MeSH Review:
Genes, vif
- Function of E. coli RNA polymerase sigma factor sigma 70 in promoter-proximal pausing. Ring, B.Z., Yarnell, W.S., Roberts, J.W. Cell (1996)
- Epigenetic inheritance at the agouti locus in the mouse. Morgan, H.D., Sutherland, H.G., Martin, D.I., Whitelaw, E. Nat. Genet. (1999)
- Identification of HTLV-III/LAV sor gene product and detection of antibodies in human sera. Kan, N.C., Franchini, G., Wong-Staal, F., DuBois, G.C., Robey, W.G., Lautenberger, J.A., Papas, T.S. Science (1986)
- Heterogeneous Helicobacter pylori isolates from members of a family with a history of peptic ulcer disease. van der Ende, A., Rauws, E.A., Feller, M., Mulder, C.J., Tytgat, G.N., Dankert, J. Gastroenterology (1996)
- Intimate adhesion of Neisseria meningitidis to human epithelial cells is under the control of the crgA gene, a novel LysR-type transcriptional regulator. Deghmane, A.E., Petit, S., Topilko, A., Pereira, Y., Giorgini, D., Larribe, M., Taha, M.K. EMBO J. (2000)
- Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2. Afzal, A.R., Rajab, A., Fenske, C.D., Oldridge, M., Elanko, N., Ternes-Pereira, E., Tüysüz, B., Murday, V.A., Patton, M.A., Wilkie, A.O., Jeffery, S. Nat. Genet. (2000)
- The peroxisome proliferator-activated receptor-gamma is a negative regulator of macrophage activation. Ricote, M., Li, A.C., Willson, T.M., Kelly, C.J., Glass, C.K. Nature (1998)
- The combination of dissimilar alleles of the A alpha and A beta gene complexes, whose proteins contain homeo domain motifs, determines sexual development in the mushroom Coprinus cinereus. Kües, U., Richardson, W.V., Tymon, A.M., Mutasa, E.S., Göttgens, B., Gaubatz, S., Gregoriades, A., Casselton, L.A. Genes Dev. (1992)
- Self-fusion of the ALL1 gene. A new genetic mechanism for acute leukemia. Schichman, S.A., Canaani, E., Croce, C.M. JAMA (1995)
- Identification of a recombinogenic major histocompatibility complex Q gene with diverse alleles. Cullen, M.K., Lapierre, L.A., Kesari, K.V., Geliebter, J. J. Exp. Med. (1993)
- Oxygen-regulated control elements in the phosphoglycerate kinase 1 and lactate dehydrogenase A genes: similarities with the erythropoietin 3' enhancer. Firth, J.D., Ebert, B.L., Pugh, C.W., Ratcliffe, P.J. Proc. Natl. Acad. Sci. U.S.A. (1994)
- Clinical correlations of osteoarthritis associated with a single-base mutation (arginine519 to cysteine) in type II procollagen gene. A newly defined pathogenesis. Pun, Y.L., Moskowitz, R.W., Lie, S., Sundstrom, W.R., Block, S.R., McEwen, C., Williams, H.J., Bleasel, J.F., Holderbaum, D., Haqqi, T.M. Arthritis Rheum. (1994)
- Preference for guanosine at first codon position in highly expressed Escherichia coli genes. A relationship with translational efficiency. Gutiérrez, G., Márquez, L., Marín, A. Nucleic Acids Res. (1996)
- Cloning of the Escherichia coli sor genes for L-sorbose transport and metabolism and physical mapping of the genes near metH and iclR. Wehmeier, U.F., Nobelmann, B., Lengeler, J.W. J. Bacteriol. (1992)
- Transversion-specific purine analogue mutagens and the mechanism of hydroxylaminopurine mutagenesis. Murray, V. Mutat. Res. (1987)
- Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes. Braun, A., Ambach, H., Kammerer, S., Rolinski, B., Stöckler, S., Rabl, W., Gärtner, J., Zierz, S., Roscher, A.A. Am. J. Hum. Genet. (1995)
- A dimorphic 4-bp repeat in the cystic fibrosis gene is in absolute linkage disequilibrium with the delta F508 mutation: implications for prenatal diagnosis and mutation origin. Chehab, F.F., Johnson, J., Louie, E., Goossens, M., Kawasaki, E., Erlich, H. Am. J. Hum. Genet. (1991)
- Autoregulation of simian virus 40 gene A by T antigen. Reed, S.I., Stark, G.R., Alwine, J.C. Proc. Natl. Acad. Sci. U.S.A. (1976)
- Male-specific transcription initiation of the C4-Slp gene in mouse liver follows activation of STAT5. Varin-Blank, N., Dondi, E., Tosi, M., Hernandez, C., Boucontet, L., Gotoh, H., Shiroishi, T., Moriwaki, K., Meo, T. Proc. Natl. Acad. Sci. U.S.A. (1998)
- Fibrinogen Philadelphia, a hypodysfibrinogenemia characterized by abnormal polymerization and fibrinogen hypercatabolism due to gamma S378P mutation. Keller, M.A., Martinez, J., Baradet, T.C., Nagaswami, C., Chernysh, I.N., Borowski, M.K., Surrey, S., Weisel, J.W. Blood (2005)
- Male-enhanced antigen gene is phylogenetically conserved and expressed at late stages of spermatogenesis. Lau, Y.F., Chan, K.M., Sparkes, R. Proc. Natl. Acad. Sci. U.S.A. (1989)
- Altered epithelial cell proportions in the fetal lung of glucocorticoid receptor null mice. Cole, T.J., Solomon, N.M., Van Driel, R., Monk, J.A., Bird, D., Richardson, S.J., Dilley, R.J., Hooper, S.B. Am. J. Respir. Cell Mol. Biol. (2004)
- Characterization of the gene encoding human TAFI (thrombin-activable fibrinolysis inhibitor; plasma procarboxypeptidase B). Boffa, M.B., Reid, T.S., Joo, E., Nesheim, M.E., Koschinsky, M.L. Biochemistry (1999)
- Postnatal expression of the plasticity-related nerve growth factor-induced gene A (NGFI-A) protein in the superficial layers of the rat superior colliculus: relation to N-methyl-D-aspartate receptor function. Giraldi-Guimarães, A., de Bittencourt-Navarrete, R.E., Nascimento, I.C., Salazar, P.R., Freitas-Campos, D., Mendez-Otero, R. Neuroscience (2004)
- The carboxyl-half of the rotavirus nonstructural protein NS53 (NSP1) is not required for virus replication. Hua, J., Patton, J.T. Virology (1994)
- In vivo formation of gene fusions encoding hybrid beta-galactosidase proteins in one step with a transposable Mu-lac transducing phage. Casadaban, M.J., Chou, J. Proc. Natl. Acad. Sci. U.S.A. (1984)
- An exonic point mutation of the androgen receptor gene in a family with complete androgen insensitivity. Sai, T.J., Seino, S., Chang, C.S., Trifiro, M., Pinsky, L., Mhatre, A., Kaufman, M., Lambert, B., Trapman, J., Brinkmann, A.O. Am. J. Hum. Genet. (1990)
- Thyroid hormone up-regulates NGFI-A gene expression in rat brain during development. Pipaon, C., Santos, A., Perez-Castillo, A. J. Biol. Chem. (1992)
- Purification and characterization of phiX174 gene A protein. A multifunctional enzyme of duplex DNA replication. Eisenberg, S., Kornberg, A. J. Biol. Chem. (1979)
- Transcriptional regulation of neuronal nicotinic acetylcholine receptor genes. A possible role for the DNA-binding protein Puralpha. Du, Q., Tomkinson, A.E., Gardner, P.D. J. Biol. Chem. (1997)
- The A-type cyclin CYCA2;3 is a key regulator of ploidy levels in Arabidopsis endoreduplication. Imai, K.K., Ohashi, Y., Tsuge, T., Yoshizumi, T., Matsui, M., Oka, A., Aoyama, T. Plant Cell (2006)
- A Ufd2/D4Cole1e chimeric protein and overexpression of Rbp7 in the slow Wallerian degeneration (WldS) mouse. Conforti, L., Tarlton, A., Mack, T.G., Mi, W., Buckmaster, E.A., Wagner, D., Perry, V.H., Coleman, M.P. Proc. Natl. Acad. Sci. U.S.A. (2000)
- Characterization of a YAC containing part or all of the Norrie disease locus. Chen, Z.Y., Sims, K.B., Coleman, M., Donnai, D., Monaco, A., Breakefield, X.O., Davies, K.E., Craig, I.W. Hum. Mol. Genet. (1992)
- Is the mitochondrial complex I ND5 gene a hot-spot for MELAS causing mutations? Liolitsa, D., Rahman, S., Benton, S., Carr, L.J., Hanna, M.G. Ann. Neurol. (2003)
- Variation of hepatic glucuronidation: Novel functional polymorphisms of the UDP-glucuronosyltransferase UGT1A4. Ehmer, U., Vogel, A., Schütte, J.K., Krone, B., Manns, M.P., Strassburg, C.P. Hepatology (2004)
- Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients. Arruda, V.R., Pieneman, W.C., Reitsma, P.H., Deutz-Terlouw, P.P., Annichino-Bizzacchi, J.M., Briët, E., Costa, F.F. Blood (1995)
- Human interferon-alpha A, -alpha 2, and -alpha 2(Arg) genes in genomic DNA. Emanuel, S.L., Pestka, S. J. Biol. Chem. (1993)
- Studies of the recognition sequence of phi X174 gene A protein. Cleavage site of phi X gene A protein in St-1 RFI DNA. Heidekamp, F., Langeveld, S.A., Baas, P.D., Jansz, H.S. Nucleic Acids Res. (1980)
- The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events. D'Angelo, A., Coppola, A., Madonna, P., Fermo, I., Pagano, A., Mazzola, G., Galli, L., Cerbone, A.M. Thromb. Haemost. (2000)
- Transcript map of the 8p23 putative tumor suppressor region. Sun, P.C., Uppaluri, R., Schmidt, A.P., Pashia, M.E., Quant, E.C., Sunwoo, J.B., Gollin, S.M., Scholnick, S.B. Genomics (2001)