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MicroRNA-339-5p Down-regulates Protein Expression of β-Site Amyloid Precursor Protein-Cleaving Enzyme 1 (BACE1) in Human Primary Brain Cultures and Is Reduced in Brain Tissue Specimens of Alzheimer Disease Subjects
Long, Justin M., Ray, Balmiki, Lahiri, Debomoy K.
Published in The Journal of biological chemistry (21.02.2014)
Published in The Journal of biological chemistry (21.02.2014)
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Decline in genomic DNA methylation through aging in a cohort of elderly subjects
Bollati, Valentina, Schwartz, Joel, Wright, Robert, Litonjua, Augusto, Tarantini, Letizia, Suh, Helen, Sparrow, David, Vokonas, Pantel, Baccarelli, Andrea
Published in Mechanisms of ageing and development (01.04.2009)
Published in Mechanisms of ageing and development (01.04.2009)
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Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome
Bonaglia, Maria Clara, Giorda, Roberto, Beri, Silvana, De Agostini, Cristina, Novara, Francesca, Fichera, Marco, Grillo, Lucia, Galesi, Ornella, Vetro, Annalisa, Ciccone, Roberto, Bonati, Maria Teresa, Giglio, Sabrina, Guerrini, Renzo, Osimani, Sara, Marelli, Susan, Zucca, Claudio, Grasso, Rita, Borgatti, Renato, Mani, Elisa, Motta, Cristina, Molteni, Massimo, Romano, Corrado, Greco, Donatella, Reitano, Santina, Baroncini, Anna, Lapi, Elisabetta, Cecconi, Antonella, Arrigo, Giulia, Patricelli, Maria Grazia, Pantaleoni, Chiara, D'Arrigo, Stefano, Riva, Daria, Sciacca, Francesca, Dalla Bernardina, Bernardo, Zoccante, Leonardo, Darra, Francesca, Termine, Cristiano, Maserati, Emanuela, Bigoni, Stefania, Priolo, Emanuela, Bottani, Armand, Gimelli, Stefania, Bena, Frederique, Brusco, Alfredo, di Gregorio, Eleonora, Bagnasco, Irene, Giussani, Ursula, Nitsch, Lucio, Politi, Pierluigi, Martinez-Frias, Maria Luisa, Martínez-Fernández, Maria Luisa, Martínez Guardia, Nieves, Bremer, Anna, Anderlid, Britt-Marie, Zuffardi, Orsetta
Published in PLoS genetics (01.07.2011)
Published in PLoS genetics (01.07.2011)
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A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment
del Castillo, F J, Rodríguez-Ballesteros, M, Álvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M R, Marlin, S, Pandya, A, Shahin, H, Siemering, K R, Weil, D, Wuyts, W, Aguirre, L A, Martín, Y, Moreno-Pelayo, M A, Villamar, M, Avraham, K B, Dahl, H-H M, Kanaan, M, Nance, W E, Petit, C, Smith, R J H, Van Camp, G, Sartorato, E L, Murgia, A, Moreno, F, del Castillo, I
Published in Journal of medical genetics (01.07.2005)
Published in Journal of medical genetics (01.07.2005)
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Genetic Determinants of the Gut Microbiome in UK Twins
Goodrich, Julia K., Davenport, Emily R., Beaumont, Michelle, Jackson, Matthew A., Knight, Rob, Ober, Carole, Spector, Tim D., Bell, Jordana T., Clark, Andrew G., Ley, Ruth E.
Published in Cell host & microbe (11.05.2016)
Published in Cell host & microbe (11.05.2016)
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Human B-cell isotype switching origins of IgE
Looney, Timothy J., Lee, Ji-Yeun, Roskin, Krishna M., Hoh, Ramona A., King, Jasmine, Glanville, Jacob, Liu, Yi, Pham, Tho D., Dekker, Cornelia L., Davis, Mark M., Boyd, Scott D.
Published in Journal of allergy and clinical immunology (01.02.2016)
Published in Journal of allergy and clinical immunology (01.02.2016)
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Next-Generation Sequencing: From Basic Research to Diagnostics
Voelkerding, Karl V, Dames, Shale A, Durtschi, Jacob D
Published in Clinical chemistry (Baltimore, Md.) (01.04.2009)
Published in Clinical chemistry (Baltimore, Md.) (01.04.2009)
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Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Bilgüvar, Kaya, Öztürk, Ali Kemal, Louvi, Angeliki, Kwan, Kenneth Y., Choi, Murim, Tatlı, Burak, Yalnızoğlu, Dilek, Tüysüz, Beyhan, Çağlayan, Ahmet Okay, Gökben, Sarenur, Kaymakçalan, Hande, Barak, Tanyeri, Bakırcıoğlu, Mehmet, Yasuno, Katsuhito, Ho, Winson, Sanders, Stephan, Zhu, Ying, Yılmaz, Sanem, Dinçer, Alp, Johnson, Michele H., Bronen, Richard A., Koçer, Naci, Per, Hüseyin, Mane, Shrikant, Pamir, Mehmet Necmettin, Yalçınkaya, Cengiz, Kumandaş, Sefer, Topçu, Meral, Özmen, Meral, Šestan, Nenad, Lifton, Richard P., State, Matthew W., Günel, Murat
Published in Nature (London) (09.09.2010)
Published in Nature (London) (09.09.2010)
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Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella
Tang, Shuyan, Wang, Xiong, Li, Weiyu, Yang, Xiaoyu, Li, Zheng, Liu, Wangjie, Li, Caihua, Zhu, Zijue, Wang, Lingxiang, Wang, Jiaxiong, Zhang, Ling, Sun, Xiaoling, Zhi, Erlei, Wang, Hongyan, Li, Hong, Jin, Li, Luo, Yang, Wang, Jian, Yang, Shenmin, Zhang, Feng
Published in American journal of human genetics (01.06.2017)
Published in American journal of human genetics (01.06.2017)
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Composition, variability, and temporal stability of the intestinal microbiota of the elderly
Claesson, Marcus J, Cusack, Siobhán, O'Sullivan, Orla, Greene-Diniz, Rachel, de Weerd, Heleen, Flannery, Edel, Marchesi, Julian R, Falush, Daniel, Dinan, Timothy, Fitzgerald, Gerald, Stanton, Catherine, van Sinderen, Douwe, O'Connor, Michael, Harnedy, Norma, O'Connor, Kieran, Henry, Colm, O'Mahony, Denis, Fitzgerald, Anthony P, Shanahan, Fergus, Twomey, Cillian, Hill, Colin, Ross, R. Paul, O'Toole, Paul W
Published in Proceedings of the National Academy of Sciences - PNAS (15.03.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (15.03.2011)
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Gut microbial colonisation in premature neonates predicts neonatal sepsis
Madan, Juliette C, Salari, Richard Cowper, Saxena, Deepti, Davidson, Lisa, O'Toole, George A, Moore, Jason H, Sogin, Mitchell L, Foster, James A, Edwards, William H, Palumbo, Paul, Hibberd, Patricia L
Published in Archives of disease in childhood. Fetal and neonatal edition (01.11.2012)
Published in Archives of disease in childhood. Fetal and neonatal edition (01.11.2012)
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Lactoferrin a multiple bioactive protein: An overview
García-Montoya, Isui Abril, Cendón, Tania Siqueiros, Arévalo-Gallegos, Sigifredo, Rascón-Cruz, Quintín
Published in Biochimica et biophysica acta (01.03.2012)
Published in Biochimica et biophysica acta (01.03.2012)
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Commonality despite exceptional diversity in the baseline human antibody repertoire
Briney, Bryan, Inderbitzin, Anne, Joyce, Collin, Burton, Dennis R.
Published in Nature (London) (01.02.2019)
Published in Nature (London) (01.02.2019)
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The relationship of 5HTT (SLC6A4) methylation and genotype on mRNA expression and liability to major depression and alcohol dependence in subjects from the Iowa Adoption Studies
Philibert, Robert A., Sandhu, Harinder, Hollenbeck, Nancy, Gunter, Tracy, Adams, William, Madan, Anup
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.07.2008)
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Isolation of a high‐affinity Bet v 1‐specific IgG‐derived ScFv from a subject vaccinated with hypoallergenic Bet v 1 fragments
Gadermaier, E., Marth, K., Lupinek, C., Campana, R., Hofer, G., Blatt, K., Smiljkovic, D., Roder, U., Focke‐Tejkl, M., Vrtala, S., Keller, W., Valent, P., Valenta, R., Flicker, S.
Published in Allergy (Copenhagen) (01.07.2018)
Published in Allergy (Copenhagen) (01.07.2018)
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APOΕ4 lowers energy expenditure in females and impairs glucose oxidation by increasing flux through aerobic glycolysis
Farmer, Brandon C., Williams, Holden C., Devanney, Nicholas A., Piron, Margaret A., Nation, Grant K., Carter, David J., Walsh, Adeline E., Khanal, Rebika, Young, Lyndsay E. A., Kluemper, Jude C., Hernandez, Gabriela, Allenger, Elizabeth J., Mooney, Rachel, Golden, Lesley R., Smith, Cathryn T., Brandon, J. Anthony, Gupta, Vedant A., Kern, Philip A., Gentry, Matthew S., Morganti, Josh M., Sun, Ramon C., Johnson, Lance A.
Published in Molecular neurodegeneration (06.09.2021)
Published in Molecular neurodegeneration (06.09.2021)
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