AAAAAA
Results: 1-25/28
Authors:
ZUKIN S
BASKERVILLE R
GREENBERG M
GUTHREAU C
HALLEY J
HALLING M
LAWLER K
NERIO R
STACK R
VITALE A
WISSINGER B
Citation: S. Zukin et al., FROM CONEY ISLAND TO LAS-VEGAS IN THE URBAN IMAGINARY - DISCURSIVE PRACTICES OF GROWTH AND DECLINE, Urban affairs review, 33(5), 1998, pp. 627-654
Authors:
KOHL S
MARX T
GIDDINGS I
JAGLE H
JACOBSON SG
APFELSTEDTSYLLA E
ZRENNER E
SHARPE LT
WISSINGER B
Citation: S. Kohl et al., TOTAL COLOURBLINDNESS IS CAUSED BY MUTATIONS IN THE GENE ENCODING THEALPHA-SUBUNIT OF THE CONE PHOTORECEPTOR CGMP-GATED CATION CHANNEL, Nature genetics, 19(3), 1998, pp. 257-259
Authors:
LEOKOTTLER B
CHRISTADLER M
WISSINGER B
ZRENNER E
Citation: B. Leokottler et al., MISDIAGNOSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) - ROLE OF CLINICAL AND MOLECULAR-GENETIC EXAMINATIONS, Der Ophthalmologe, 95(8), 1998, pp. 549-554
Authors:
WISSINGER B
JAGLE H
KOHL S
BROGHAMMER M
BAUMANN B
HANNA DB
HEDELS C
APFELSTEDTSYLLA E
RANDAZZO G
JACOBSON SG
ZRENNER E
SHARPE LT
Citation: B. Wissinger et al., HUMAN ROD MONOCHROMACY - LINKAGE ANALYSIS AND MAPPING OF A CONE PHOTORECEPTOR EXPRESSED CANDIDATE GENE ON CHROMOSOME 2Q11, Genomics (San Diego, Calif.), 51(3), 1998, pp. 325-331
Authors:
WOLF S
SHARPE LT
KNAU H
WISSINGER B
Citation: S. Wolf et al., NUMBERS AND RATIOS OF X-CHROMOSOMAL-LINKED OPSIN GENES, Vision research (Oxford), 38(21), 1998, pp. 3227-3231
Authors:
WISSINGER B
SHARPE LT
Citation: B. Wissinger et Lt. Sharpe, NEW ASPECTS OF AN OLD THEME - THE GENETIC-BASIS OF HUMAN COLOR-VISION, American journal of human genetics, 63(5), 1998, pp. 1257-1262
Authors:
STRAUSS B
MEERKOETTER R
WISSINGER B
WENDLING P
HESS M
Citation: B. Strauss et al., ON THE REGIONAL CLIMATIC IMPACT OF CONTRAILS - MICROPHYSICAL AND RADIATIVE PROPERTIES OF CONTRAILS AND NATURAL CIRRUS CLOUDS, Annales geophysicae, 15(11), 1997, pp. 1457-1467
Authors:
WISSINGER B
MULLER F
WEYAND I
SCHUFFENHAUER S
THANOS S
KAUPP UB
ZRENNER E
Citation: B. Wissinger et al., CLONING, CHROMOSOMAL LOCALIZATION AND FUNCTIONAL EXPRESSION OF THE GENE ENCODING THE ALPHA-SUBUNIT OF THE CGMP-GATED CHANNEL IN HUMAN CONE PHOTORECEPTORS, European journal of neuroscience, 9(12), 1997, pp. 2512-2521
Authors:
BLIN N
SCHOLZ M
WISSINGER B
MULLENBACH R
PUSCH C
Citation: N. Blin et al., EXPRESSED SEQUENCES WITHIN PERICENTROMERIC HETEROCHROMATIN OF HUMAN-CHROMOSOME-22, Mammalian genome, 8(11), 1997, pp. 859-862
Authors:
FAUSER S
WISSINGER B
Citation: S. Fauser et B. Wissinger, SIMULTANEOUS DETECTION OF MULTIPLE POINT MUTATIONS USING FLUORESCENCE-COUPLED COMPETITIVE PRIMER EXTENSION, BioTechniques, 22(5), 1997, pp. 964-968
Authors:
KOEHLER MR
WISSINGER B
GORBOULEV V
KOEPSELL H
SCHMID M
Citation: Mr. Koehler et al., THE 2 HUMAN ORGANIC CATION TRANSPORTER GENES SLC22A1 AND SLC22A2 ARE LOCATED ON CHROMOSOME 6Q26, Cytogenetics and cell genetics, 79(3-4), 1997, pp. 198-200
Authors:
BESCH D
CHRISTADLER M
LEOKOTTLER B
ZRENNER E
WISSINGER B
Citation: D. Besch et al., SCREEN FOR MUTATIONS OF THE MITOCHONDRIAL-DNA IN PATIENTS WITH LEBERS-HEREDITARY-OPTIC-NEUROPATHY (LHON), Investigative ophthalmology & visual science, 38(4), 1997, pp. 3699-3699
Authors:
APFELSTEDTSYLLA E
MEITINGER T
MEINDL A
HERMANN K
BRANDAU O
WISSINGER B
ENGEL C
ZRENNER E
Citation: E. Apfelstedtsylla et al., RPGR MISSENSE MUTATION IN CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB), Investigative ophthalmology & visual science, 38(4), 1997, pp. 3702-3702
Authors:
WISSINGER B
WOLF S
KNAU H
ZRENNER E
SHARPE LT
Citation: B. Wissinger et al., NUMBERS AND RATIOS OF L-OPSIN AND M-OPSIN GENES IN HUMANS - EVALUATION OF DIFFERENT TECHNICAL APPROACHES, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1049-1049
Authors:
MEERKOETTER R
WISSINGER B
SECKMEYER G
Citation: R. Meerkoetter et al., SURFACE UV FROM ERS-2 GOME AND NOAA/AVHRR DATA - A CASE-STUDY/, Geophysical research letters, 24(15), 1997, pp. 1939-1942
Authors:
KOHL S
CHRISTADLER M
APFELSTEDTSYLLA E
KELLNER U
ECKSTEIN A
ZRENNER E
WISSINGER B
Citation: S. Kohl et al., RDS PERIPHERIN GENE-MUTATIONS ARE FREQUENT CAUSES OF CENTRAL RETINAL DYSTROPHIES/, Journal of Medical Genetics, 34(8), 1997, pp. 620-626
Authors:
WISSINGER B
BESCH D
BAUMANN B
FAUSER S
CHRISTADLER M
JURKLIES B
ZRENNER E
LEOKOTTLER B
Citation: B. Wissinger et al., MUTATION ANALYSIS OF THE ND6 GENE IN PATIENTS WITH LEBERS HEREDITARY OPTIC NEUROPATHY, Biochemical and biophysical research communications, 234(2), 1997, pp. 511-515
Authors:
WISSINGER B
SEELIGER MW
FRANK J
BROGHAMMER M
BIESALSKI HK
ZRENNER E
Citation: B. Wissinger et al., MUTATIONS IN THE GENE FOR SERUM RETINOL-BINDING PROTEIN IN A FAMILY WITH RETINAL DYSTROPHY, American journal of human genetics, 61(4), 1997, pp. 135-135
Authors:
LEOKOTTLER B
CHRISTADLER M
BAUMANN B
ZRENNER E
WISSINGER B
Citation: B. Leokottler et al., LEBERS HEREDITARY OPTIC NEUROPATHY - CLINICAL AND MOLECULAR-GENETIC RESULTS OBTAINED IN A FAMILY WITH A NEW POINT MUTATION AT NUCLEOTIDE POSITION-14498 IN THE ND-6 GENE, German journal of ophthalmology, 5(4), 1996, pp. 233-240
Authors:
ARNING S
APFELSTEDTSYLLA E
SEELIGER M
GENDO K
WISSINGER B
ZRENNER E
Citation: S. Arning et al., RHODOPSIN MUTATIONS IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA, Vision research, 36, 1996, pp. 439-439
Authors:
WISSINGER B
PREUSS S
CHRISTADLER M
APFELSTEDTSYLLA E
KELLNER U
ZRENNER E
Citation: B. Wissinger et al., ANALYSIS OF THE PERIPHERIN RDS-GENE IN CENTRAL RETINAL DISEASES/, Vision research, 36, 1996, pp. 441-441
Authors:
ZRENNER E
LORENZ B
WITTWER B
APFELSTEDT E
WISSINGER B
HERGERSBERG M
RUDOLPH G
HERRMANN K
ACHATZ H
MEINDL A
MEITINGER T
Citation: E. Zrenner et al., MUTATION ANALYSIS IN PATIENTS WITH X-LINKED RETINITIS-PIGMENTOSA, Vision research, 36, 1996, pp. 3231-3231
Authors:
WEBER BHF
SANDER S
KOPP C
WALKER D
ECKSTEIN A
WISSINGER B
ZRENNER E
GRIMM T
Citation: Bhf. Weber et al., ANALYSIS OF 21 STARGARDTS-DISEASE FAMILIES CONFIRMS A MAJOR LOCUS ON CHROMOSOME 1P WITH EVIDENCE FOR NON-ALLELIC HETEROGENEITY IN A MINORITY OF CASES, British journal of ophthalmology, 80(8), 1996, pp. 745-749
Authors:
WISSINGER B
ZRENNER E
Citation: B. Wissinger et E. Zrenner, IDENTIFICATION OF THE GENE ENCODING THE ALPHA-SUBUNIT OF THE CGMP GATED CATION CHANNEL IN HUMAN CONE PHOTORECEPTORS, Investigative ophthalmology & visual science, 36(4), 1995, pp. 278-278
Authors:
CHRISTADLER M
LEOKOTTLER B
BAUMANN B
FAUSER S
ZRENNER E
WISSINGER B
Citation: M. Christadler et al., A NEW MUTATION IN THE MITOCHONDRIAL ND6 GENE IN A FAMILY WITH LEBERS HEREDITARY OPTIC NEUROPATHY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 675-675