MLT-10 Defines a Family of DUF644 and Proline-rich Repeat Proteins Involved in the Molting Cycle of Caenorhabditis elegans

por Meli, Vijaykumar S., Osuna, Beatriz, Ruvkun, Gary, Frand, Alison R.
Publicado 2010

Host and viral factors associated with severity of human rhinovirus–associated infant respiratory tract illness

por Miller, E. Kathryn, Williams, John V., Gebretsadik, Tebeb, Carroll, Kecia N., Dupont, William D., Mohamed, Yassir A., Morin, Laura-Lee, Heil, Luke, Minton, Patricia A., Woodward, Kimberly, Liu, Zhouwen, Hartert, Tina V.
Publicado 2011

SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families

por Cornejo-Sanchez, Diana M., Acharya, Anushree, Bharadwaj, Thashi, Marin-Gomez, Lizeth, Pereira-Gomez, Pilar, Nouel-Saied, Liz M., Nickerson, Deborah A., Bamshad, Michael J., Mefford, Heather C., Schrauwen, Isabelle, Carrizosa-Moog, Jaime, Cornejo-Ochoa, William, Pineda-Trujillo, Nicolas, Leal, Suzanne M.
Publicado 2022

Close Encounters of the First Kind: An Interdisciplinary Ethics of Care Approach Mitigates Moral Injury and Family Division in the Midst of Covid-19

por Berlin, Ana
Publicado 2022

Upregulated SPAG6 promotes acute myeloid leukemia progression through MYO1D that regulates the EGFR family expression

por Mu, Jiao, Yuan, Peng, Luo, Jie, Chen, Yafan, Tian, Yiyuan, Ding, Li, Zhao, Beibei, Wang, Xiaocheng, Wang, Bao, Liu, Lin
Publicado 2022

Genome-wide association study of Tourette Syndrome

por Scharf, Jeremiah M., Yu, Dongmei, Mathews, Carol A., Neale, Benjamin M., Stewart, S. Evelyn, Fagerness, Jesen A, Evans, Patrick, Gamazon, Eric, Edlund, Christopher K., Service, Susan, Tikhomirov, Anna, Osiecki, Lisa, Illmann, Cornelia, Pluzhnikov, Anna, Konkashbaev, Anuar, Davis, Lea K, Han, Buhm, Crane, Jacquelyn, Moorjani, Priya, Crenshaw, Andrew T., Parkin, Melissa A., Reus, Victor I., Lowe, Thomas L., Rangel-Lugo, Martha, Chouinard, Sylvain, Dion, Yves, Girard, Simon, Cath, Danielle C, Smit, Jan H, King, Robert A., Fernandez, Thomas, Leckman, James F., Kidd, Kenneth K., Kidd, Judith R., Pakstis, Andrew J., State, Matthew, Herrera, Luis Diego, Romero, Roxana, Fournier, Eduardo, Sandor, Paul, Barr, Cathy L, Phan, Nam, Gross-Tsur, Varda, Benarroch, Fortu, Pollak, Yehuda, Budman, Cathy L., Bruun, Ruth D., Erenberg, Gerald, Naarden, Allan L, Lee, Paul C, Weiss, Nicholas, Kremeyer, Barbara, Berrío, Gabriel Bedoya, Campbell, Desmond, Silgado, Julio C. Cardona, Ochoa, William Cornejo, Restrepo, Sandra C. Mesa, Muller, Heike, Duarte, Ana V. Valencia, Lyon, Gholson J, Leppert, Mark, Morgan, Jubel, Weiss, Robert, Grados, Marco A., Anderson, Kelley, Davarya, Sarah, Singer, Harvey, Walkup, John, Jankovic, Joseph, Tischfield, Jay A., Heiman, Gary A., Gilbert, Donald L., Hoekstra, Pieter J., Robertson, Mary M., Kurlan, Roger, Liu, Chunyu, Gibbs, J. Raphael, Singleton, Andrew, Hardy, John, Strengman, Eric, Ophoff, Roel, Wagner, Michael, Moessner, Rainald, Mirel, Daniel B., Posthuma, Danielle, Sabatti, Chiara, Eskin, Eleazar, Conti, David V., Knowles, James A., Ruiz-Linares, Andres, Rouleau, Guy A., Purcell, Shaun, Heutink, Peter, Oostra, Ben A., McMahon, William, Freimer, Nelson, Cox, Nancy J., Pauls, David L.
Publicado 2012

Engagement With Tailored Physical Activity Content: Secondary Findings From the Families Improving Together for Weight Loss Randomized Controlled Trial

por Sweeney, Allison M, Wilson, Dawn K, Resnicow, Kenneth, Van Horn, M Lee, Kitzman, Heather
Publicado 2023

Pan-cancer analysis reveals distinct clinical, genomic, and immunological features of the LILRB immune checkpoint family in acute myeloid leukemia

por Xu, Zi-jun, Zhang, Xin-long, Jin, Ye, Wang, Shi-sen, Gu, Yu, Ma, Ji-chun, Wen, Xiang-mei, Leng, Jia-yan, Mao, Zhen-wei, Lin, Jiang, Qian, Jun
Publicado 2022

SUN-085 Clinical and Hormonal Features of 37 Families with Central Precocious Puberty Due to MKRN3 Loss-Of -Function Mutations

por Seraphim, Carlos Eduardo, Canton, Ana Pinheiro Machado, Montenegro, Luciana Ribeiro, Piovesan, Maiara Ribeiro, Bohlen, Tabata Mariz, Frazao, Renata, Macedo, Delanie Bulcão, de Faria, Aline Guimarães, Ramos, Carolina, Gagliardi, Priscila Carvalho, Abreu, Ana Paula, Leal, Andrea de Castro, Castro, Margaret De, Antonini, Sonir Roberto Rauber, Soriano-Guillén, Leandro, Escribano-Muñoz, Arancha, Collado, Raquel Corripio, Labarta, Jose Ignacio, Lourdes, Travieso-Suárez, Ortiz-Cabrera, Neimar Valentina, Argente, Jesús, Mendonca, Berenice Bilharinho, Kaiser, Ursula B, Brito, Vinicius Nahime, Latronico, Ana Claudia
Publicado 2020

TBC1D3 family is a prognostic biomarker and correlates with immune infiltration in kidney renal clear cell carcinoma

por Wang, Bei, Chen, Dandan, Hua, Haiying
Publicado 2021

Glutamate helps unmask the differences in driving forces for phase separation versus clustering of FET family proteins in sub-saturated solutions

por Kar, Mrityunjoy, Vogel, Laura T., Chauhan, Gaurav, Ausserwöger, Hannes, Welsh, Timothy J., Kamath, Anjana R., Knowles, Tuomas P. J., Hyman, Anthony A., Seidel, Claus A. M., Pappu, Rohit V.
Publicado 2023

Multiple Symmetric Lipomatosis (Madelung Disease) in a Large Canadian Family With the Mitochondrial MTTK c.8344A>G Variant

por Perera, Uththara, Kennedy, Brooke A., Hegele, Robert A.
Publicado 2018

Dual Roles for the TSPYL Family in Mediating Serotonin Transport and the Metabolism of Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder

por Qin, Sisi, Eugene, Andy R., Liu, Duan, Zhang, Lingxin, Neavin, Drew, Biernacka, Joanna M., Yu, Jia, Weinshilboum, Richard M., Wang, Liewei
Publicado 2019

Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy

por Kuroha, Yasuko, Ishiguro, Takanobu, Tada, Mari, Hara, Norikazu, Murayama, Kei, Kawachi, Izumi, Kasuga, Kensaku, Miyashita, Akinori, Hasegawa, Arika, Takahashi, Tetsuya, Matsubara, Nae, Onodera, Osamu, Kakita, Akiyoshi, Koike, Ryoko, Ikeuchi, Takeshi
Publicado 2022

The CHEK2 1100delC allelic variant is not present in familial and sporadic breast cancer cases from Moroccan population

por Marouf, Chaymaa, Hajji, Omar, Diakité, Brehima, Tazzite, Amal, Jouhadi, Hassan, Benider, Abdellatif, Nadifi, Sellama
Publicado 2015

Age-Dependent Differences in Frequent Mental Distress (FMD) of US Older Adults Living in Multigenerational Families versus Living Alone

por Das Gupta, Debasree, Wong, David W. S.
Publicado 2023

A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

por Zaib, Tahir, Ji, Wei, Saleem, Komal, Nie, Guangchen, Li, Chao, Cao, Lin, Xu, Baijun, Dong, Kexian, Yu, Hanfei, Hao, Xuguang, Xue, Yan, Si, Shuhan, Jia, Xueyuan, Wu, Jie, Zhang, Xuelong, Guan, Rongwei, Ji, Guohua, Bai, Jing, Chen, Feng, Liu, Yong, Sun, Wenjing, Fu, Songbin
Publicado 2019

A new perspective on the evolution and diversity of the genus Amdoparvovirus (family Parvoviridae) through genetic characterization, structural homology modeling, and phylogenetics

por Canuti, Marta, Pénzes, Judit J, Lang, Andrew S
Publicado 2022

mobileOG-db: a Manually Curated Database of Protein Families Mediating the Life Cycle of Bacterial Mobile Genetic Elements

por Brown, Connor L., Mullet, James, Hindi, Fadi, Stoll, James E., Gupta, Suraj, Choi, Minyoung, Keenum, Ishi, Vikesland, Peter, Pruden, Amy, Zhang, Liqing
Publicado 2022

Effect of a Family-Based Intervention on Nutrient Biomarkers, Desaturase Enzyme Activities, and Cardiometabolic Risk Factors in Children with Overweight and Obesity

por Matthan, Nirupa R, Wylie-Rosett, Judith, Xue, Xiaonan, Gao, Qi, Groisman-Perelstein, Adriana E, Diamantis, Pamela M, Ginsberg, Mindy, Mossavar-Rahmani, Yasmin, Barger, Kathryn, Lichtenstein, Alice H
Publicado 2019