Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever
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F. Collins | L. Deaven | R. Moyzis | D. Ricke | A. Baxevanis | Z. Deng | A. Cercek | D. Krizman | R. Richards | C. Robbins | M. Mangelsdorf | E. Pras | M. Centola | N. Raben | R. Sood | M. Shohat | J. Buckingham | D. Gumucio | J. Balow | Y. Yokoyama | I. Aksentijevich | N. Doggett | P. Liu | T. Blake | M. Hamon | N. Shafran | N. Zaks | N. Richards | G. Wood | E. Mansfield | A. Vedula | T. Kahan | S. Eisenberg | D. Kastner | Xing Chen | M. Pras | Xuejun Chen | J. Rotter | N. FischelGhodsian | D. A. Shelton | A. Orsborn
[1] L B YUSHKEVICH,et al. On hemoglobinopathies. , 1961, Problemy gematologii i perelivaniia krovi.
[2] Graham-Stewart Cw. Hereditary Factor VII Deficiency , 1964 .
[3] E. Sohar,et al. FAMILIAL MEDITERRANEAN FEVER , 1959, Definitions.
[4] D. Zemer,et al. Variable incidence of amyloidosis in familial Mediterranean fever among different ethnic groups. , 1982, The Johns Hopkins medical journal.
[5] J. Sambrook,et al. Molecular Cloning: A Laboratory Manual , 2001 .
[6] Y. Matzner,et al. C5a-inhibitor deficiency in peritoneal fluids from patients with familial Mediterranean fever. , 1984, The New England journal of medicine.
[7] P. Aisen,et al. Circulating hydroxy fatty acids in familial Mediterranean fever. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[8] R. Kyle,et al. Autosomal dominant familial Mediterranean fever-like syndrome with amyloidosis. , 1987, Mayo Clinic proceedings.
[9] G. Freeman,et al. rpt-1, an intracellular protein from helper/inducer T cells that regulates gene expression of interleukin 2 receptor and human immunodeficiency virus type 1. , 1988, Proceedings of the National Academy of Sciences of the United States of America.
[10] H. Hiai,et al. Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene , 1988, Molecular and cellular biology.
[11] F. Fenech,et al. PLASMA DOPAMINE BETA-HYDROXYLASE: RAPID DIAGNOSTIC TEST FOR RECURRENT HEREDITARY POLYSEROSITIS , 1988, The Lancet.
[12] J. Rotter,et al. Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequency. , 1989, American journal of medical genetics.
[13] H. Sambrook. Molecular cloning : a laboratory manual. Cold Spring Harbor, NY , 1989 .
[14] E. Myers,et al. Basic local alignment search tool. , 1990, Journal of molecular biology.
[15] S. McKnight,et al. Evidence of changes in protease sensitivity and subunit exchange rate on DNA binding by C/EBP. , 1990, Science.
[16] I. Mather,et al. Cloning and analysis of cDNA encoding bovine butyrophilin, an apical glycoprotein expressed in mammary tissue and secreted in association with the milk-fat globule membrane during lactation. , 1990, The Journal of biological chemistry.
[17] S. Weissman,et al. cDNA selection: efficient PCR approach for the selection of cDNAs encoded in large chromosomal DNA fragments. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[18] Margaret Robertson,et al. Identification of a mutation in the gene causing hyperkalemic periodic paralysis , 1991, Cell.
[19] M. B. Frank,et al. Protein heterogeneity in the human Ro/SSA ribonucleoproteins. The 52- and 60-kD Ro/SSA autoantigens are encoded by separate genes. , 1991, The Journal of clinical investigation.
[20] R. Laskey,et al. Two interdependent basic domains in nucleoplasmin nuclear targeting sequence: Identification of a class of bipartite nuclear targeting sequence , 1991, Cell.
[21] M. Kloc,et al. The cloning and characterization of a maternally expressed novel zinc finger nuclear phosphoprotein (xnf7) in Xenopus laevis. , 1991, Developmental biology.
[22] P. Sharp,et al. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[23] Y. Nakamura,et al. The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity. , 1992, American journal of human genetics.
[24] M. Kanehisa,et al. A knowledge base for predicting protein localization sites in eukaryotic cells , 1992, Genomics.
[25] P. Freemont,et al. A novel zinc finger coiled-coil domain in a family of nuclear proteins. , 1992, Trends in biochemical sciences.
[26] D. Kastner,et al. Mapping of a gene causing familial Mediterranean fever to the short arm of chromosome 16. , 1992, The New England journal of medicine.
[27] T. Pettersson,et al. Autosomal dominant ‘Mediterranean fever’ in a Finnish family , 1992, Journal of internal medicine.
[28] B. Rost,et al. Prediction of protein secondary structure at better than 70% accuracy. , 1993, Journal of molecular biology.
[29] R. Richards,et al. Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis. , 1993, American journal of human genetics.
[30] J. Gall,et al. A putative zinc‐binding protein on lampbrush chromosome loops. , 1993, The EMBO journal.
[31] B. Rost,et al. Combining evolutionary information and neural networks to predict protein secondary structure , 1994, Proteins.
[32] John C. Wootton,et al. Non-globular Domains in Protein Sequences: Automated Segmentation Using Complexity Measures , 1994, Comput. Chem..
[33] N. Mechti,et al. Molecular Cloning of a New Interferon-induced Factor That Represses Human Immunodeficiency Virus Type 1 Long Terminal Repeat Expression (*) , 1995, The Journal of Biological Chemistry.
[34] N. Doggett,et al. An integrated physical map of human chromosome 16. , 1995, Nature.
[35] Y. Yuval,et al. Dominant inheritance in two families with familial Mediterranean fever (FMF). , 1995, American journal of medical genetics.
[36] T. Shohat,et al. Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in Israel. , 1995, American journal of medical genetics.
[37] L. Kruglyak,et al. Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246. , 1996, American journal of human genetics.
[38] K. Klinger,et al. The region surrounding the PKD1 gene: a 700-kb P1 contig from a YAC-deficient interval. , 1996, Genome research.
[39] P. Pontarotti,et al. B30.2-like domain proteins: a growing family. , 1997, Biochemical and biophysical research communications.
[40] L. Deaven,et al. Construction of a 1.2-Mb contig surrounding, and molecular analysis of, the human CREB-binding protein (CBP/CREBBP) gene on chromosome 16p13.3. , 1997, Genomics.
[41] F. Collins,et al. A high-resolution genetic map of the familial Mediterranean fever candidate region allows identification of haplotype-sharing among ethnic groups. , 1997, Genomics.
[42] Amos Bairoch,et al. The PROSITE database, its status in 1997 , 1997, Nucleic Acids Res..
[43] L. Deaven,et al. Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3. , 1997, Genomics.
[44] M. Pras,et al. Clinical differences between North African and Iraqi Jews with familial Mediterranean fever. , 1998, American journal of medical genetics.