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FORMATION OF 22-KETO-CHOLESTEROL FROM 22S-HYDROXY-CHOLESTEROL BY A NADPH AND O2 DEPENDENT, CO-INSENSITIVE ENZYME IN BOVINE ADRENAL CORTEX MITOCHONDRIAALSEMA GJ; DEGENHART HJ; HOOGERBRUGGE J et al.1982; J. STEROID BIOCHEM.; ISSN 0022-4731; GBR; DA. 1982; VOL. 17; NO 1; PP. 37-40; BIBL. 19 REF.Article

New case of contiguous gene syndrome at chromosome 8p11.2p12CAU, M; CONGIU, R; ORIGA, R et al.American journal of medical genetics. 2005, Vol 136A, Num 2, pp 221-222, issn 0148-7299, 2 p.Article

Miller-Dieker syndrome: Analysis of a human contiguous gene syndrome in the mouseYINGLING, Jessica; TOYO-OKA, Kazuhito; WYNSHAW-BORIS, Anthony et al.American journal of human genetics. 2003, Vol 73, Num 3, pp 475-488, issn 0002-9297, 14 p.Article

The effects of scale: variation in the APOA1/C3/A4/A5 gene clusterFULLERTON, Stephanie M; BUCHANAN, Anne V; NICKERSON, Deborah A et al.Human genetics. 2004, Vol 115, Num 1, pp 36-56, issn 0340-6717, 21 p.Article

Leaf rust of spring wheat in Northern Kazakhstan and Siberia : incidence, virulence, and breeding for resistanceMORGOUNOV, A; ROSSEEVA, L; KOYSHIBAYEV, M et al.Australian journal of agricultural research. 2007, Vol 58, Num 9, pp 847-853, issn 0004-9409, 7 p.Article

Intrinsic Bent DNA Sites in the Developmentally Amplified C3-22 Gene Promoter of Rhynchosciara americana (Diptera: Sciaridae)DE SOUZA GOUVEIA, Fabiana; GIMENES, Fabricia; FIORINI, Adriana et al.Bioscience, biotechnology, and biochemistry. 2008, Vol 72, Num 5, pp 1190-1198, issn 0916-8451, 9 p.Article

A Hybrid CFHR3-1 Gene Causes Familial C3 GlomerulopathyMALIK, Talat H; LAVIN, Peter J; PICKERING, Matthew C et al.Journal of the American Society of Nephrology. 2012, Vol 23, Num 7, pp 1155-1160, issn 1046-6673, 6 p.Article

COMPARATIVE ELECTROPHORESIS OF THE 18-22S RNAS OF NEWCASTLE DISEASE VIRUSWEISS SR; BRATT MA.1976; J. VIROL.; U.S.A.; DA. 1976; VOL. 18; NO 1; PP. 316-323; BIBL. 16 REF.Article

The 22 S cylinder particles of Xenopus laevis. II: Immunological characterization and localization of their proteins in tissues and cultures cellsHÜGLE, B; KLEINSCHMIDT, J. A; FRANKE, W. W et al.European journal of cell biology. 1983, Vol 32, Num 1, pp 157-163, issn 0171-9335Article

A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHDBOYCOTT, Kym M; PARSLOW, Malcolm I; ROSS, Judith L et al.American journal of medical genetics. 2003, Vol 122A, Num 2, pp 139-147, issn 0148-7299, 9 p.Article

Structural features of the human C3 gene : intron/exon organization, transcriptional start site, and promoter region sequenceVIK, D. P; AMIGUET, P; MOFFAT, G. J et al.Biochemistry (Easton). 1991, Vol 30, Num 4, pp 1080-1085, issn 0006-2960, 6 p.Article

Contiguous ∼16 Mb 1p36 Deletion: Dominant Features of Classical Distal 1p36 Monosomy With Hapio-LethalityNICOULAZ, A; RUBI, F; CONRAD, B et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1964-1968, issn 1552-4825, 5 p.Article

Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseMICALE, Lucia; FUSCO, Carmela; AUGELLO, Bartolomeo et al.European journal of human genetics. 2008, Vol 16, Num 9, pp 1038-1049, issn 1018-4813, 12 p.Article

Complement component C3 : molecular basis of the C3*SO25 variant and evidence for molecular heterogeneity of other variantsHÖHLER, T; BOTTO, M; RITTNER, C et al.Human genetics. 1995, Vol 96, Num 5, pp 539-541, issn 0340-6717Article

The Xp Contiguous Deletion Syndrome and AutismSHINAWI, Marwan; PATEL, Ankita; PANICHKUL, Prisana et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1138-1148, issn 1552-4825, 11 p.Article

Sensorineural deafness and male infertility : a contiguous gene deletion syndromeYUZHOU ZHANG; MALEKPOUR, Mahdi; AL-MADANI, Navid et al.Journal of medical genetics. 2007, Vol 44, Num 4, pp 233-240, issn 0022-2593, 8 p.Article

Complete intron/exon organization of DNA encoding the α' chain of human C3BARNUM, S. R; AMIGUET, P; AMIGUET-BARRAS, F et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 15, pp 8471-8474, issn 0021-9258Article

Détermination du polymorphisme génétique du complément C'3 chez l'homme par une méthode l'électrophorèse verticale sur gel de polyacrylamideBATSUUR, ZH; PETRISHCHEV, V. N; RAUTIAN, G. S et al.Genetika. 1985, Vol 21, Num 4, pp 658-663, issn 0016-6758Article

C3, BF and C4 polymorphisms in TunisiansAYED, K; GORGI, Y.Human heredity. 1990, Vol 40, Num 6, pp 363-367, issn 0001-5652Article

Approximate linkage equilibrium between two polymorphic sites within the gene for human complement component 3DONALD, J. A; BALL, S. P.Annals of human genetics. 1984, Vol 48, Num 3, pp 269-273, issn 0003-4800Article

Development of a strategy for transgenic studies and monitoring of transgene expression in two closely related Moricandia species possessing a C3 or C3-C4 intermediate photosynthetic phenotypeTHOLE, Vera; RAWSTHORNE, Stephen.Physiologia Plantarum (København. 1948). 2003, Vol 119, Num 1, pp 155-164, issn 0031-9317, 10 p.Article

Homozygous hereditary C3 deficiency due to a partial gene deletionBOTTO, M; FONG, K. Y; SO, A. K et al.Proceedings of the National Academy of Sciences of the United States of America. 1992, Vol 89, Num 11, pp 4957-4961, issn 0027-8424Article

Molecular characterization of human complement factor B subtypesDAVRINCHE, C; ABBAL, M; CLERC, A et al.Immunogenetics (New York, NY). 1990, Vol 32, Num 5, pp 309-312, issn 0093-7711, 4 p.Article

C3 POLYMORPHISM IN SOME INDIAN POPULATIONSPAPIHA SS; BERNAL JE; ROBERTS DF et al.1979; HUM. HERED.; CHE; DA. 1979; VOL. 29; NO 4; PP. 193-196; BIBL. 14 REF.Article

Differentially expressed wheat genes in response to powdery mildew infectionLI, C. X; HU, L; XU, W. G et al.Annals of applied biology. 2013, Vol 163, Num 2, pp 209-217, issn 0003-4746, 9 p.Article

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