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收藏分享 收藏 分享 收藏 分享 收藏 SARS-CoV-2 Viral Replication Persists in the Human Lung for Several Weeks after Symptom Onset症状发作后，SARS-CoV-2病毒复制在人肺中持续数周
Tomasicchio, Michele; Jaumdally, Shameem; Wilson, Lindsay; Kotze, Andrea; Semple, Lynn; Meier, Stuart; Pooran, Anil; Esmail, Aliasgar; Pillay, Komala; Roberts, Riyaadh; Kriel, Raymond; Meldau, Richard; Oelofse, Suzette; Mandviwala, Carley; Burns, Jessica; Londt, Rolanda; Davids, Malika; van der Merwe, Charnay; Roomaney, Aqeedah; Kuhn, Loui; Perumal, Tahlia; Scott, Alex J.; Hale, Martin J.; Baillie, Vicky; Mahtab, Sana; Williamson, Carolyn; Joseph, Rageema; Sigal, Alex; Joubert, Ivan; Piercy, Jenna; Thomson, David; Fredericks, David L.; Miller, Malcolm G. A.; Nunes, Marta C.; Madhi, Shabir A.; Dheda, Keertan 分享 收藏 分享 收藏 分享 收藏 T-Cell Homeostatic Imbalance in Placentas From Women With Human Immunodeficiency Virus in the Absence of Vertical TransmissionIkumi, Nadia M.; Pillay, Komala; Tilburgs, Tamara; Malaba, Thokozile R.; Dzanibe, Sonwabile; Enninga, Elizabeth Ann L.; Chakraborty, Rana; Lamorde, Mohammed; Myer, Landon; Khoo, Saye; Jaspan, Heather B.; Gray, Clive M. 分享 收藏 Differential impact of antiretroviral therapy initiated before or during pregnancy on placenta pathology in HIV-positive womenIkumi, Nadia M.; Malaba, Thokozile R.; Pillay, Komala; Cohen, Marta C.; Madlala, Hlengiwe P.; Matjila, Mushi; Anumba, Dilly; Myer, Landon; Newell, Marie-Louise; Gray, Clive M. 分享 收藏 分享 收藏 Renal dysfunction, rod-cone dystrophy, and sensorineural hearing loss caused by a mutation inRRM2BRoberts, Lisa; Julius, Stephanie; Dawlat, Shrinav; Yildiz, Safiye; Rebello, George; Meldau, Surita; Pillay, Komala; Esterhuizen, Alina; Vorster, Alvera; Benefeld, Gameda; da Rocha, Jorge; Beighton, Peter; Sellars, Sean L.; Thandrayen, Kebashni; Pettifor, John M.; Ramesar, Raj S. 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Epigenetic changes as a common trigger of muscle weakness in congenital myopathiesRokach, Ori; Sekulic-Jablanovic, Marijana; Voermans, Nicol; Wilmshurst, Jo; Pillay, Komala; Heytens, Luc; Zhou, Haiyan; Muntoni, Francesco; Gautel, Mathias; Nevo, Yoram; Mitrani-Rosenbaum, Stella; Attali, Ruben; Finotti, Alessia; Gambari, Roberto; Mosca, Barbara; Jungbluth, Heinz; Zorzato, Francesco; Treves, Susan 分享 收藏 Mutations in FAM111B Cause Hereditary Fibrosing Poikiloderma with Tendon Contracture, Myopathy, and Pulmonary FibrosisMercier, Sandra; Kuery, Sebastien; Shaboodien, Gasnat; Houniet, Darren T.; Khumalo, Nonhlanhla P.; Bou-Hanna, Chantal; Bodak, Nathalie; Cormier-Daire, Valerie; David, Albert; Faivre, Laurence; Figarella-Branger, Dominique; Gherardi, Romain K.; Glen, Elise; Hamel, Antoine; Laboisse, Christian; Le Caignec, Cedric; Lindenbaum, Pierre; Magot, Armelle; Munnich, Arnold; Mussini, Jean-Marie; Pillay, Komala; Rahman, Thahira; Redon, Richard; Salort-Campana, Emmanuelle; Santibanez-Koref, Mauro; Thauvin, Christel; Barbarot, Sebastien; Keavney, Bernard; Bezieau, Stephane; Mayosi, Bongani M. 分享 收藏 RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling先天性肌病中的RyR1缺乏会破坏兴奋-收缩耦合Zhou, Haiyan; Rokach, Ori; Feng, Lucy; Munteanu, Iulia; Mamchaoui, Kamel; Wilmshurst, Jo M.; Sewry, Caroline; Manzur, Adnan Y.; Pillay, Komala; Mouly, Vincent; Duchen, Michael; Jungbluth, Heinz; Treves, Susan; Muntoni, Francesco 分享 收藏 分享 收藏 RYR1 Mutations Are a Common Cause of Congenital Myopathies with Central NucleiWilmshurst, J. M.; Lillis, S.; Zhou, H.; Pillay, K.; Henderson, H.; Kress, W.; Mueller, C. R.; Ndondo, A.; Cloke, V.; Cullup, T.; Bertini, E.; Boennemann, C.; Straub, V.; Quinlivan, R.; Dowling, J. J.; Al-Sarraj, S.; Treves, S.; Abbs, S.; Manzur, A. Y.; Sewry, C. A.; Muntoni, F.; Jungbluth, H. 分享 收藏 分享 收藏 
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