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Page 1
Location of mutations within the PKD2 gene influences clinical outcome.
Hateboer N, Veldhuisen B, Peters D, Breuning MH, San-Millán JL, Bogdanova N, Coto E, van Dijk MA, Afzal AR, Jeffery S, Saggar-Malik AK, Torra R, Dimitrakov D, Martinez I, de Castro SS, Krawczak M, Ravine D. Hateboer N, et al. Among authors: bogdanova n. Kidney Int. 2000 Apr;57(4):1444-51. doi: 10.1046/j.1523-1755.2000.00989.x. Kidney Int. 2000. PMID: 10760080 Free article.
A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2).
Veldhuisen B, Saris JJ, de Haij S, Hayashi T, Reynolds DM, Mochizuki T, Elles R, Fossdal R, Bogdanova N, van Dijk MA, Coto E, Ravine D, Nørby S, Verellen-Dumoulin C, Breuning MH, Somlo S, Peters DJ. Veldhuisen B, et al. Among authors: bogdanova n. Am J Hum Genet. 1997 Sep;61(3):547-55. doi: 10.1086/515497. Am J Hum Genet. 1997. PMID: 9326320 Free PMC article.
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney disease.
Schiavello T, Burke V, Bogdanova N, Jasik P, Melsom S, Boudville N, Robertson K, Angelicheva D, Dworniczak B, Lemmens M, Horst J, Todorov V, Dimitrakov D, Sulowicz W, Krasniak A, Stompor T, Beilin L, Hallmayer J, Kalaydjieva L, Thomas M. Schiavello T, et al. Among authors: bogdanova n. Nephrol Dial Transplant. 2001 Dec;16(12):2323-7. doi: 10.1093/ndt/16.12.2323. Nephrol Dial Transplant. 2001. PMID: 11733623
Genetic heterogeneity of polycystic kidney disease in Bulgaria.
Bogdanova N, Dworniczak B, Dragova D, Todorov V, Dimitrakov D, Kalinov K, Hallmayer J, Horst J, Kalaydjieva L. Bogdanova N, et al. Hum Genet. 1995 Jun;95(6):645-50. doi: 10.1007/BF00209481. Hum Genet. 1995. PMID: 7789949
Chromosomal evolution of the PKD1 gene family in primates.
Kirsch S, Pasantes J, Wolf A, Bogdanova N, Münch C, Markoff A, Pennekamp P, Krawczak M, Dworniczak B, Schempp W. Kirsch S, et al. Among authors: bogdanova n. BMC Evol Biol. 2008 Sep 26;8:263. doi: 10.1186/1471-2148-8-263. BMC Evol Biol. 2008. PMID: 18822117 Free PMC article.
Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in russian charcot-marie-tooth neuropathy patients; irina V. Mersiyanova, sookhrat M. Ismailov, alexandr V. Polyakov, elena L. Dadali, valeriy P. Fedotov, eva nelis, ann Lofgren, vincent timmerman, christine van broeckhoven, and oleg V. Evgrafov (Article was originally published in human mutation 15:340-347, 2000).
Bogdanova N, McCluskey M, Sikmann K, Markoff A, Todorov V V, Dimitrakov D, Schiavello T, Thomas M, Kalaydjieva L, Dworniczak B, Horst J. Bogdanova N, et al. Hum Mutat. 2000;16(2):175. doi: 10.1002/1098-1004(200008)16:2<175::AID-HUMU10>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10923039
400 results