Addressing the age-old question of old age

por McElwee, Joshua J
Publicado 2004

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies

por Hao, Ke, Chudin, Eugene, McElwee, Joshua, Schadt, Eric E
Publicado 2009

Magnesium Restores Activity to Peripheral Blood Cells in a Patient With Functionally Impaired Interleukin-2-Inducible T Cell Kinase

por Howe, Matthew K., Dowdell, Kennichi, Roy, Amitava, Niemela, Julie E., Wilson, Wyndham, McElwee, Joshua J., Hughes, Jason D., Cohen, Jeffrey I.
Publicado 2019

Evolutionary conservation of regulated longevity assurance mechanisms

por McElwee, Joshua J, Schuster, Eugene, Blanc, Eric, Piper, Matthew D, Thomas, James H, Patel, Dhaval S, Selman, Colin, Withers, Dominic J, Thornton, Janet M, Partridge, Linda, Gems, David
Publicado 2007

DamID in C. elegans reveals longevity-associated targets of DAF-16/FoxO

por Schuster, Eugene, McElwee, Joshua J, Tullet, Jennifer M A, Doonan, Ryan, Matthijssens, Filip, Reece-Hoyes, John S, Hope, Ian A, Vanfleteren, Jacques R, Thornton, Janet M, Gems, David
Publicado 2010

Heterozygous splice mutation in PIK3R1 causes human immunodeficiency with lymphoproliferation due to dominant activation of PI3K

por Lucas, Carrie L., Zhang, Yu, Venida, Anthony, Wang, Ying, Hughes, Jason, McElwee, Joshua, Butrick, Morgan, Matthews, Helen, Price, Susan, Biancalana, Matthew, Wang, Xiaochuan, Richards, Michael, Pozos, Tamara, Barlan, Isil, Ozen, Ahmet, Rao, V. Koneti, Su, Helen C., Lenardo, Michael J.
Publicado 2014

Structural basis for isoform-specific inhibition of human CTPS1

por Lynch, Eric M., DiMattia, Michael A., Albanese, Steven, van Zundert, Gydo C. P., Hansen, Jesse M., Quispe, Joel D., Kennedy, Madison A., Verras, Andreas, Borrelli, Kenneth, Toms, Angela V., Kaila, Neelu, Kreutter, Kevin D., McElwee, Joshua J., Kollman, Justin M.
Publicado 2021

Common dysregulation network in the human prefrontal cortex underlies two neurodegenerative diseases

por Narayanan, Manikandan, Huynh, Jimmy L, Wang, Kai, Yang, Xia, Yoo, Seungyeul, McElwee, Joshua, Zhang, Bin, Zhang, Chunsheng, Lamb, John R, Xie, Tao, Suver, Christine, Molony, Cliona, Melquist, Stacey, Johnson, Andrew D, Fan, Guoping, Stone, David J, Schadt, Eric E, Casaccia, Patrizia, Emilsson, Valur, Zhu, Jun
Publicado 2014

Absence of effects of Sir2 over-expression on lifespan in C. elegans and Drosophila

por Burnett, Camilla, Valentini, Sara, Cabreiro, Filipe, Goss, Martin, Somogyvári, Milán, Piper, Matthew D., Hoddinott, Matthew, Sutphin, George L., Leko, Vid, McElwee, Joshua J., Vazquez, Rafael, Orfila, Anne-Marie, Ackerman, Daniel, Au, Catherine, Vinti, Giovanna, Riesen, Michèle, Howard, Ken, Neri, Christian, Bedalov, Antonio, Kaeberlein, Matt, Söti, Csaba, Partridge, Linda, Gems, David
Publicado 2011

Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology

por Takeda, Andrew J., Maher, Timothy J., Zhang, Yu, Lanahan, Stephen M., Bucklin, Molly L., Compton, Susan R., Tyler, Paul M., Comrie, William A., Matsuda, Makoto, Olivier, Kenneth N., Pittaluga, Stefania, McElwee, Joshua J., Long Priel, Debra A., Kuhns, Douglas B., Williams, Roger L., Mustillo, Peter J., Wymann, Matthias P., Koneti Rao, V., Lucas, Carrie L.
Publicado 2019

Recurrent rhinovirus infections in a child with inherited MDA5 deficiency

por Lamborn, Ian T., Jing, Huie, Zhang, Yu, Drutman, Scott B., Abbott, Jordan K., Munir, Shirin, Bade, Sangeeta, Murdock, Heardley M., Santos, Celia P., Brock, Linda G., Masutani, Evan, Fordjour, Emmanuel Y., McElwee, Joshua J., Hughes, Jason D., Nichols, Dave P., Belkadi, Aziz, Oler, Andrew J., Happel, Corinne S., Matthews, Helen F., Abel, Laurent, Collins, Peter L., Subbarao, Kanta, Gelfand, Erwin W., Ciancanelli, Michael J., Casanova, Jean-Laurent, Su, Helen C.
Publicado 2017

Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

por Abolhassani, Hassan, Edwards, Emily S.J., Ikinciogullari, Aydan, Jing, Huie, Borte, Stephan, Buggert, Marcus, Du, Likun, Matsuda-Lennikov, Mami, Romano, Rosa, Caridha, Rozina, Bade, Sangeeta, Zhang, Yu, Frederiksen, Juliet, Fang, Mingyan, Bal, Sevgi Kostel, Haskologlu, Sule, Dogu, Figen, Tacyildiz, Nurdan, Matthews, Helen F., McElwee, Joshua J., Gostick, Emma, Price, David A., Palendira, Umaimainthan, Aghamohammadi, Asghar, Boisson, Bertrand, Rezaei, Nima, Karlsson, Annika C., Lenardo, Michael J., Casanova, Jean-Laurent, Hammarström, Lennart, Tangye, Stuart G., Su, Helen C., Pan-Hammarström, Qiang
Publicado 2017

BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency

por Afzali, Behdad, Grönholm, Juha, Vandrovcova, Jana, O’Brien, Charlotte, Sun, Hong-Wei, Vanderleyden, Ine, Davis, Fred P, Khoder, Ahmad, Zhang, Yu, Hegazy, Ahmed N, Villarino, Alejandro V, Palmer, Ira W, Kaufman, Joshua, Watts, Norman R, Kazemian, Majid, Kamenyeva, Olena, Keith, Julia, Sayed, Anwar, Kasperaviciute, Dalia, Mueller, Michael, Hughes, Jason D., Fuss, Ivan J., Sadiyah, Mohammed F, Montgomery-Recht, Kim, McElwee, Joshua, Restifo, Nicholas P, Strober, Warren, Linterman, Michelle A, Wingfield, Paul T, Uhlig, Holm H, Roychoudhuri, Rahul, Aitman, Timothy J., Kelleher, Peter, Lenardo, Michael J, O’Shea, John J, Cooper, Nichola, Laurence, Arian DJ
Publicado 2017

Phenome-wide association studies across large population cohorts support drug target validation

por Diogo, Dorothée, Tian, Chao, Franklin, Christopher S., Alanne-Kinnunen, Mervi, March, Michael, Spencer, Chris C. A., Vangjeli, Ciara, Weale, Michael E., Mattsson, Hannele, Kilpeläinen, Elina, Sleiman, Patrick M. A., Reilly, Dermot F., McElwee, Joshua, Maranville, Joseph C., Chatterjee, Arnaub K., Bhandari, Aman, Nguyen, Khanh-Dung H., Estrada, Karol, Reeve, Mary-Pat, Hutz, Janna, Bing, Nan, John, Sally, MacArthur, Daniel G., Salomaa, Veikko, Ripatti, Samuli, Hakonarson, Hakon, Daly, Mark J., Palotie, Aarno, Hinds, David A., Donnelly, Peter, Fox, Caroline S., Day-Williams, Aaron G., Plenge, Robert M., Runz, Heiko
Publicado 2018

Germline hypomorphic CARD11 mutations in severe atopic disease

por Ma, Chi A, Stinson, Jeffrey R, Zhang, Yuan, Abbott, Jordan K, Weinreich, Michael A, Hauk, Pia J, Reynolds, Paul R, Lyons, Jonathan J, Nelson, Celeste G, Ruffo, Elisa, Dorjbal, Batsukh, Glauzy, Salomé, Yamakawa, Natsuko, Arjunaraja, Swadhinya, Voss, Kelsey, Stoddard, Jennifer, Niemela, Julie, Zhang, Yu, Rosenzweig, Sergio D, McElwee, Joshua J, DiMaggio, Thomas, Matthews, Helen F, Jones, Nina, Stone, Kelly D, Palma, Alejandro, Oleastro, Matías, Prieto, Emma, Bernasconi, Andrea R, Dubra, Geronimo, Danielian, Silvia, Zaiat, Jonathan, Marti, Marcelo A, Kim, Brian, Cooper, Megan A, Romberg, Neil D, Meffre, Eric, Gelfand, Erwin W, Snow, Andrew L, Milner, Joshua D
Publicado 2017

Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms

por Chovanec, Jack, Tunc, Ilker, Hughes, Jason, Halstead, Joseph, Mateja, Allyson, Liu, Yihui, O’Connell, Michael P., Kim, Jiwon, Park, Young Hwan, Wang, Qinlu, Le, Quang, Pirooznia, Mehdi, Trivedi, Neil N., Bai, Yun, Yin, Yuzhi, Hsu, Amy P., McElwee, Joshua, Lassiter, Sheryce, Nelson, Celeste, Bandoh, Judy, DiMaggio, Thomas, Šelb, Julij, Rijavec, Matija, Carter, Melody C., Komarow, Hirsh D., Sabato, Vito, Steinberg, Joshua, Hafer, Kurt M., Feuille, Elizabeth, Hourigan, Christopher S., Lack, Justin, Khoury, Paneez, Maric, Irina, Zanotti, Roberta, Bonadonna, Patrizia, Schwartz, Lawrence B., Milner, Joshua D., Glover, Sarah C., Ebo, Didier G., Korošec, Peter, Caughey, George H., Brittain, Erica H., Busby, Ben, Metcalfe, Dean D., Lyons, Jonathan J.
Publicado 2022