.
[9] D. Tollervey,et al. Function and synthesis of small nucleolar RNAs. , 1997, Current opinion in cell biology.
[10] Tamás Kiss,et al. Site-Specific Pseudouridine Formation in Preribosomal RNA Is Guided by Small Nucleolar RNAs , 1997, Cell.
[11] J. Ni,et al. Small Nucleolar RNAs Direct Site-Specific Synthesis of Pseudouridine in Ribosomal RNA , 1997, Cell.
[12] I. Dokal. Dyskeratosis congenita: an inherited bone marrow failure syndrome , 1996, British journal of haematology.
[13] et al.,et al. The RNA component of human telomerase , 1995, Science.
[14] R. Reddel,et al. Telomere elongation in immortal human cells without detectable telomerase activity. , 1995, The EMBO journal.
[15] C. Greider,et al. Developmental and tissue-specific regulation of mouse telomerase and telomere length. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[16] C B Harley,et al. Specific association of human telomerase activity with immortal cells and cancer. , 1994, Science.
[17] G. Blobel,et al. NAP57, a mammalian nucleolar protein with a putative homolog in yeast and bacteria [published erratum appears in J Cell Biol 1998 Jan 26;140(2):447] , 1994, The Journal of cell biology.
[18] C. Harley,et al. Stabilization of short telomeres and telomerase activity accompany immortalization of Epstein-Barr virus-transformed human B lymphocytes , 1994, Journal of virology.
[19] J Ofengand,et al. Four newly located pseudouridylate residues in Escherichia coli 23S ribosomal RNA are all at the peptidyltransferase center: analysis by the application of a new sequencing technique. , 1993, Biochemistry.
[20] L. Luzzatto,et al. Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangements. , 1992, Blood.
[21] B. Alter,et al. Dyskeratosis Congenita: Clinical and Genetic Heterogeneity Report of a New Case and Review of the Literature , 1992, The American journal of pediatric hematology/oncology.
[22] T. Dexter,et al. "Stem cell" origin of the hematopoietic defect in dyskeratosis congenita. , 1992, Blood.
[23] Robin C. Allshire,et al. Telomere reduction in human colorectal carcinoma and with ageing , 1990, Nature.
[24] C. Harley,et al. Telomeres shorten during ageing of human fibroblasts , 1990, Nature.
[25] E. Blackburn,et al. In vivo alteration of telomere sequences and senescence caused by mutated Tetrahymena telomerase RNAs , 1990, Nature.
[26] A. Trowbridge,et al. Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature. , 1975, Journal of medical genetics.
[27] A. Trowbridge,et al. Dyskeratosis congenita: Hematologic evaluation of a sibship and review of the literature , 1977, American journal of hematology.