Molecular Genetics of the Human MHC Complement Gene Cluster
暂无分享,去创建一个
C. Y. Yu | C. Yung Yu | C. Y. Yu | C. Yung Yu
[1] J. Klein,et al. Molecular Evolution of the Major Histocompatibility Complex , 2011, NATO ASI Series.
[2] C. Y. Yu,et al. An Unequal Crossover between the RCCX Modules of the Human MHC Leading to the Presence of a CYP21B Gene and a Tenascin TNXB/TNXA-RP2 Recombinant between C4A and C4B Genes in a Patient with Juvenile Rheumatoid Arthritis , 1999, Experimental and Clinical Immunogenetics.
[3] T. R. Welch,et al. Modular Variations of the Human Major Histocompatibility Complex Class III Genes for Serine/Threonine Kinase RP, Complement Component C4, Steroid 21-Hydroxylase CYP21, and Tenascin TNX (the RCCX Module) , 1999, The Journal of Biological Chemistry.
[4] H. Colten,et al. Deficiency of human complement protein C4 due to identical frameshift mutations in the C4A and C4B genes. , 1999, Journal of immunology.
[5] P. Schneider,et al. Reference Typing Report for Complement Component C4 , 1999, Experimental and Clinical Immunogenetics.
[6] P. M. Schneider,et al. Reference Typing Report for Complement Factor B , 1999, Experimental and Clinical Immunogenetics.
[7] L. Truedsson,et al. Characterization of non-expressed C4 genes in a case of complete C4 deficiency: identification of a novel point mutation leading to a premature stop codon. , 1998, Human immunology.
[8] C. Y. Yu,et al. Four ubiquitously expressed genes, RD (D6S45)-SKI2W (SKIV2L)-DOM3Z-RP1 (D6S60E), are present between complement component genes factor B and C4 in the class III region of the HLA. , 1998, Genomics.
[9] C. Y. Yu,et al. The human DEVH-box protein Ski2w from the HLA is localized in nucleoli and ribosomes. , 1998, Nucleic acids research.
[10] H. Colten,et al. Genetic deficiencies of complement. , 1998, Annals of medicine.
[11] J. Volanakis,et al. A novel type II complement C2 deficiency allele in an African-American family. , 1998, Journal of immunology.
[12] R. Parker,et al. The 3′ to 5′ degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3′ to 5′ exonucleases of the exosome complex , 1998, The EMBO journal.
[13] Lokki,et al. Molecular heterogeneity in deficiency of complement protein C2 type I , 1998, Immunology.
[14] P. Taylor,et al. A Targeted Disruption of the Murine Complement Factor B Gene Resulting in Loss of Expression of Three Genes in Close Proximity, Factor B, C2, and D17H6S45 * , 1998, The Journal of Biological Chemistry.
[15] J. Bristow,et al. Tenascin–X deficiency is associated with Ehlers–Danlos syndrome , 1997, Nature Genetics.
[16] M. Petzl-Erler,et al. Major histocompatibility complex (MHC) class III genetics in two Amerindian tribes from Southern Brazil: the Kaingang and the Guarani , 1997, Human Genetics.
[17] B. Conrad,et al. A Human Endogenous Retroviral Superantigen as Candidate Autoimmune Gene in Type I Diabetes , 1997, Cell.
[18] L. Harrison,et al. The Potential Roles of Endogenous Retroviruses in Autoimmunity , 1996, Immunological reviews.
[19] C. Auffray,et al. The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression. , 1996, Genomics.
[20] H. Colten,et al. Type II Human Complement C2 Deficiency , 1996, The Journal of Biological Chemistry.
[21] A. Willis,et al. The reaction mechanism of the internal thioester in the human complement component C4 , 1996, Nature.
[22] S. Strome,et al. Phenotypic and molecular analysis of mes-3, a maternal-effect gene required for proliferation and viability of the germ line in C. elegans. , 1995, Genetics.
[23] S. Gitelman,et al. A promoter within intron 35 of the human C4A gene initiates abundant adrenal-specific transcription of a 1 kb RNA: location of a cryptic CYP21 promoter element? , 1995, Human molecular genetics.
[24] P. Donohoue,et al. The HLA-A3, Cw6,B47,DR7 extended haplotypes in salt losing 21-hydroxylase deficiency and in the Old Order Amish: identical class I antigens and class II alleles with at least two crossover sites in the class III region. , 1995, Tissue antigens.
[25] H. Colten,et al. Genetic Deficiencies of Complement , 1995 .
[26] M. Bedolli,et al. Embryonic expression of tenascin‐X suggests a role in limb, muscle, and heart development , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.
[27] J. Bristow,et al. Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of tenascin-X. , 1995, Genomics.
[28] J. Garrido,et al. Distinct tissue distribution in pigs of tenascin-X and tenascin-C transcripts. , 1995, European journal of biochemistry.
[29] C. Y. Yu,et al. Human helicase gene SKI2W in the HLA class III region exhibits striking structural similarities to the yeast antiviral gene SKI2 and to the human gene KIAA0052: emergence of a new gene family. , 1995, Nucleic acids research.
[30] N. Sonenberg,et al. Decoying the cap- mRNA degradation system by a double-stranded RNA virus and poly(A)- mRNA surveillance by a yeast antiviral system , 1995, Molecular and cellular biology.
[31] D. Valle,et al. Hemolytically inactive C4B complement allotype caused by a proline to leucine mutation in the C5-binding site. , 1994, The Journal of biological chemistry.
[32] F. Fuller-Pace,et al. RNA helicases: modulators of RNA structure. , 1994, Trends in cell biology.
[33] T. Ikemura,et al. The distribution of tenascin-X is distinct and often reciprocal to that of tenascin-C , 1994, The Journal of cell biology.
[34] C. Y. Yu,et al. Structure and genetics of the partially duplicated gene RP located immediately upstream of the complement C4A and the C4B genes in the HLA class III region. Molecular cloning, exon-intron structure, composite retroposon, and breakpoint of gene duplication. , 1994, The Journal of biological chemistry.
[35] R. Campbell,et al. Characterisation of the novel gene G11 lying adjacent to the complement C4A gene in the human major histocompatibility complex. , 1994, Human molecular genetics.
[36] J. Volanakis,et al. cDNA cloning and characterization of the protein encoded by RD, a gene located in the class III region of the human major histocompatibility complex. , 1993, The Biochemical journal.
[37] S. Gitelman,et al. Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B , 1993, The Journal of cell biology.
[38] R. Wickner,et al. Evidence that the SKI antiviral system of Saccharomyces cerevisiae acts by blocking expression of viral mRNA , 1993, Molecular and cellular biology.
[39] J. Volanakis,et al. Structure of the human C2 gene. , 1993, Journal of immunology.
[40] S. Gitelman,et al. Abundant adrenal-specific transcription of the human P450c21A "pseudogene". , 1993, The Journal of biological chemistry.
[41] P. Schneider,et al. Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression. , 1993, The Journal of clinical investigation.
[42] J. Dausset. The Major Histocompatibility Complex in Man , 1992 .
[43] D R Bentley,et al. A variable number of tandem repeats locus within the human complement C2 gene is associated with a retroposon derived from a human endogenous retrovirus , 1992, The Journal of experimental medicine.
[44] H. Colten,et al. Type I human complement C2 deficiency. A 28-base pair gene deletion causes skipping of exon 6 during RNA splicing. , 1992, The Journal of biological chemistry.
[45] R. Campbell,et al. The coding sequence of the hemolytically inactive C4A6 allotype of human complement component C4 reveals that a single arginine to tryptophan substitution at beta-chain residue 458 is the likely cause of the defect. , 1992, Journal of immunology.
[46] S. Gitelman,et al. Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus , 1992, Molecular and cellular biology.
[47] R. Campbell,et al. A single arginine to tryptophan interchange at beta-chain residue 458 of human complement component C4 accounts for the defect in classical pathway C5 convertase activity of allotype C4A6. Implications for the location of a C5 binding site in C4. , 1992, Journal of immunology.
[48] C. Y. Yu,et al. The complete exon-intron structure of a human complement component C4A gene. DNA sequences, polymorphism, and linkage to the 21-hydroxylase gene. , 1991, Journal of immunology.
[49] M. Carroll,et al. Substitution of a single amino acid (aspartic acid for histidine) converts the functional activity of human complement C4B to C4A. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[50] J. Klein,et al. Organization of the chimpanzee C4‐CYP21 region: Implications for the evolution of human genes , 1990, European journal of immunology.
[51] P. Schneider,et al. Null alleles of human complement C4. Evidence for pseudogenes at the C4A locus and for gene conversion at the C4B locus , 1990, The Journal of experimental medicine.
[52] P. White,et al. Structure of the human RD gene: a highly conserved gene in the class III region of the major histocompatibility complex. , 1989, DNA.
[53] S. Gitelman,et al. Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[54] B. Uring-Lambert,et al. Molecular basis of complete C4 deficiency. A study of three patients. , 1989, Human immunology.
[55] M. Steinmetz,et al. A previously undetected MHC gene with an unusual periodic structure. , 1988, Science.
[56] I. Dunham,et al. Molecular characterization of the HLA‐linked steroid 21‐hydroxylase B gene from an individual with congenital adrenal hyperplasia. , 1987, The EMBO journal.
[57] J. Schifferli,et al. Complement‐mediated adherence of immune complexes to human erythrocytes , 1987, FEBS letters.
[58] R. Campbell,et al. Cell-specific expression of the human complement protein Factor B gene: Evidence for the role of two distinct 5′-flanking elements , 1987, Cell.
[59] R. Campbell,et al. Structural basis of the polymorphism of human complement components C4A and C4B: gene size, reactivity and antigenicity. , 1986, The EMBO journal.
[60] D. Bentley. Primary structure of human complement component C2. Homology to two unrelated protein families. , 1986, The Biochemical journal.
[61] H. Colten,et al. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants. , 1986, The Journal of clinical investigation.
[62] P. White,et al. Structure of human steroid 21-hydroxylase genes. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[63] O. Gotoh,et al. Complete nucleotide sequence of two steroid 21-hydroxylase genes tandemly arranged in human chromosome: a pseudogene and a genuine gene. , 1986, Proceedings of the National Academy of Sciences of the United States of America.
[64] J. Young,et al. Covalent binding properties of the C4A and C4B isotypes of the fourth component of human complement on several C1-bearing cell surfaces. , 1986, Journal of immunology.
[65] K. Belt,et al. Deletion of complement C4 and steroid 21‐hydroxylase genes in the HLA class III region. , 1985, The EMBO journal.
[66] R. Porter,et al. The origin of the very variable haemolytic activities of the common human complement component C4 allotypes including C4‐A6. , 1985, The EMBO journal.
[67] J. Strominger,et al. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[68] D. Bentley,et al. The factor B and C2 genes. , 1984, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.
[69] R. Porter,et al. A comparison of the properties of two classes, C4A and C4B, of the human complement component C4. , 1984, The EMBO journal.
[70] J. Young,et al. The molecular basis for the difference in immune hemolysis activity of the Chido and Rodgers isotypes of human complement component C4. , 1984, Journal of immunology.
[71] L. Strong,et al. Human C4 haplotypes with duplicated C4A or C4B. , 1984, American journal of human genetics.
[72] D. Bentley,et al. A molecular map of the human major histocompatibility complex class III region linking complement genes C4, C2 and factor B , 1984, Nature.
[73] L. Abraham,et al. Comparative analysis of the disease-associated complement C4 gene from the HLA-A1, B8, DR3 haplotype. , 1996, Experimental and clinical immunogenetics.
[74] R. Campbell,et al. Genes of the MHC class III region and the functions of the proteins they encode , 1996 .
[75] P. Schneider,et al. Length polymorphism of the human complement component C4 gene is due to an ancient retroviral integration. , 1995, Experimental and clinical immunogenetics.
[76] M. Tassabehji,et al. Identification of a novel family of human endogenous retroviruses and characterization of one family member, HERV-K(C4), located in the complement C4 gene cluster. , 1994, Nucleic acids research.
[77] P. Schneider,et al. Identification of the recombination site within the steroid 21-hydroxylase gene (CYP21) of the HLA-B47,DR7 haplotype. , 1992, Experimental and clinical immunogenetics.
[78] L. Truedsson,et al. DNA analysis in a MHC heterozygous patient with complete C4 deficiency--homozygosity for C4 gene deletion and C4 pseudogene. , 1991, Experimental and clinical immunogenetics.
[79] J. Klein,et al. Evolution of Primate C4 and CYP21 Genes , 1991 .
[80] P. M. Schneider. C4 DNA RFLP reference typing report. , 1990, Complement and inflammation.
[81] P. Schneider,et al. C4 nomenclature statement (1990). , 1990, Complement and inflammation.
[82] C. Giles. C4: Rodgers and Chido typing. , 1990, Complement and inflammation.
[83] R. Spritz,et al. The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conserved. , 1990, Gene.
[84] P. Schneider,et al. C4 reference typing report. , 1990, Complement and inflammation.
[85] I. Dunham,et al. Polymorphism of the human complement component C4. , 1990, Experimental and clinical immunogenetics.
[86] Yves Morel,et al. The molecular genetics of 21-hydroxylase deficiency. , 1989, Annual review of genetics.
[87] P. Donohoue,et al. Restriction fragment analysis of duplication of the fourth component of complement (C4A). , 1988, Genomics.
[88] G. Hauptmann,et al. Inherited deficiency of the fourth component of human complement. , 1988, Immunodeficiency reviews.
[89] R. Campbell,et al. Mapping of steroid 21-hydroxylase genes adjacent to complement component C4 genes in HLA, the major histocompatibility complex in man. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[90] P. Schneider,et al. NULL ALLELES OF HUMAN COMPLEMENT C 4 Evidence for Pseudogenes at the C 4 A Locus and for Gene Conversion at the C 4 B Locus BY LIANE BRAUN , ' , 2022 .