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Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes
Corre, Tanguy, Arjona, Francisco J., Hayward, Caroline, Youhanna, Sonia, de Baaij, Jeroen H.F., Belge, Hendrica, Nägele, Nadine, Debaix, Huguette, Blanchard, Maxime G., Traglia, Michela, Harris, Sarah E., Ulivi, Sheila, Rueedi, Rico, Lamparter, David, Macé, Aurélien, Sala, Cinzia, Lenarduzzi, Stefania, Ponte, Belen, Pruijm, Menno, Ackermann, Daniel, Ehret, Georg, Baptista, Daniela, Polasek, Ozren, Rudan, Igor, Hurd, Toby W., Hastie, Nicholas D., Vitart, Veronique, Waeber, Geràrd, Kutalik, Zoltán, Bergmann, Sven, Vargas-Poussou, Rosa, Konrad, Martin, Gasparini, Paolo, Deary, Ian J., Starr, John M., Toniolo, Daniela, Vollenweider, Peter, Hoenderop, Joost G.J., Bindels, René J.M., Bochud, Murielle, Devuyst, Olivier
Published in Journal of the American Society of Nephrology (01.01.2018)
Published in Journal of the American Society of Nephrology (01.01.2018)
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Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing
Zenteno, Juan C., García‐Montaño, Leopoldo A., Cruz‐Aguilar, Marisa, Ronquillo, Josué, Rodas‐Serrano, Agustín, Aguilar‐Castul, Luis, Matsui, Rodrigo, Vencedor‐Meraz, Carlos I., Arce‐González, Rocío, Graue‐Wiechers, Federico, Gutiérrez‐Paz, Mario, Urrea‐Victoria, Tatiana, Dios Cuadras, Ulises, Chacón‐Camacho, Oscar F.
Published in Molecular genetics & genomic medicine (01.01.2020)
Published in Molecular genetics & genomic medicine (01.01.2020)
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Association of the ARL15 rs6450176 SNP and serum lipid levels in the Jing and Han populations
Sun, Jia-Qi, Yin, Rui-Xing, Shi, Guang-Yuan, Shen, Shao-Wen, Chen, Xia, Bin, Yuan, Huang, Feng, Wang, Wei, Lin, Wei-Xiong, Pan, Shang-Ling
Published in International journal of clinical and experimental pathology (01.01.2015)
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Published in International journal of clinical and experimental pathology (01.01.2015)
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Hippocampal dysgenesis and variable neuropsychiatric phenotypes in patients with Bardet-Biedl syndrome underline complex CNS impact of primary cilia
Bennouna-Greene, V, Kremer, S, Stoetzel, C, Christmann, D, Schuster, C, Durand, M, Verloes, A, Sigaudy, S, Holder-Espinasse, M, Godet, J, Brandt, C, Marion, V, Danion, A, Dietemann, J-L, Dollfus, H
Published in Clinical genetics (01.12.2011)
Published in Clinical genetics (01.12.2011)
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Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene
Wassink, Thomas H., Piven, Joseph, Vieland, Veronica J., Jenkins, Laura, Frantz, Rebecca, Bartlett, Christopher W., Goedken, Rhinda, Childress, Deb, Spence, M. Anne, Smith, Moyra, Sheffield, Val C.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2005)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2005)
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A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity
Adams, Ted D., Lewis, Tracey, Mao, Rong, Xin, Yuanpei, Hasstedt, Sandra J., Hunt, Steven C.
Published in Journal of Obesity (01.01.2015)
Published in Journal of Obesity (01.01.2015)
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ARLTS1 variants and melanoma risk
Frank, Bernd, Meyer, Peter, Boettger, Melanie Barbara, Hemminki, Kari, Stapelmann, Henrike, Gast, Andreas, Schmitt, Christina, Kumar, Rajiv, Sergi, Consolato, Burwinkel, Barbara
Published in INTERNATIONAL JOURNAL OF CANCER (01.10.2006)
Published in INTERNATIONAL JOURNAL OF CANCER (01.10.2006)
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Membrane metabolism mediated by Sec14 family members influences Arf GTPase activating protein activity for transport from the trans-Golgi
Wong, T.A, Fairn, G.D, Poon, P.P, Shmulevitz, M, McMaster, C.R, Singer, R.A, Johnston, G.C
Published in Proceedings of the National Academy of Sciences - PNAS (06.09.2005)
Published in Proceedings of the National Academy of Sciences - PNAS (06.09.2005)
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