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Defects in IL-2R Signaling Contribute to Diminished Maintenance of FOXP3 Expression in CD4+CD25+ Regulatory T-Cells of Type 1 Diabetic Subjects
Long, S. Alice, Cerosaletti, Karen, Bollyky, Paul L., Tatum, Megan, Shilling, Heather, Zhang, Sheng, Zhang, Zhong-Yin, Pihoker, Catherine, Sanda, Srinath, Greenbaum, Carla, Buckner, Jane H.
Published in Diabetes (New York, N.Y.) (01.02.2010)
Published in Diabetes (New York, N.Y.) (01.02.2010)
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Plasma Microbiome in COVID-19 Subjects: An Indicator of Gut Barrier Defects and Dysbiosis
Prasad, Ram, Patton, Michael John, Floyd, Jason Levi, Fortmann, Seth, DuPont, Mariana, Harbour, Angela, Wright, Justin, Lamendella, Regina, Stevens, Bruce R., Oudit, Gavin Y., Grant, Maria B.
Published in International journal of molecular sciences (15.08.2022)
Published in International journal of molecular sciences (15.08.2022)
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.
Published in American journal of human genetics (02.01.2020)
Published in American journal of human genetics (02.01.2020)
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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
Salpietro, Vincenzo, Dixon, Christine L., Guo, Hui, Bello, Oscar D., Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Heimer, Gali, Burglen, Lydie, Valence, Stephanie, Torti, Erin, Hacke, Moritz, Rankin, Julia, Tariq, Huma, Colin, Estelle, Procaccio, Vincent, Striano, Pasquale, Mankad, Kshitij, Lieb, Andreas, Chen, Sharon, Pisani, Laura, Bettencourt, Conceicao, Männikkö, Roope, Manole, Andreea, Brusco, Alfredo, Grosso, Enrico, Ferrero, Giovanni Battista, Armstrong-Moron, Judith, Gueden, Sophie, Bar-Yosef, Omer, Tzadok, Michal, Monaghan, Kristin G., Santiago-Sim, Teresa, Person, Richard E., Cho, Megan T., Willaert, Rebecca, Yoo, Yongjin, Chae, Jong-Hee, Quan, Yingting, Wu, Huidan, Wang, Tianyun, Bernier, Raphael A., Xia, Kun, Blesson, Alyssa, Jain, Mahim, Motazacker, Mohammad M., Jaeger, Bregje, Schneider, Amy L., Boysen, Katja, Muir, Alison M., Myers, Candace T., Gavrilova, Ralitza H., Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W., Dyment, David, Osmond, Matthew, Parellada, Mara, Llorente, Cloe, Gonzalez-Peñas, Javier, Carracedo, Angel, Van Haeringen, Arie, Ruivenkamp, Claudia, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Minetti, Carlo, Skabar, Aldo, Fabretto, Antonella, Raspall-Chaure, Miquel, Chez, Michael, Tsai, Anne, Fassi, Emily, Shinawi, Marwan, Constantino, John N., De Zorzi, Rita, Fortuna, Sara, Kok, Fernando, Keren, Boris, Bonneau, Dominique, Choi, Murim, Benzeev, Bruria, Zara, Federico, Mefford, Heather C., Scheffer, Ingrid E., Clayton-Smith, Jill, Macaya, Alfons, Rothman, James E., Eichler, Evan E., Kullmann, Dimitri M., Houlden, Henry
Published in Nature communications (12.07.2019)
Published in Nature communications (12.07.2019)
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Dual Metabolic Defects Are Required to Produce Hypertriglyceridemia in Obese Subjects
Taskinen, Marja-Riitta, Adiels, Martin, Westerbacka, Jukka, Söderlund, Sanni, Kahri, Juhani, Lundbom, Nina, Lundbom, Jesper, Hakkarainen, Antti, Olofsson, Sven-Olof, Orho-Melander, Marju, Borén, Jan
Published in Arteriosclerosis, thrombosis, and vascular biology (01.09.2011)
Published in Arteriosclerosis, thrombosis, and vascular biology (01.09.2011)
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Tumour necrosis factor-α −308G/A polymorphism is associated with insulin secretory defects in Bangladeshi prediabetic/diabetic subjects
Hossain, Muhammad M., Paul, Sunanda, Das, Manisha, Saha, Trissa, Faruque, Md O., Hassan, Zahid
Published in Journal of Taibah University Medical Sciences (01.04.2022)
Published in Journal of Taibah University Medical Sciences (01.04.2022)
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Patient-Specific Computational Simulations of Hyperpolarized ^3He MRI Ventilation Defects in Healthy and Asthmatic Subjects
Oakes, Jessica M., Mummy, David G., Poorbahrami, Kamran, Zha, Wei, Fain, Sean B.
Published in IEEE transactions on biomedical engineering (01.05.2019)
Published in IEEE transactions on biomedical engineering (01.05.2019)
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Evaluation of the potential utility of the total thrombus‐formation analysis system in comparison to the platelet function analyser in subjects with primary haemostatic defects
Charpy, Juliette, Chaghouri, Pierre‐Elian, Benattar, Norbert, Castet, Sabine‐Marie, Huguenin, Yoann, James, Chloé, Fiore, Mathieu
Published in British journal of haematology (01.10.2020)
Published in British journal of haematology (01.10.2020)
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Prenatal Exposure to Toxic Metals and Neural Tube Defects: A Systematic Review of the Epidemiologic Evidence
Eaves, Lauren A., Choi, Giehae, Hall, Emily, Sillé, Fenna C.M., Fry, Rebecca C., Buckley, Jessie P., Keil, Alexander P.
Published in Environmental health perspectives (01.08.2023)
Published in Environmental health perspectives (01.08.2023)
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What are ventilation defects in asthma?
Svenningsen, Sarah, Kirby, Miranda, Starr, Danielle, Coxson, Harvey O, Paterson, Nigel A M, McCormack, David G, Parraga, Grace
Published in Thorax (01.01.2014)
Published in Thorax (01.01.2014)
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