日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Longitudinal Study on the Antimicrobial Performance of a Polyhexamethylene Biguanide (PHMB)-Treated Textile Fabric in a Hospital Environment

医院环境中聚六亚甲基双胍(PHMB)处理纺织织物抗菌性能的纵向研究

Yim, Sui-Lung; Cheung, Jessie Wing-Yi; Cheng, Iris Yuk-Ching; Ho, Lewis Wai-Hong; Szeto, Suet-Yee Sandy; Chan, Pinky; Lam, Yin-Ling; Kan, Chi-Wai

Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis

用于基因组分析的环境微生物真核生物单细胞分离和基因组扩增的协议

Doina Ciobanu, Sandy Chan, Steven Ahrendt, C Alisha Quandt, Gerald L Benny, Matthew E Smith, Timothy Y James, Jan-Fang Cheng

Primary brain calcification: an international study reporting novel variants and associated phenotypes

原发性脑钙化:一项报告新变异及相关表型的国际研究

Ramos, Eliana Marisa; Carecchio, Miryam; Lemos, Roberta; Ferreira, Joana; Legati, Andrea; Sears, Renee Louise; Hsu, Sandy Chan; Panteghini, Celeste; Magistrelli, Luca; Salsano, Ettore; Esposito, Silvia; Taroni, Franco; Richard, Anne-Claire; Tranchant, Christine; Anheim, Mathieu; Ayrignac, Xavier; Goizet, Cyril; Vidailhet, Marie; Maltete, David; Wallon, David; Frebourg, Thierry; Pimentel, Lylyan; Geschwind, Daniel H; Vanakker, Olivier; Galasko, Douglas; Fogel, Brent L; Innes, A Micheil; Ross, Alison; Dobyns, William B; Alcantara, Diana; O'Driscoll, Mark; Hannequin, Didier; Campion, Dominique; Oliveira, João R; Garavaglia, Barbara; Coppola, Giovanni; Nicolas, Gaël

A novel mutation P112H in the TARDBP gene associated with frontotemporal lobar degeneration without motor neuron disease and abundant neuritic amyloid plaques

TARDBP基因中的一种新型突变P112H与额颞叶变性相关,但无运动神经元疾病,且伴有大量神经炎性淀粉样斑块。

Moreno, Fermin; Rabinovici, Gil D; Karydas, Anna; Miller, Zachary; Hsu, Sandy Chan; Legati, Andrea; Fong, Jamie; Schonhaut, Daniel; Esselmann, Hermann; Watson, Christa; Stephens, Melanie L; Kramer, Joel; Wiltfang, Jens; Seeley, William W; Miller, Bruce L; Coppola, Giovanni; Grinberg, Lea Tenenholz

TDP-43 frontotemporal lobar degeneration and autoimmune disease

TDP-43额颞叶变性和自身免疫性疾病

Miller, Zachary A; Rankin, Katherine P; Graff-Radford, Neill R; Takada, Leonel T; Sturm, Virginia E; Cleveland, Clare M; Criswell, Lindsey A; Jaeger, Philipp A; Stan, Trisha; Heggeli, Kristin A; Hsu, Sandy Chan; Karydas, Anna; Khan, Baber K; Grinberg, Lea T; Gorno-Tempini, Maria Luisa; Boxer, Adam L; Rosen, Howard J; Kramer, Joel H; Coppola, Giovanni; Geschwind, Daniel H; Rademakers, Rosa; Seeley, William W; Wyss-Coray, Tony; Miller, Bruce L

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification

SLC20A2基因突变是家族性特发性基底节钙化的主要原因。

Hsu, Sandy Chan; Sears, Renee L; Lemos, Roberta R; Quintáns, Beatriz; Huang, Alden; Spiteri, Elizabeth; Nevarez, Lisette; Mamah, Catherine; Zatz, Mayana; Pierce, Kerrie D; Fullerton, Janice M; Adair, John C; Berner, Jon E; Bower, Matthew; Brodaty, Henry; Carmona, Olga; Dobricić, Valerija; Fogel, Brent L; García-Estevez, Daniel; Goldman, Jill; Goudreau, John L; Hopfer, Suellen; Janković, Milena; Jaumà, Serge; Jen, Joanna C; Kirdlarp, Suppachok; Klepper, Joerg; Kostić, Vladimir; Lang, Anthony E; Linglart, Agnès; Maisenbacher, Melissa K; Manyam, Bala V; Mazzoni, Pietro; Miedzybrodzka, Zofia; Mitarnun, Witoon; Mitchell, Philip B; Mueller, Jennifer; Novaković, Ivana; Paucar, Martin; Paulson, Henry; Simpson, Sheila A; Svenningsson, Per; Tuite, Paul; Vitek, Jerrold; Wetchaphanphesat, Suppachok; Williams, Charles; Yang, Michele; Schofield, Peter R; de Oliveira, João R M; Sobrido, María-Jesús; Geschwind, Daniel H; Coppola, Giovanni