Molecular genetics of hereditary nephritisREEDERS, S. T.Kidney international. 1992, Vol 42, Num 3, pp 783-792, issn 0085-2538Article

A modification of the ALIGN program to assist visual interpretation of mutated sequencesNADKARNI, P. M; REEDERS, S. T; JING ZHOU et al.Computer applications in the biosciences (Print). 1994, Vol 10, Num 3, pp 361-362, issn 0266-7061Article

Type IV collagen : structure, gene organization, and role in human diseases : molecular basis of goodpasture and alport syndromes and diffuse leiomyomatosisHUDSON, B. G; REEDERS, S. T; TRYGGVASON, K et al.The Journal of biological chemistry (Print). 1993, Vol 268, Num 35, pp 26033-26036, issn 0021-9258Article

Structure of the human type IV collagen COL4A6 gene, which is mutated in Alport syndrome-associated leiomyomatosisZHANG, X; ZHOU, J; REEDERS, S. T et al.Genomics (San Diego, Calif.). 1996, Vol 33, Num 3, pp 473-479, issn 0888-7543Article

Polymorphism in the APNH gene, detected by denaturing gradient gel electrophoresisDUDLEY, C. R. K; GIUFFRA, L. A; REEDERS, S. T et al.Nucleic acids research. 1990, Vol 18, Num 17, issn 0305-1048, p. 5326Article

Recent advances in the genetics of renal cystic diseaseREEDERS, S. T; GERMINO, G. G; GILLESPIE, G. A. J et al.Molecular biology & medicine. 1989, Vol 6, Num 1, pp 81-86, issn 0735-1313Article

The α4(IV) chain of basement membrane collagen : isolation of cDNAs encoding bovine α4(IV) and comparison with other type IV collagensMARIYAMA, M; KALLURI, R; HUDSON, B. G et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 2, pp 1253-1258, issn 0021-9258Article

Report of the committee on the constitution of chromosome 16REEDERS, S. T; HILDEBRAND, C. E; SUTHERLAND, G. R et al.Cytogenetics and cell genetics. 1990, Vol 55, Num 1-4, pp 194-197, issn 0301-0171, 4 p.Conference Paper

Mapping the locus of autosomal dominant polycystic kidney disease: diagnostic applicationREEDERS, S. T; GERMINO, G. G; GILLESPIE, G. A. J et al.Clinical chemistry (Baltimore, Md.). 1989, Vol 35, Num 7, pp B13-B16, issn 0009-9147Conference Paper

Complete primary structure of the sixth chain of human basement membrane collagen, α6(IV) : isolation of the cDNAS for α6(IV) and comparison with five other type IV collagen chainsJING ZHOU; MING DING; ZHIHUI ZHAO et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 18, pp 13193-13199, issn 0021-9258Article

Use of the polymerase chain reaction to clone and sequence a cDNA encoding the bovine α3 chain of type IV collagenMORRISON, K. E; GERMINO, G. G; REEDERS, S. T et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 1, pp 34-39, issn 0021-9258, 6 p.Article

Localisation of a mutation producing autosomal dominant polycystic kidney disease without renal failureRYYNANEN, M; DOLATA, M. M; LAMPAINEN, E et al.Journal of medical genetics. 1987, Vol 24, Num 8, pp 462-465, issn 0022-2593Article

Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markersSOMLO, S; WIRTH, B; COTO, E et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 1, pp 152-158, issn 0888-7543Article

Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1)HIMMELBAUER, H; POHLSCHMIDT, M; SNAREY, A et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 1, pp 35-38, issn 0888-7543Article

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)BREUNING, M. H; SNIJDEWINT, F. G. M; HYLAND, V. J et al.Journal of medical genetics. 1990, Vol 27, Num 10, pp 603-613, issn 0022-2593, 11 p.Article

45 X Turner's syndrome in association with polycystic ovaries: case reportHAGUE, W. M; ADAMS, J; REEDERS, S. T et al.British journal of obstetrics and gynaecology (Print). 1989, Vol 96, Num 5, pp 613-618, issn 0306-5456Article

Mutations in the type IV collagen α3 (COL4A3) gene in autosomal recessive Alport syndromeLEMMINK, H. H; MOCHIZUKI, T; VAN DEN HEUVEL, L. P. W et al.Human molecular genetics (Print). 1994, Vol 3, Num 8, pp 1269-1273, issn 0964-6906Article

FRA2B is distinct from inverted telomere repeat arrays at 2q13IJDO, J. W; BALDINI, A; WELLS, R. A et al.Genomics (San Diego, Calif.). 1992, Vol 12, Num 4, pp 833-835, issn 0888-7543Article

Detection of breakpoints in submicroscopic chromosomal translocation, illustrating an important mechanism for genetic diseaseLAMB, J; WILKIE, A. O. M; HARRIS, P. C et al.Lancet (British edition). 1989, Num 8667, pp 819-823, issn 0140-6736Article

Evidence linking familial thrombosis with a defective antithrombin III gene in two British kindredsSACKS, S. H; OLD, J. M; REEDERS, S. T et al.Journal of medical genetics. 1988, Vol 25, Num 1, pp 20-25, issn 0022-2593Article

Polycystin-L is a calcium-regulated cation channel permeable to calcium ionsCHEN, X.-Z; VASSILEV, P. M; BASORA, N et al.Nature (London). 1999, Vol 401, Num 6751, pp 383-386, issn 0028-0836Article

Deletion of the paired α5(IV) and α6(IV) collagen genes in inherited smooth muscle tumorsJING ZHOU; MICHIZUKI, T; SMEETS, H et al.Science (Washington, D.C.). 1993, Vol 261, Num 5125, pp 1167-1169, issn 0036-8075Article

Goodpasture syndrome : localization of the epitope for the autoantibodies to the carboxyl-terminal region of the α3(IV) chain of basement membrane collagenKALLURI, R; GUNWAR, S; REEDERS, S. T et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 35, pp 24018-24024, issn 0021-9258Article

Presymptomatic testing for adult onset polycystic kidney disease in at-risk kidney transplant donorsHANNIG, V. L; HOPKINS, J. R; JOHNSON, H. K et al.American journal of medical genetics. 1991, Vol 40, Num 4, pp 425-428, issn 0148-7299Article

Genetic linkage map of 46 DNA markers on human chromosome 16KEITH, T. P; GREEN, P; NELSON, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 15, pp 5754-5758, issn 0027-8424, 5 p.Article