The polymerase chain reaction: an improved method for the analysis of nucleic acidsVOSBERG, H.-P.Human genetics. 1989, Vol 83, Num 1, pp 1-15, issn 0340-6717Article

Characterization of a human genomic DNA fragment coding for a myosin heavy chainAPPELHANS, H; VOSBERG, H.-P.Human genetics. 1983, Vol 65, Num 2, pp 198-203, issn 0340-6717Article

Characterisation of size variants of type I DNA topoisomerase isolated from calf thymusSCHMITT, B; BUHRE, U; VOSBERG, H.-P et al.European journal of biochemistry (Print). 1984, Vol 144, Num 1, pp 127-134, issn 0014-2956Article

The regulation of the human β myosin heavy-chain geneVOSBERG, H.-P; HORSTMANN-HEROLD, U; WETTSTEIN, A et al.Basic research in cardiology. 1992, Vol 87, pp 161-173, issn 0300-8428, SUP1Article

Relaxation of supercoiled phosphorothioate DNA by mammalian topoisomerases is inhibited in a base-specific mannerDARBY, N. K; VOSBERG, H.-P.The Journal of biological chemistry (Print). 1985, Vol 260, Num 7, pp 4501-4507, issn 0021-9258Article

Chromosomal localization of a human myosin heavy-chain gene by in situ hybridizationRAPPOLD, G. A; VOSBERG, H.-P.Human genetics. 1983, Vol 65, Num 2, pp 195-197, issn 0340-6717Article

A polymorphism of the MYH7 geneSIEWERSTEN, M. A; VOSBERG, H.-P; COX, D. W et al.Nucleic acids research. 1990, Vol 18, Num 20, issn 0305-1048, p. 6173Article

Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the β-myosin heavy chain gene and cardiac arrest in childhood a case report and family studyDOHLEMANN, C; HEBE, J; MEITINGER, T et al.Zeitschrift für Kardiologie (Print). 2000, Vol 89, Num 7, pp 612-619, issn 0300-5860Article

Mapping of the actomyosin interfacesELDIN, P; LE CUNFF, M; VOSBERG, H. P et al.Proceedings of the National Academy of Sciences of the United States of America. 1994, Vol 91, Num 7, pp 2772-2776, issn 0027-8424Conference Paper

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C geneORTLEPP, J. R; VOSBERG, H. P; REITH, S et al.Heart (London 1996). 2002, Vol 87, Num 3, pp 270-275, issn 1355-6037Article

Regulation of myosin heavy chain expression in the hearts of hypertension rats by testosteroneMORANO, I; GERSTNER, J; RUÊEGG, J. C et al.Circulation research. 1990, Vol 66, Num 6, pp 1585-1590, issn 0009-7330, 6 p.Article

Direct sequencing of polymerase chain reaction amplified DNA fragments through the incorporation of deoxynucleoside α-thiotriphosphatesNAKAMAYE, K. L; GISH, G; ECKSTEIN, F et al.Nucleic acids research. 1988, Vol 16, Num 21, pp 9947-9959, issn 0305-1048Article

Identification of gene defects by linkage analysis : use in inherited cardiomyopathiesVOSBERG, H.-P.European heart journal. 1994, Vol 15, Num DEC, pp 20-23, issn 0195-668X, SUPDConference Paper

Isolation and characterization of the complete human β-myosin heavy chain geneDIEDERICH, K. W; EISELE, I; RIED, T et al.Human genetics. 1989, Vol 81, Num 3, pp 214-220, issn 0340-6717Article

DNA topoisomerase II cleaves at specific sites in the 5' flanking region of c-fos proto-oncogenes in vitroDARBY, M. K; HERRERA, R. F; VOSBERG, H.-P et al.EMBO journal (Print). 1986, Vol 5, Num 9, pp 2257-2265, issn 0261-4189Article

Partial characterization of the human β-myosin heavy-chain gene which is expressed in heart and skeletal muscleLICHTER, P; UMEDA, P. K; LEVIN, J. E et al.European journal of biochemistry (Print). 1986, Vol 160, Num 2, pp 419-426, issn 0014-2956Article

Inhibition of calf thymus type II DNA topoisomerase by poly(ADP-ribosylation)DARBY, M. K; SCHMITT, B; JONGSTRA-BILEN, J et al.EMBO journal (Print). 1985, Vol 4, Num 8, pp 2129-2134, issn 0261-4189Article

Analysis of a dystrophin gene deletion by amplification of mRNA isolated from DMD myotubes cultured in vitroEHRENPREIS, J; HILLERS, M; JUNKES, B et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 3, pp 551-557, issn 0888-7543, 7 p.Article

A molecular basis for familial hypertrophic cardiomyopathy : a β cardiac myosin heavy chain gene missense mutationGEISTERFER-LOWRANCE, A. A. T; KASS, S; TANIGAWA, G et al.Cell (Cambridge). 1990, Vol 62, Num 5, pp 999-1006, issn 0092-8674, 8 p.Article

Scl 70 autoantibodies from scleroderma patients recognize a 95 kDa protein identified as DNA topoisomerase IGULDNER, H.-H; SZOSTECKI, C; VOSBERG, H.-P et al.Chromosoma (Berlin. Print). 1986, Vol 94, Num 2, pp 132-138, issn 0009-5915Article

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated β-myosin heavy chain genesJESCHKE, B; UHL, K; WEIST, B et al.Human genetics. 1998, Vol 102, Num 3, pp 299-304, issn 0340-6717Article

A molecular basis for familial hypertrophic cardiomyopathy : an α/β cardiac myosin heavy chain hybrid geneTANIGAWA, G; JARCHO, J. A; KASS, S et al.Cell (Cambridge). 1990, Vol 62, Num 5, pp 991-998, issn 0092-8674, 8 p.Article

Expression of human β-myosin heavy chain fragments in Escherichia coli ; localization of actin interfaces on cardiac myosinELDIN, P; LE CUNFF, M; DIEDERICH, K. W et al.Journal of muscle research and cell motility. 1990, Vol 11, Num 5, pp 378-391, issn 0142-4319, 14 p.Article

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetranceMOOLMAN, J. A; REITH, S; VOSBERG, H.-P et al.Circulation (New York, N.Y.). 2000, Vol 101, Num 12, pp 1396-1402, issn 0009-7322Article

Clinical features of hypertrophic cardiomyopathy caused by mutation of a hot spot in the alpha-tropomyosin geneCOVIELLO, D. A; MARON, B. J; SPIRITO, P et al.Journal of the American College of Cardiology. 1997, Vol 29, Num 3, pp 635-640, issn 0735-1097Article