mutation
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Comprehensive Analysis of PTEN in Primary Cutaneous Melanoma
Kristýna Němejcová, P. Dundr, R. Jakša, M. Bártů, I. Stružinská, J. Hojný, N. Hájková, O. Kodet
2020, Vol. 66, Issue 1, pp. 7-16 -
Mutational Analysis of the NPHS2 Gene in Czech Patients with Idiopathic Nephrotic Syndrome
Jana Reiterová, H. Šafránková, L. Obeidová, J. Štekrová, D. Maixnerová, M. Merta, V. Tesař
2012, Vol. 58, Issue 2, pp. 64-68 -
CCAAT/Enhancer-Binding Protein α (CEBPA) Polymorphisms and Mutations in Healthy Individuals and in Patients with Peripheral Artery Disease, Ischaemic Heart Disease and Hyperlipidaemia
Ota Fuchs, A. Kostečka, D. Provazníková, B. Krásná, R. Kotlín, M. Staňková, P. Kobylka, G. Dostálová, M. Zeman, M. Chochola
2010, Vol. 56, Issue 2, pp. 51-57 -
Apolipoprotein E Arg136 → Cys in Individuals with Premature Myocardial Infarction
Jaroslav A. Hubáček, R. Poledne, J. Piťha, M. Aschermann, H. Skalická, V. Staněk
2009, Vol. 55, Issue 3, pp. 116-118 -
Leukaemia Inhibitory Factor (LIF) Gene Mutations in Women Diagnosed with Unexplained Infertility and Endometriosis Have a Negative Impact on the IVF Outcome A Pilot Study
Z. Novotný, J. Křížan, R. Šíma, P. Šíma, P. Uher, N. Zech, R. Hüttelová, P. Baborová, Z. Ulčová-Gallová, I. Šubrt, E. Ulmanová, Z. Houdek, Z. Rokyta, V. Babuška, Milena Králíčková
2009, Vol. 55, Issue 3, pp. 92-97 -
Lack of B-RAF Mutations in Head and Neck Squamous Cell Carcinoma
M. Al Sheikh Ali, Mehmet Gunduz, E. Gunduz, R. Tamamura, L. Beder, S. Tominaga, T. Onoda, N. Yamanaka, R. Grenman, K. Shimizu, N. Nagai, H. Nagatsuka
2008, Vol. 54, Issue 5, pp. 157-161
