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694 HLA CLASS I ALLELES ASSOCIATED WITH HCV POLYMORPHISMS AND RESPONSE TO ANTIVIRAL THERAPY IN HCV GENOTYPE 1-INFECTED PATIENTS
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ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels
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Association Between Non-Alcoholic Fatty Liver Disease (NAFLD) and Iron Metabolism in Obese Children and Adolescents: Results of the Beta-JUDO Study
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Staaf, Johan, Labmayr, V., Paulmichl, K., Ohlsson, H., Cen, Jing, Ciba, Iris, Dahlbom, Marie, Roomp, K., Anderwald, C-H, Ladinger, A., Schneider, R., Forslund, Anders, Widhalm, K., Bergquist, Jonas, Ahlström, Håkan, Bergsten, Peter, Weghuber, D., Kullberg, Joel
Published in Acta Paediatrica (2015)
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Clee, S M, Kastelein, J J, van Dam, M, Marcil, M, Roomp, K, Zwarts, K Y, Collins, J A, Roelants, R, Tamasawa, N, Stulc, T, Suda, T, Ceska, R, Boucher, B, Rondeau, C, DeSouich, C, Brooks-Wilson, A, Molhuizen, H O, Frohlich, J, Genest, Jr, J, Hayden, M R
Published in The Journal of clinical investigation (01.11.2000)
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Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease
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Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
MARCIL, M, BROOKS-WILSON, A, OUELLETTE, B. F. F, SENSEN, C. W, FICHTER, K, MOTT, S, DENIS, M, BOUCHER, B, PIMSTONE, S, GENEST, J. JR, KASTELEIN, J. J. P, HAYDEN, M. R, CLEE, S. M, ROOMP, K, ZHANG, L.-H, LU YU, COLLINS, J. A, VAN DAM, M, MOLHUIZEN, H. O. F, LOUBSTER, O
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Systems biomedicine approach to diabetic nephropathy: role of coagulation protease-activated protein C
Schneider, JG, Rybacka, E, Madhusudhan, T, Roomp, K, Isermann, BH
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Short communication: selection of thymidine analogue resistance mutational patterns in children infected from a common HIV type 1 subtype G source
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Published in AIDS research and human retroviruses (01.03.2010)
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PPAR[gamma] population shift produces disease-related changes in molecular networks associated with metabolic syndrome
Jurkowski, W, Roomp, K, Crespo, I, Schneider, J G, Del Sol, A
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Expression and Functional Analyses of Novel Mutations of ATP-Binding Cassette Transporter-1 in Japanese Patients with High-Density Lipoprotein Deficiency
Nishida, Yoshiharu, Hirano, Ken-ichi, Tsukamoto, Kosuke, Nagano, Makoto, Ikegami, Chiaki, Roomp, Kirsten, Ishihara, Mitsuaki, Sakane, Naoki, Zhang, Zhongyan, Tsujii, Ken-ichi, Matsuyama, Akifumi, Ohama, Tohru, Matsuura, Fumihiko, Ishigami, Masato, Sakai, Naohiko, Hiraoka, Hisatoyo, Hattori, Hiroaki, Wellington, Cheryl, Yoshida, Yoshihide, Misugi, Susumu, Hayden, Michael R., Egashira, Toru, Yamashita, Shizuya, Matsuzawa, Yuji
Published in Biochemical and biophysical research communications (18.01.2002)
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Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol
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Assoziation bestimmter HLA Klasse I-Allele mit dem Ansprechen auf eine antivirale Therapie bei Patienten mit chronischer Hepatitis C
Lange, CM, Dragan, A, Roomp, K, Nattermann, J, Nattermann, J, Michalk, M, Michalk, M, Spengler, U, Berg, T, Langauer, T, Zeuzem, S, Sarrazin, C
Published in Zeitschrift für Gastroenterologie (12.01.2010)
Published in Zeitschrift für Gastroenterologie (12.01.2010)
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Conference Proceeding
Mutations in the ABC1 gene in familial HDL deficiency with defective cholesterol efflux
Marcil, M, Brooks-Wilson, A, Clee, S M, Roomp, K, Zhang, L-H, Yu, L, Collins, JA, van Dam, M, Molhuizen, HOF, Loubster, O, Ouellette, BFF, Sensen, C W, Fichter, K, Hayden, M R
Published in The Lancet (North American edition) (16.10.1999)
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Published in The Lancet (North American edition) (16.10.1999)
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