Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: DAK[original query] |
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Lipoprotein lipase gene polymorphism and lipid profile in coronary artery disease. Archives of pathology & laboratory medicine 2004 Aug 128 (8): 869-74. Duman Belgin Süsleyici, Türko?lu Cavlan, Akpinar Belhhan, Güden Mustafa, Vertii Anastassia, Dak Esranur, Ca?atay Penbe, Günay Demet, Büyükdevrim A Sev |
M34T and V37I mutations in GJB2 associated hearing impairment: evidence for pathogenicity and reduced penetrance. American journal of medical genetics. Part A 2007 Nov 143A (21): 2534-43. Pollak Agnieszka, Skórka Agata, Mueller-Malesi?ska Ma?gorzata, Kostrzewa Grazyna, Kisiel Bart?omiej, Waligóra Jaros?aw, Krajewski Pawe?, O?dak Monika, Korniszewski Lech, Skarzy?ski Henryk, Ploski Raf |
GJB2 and hearing impairment: promoter defects do not explain the excess of monoallelic mutations. Journal of medical genetics 2008 Sep 45 (9): 607-8. Pollak A, Mueller-Malesinska M, Skórka A, Kostrzewa G, O?dak M, Korniszewski L, Skarzý?ski H, Ploski |
Multidrug resistance-associated protein 2 gene (ABCC2) variant in kidney allograft recipients. Transplantation proceedings 2009 Oct 41 (8): 3009-10. Pazik J, O?dak M, Sitarek E, Lewandowski Z, Maksym R, Slubowska K, P?oski R, Malejczyk J, Durlik |
Mutation analysis of mitochondrial 12S rRNA gene in Polish patients with non-syndromic and aminoglycoside-induced hearing loss. Biochemical and biophysical research communications 2010 Mar . Rydzanicz M, Wróbel M, Pollak A, Gaw?cki W, Brauze D, Kostrzewska-Poczekaj M, Wojsyk-Banaszak I, Lechowicz U, Mueller-Malesi?ska M, O?dak M, P?oski R, Skar?y?ski H, Szyfter K |
Neurotransmitter and neuromodulator genes associated with a history of depressive symptoms in individuals with alcohol dependence. Alcoholism, clinical and experimental research 2011 Mar 35 (3): 496-505. Kertes Darlene A, Kalsi Gursharan, Prescott Carol A, Kuo Po-Hsiu, Patterson Diana G, Walsh Dermot, Kendler Kenneth S, Riley Brien |
The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients. Molecular genetics and metabolism 0 104 (1-2): 153-9. Rydzanicz Ma?gorzata, Cywi?ska Karolina, Wróbel Maciej, Pollak Agnieszka, Gaw?cki Wojciech, Wojsyk-Banaszak Irena, Lechowicz Urszula, Mueller-Malesi?ska Ma?gorzata, O?dak Monika, P?oski Rafa?, Skar?y?ski Henryk, Szyfter Krzysztof, Szyfter Wito |
Lymphocyte counts in kidney allograft recipients are associated with IMPDH2 3757T>C gene polymorphism. Transplantation proceedings 2011 Oct 43 (8): 2943-5. Pazik J, O?dak M, Podgórska M, Lewandowski Z, Sitarek E, P?oski R, Szmidt J, Chmura A, Durlik M, Malejczyk |
Association of UDP-glucuronosyltransferase 1A9 (UGT1A9) gene polymorphism with kidney allograft function. Annals of transplantation : quarterly of the Polish Transplantation Society 0 16 (4): 69-73. Pazik Joanna, O?dak Monika, D?browski Marcin, Lewandowski Zbigniew, Sitarek El?bieta, Podgórska Marta, Wa?na Ewa, P?oski Rafa?, Szmidt Jacek, Chmura Andrzej, Durlik Magdalena, Malejczyk Jac |
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa. Transfusion 2013 Nov 53 (11 Suppl 2): 3009-17. Granier Thomas, Beley Sophie, Chiaroni Jacques, Bailly Pascal, Silvy Moniq |
Uridine diphosphate glucuronosyltransferase 2B7 variant p.His268Tyr as a predictor of kidney allograft early acute rejection. Transplantation proceedings 2013 May 45 (4): 1516-9. Pazik J, O?dak M, Lewandowski Z, Podgórska M, Sitarek E, P?oski R, Ga?azka Z, Kwiatkowski A, Malejczyk J, Durlik |
Recipient uridine 5'-diphospho-glucuronosyltransferase UGT1A9 c.98T>C variant determines transplanted kidney filtration rate. Transplantation proceedings 2014 Oct 46 (8): 2678-82. Pazik J, O?dak M, Lewandowski Z, D?browski M, Podgórska M, Sitarek E, Malejczyk J, P?oski R, Durlik |
Next-generation sequencing of ABCA4: High frequency of complex alleles and novel mutations in patients with retinal dystrophies from Central Europe. Experimental eye research 2015 Nov . ?cie?y?ska Aneta, Ozi?b?o Dominika, Ambroziak Anna M, Korwin Magdalena, Szulborski Kamil, Krawczy?ski Maciej, Stawi?ski Piotr, Szaflik Jerzy, Szaflik Jacek P, P?oski Rafa?, O?dak Moni |
Novel sporadic and recurrent mutations in KRT5 and KRT14 genes in Polish epidermolysis bullosa simplex patients: further insights into epidemiology and genotype-phenotype correlation. Journal of applied genetics 2015 Oct . Wertheim-Tysarowska K, O?dak M, Giza A, Kutkowska-Ka?mierczak A, Sota J, Przybylska D, Wo?niak K, ?niegórska D, Niepokój K, Sobczy?ska-Tomaszewska A, Rygiel A M, P?oski R, Bal J, Kowalewski |
Fuchs Endothelial Corneal Dystrophy: Strong Association with rs613872 Not Paralleled by Changes in Corneal Endothelial TCF4 mRNA Level. BioMed research international 2015 2015 640234. O?dak Monika, Ruszkowska Ewelina, Udziela Monika, Ozi?b?o Dominika, Bi?czyk Ewelina, ?cie?y?ska Aneta, P?oski Rafa?, Szaflik Jacek |
Application of next?generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss. Molecular medicine reports 2018 Jan 17 (1): 1782-1790. Lechowicz Urszula, Pollak Agnieszka, Fr?czak Agnieszka, Rydzanicz Ma?gorzata, Stawi?ski Piotr, Lorens Artur, Skar?y?ski Piotr H, Skar?y?ski Henryk, P?oski Rafa?, O?dak Moni |
Malnutrition Risk in Kidney Recipients Treated With Mycophenolate Mofetil Is Associated With IMPDH1 rs2278294 Polymorphism. Transplantation proceedings 0 50 (6): 1794-1797. Pazik J, Lewandowski Z, Nowacka Cieciura E, O?dak M, Podgórska M, Sadowska A, D?borska Materkowska D, Durlik |
Tinnitus in patients with hearing loss due to mitochondrial DNA pathogenic variants. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2018 Jun . Lechowicz Urszula, Pollak Agnieszka, Raj-Koziak Danuta, Dziendziel Beata, Skar?y?ski Piotr Henryk, Skar?y?ski Henryk, O?dak Moni |
Mitochondrial genome variation in male LHON patients with the m.11778G?>?A mutation. Metabolic brain disease 2020 8 35 (8): 1317-1327. Piotrowska-Nowak Agnieszka, Krawczy?ski Maciej R, Kosior-Jarecka Ewa, Ambroziak Anna M, Korwin Magdalena, O?dak Monika, To?ska Katarzyna, Bartnik E |
Prevalence, incidence and presence of comorbidities in patients with prurigo and pruritus in Germany: A population-based claims data analysis. Journal of the European Academy of Dermatology and Venereology : JEADV 2021 6 35 (11): 2270-2276. Augustin M, Garbe C, Hagenström K, Petersen J, Pereira M P, Ständer |
Functional Polymorphism of MMP9 and BDNF as Potential Biomarker of Auditory Neuroplasticity in Prelingual Deafness Treatment With Cochlear Implantation-A Retrospective Cohort Analysis. Trends in hearing 2021 3 25 23312165211002140. Matusiak Monika, Ozi?b?o Dominika, Obrycka Anita, O?dak Monika, Kaczmarek Leszek, Skar?y?ski Piotr, Skar?y?ski Henr |
Searching for the Molecular Basis of Partial Deafness. International journal of molecular sciences 2022 6 23 (11): . Ozi?b?o Dominika, Ba?dyga Natalia, Leja Marcin L, Skar?y?ski Henryk, O?dak Moni |
Prospective cohort study reveals MMP-9, a neuroplasticity regulator, as a prediction marker of cochlear implantation outcome in prelingual deafness treatment. Molecular neurobiology 2022 Jan . Matusiak Monika, Ozi?b?o Dominika, O?dak Monika, Rejmak Emilia, Kaczmarek Leszek, Skar?y?ski Piotr Henryk, Skar?y?ski Henr |
The Genetic Background of Hearing Loss in Patients with EVA and Cochlear Malformation. Genes 2023 2 14 (2): . Ba?dyga Natalia, Ozi?b?o Dominika, Gan Nina, Furmanek Mariusz, Leja Marcin L, Skar?y?ski Henryk, O?dak Moni |
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