New aspects of an old theme : The genetic basis of human color visionWISSINGER, B; SHARPE, L. T.American journal of human genetics. 1998, Vol 63, Num 5, pp 1257-1262, issn 0002-9297Article

Simultaneous detection of multiple point mutations using fluorescence-coupled competitive primer extensionFAUSER, S; WISSINGER, B.BioTechniques. 1997, Vol 22, Num 5, pp 964-968, issn 0736-6205Article

Regenerating good sense: RNA editing and trans splicing in plant mitochondriaWISSINGER, B; BRENNICKE, A; SCHUSTER, W et al.Trends in genetics (Regular ed.). 1992, Vol 8, Num 9, pp 322-328, issn 0168-9525Article

RNA editing in the cytochrome b locus of the higher plant Oenothera berteriana includes a U-to-C transitionSCHUSTER, W; HIESEL, R; WISSINGER, B et al.Molecular and cellular biology (Print). 1990, Vol 10, Num 5, pp 2428-2431, issn 0270-7306, 4 p.Article

RNA editing in trans-splicing intron sequences of nad2 mRNAs in Oenothera mitochondriaBINDER, S; MARCHFELDER, A; BRENNICKE, A et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 11, pp 7615-7623, issn 0021-9258Article

The coxII gene in carrot mitochondria contains two intronsLIPPOK, B; BRENNICKE, A; WISSINGER, B et al.MGG. Molecular & general genetics. 1992, Vol 232, Num 2, pp 322-327, issn 0026-8925Article

Trans splicing in oenothera mitochondrial : nad1 mRNAs are edited in exon and trans-splicing group II intron sequencesWISSINGER, B; SCHUSTER, W; BRENNICKE, A et al.Cell (Cambridge). 1991, Vol 65, Num 3, pp 473-482, issn 0092-8674, 10 p.Article

Transcripts of the NADH-dehydrogenase subunit 3 gene are differentially edited in Oenothera mitochondriaSCHUSTER, W; WISSINGER, B; UNSELD, M et al.EMBO journal (Print). 1990, Vol 9, Num 1, pp 263-269, issn 0261-4189Article

Species-specific RNA editing patterns in the mitochondrial rps13 transcripts of Oenothera and DaucusWISSINGER, B; SCHUSTER, W; BRENNICKE, A et al.MGG. Molecular & general genetics. 1990, Vol 224, Num 3, pp 389-395, issn 0026-8925, 7 p.Article

Cytochrome oxidase subunit II mRNAs in Oenothera mitochondria are edited at 24 sitesHIESEL, R; WISSINGER, B; BRENNICKE, A et al.Current genetics. 1990, Vol 18, Num 4, pp 371-375, issn 0172-8083, 5 p.Article

Surface UV from ERS-2/GOME and NOAA/AVHHR data : A case studyMEERKOETTER, R; WISSINGER, B; SECKMEYER, G et al.Geophysical research letters. 1997, Vol 24, Num 15, pp 1939-1942, issn 0094-8276Article

Differential RNA editing in closely related introns in Oenothera mitochondriaLIPPOK, B; BRENNICKE, A; WISSINGER, B et al.MGG. Molecular & general genetics. 1994, Vol 243, Num 1, pp 39-46, issn 0026-8925Article

Trans splicing integrates an exon of 22 nucleotides into the nad5 mRNA in higher plant mitochondriaKNOOP, V; SCHUSTER, W; WISSINGER, B et al.EMBO journal (Print). 1991, Vol 10, Num 11, pp 3483-3493, issn 0261-4189Article

RNA editing in plant mitochondriaHIESEL, R; WISSINGER, B; SCHUSTER, W et al.Science (Washington, D.C.). 1989, Vol 246, Num 4937, pp 1632-1634, issn 0036-8075, 3 p.Article

The NADH-dehydrogenae subunit 5 gene in Oenothera mitochondria contains two introns and is co-transcribed with the 5 S rRNA geneWISSINGER, B; HIESEL, R; SCHUSTER, W et al.MGG. Molecular & general genetics. 1988, Vol 212, Num 1, pp 56-65, issn 0026-8925Article

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyWEISSCHUH, N; WOLF, C; WISSINGER, B et al.Clinical genetics. 2008, Vol 74, Num 5, pp 476-480, issn 0009-9163, 5 p.Article

Ribosomal protein S14 transcripts are edited in Oenothera mitochondriaSCHUSTER, W; UNSELD, M; WISSINGER, B et al.Nucleic acids research. 1990, Vol 18, Num 2, pp 229-233, issn 0305-1048Article

Genotype-phenotype correlation in a german family with a novel complex CRX mutation extending the open reading framePAUNESCU, K; PREISING, M. N; JANKE, B et al.Ophthalmology (Rochester, MN). 2007, Vol 114, Num 7, pp 1348-1357, issn 0161-6420, 10 p.Article

M-cone opsin gene number does not correlate with variation in L/M-cone sensitivityKNAU, H; KREMERS, J; SCHMIDT, H.-J et al.Vision research (Oxford). 2002, Vol 42, Num 15, pp 1888-1896, issn 0042-6989Article

Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding proteinBIESALSKI, H. K; FRANK, J; BECK, S. C et al.The American journal of clinical nutrition. 1999, Vol 69, Num 5, pp 931-936, issn 0002-9165Conference Paper

Human rod monochromacy : Linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11WISSINGER, B; JÄGLE, H; ZRENNER, E et al.Genomics (San Diego, Calif.). 1998, Vol 51, Num 3, pp 325-331, issn 0888-7543Article

Fehldiagnose Lebersche Optikusneuropathie (LHON): Stellenwert klinischer und molekulargenetischer Untersuchungen = Misdiagnosis of leber's hereditary optic neuropathy (LHON) : role of clinical and molecular genetic examinationsLEO-KOTTLER, B; CHRIST-ADLER, M; WISSINGER, B et al.Der Ophthalmologe (Berlin. Print). 1998, Vol 95, Num 8, pp 549-554, issn 0941-293XConference Paper

The two human organic cation transporter genes SLC22A1 and SLC22A2 are located on chromosome 6q26KOEHLER, M. R; WISSINGER, B; GORBOULEV, V et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 3-4, pp 198-200, issn 0301-0171Article

Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutationKITIRATSCHKY, V. B. D; NAGY, D; ZABEL, T et al.British journal of ophthalmology. 2008, Vol 92, Num 8, pp 1086-1091, issn 0007-1161, 6 p.Article

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaSCHUSTER, A; WEISSCHUH, N; JÄGLE, H et al.British journal of ophthalmology. 2005, Vol 89, Num 10, pp 1258-1264, issn 0007-1161, 7 p.Article