Markus Pfister, M.D. - Publications

Faculty of Medicine Eberhard Karls Universität Tübingen, Tübingen, Baden-Württemberg, Germany 

62 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2020 Budde BS, Aly MA, Mohamed MR, Breß A, Altmüller J, Motameny S, Kawalia A, Thiele H, Konrad K, Becker C, Toliat MR, Nürnberg G, Sayed EAF, Mohamed ES, Pfister M, et al. Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clinical Genetics. PMID 32279305 DOI: 10.1111/Cge.13754  0.392
2017 Neuhaus C, Eisenberger T, Decker C, Nagl S, Blank C, Pfister M, Kennerknecht I, Müller-Hofstede C, Charbel Issa P, Heller R, Beck B, Rüther K, Mitter D, Rohrschneider K, Steinhauer U, et al. Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and PEX26 mutated in Heimler syndrome. Molecular Genetics & Genomic Medicine. 5: 531-552. PMID 28944237 DOI: 10.1002/Mgg3.312  0.362
2015 Hassan MA, Shah AA, Szmida E, Smigiel R, Sasiadek MM, Pfister M, Blin N, Bress A. A TMC1 (transmembrane channel-like 1) mutation (p.S320R) in a Polish family with hearing impairment. Journal of Applied Genetics. PMID 25560804 DOI: 10.1007/S13353-014-0263-4  0.417
2014 Dettling J, Franz C, Zimmermann U, Lee SC, Bress A, Brandt N, Feil R, Pfister M, Engel J, Flamant F, Rüttiger L, Knipper M. Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells. Molecular and Cellular Endocrinology. 382: 26-37. PMID 24012852 DOI: 10.1016/J.Mce.2013.08.025  0.355
2011 Lubka-Pathak M, Shah AA, Gallozzi M, Müller M, Zimmermann U, Löwenheim H, Pfister M, Knipper M, Blin N, Schimmang T. Altered expression of securin (Pttg1) and serpina3n in the auditory system of hearing-impaired Tff3-deficient mice. Cellular and Molecular Life Sciences : Cmls. 68: 2739-49. PMID 21076990 DOI: 10.1007/S00018-010-0586-1  0.355
2010 Mohamed MR, Alesutan I, Föller M, Sopjani M, Bress A, Baur M, Salama RH, Bakr MS, Mohamed MA, Blin N, Lang F, Pfister M. Functional analysis of a novel I71N mutation in the GJB2 gene among Southern Egyptians causing autosomal recessive hearing loss. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 26: 959-66. PMID 21220926 DOI: 10.1159/000324004  0.408
2010 Xia A, Gao SS, Yuan T, Osborn A, Bress A, Pfister M, Maricich SM, Pereira FA, Oghalai JS. Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation. Disease Models & Mechanisms. 3: 209-23. PMID 20142329 DOI: 10.1242/Dmm.004135  0.404
2010 Mallur PS, Weisstuch A, Pfister M, Mhatre AN, Lalwani AK. Aquaporin-2 and -4: Single nucleotide polymorphisms in Ménire's disease patients Audiological Medicine. 8: 18-23. DOI: 10.3109/16513860903574232  0.303
2010 Zak M, Bress A, Pfister M, Knipper M, Blin N. ERGIC2, a new member of the OTOF interactome connected with the DFNB9 form of hearing impairment New Biotechnology. 27. DOI: 10.1016/J.Nbt.2010.01.172  0.323
2009 Baur M, Fransen E, Tropitzsch A, van Laer L, Mauz PS, Van Camp G, Blin N, Pfister M. [Influence of exogenic factors on age-related hearing impairment]. Hno. 57: 1023-8. PMID 19730805 DOI: 10.1007/S00106-009-1900-9  0.311
2009 Winter H, Rüttiger L, Müller M, Kuhn S, Brandt N, Zimmermann U, Hirt B, Bress A, Sausbier M, Conscience A, Flamant F, Tian Y, Zuo J, Pfister M, Ruth P, et al. Deafness in TRbeta mutants is caused by malformation of the tectorial membrane. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2581-7. PMID 19244534 DOI: 10.1523/Jneurosci.3557-08.2009  0.351
2009 Friedman RA, Van Laer L, Huentelman MJ, Sheth SS, Van Eyken E, Corneveaux JJ, Tembe WD, Halperin RF, Thorburn AQ, Thys S, Bonneux S, Fransen E, Huyghe J, Pyykkö I, Cremers CW, ... ... Pfister M, et al. GRM7 variants confer susceptibility to age-related hearing impairment. Human Molecular Genetics. 18: 785-96. PMID 19047183 DOI: 10.1093/Hmg/Ddn402  0.317
2008 Heidrych P, Zimmermann U, Bress A, Pusch CM, Ruth P, Pfister M, Knipper M, Blin N. Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form. Human Molecular Genetics. 17: 3814-21. PMID 18772196 DOI: 10.1093/Hmg/Ddn279  0.312
2008 Huyghe JR, Van Laer L, Hendrickx JJ, Fransen E, Demeester K, Topsakal V, Kunst S, Manninen M, Jensen M, Bonaconsa A, Mazzoli M, Baur M, Hannula S, Mäki-Torkko E, Espeso A, ... ... Pfister M, et al. Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. American Journal of Human Genetics. 83: 401-7. PMID 18760390 DOI: 10.1016/J.Ajhg.2008.08.002  0.302
2008 Fransen E, Topsakal V, Hendrickx JJ, Van Laer L, Huyghe JR, Van Eyken E, Lemkens N, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Tropitzsch A, Bonaconsa A, Mazzoli M, Espeso A, ... ... Pfister M, et al. Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study. Journal of the Association For Research in Otolaryngology : Jaro. 9: 264-76; discussion 2. PMID 18543032 DOI: 10.1007/S10162-008-0123-1  0.341
2008 Lubka M, Müller M, Baus-Loncar M, Hinz M, Blaschke K, Hoffmann W, Pfister M, Löwenheim H, Pusch CM, Knipper M, Blin N. Lack of Tff3 peptide results in hearing impairment and accelerated presbyacusis. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 21: 437-44. PMID 18453751 DOI: 10.1159/000129636  0.378
2008 Van Laer L, Van Eyken E, Fransen E, Huyghe JR, Topsakal V, Hendrickx JJ, Hannula S, Mäki-Torkko E, Jensen M, Demeester K, Baur M, Bonaconsa A, Mazzoli M, Espeso A, Verbruggen K, ... ... Pfister M, et al. The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment. Human Molecular Genetics. 17: 159-69. PMID 17921507 DOI: 10.1093/Hmg/Ddm292  0.333
2008 Brosch S, Rauffeisen A, Baur M, Michels L, Trefz FK, Pfister M. [Propionic acidemia and sensorineural hearing loss: is there a connection at the molecular genetics level?]. Hno. 56: 37-42. PMID 17415538 DOI: 10.1007/S00106-007-1560-6  0.323
2007 Tóth T, Kupka S, Haack B, Fazakas F, Muszbek L, Blin N, Pfister M, Sziklai I. Coincidence of mutations in different connexin genes in Hungarian patients. International Journal of Molecular Medicine. 20: 315-21. PMID 17671735 DOI: 10.3892/Ijmm.20.3.315  0.381
2007 Brosch S, Baur M, Blin N, Reinert S, Pfister M. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome. International Journal of Molecular Medicine. 20: 85-9. PMID 17549393 DOI: 10.3892/Ijmm.20.1.85  0.359
2007 Van Eyken E, Van Camp G, Fransen E, Topsakal V, Hendrickx JJ, Demeester K, Van De Heyning P, Mäki-Torkko E, Hannula S, Sorri M, Jensen M, Parving A, Bille M, Baur M, Pfister M, et al. Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment Journal of Medical Genetics. 44: 570-578. PMID 17513527 DOI: 10.1136/Jmg.2007.049205  0.316
2007 Chen W, Meyer NC, Mckenna MJ, Pfister M, McBride DJ, Fukushima K, Thys M, Camp GV, Smith RJH. Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosis Clinical Genetics. 71: 406-414. PMID 17489845 DOI: 10.1111/J.1399-0004.2007.00794.X  0.372
2006 Schug N, Braig C, Zimmermann U, Engel J, Winter H, Ruth P, Blin N, Pfister M, Kalbacher H, Knipper M. Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat. The European Journal of Neuroscience. 24: 3372-80. PMID 17229086 DOI: 10.1111/J.1460-9568.2006.05225.X  0.317
2006 Vrijens K, Thys S, De Jeu MT, Postnov AA, Pfister M, Cox L, Zwijsen A, Van Hoof V, Mueller M, De Clerck NM, De Zeeuw CI, Van Camp G, Van Laer L. Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome. Neurobiology of Disease. 24: 28-40. PMID 16875832 DOI: 10.1016/J.Nbd.2006.04.016  0.372
2006 Frey A, Lampert A, Waldegger S, Jeck N, Waldegger P, Artunc F, Seebohm G, Lang UE, Kupka S, Pfister M, Hoppe J, Gerloff C, Schaeffeler E, Schwab M, Lang F. Influence of gain of function epithelial chloride channel ClC-Kb mutation on hearing thresholds. Hearing Research. 214: 68-75. PMID 16549283 DOI: 10.1016/J.Heares.2006.02.001  0.39
2006 Palmada M, Schmalisch K, Böhmer C, Schug N, Pfister M, Lang F, Blin N. Loss of function mutations of the GJB2 gene detected in patients with DFNB1-associated hearing impairment Neurobiology of Disease. 22: 112-118. PMID 16300957 DOI: 10.1016/J.Nbd.2005.10.005  0.391
2006 Tóth T, Pfister M, Zenner HP, Sziklai I. Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment. International Journal of Pediatric Otorhinolaryngology. 70: 201-6. PMID 16043233 DOI: 10.1016/J.Ijporl.2005.06.011  0.397
2005 Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, ... ... Pfister M, et al. GJB2 mutations and degree of hearing loss: a multicenter study. American Journal of Human Genetics. 77: 945-57. PMID 16380907 DOI: 10.1086/497996  0.41
2005 Yang T, Pfister M, Blin N, Zenner HP, Pusch CM, Smith RJ. Genetic heterogeneity of deafness phenotypes linked to DFNA4. American Journal of Medical Genetics. Part A. 139: 9-12. PMID 16222661 DOI: 10.1002/Ajmg.A.30989  0.375
2005 Van Laer L, Pfister M, Thys S, Vrijens K, Mueller M, Umans L, Serneels L, Van Nassauw L, Kooy F, Smith RJ, Timmermans JP, Van Leuven F, Van Camp G. Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells. Neurobiology of Disease. 19: 386-99. PMID 16023581 DOI: 10.1016/J.Nbd.2005.01.019  0.371
2005 Schulte C, Geisthoff U, Lux A, Kupka S, Zenner HP, Blin N, Pfister M. High frequency of ENG and ALK1/ACVRL1 mutations in German HHT patients. Human Mutation. 25: 595. PMID 15880681 DOI: 10.1002/Humu.9345  0.371
2005 Kupka S, Bodden-Kamps B, Baur M, Zenner HP, Pfister M. [Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment]. Hno. 52: 968-72. PMID 15309320 DOI: 10.1007/S00106-003-0994-8  0.365
2004 Rüttiger L, Sausbier M, Zimmermann U, Winter H, Braig C, Engel J, Knirsch M, Arntz C, Langer P, Hirt B, Müller M, Köpschall I, Pfister M, Münkner S, Rohbock K, et al. Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing loss. Proceedings of the National Academy of Sciences of the United States of America. 101: 12922-7. PMID 15328414 DOI: 10.1073/Pnas.0402660101  0.368
2004 Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S. A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 14: 369-76. PMID 15319541 DOI: 10.1159/000080347  0.388
2004 Riemann K, Pfister M, Blin N, Kupka S. Mitochondrial hearing impairment. Background, genetic predisposition and diagnostic possibilities | Mitochondrial bedingte schwerhörigkeiten. Hintergründe, genetische prädisposition und möglichkeiten der diagnostik Hno. 52: 503-509. PMID 15241512 DOI: 10.1007/S00106-003-0993-9  0.339
2004 Tóth T, Kupka S, Haack B, Riemann K, Braun S, Fazakas F, Zenner HP, Muszbek L, Blin N, Pfister M, Sziklai I. GJB2 mutations in patients with non-syndromic hearing loss from Northeastern Hungary. Human Mutation. 23: 631-2. PMID 15146474 DOI: 10.1002/Humu.9250  0.37
2004 Riemann K, Sotlar K, Kupka S, Braun S, Zenner HP, Preyer S, Pfister M, Pusch CM, Blin N. Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases. Cancer Genetics and Cytogenetics. 150: 128-35. PMID 15066320 DOI: 10.1016/J.Cancergencyto.2003.10.013  0.322
2004 Pusch CM, Meyer B, Kupka S, Smith RJ, Lalwani AK, Zenner HP, Blin N, Nürnberg P, Pfister M. Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33. Journal of Molecular Medicine (Berlin, Germany). 82: 398-402. PMID 15042303 DOI: 10.1007/S00109-004-0538-Z  0.356
2004 Donaudy F, Snoeckx R, Pfister M, Zenner HP, Blin N, Di Stazio M, Ferrara A, Lanzara C, Ficarella R, Declau F, Pusch CM, Nürnberg P, Melchionda S, Zelante L, Ballana E, et al. Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). American Journal of Human Genetics. 74: 770-6. PMID 15015131 DOI: 10.1086/383285  0.429
2004 Tóth T, Kupka S, Nürnberg P, Thiele H, Zenner HP, Sziklai I, Pfister M. Phenotypic characterization of a DFNA6 family showing low-frequency sensorineural hearing impairment | Phänotypische charakterisierung einer DFNA6-familie mit tieftonschwerhörigkeit Hno. 52: 132-136. PMID 14968315 DOI: 10.1007/S00106-003-0912-0  0.438
2004 Braun S, Riemann K, Pusch CM, Sotlar K, Pfister M, Kupka S. Paragangliomas of the head and neck region. Review of past and future molecular genetic research | Paragangliome der kopf-hals-region. Ein überblick über die molekulargenetische forschung Hno. 52: 11-17. PMID 14740109 DOI: 10.1007/S00106-003-0959-Y  0.307
2003 Oh N, Kupka S, Mirghomizadeh F, Arold R, Zimmermann R, Blin N, Zenner HP, Pfister M. Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3) | Klinische und molekulargenetische analyse monozygoter zwillinge mit stapes-gusher-syndrom (DFN3) Hno. 51: 629-633. PMID 12942177 DOI: 10.1007/S00106-002-0777-7  0.33
2003 Tóth T, Kupka S, Sziklai I, Blin N, Zenner HP, Pfister M. Phenotype of patients showing hearing impairment based on the 35delG mutation in the connexin 26 gene | Phänotypische charakterisierung schwerhöriger patienten mit homozygoter 35delG-mutation im connexin-26-gen Hno. 51: 400-404. PMID 12835856 DOI: 10.1007/S00106-002-0737-2  0.4
2003 Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJ, Timmermans JP, Van Camp G. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochemistry and Cell Biology. 119: 247-56. PMID 12649740 DOI: 10.1007/S00418-003-0495-6  0.411
2003 Mirghomizadeh F, Pfister M, Blin N, Pusch CM. Uncommon cytidine-homopolymer dimorphism in 5'-UTR of the human otoferlin gene. International Journal of Molecular Medicine. 11: 63-4. PMID 12469219 DOI: 10.3892/Ijmm.11.1.63  0.373
2002 Pfister M, Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S. A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10. Molecular Medicine (Cambridge, Mass.). 8: 607-11. PMID 12477971 DOI: 10.1007/Bf03402171  0.379
2002 Maassen MM, Pfister M, Plontke S, Koitschev A, Vögler A, Löwenheim H. Recovery of hearing: Results of delayed medical treatment in patients with idiopathic sudden hearing loss | Erholung der hörschwelle bei verzögert einsetzender therapie des hörsturzes Hno. 50: 1062-1067. PMID 12474128 DOI: 10.1007/S00106-002-0653-5  0.34
2002 Tóth T, Kupka S, Blin N, Pfister M, Sziklai I. [Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary]. Orvosi Hetilap. 143: 2285-9. PMID 12420583  0.314
2002 Mirghomizadeh F, Pfister M, Apaydin F, Petit C, Kupka S, Pusch CM, Zenner HP, Blin N. Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness. Neurobiology of Disease. 10: 157-64. PMID 12127154 DOI: 10.1006/Nbdi.2002.0488  0.367
2002 Kupka S, Braun S, Aberle S, Haack B, Ebauer M, Zeissler U, Zenner HP, Blin N, Pfister M. Frequencies of GJB2 mutations in German control individuals and patients showing sporadic non-syndromic hearing impairment. Human Mutation. 20: 77-8. PMID 12112666 DOI: 10.1002/Humu.9044  0.404
2002 Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, et al. Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110: 389-94. PMID 12073007 DOI: 10.1007/S00439-002-0719-1  0.425
2002 Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N. Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation. European Journal of Human Genetics : Ejhg. 10: 95-9. PMID 11938438 DOI: 10.1038/Sj.Ejhg.5200769  0.342
2002 Kupka S, Tóth T, Wróbel M, Zeissler U, Szyfter W, Szyfter K, Niedzielska G, Bal J, Zenner HP, Sziklai I, Blin N, Pfister M. Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients. Human Mutation. 19: 308-9. PMID 11857751 DOI: 10.1002/Humu.9017  0.409
2001 Tóth T, Kupka S, Esmer H, Zeissler U, Sziklai I, Zenner HP, Blin N, Pfister M. Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairment International Journal of Molecular Medicine. 8: 189-192. PMID 11445873 DOI: 10.3892/Ijmm.8.2.189  0.438
2001 Lin D, Goldstein JA, Mhatre AN, Lustig LR, Pfister M, Lalwani AK. Assessment of denaturing high-performance liquid chromatography (DHPLC) in screening for mutations in connexin 26 (GJB2). Human Mutation. 18: 42-51. PMID 11438992 DOI: 10.1002/Humu.1148  0.339
2000 Pfister M, Lalwani AK. DFN4: non-syndromic autosomal dominant X-linked sensorineural hearing impairment. Advances in Oto-Rhino-Laryngology. 56: 196-9. PMID 10868235 DOI: 10.1159/000059102  0.327
1999 Seeliger M, Pfister M, Gendo K, Paasch S, Apfelstedt-Sylla E, Plinkert P, Zenner HP, Zrenner E. Comparative study of visual, auditory, and olfactory function in Usher syndrome. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fã¼R Klinische Und Experimentelle Ophthalmologie. 237: 301-7. PMID 10208263 DOI: 10.1007/S004170050237  0.326
1998 Apaydin F, Pfister M, Iber M, Kandogan T, Leal SM, Brändle U, Cura O, Zenner HP. Initial experience with the identification of families with hereditary hearing loss in Turkey | Hereditare schwerhorigkeit in der Turkei erste ergebnisse Hno. 46: 809-814. PMID 9816535 DOI: 10.1007/S001060050317  0.382
1998 Leal SM, Apaydin F, Barnwell C, Iber M, Kandogan T, Pfister M, Braendle U, Cura O, Schwalb M, Zenner HP, Vitale E. A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9 European Journal of Human Genetics. 6: 341-344. PMID 9781041 DOI: 10.1038/Sj.Ejhg.5200201  0.344
1997 Pfister M, Maier H, Gummer AW, Preyer S. [In vivo cochleoscopy through the round window]. Hno. 45: 216-21. PMID 9221261 DOI: 10.1007/S001060050107  0.577
1994 Preyer S, Hemmert W, Pfister M, Zenner HP, Gummer AW. Frequency response of mature guinea-pig outer hair cells to stereociliary displacement. Hearing Research. 77: 116-24. PMID 7928723 DOI: 10.1016/0378-5955(94)90259-3  0.667
1993 Preyer S, Pfister M, Hemmert W. [Mechanical stimulation of isolated outer hair cells as a test system. Inhibition of transduction by streptomycin treatment]. Hno. 41: 471-4. PMID 7693630  0.581
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