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Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience
Hofman, Nynke, Tan, Hanno L., Alders, Mariëlle, Kolder, Iris, de Haij, Simone, Mannens, Marcel M.A.M., Lombardi, Maria Paola, dit Deprez, Ronald H. Lekanne, van Langen, Irene, Wilde, Arthur A.M.
Published in Circulation (New York, N.Y.) (01.10.2013)
Published in Circulation (New York, N.Y.) (01.10.2013)
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Evaluation the Presence of SERPINA5 (Exon 3) and FTO rs9939609 Polymorphisms in Papillary Thyroid Cancer Patients
Moshtaghioun, Seyed Mohammad, Fazel-Yazdi, Nasim, Mandegari, Mohammad, Shirinzadeh-Dastgiri, Ahmad, Vakili, Mohammad, Fazel-Yazdi, Habib
Published in Asian Pacific journal of cancer prevention : APJCP (01.11.2021)
Published in Asian Pacific journal of cancer prevention : APJCP (01.11.2021)
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Genetic polymorphism of interleukin-17A and -17F genes in gastric carcinogenesis
Shibata, Tomoyuki, Tahara, Tomomitsu, Hirata, Ichiro, Arisawa, Tomiyasu
Published in Human immunology (01.07.2009)
Published in Human immunology (01.07.2009)
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Central Role of Reverting Mutations in HLA Associations with Human Immunodeficiency Virus Set Point
Matthews, Philippa C., Prendergast, Andrew, Leslie, Alasdair, Crawford, Hayley, Payne, Rebecca, Rousseau, Christine, Rolland, Morgane, Honeyborne, Isobella, Carlson, Jonathan, Kadie, Carl, Brander, Christian, Bishop, Karen, Mlotshwa, Nonkululeko, Mullins, James I., Coovadia, Hoosen, Ndung'u, Thumbi, Walker, Bruce D., Heckerman, David, Goulder, Philip J. R.
Published in Journal of Virology (01.09.2008)
Published in Journal of Virology (01.09.2008)
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Helicobacter pylori and Interleukin 1 Genotyping: An Opportunity to Identify High-Risk Individuals for Gastric Carcinoma
Figueiredo, Céu, Machado, José Carlos, Pharoah, Paul, Seruca, Raquel, Sousa, Sónia, Carvalho, Ralph, Capelinha, Ana Filipa, Quint, Wim, Caldas, Carlos, van Doorn, Leen-Jan, Carneiro, Fátima, Sobrinho-Simões, Manuel
Published in JNCI : Journal of the National Cancer Institute (20.11.2002)
Published in JNCI : Journal of the National Cancer Institute (20.11.2002)
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Extended haplotypes in the complement factor H (CFH) and CFH-related (CFHR) family of genes protect against age-related macular degeneration: characterization, ethnic distribution and evolutionary implications
Hageman, Gregory S, Hancox, Lisa S, Taiber, Andrew J, Gehrs, Karen M, Anderson, Don H, Johnson, Lincoln V, Radeke, Monte J, Kavanagh, David, Richards, Anna, Atkinson, John, Meri, Seppo, Bergeron, Julie, Zernant, Jana, Merriam, Joanna, Gold, Bert, Allikmets, Rando, Dean, Michael
Published in Annals of medicine (Helsinki) (2006)
Published in Annals of medicine (Helsinki) (2006)
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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Ackerman, Michael J, Splawski, Igor, Makielski, Jonathan C, Tester, David J, Will, Melissa L, Timothy, Katherine W, Keating, Mark T, Jones, Gregg, Chadha, Monica, Burrow, Christopher R, Stephens, J Claiborne, Xu, Chuanbo, Judson, Richard, Curran, Mark E
Published in Heart rhythm (01.11.2004)
Published in Heart rhythm (01.11.2004)
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Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease
Caprioli, Jessica, Castelletti, Federica, Bucchioni, Sara, Bettinaglio, Paola, Bresin, Elena, Pianetti, Gaia, Gamba, Sara, Brioschi, Simona, Daina, Erica, Remuzzi, Giuseppe, Noris, Marina
Published in Human molecular genetics (15.12.2003)
Published in Human molecular genetics (15.12.2003)
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High-dose methotrexate in pediatric acute lymphoblastic leukemia: impact of ABCC2 polymorphisms on plasma concentrations
Rau, Thomas, Erney, Birgit, Göres, Ralf, Eschenhagen, Thomas, Beck, Jörn, Langer, Thorsten
Published in Clinical pharmacology and therapeutics (01.11.2006)
Published in Clinical pharmacology and therapeutics (01.11.2006)
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PAX4 Mutations in Thais with Maturity Onset Diabetes of the Young
Plengvidhya, Nattachet, Kooptiwut, Suwattanee, Songtawee, Napat, Doi, Asako, Furuta, Hiroto, Nishi, Masahiro, Nanjo, Kishio, Tantibhedhyangkul, Wiwit, Boonyasrisawat, Watip, Yenchitsomanus, Pa-thai, Doria, Alessandro, Banchuin, Napatawn
Published in The journal of clinical endocrinology and metabolism (01.07.2007)
Published in The journal of clinical endocrinology and metabolism (01.07.2007)
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A coding variant in NLRP1 is associated with autoimmune Addison's disease
Żurawek, Magdalena, Fichna, Marta, Januszkiewicz-Lewandowska, Danuta, Gryczyńska, Maria, Fichna, Piotr, Nowak, Jerzy
Published in Human immunology (01.05.2010)
Published in Human immunology (01.05.2010)
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MDM2 Promoter Polymorphism Is Associated With Both an Increased Susceptibility to Gastric Carcinoma and Poor Prognosis
Ohmiya, Naoki, Taguchi, Ayumu, Mabuchi, Nobuyuki, Itoh, Akihiro, Hirooka, Yoshiki, Niwa, Yasumasa, Goto, Hidemi
Published in Journal of clinical oncology (20.09.2006)
Published in Journal of clinical oncology (20.09.2006)
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Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome
Ebisawa, Takashi, Uchiyama, Makoto, Kajimura, Naofumi, Mishima, Kazuo, Kamei, Yuichi, Katoh, Masaaki, Watanabe, Tsuyoshi, Sekimoto, Masanori, Shibui, Kayo, Kim, Keiko, Kudo, Yoshinao, Ozeki, Yuji, Sugishita, Mariko, Toyoshima, Ryoichi, Inoue, Yuichi, Yamada, Naoto, Nagase, Takahiro, Ozaki, Norio, Ohara, Osamu, Ishida, Norio, Okawa, Masako, Takahashi, Kiyohisa, Yamauchi, Toshio
Published in EMBO reports (01.04.2001)
Published in EMBO reports (01.04.2001)
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Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucoma
Alward, Wallace L.M, Kwon, Young H, Kawase, Kazuhide, Craig, Jamie E, Hayreh, Sohan S, Johnson, A.Tim, Khanna, Cheryl L, Yamamoto, Tetsuya, Mackey, David A, Roos, Benjamin R, Affatigato, Louisa M, Sheffield, Val C, Stone, Edwin M
Published in American journal of ophthalmology (01.11.2003)
Published in American journal of ophthalmology (01.11.2003)
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Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color
Kennedy, Cornelis, ter Huurne, Jeanet, Berkhout, Marjo, Gruis, Nelleke, Bastiaens, Maarten, Bergman, W., Willemze, R., Bouwes Bavinck, Jan Nico
Published in Journal of investigative dermatology (01.08.2001)
Published in Journal of investigative dermatology (01.08.2001)
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Congenital leptin deficiency is associated with severe early-onset obesity in humans
Montague, Carl T., Farooqi, I. Sadaf, Whitehead, Jonathan P., Soos, Maria A., Rau, Harald, Wareham, Nicholas J., Sewter, Ciaran P., Digby, Janet E., Mohammed, Shehla N., Hurst, Jane A., Cheetham#, Christopher H., Earley#, Alison R., Barnett, Anthony H., Prins, Johannes B., O'Rahilly, Stephen
Published in Nature (London) (26.06.1997)
Published in Nature (London) (26.06.1997)
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Atopic Dermatitis Is Associated with a Functional Mutation in the Promoter of the C-C Chemokine RANTES
Nickel, Renate G, Casolaro, Vincenzo, Wahn, Ulrich, Beyer, Kirsten, Barnes, Kathleen C, Plunkett, Beverly S, Freidhoff, Linda R, Sengler, Claudia, Plitt, James R, Schleimer, Robert P, Caraballo, Luis, Naidu, Raana P, Levett, Paul N, Beaty, Terri H, Huang, Shau-Ku
Published in The Journal of immunology (1950) (01.02.2000)
Published in The Journal of immunology (1950) (01.02.2000)
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