1 - 25 of 40 results for author:"Slowik A." in Literature citations
Results Customize
› Repeat search in UniProtKB (1)
| Genetic variation at CR1 increases risk of cerebral amyloid angiopathy. Biffi A., Shulman J.M., Jagiella J.M., Cortellini L., Ayres A.M., Schwab K., Brown D.L., Silliman S.L., Selim M., Worrall B.B. et al. Neurology 78:334-341(2012) · Mapped (26) |
| Platelets display potent antimicrobial activity and release human beta-defensin 2. Tohidnezhad M., Varoga D., Wruck C.J., Podschun R., Sachweh B.H., Bornemann J., Bovi M., Sonmez T.T., Slowik A., Houben A. et al. Platelets 23:217-223(2012) · Mapped (1) |
| Paraoxonase 1 gene polymorphisms do not influence the response to treatment in Alzheimer's disease. Klimkowicz-Mrowiec A., Marona M., Spisak K., Jagiella J., Wolkow P., Szczudlik A., Slowik A. Dement Geriatr Cogn Disord 32:26-31(2011) · Mapped (3) |
| Circulating activated factor XI and active tissue factor as predictors of worse prognosis in patients following ischemic cerebrovascular events. Undas A., Slowik A., Gissel M., Mann K.G., Butenas S. Thromb. Res. 128:e62-6(2011) · Mapped (9) |
| Paraoxonase gene polymorphism and the risk for Alzheimer's disease in the polish population. Klimkowicz-Mrowiec A., Marona M., Wolkow P., Witkowski A., Maruszak A., Styczynska M., Barcikowska M., Szczudlik A., Slowik A. Dement Geriatr Cogn Disord 31:417-423(2011) · Mapped (11) |
| APOE genotype and extent of bleeding and outcome in lobar intracerebral haemorrhage: a genetic association study. International Stroke Genetics Consortium Lancet Neurol 10:702-709(2011) · Mapped (5) |
| The rs2200733 variant on chromosome 4q25 is a risk factor for cardioembolic stroke related to atrial fibrillation in Polish patients. Wnuk M., Pera J., Jagiella J., Szczygiel E., Ferens A., Spisak K., Wolkow P., Kmiec M., Burkot J., Chrzanowska-Wasko J. et al. Neurol. Neurochir. Pol. 45:148-152(2011) · Mapped (2) |
| Interleukin 6-174G>C polymorphism and risk of aneurysmal subarachnoid hemorrhage: case-control study and meta-analysis. Pera J., Dziedzic T., Adamski M., Jagiella J., Krupa M., Moskala M., Szczudlik A., Slowik A. Acta Neurol. Scand. 125:111-115(2012) · Mapped (5) |
| The formyl peptide receptor like-1 and scavenger receptor MARCO are involved in glial cell activation in bacterial meningitis. Braun B.J., Slowik A., Leib S.L., Lucius R., Varoga D., Wruck C.J., Jansen S., Podschun R., Pufe T., Brandenburg L.O. J Neuroinflammation 8:11-11(2011) · Mapped (5) |
| Interleukin-6 gene (-174 C/G ) and apolipoprotein E gene polymorphisms and the risk of Alzheimer disease in a Polish population. Klimkowicz-Mrowiec A., Wolkow P., Spisak K., Maruszak A., Styczynska M., Barcikowska M., Szczudlik A., Slowik A. Neurol. Neurochir. Pol. 44:537-541(2010) · Mapped (9) |
| Lack of association between VEGF gene polymorphisms and plasma VEGF levels and sporadic AL. Golenia A., Tomik B., Zawislak D., Wolkow P., Dziubek A., Sado M., Szczudlik A., Figlewicz D.A., Slowik A. Neurology 75:2035-2037(2010) · Mapped (7) |
| Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosis. McLaughlin R.L., Phukan J., McCormack W., Lynch D.S., Greenway M., Cronin S., Saunders J., Slowik A., Tomik B., Andersen P.M. et al. PLoS ONE 5:e15402-e15402(2010) · Mapped (1) |
| Variants at APOE influence risk of deep and lobar intracerebral hemorrhage. International Stroke Genetics Consortium Ann. Neurol. 68:934-943(2010) · Mapped (5) |
| Plasma factor and inhibitor composition contributes to thrombin generation dynamics in patients with acute or previous cerebrovascular events. Gissel M., Undas A., Slowik A., Mann K.G., Brummel-Ziedins K.E. Thromb. Res. 126:262-269(2010) · Mapped (8) |
| A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Blauw H.M., Al-Chalabi A., Andersen P.M., van Vught P.W., Diekstra F.P., van Es M.A., Saris C.G., Groen E.J., van Rheenen W., Koppers M. et al. Hum. Mol. Genet. 19:4091-4099(2010) · Mapped (13) |
| The -A162G polymorphism of the PON1 gene and the risk of sporadic amyotrophic lateral sclerosis. Zawislak D., Ostrowska M., Golenia A., Marona M., Tomik B., Wolkow P., Gryz-Kurek E., Szczudlik A., Slowik A. Neurol. Neurochir. Pol. 44:246-250(2010) · Mapped (3) |
| Tau levels do not influence human ALS or motor neuron degeneration in the SOD1G93A mouse. Taes I., Goris A., Lemmens R., van Es M.A., van den Berg L.H., Chio A., Traynor B.J., Birve A., Andersen P., Slowik A. et al. Neurology 74:1687-1693(2010) · Mapped (6) |
| Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis. Bogaert E., Goris A., Van Damme P., Geelen V., Lemmens R., van Es M.A., van den Berg L.H., Sleegers K., Verpoorten N., Timmerman V. et al. Neurobiol. Aging 33:418-420(2012) · Mapped (14) |
| Interleukin-1 gene -511 CT polymorphism and the risk of Alzheimer's disease in a Polish population. Klimkowicz-Mrowiec A., Marona M., Wolkow P., Maruszak A., Styczynska M., Barcikowska M., Zekanowski C., Szczudlik A., Slowik A. Dement Geriatr Cogn Disord 28:461-464(2009) · Mapped (8) |
| Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. van Es M.A., Veldink J.H., Saris C.G., Blauw H.M., van Vught P.W., Birve A., Lemmens R., Schelhaas H.J., Groen E.J., Huisman M.H. et al. Nat. Genet. 41:1083-1087(2009) · Mapped (8) |
| A1/A2 polymorphism of GpIIIa gene and a risk of aneurysmal subarachnoid haemorrhage. Adamski M.G., Borratynska A., Krupa M., Wloch-Kopec D., Turaj W., Wolkow P., Wnuk M., Urbanik A., Moskala M., Szczudlik A. et al. Biochem. Biophys. Res. Commun. 383:228-230(2009) · Mapped (5) |
| A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS. Wills A.M., Cronin S., Slowik A., Kasperaviciute D., Van Es M.A., Morahan J.M., Valdmanis P.N., Meininger V., Melki J., Shaw C.E. et al. Neurology 73:16-24(2009) · Mapped (3) |
| A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease. Adamski M.G., Turaj W., Slowik A., Wloch-Kopec D., Wolkow P., Szczudlik A. Acta Neurol. Scand. 120:94-100(2009) · Mapped (4) |
| Screening for replication of genome-wide SNP associations in sporadic ALS. Cronin S., Tomik B., Bradley D.G., Slowik A., Hardiman O. Eur. J. Hum. Genet. 17:213-218(2009) · Mapped (62) |
| Species differences in the expression of Ahi1, a protein implicated in the neurodevelopmental disorder Joubert syndrome, with preferential accumulation to stigmoid bodies. Doering J.E., Kane K., Hsiao Y.C., Yao C., Shi B., Slowik A.D., Dhagat B., Scott D.D., Ault J.G., Page-McCaw P.S. et al. J. Comp. Neurol. 511:238-256(2008) · Mapped (24) |