檢索結果 - Li, Samuel

Axial and appendicular body proportions for evaluation of limb and trunk asymmetry 由 Weinberg, Douglas S, Liu, Raymond W, Li, Samuel Q, Sanders, James O, Cooperman, Daniel R

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Extracellular Vesicle-Based Therapeutics: Preclinical and Clinical Investigations 由 Klyachko, Natalia L., Arzt, Camryn J., Li, Samuel M., Gololobova, Olesia A., Batrakova, Elena V.

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Identification of potent Yes1 kinase inhibitors using a library screening approach 由 Patel, Paresma R., Sun, Hongmao, Li, Samuel Q., Shen, Min, Khan, Javed, Thomas, Craig J., Davis, Mindy I.

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Targeting Wild-Type and Mutationally Activated FGFR4 in Rhabdomyosarcoma with the Inhibitor Ponatinib (AP24534) 由 Li, Samuel Q., Cheuk, Adam T., Shern, Jack F., Song, Young K., Hurd, Laura, Liao, Hongling, Wei, Jun S., Khan, Javed

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Mitochondrial DNA Content Is Linked to Cardiovascular Disease Patient Phenotypes 由 Wei,, Ruipeng, Ni,, Ying, Bazeley,, Peter, Grandhi,, Sneha, Wang,, Janet, Li,, Samuel T., Hazen,, Stanley L., Wilson Tang,, W. H., LaFramboise,, Thomas

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FoxM1c Counteracts Oxidative Stress-induced Senescence and Stimulates Bmi-1 Expression 由 Li, Samuel K. M., Smith, David K., Leung, Wai Ying, Cheung, Alice M. S., Lam, Eric W. F., Dimri, Goberdhan P., Yao, Kwok-Ming

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Extracellular Vesicles as Drug Delivery System for Treatment of Neurodegenerative Disorders: Optimization of the Cell Source 由 Haney, Matthew J., Zhao, Yuling, Fallon, John K., Yue, Wang, Li, Samuel M., Lentz, Emily E., Erie, Dorothy, Smith, Philip C., Batrakova, Elena V.

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Rare germline variant contributions to myeloid malignancy susceptibility 由 Li, Samuel T., Wang, Janet, Wei, Ruipeng, Shi, Ruqi, Adema, Vera, Nagata, Yasunobu, Kerr, Cassandra M., Kuzmanovic, Teodora, Przychodzen, Bartlomiej, Sole, Francesc, Maciejewski, Jaroslaw P., LaFramboise, Thomas

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Massively Parallel Sequencing Reveals an Accumulation of De Novo Mutations and an Activating Mutation of LPAR1 in a Patient with Metastatic Neuroblastoma 由 Wei, Jun S., Johansson, Peter, Chen, Li, Song, Young K., Tolman, Catherine, Li, Samuel, Hurd, Laura, Patidar, Rajesh, Wen, Xinyu, Badgett, Thomas C., Cheuk, Adam T. C., Marshall, Jean-Claude, Steeg, Patricia S., Vaqué Díez, José P., Yu, Yanlin, Gutkind, J. Silvio, Khan, Javed

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Single cell RNA sequencing of AML initiating cells reveals RNA-based evolution during disease progression 由 Stetson, L. C., Balasubramanian, Dheepa, Ribeiro, Susan Pereira, Stefan, Tammy, Gupta, Kalpana, Xu, Xuan, Fourati, Slim, Roe, Anne, Jackson, Zachary, Schauner, Robert, Sharma, Ashish, Tamilselvan, Banumathi, Li, Samuel, de Lima, Marcos, Hwang, Tae Hyun, Balderas, Robert, Saunthararajah, Yogen, Maciejewski, Jaroslaw, LaFramboise, Thomas, Barnholtz-Sloan, Jill S., Sekaly, Rafick-Pierre, Wald, David N.

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Germline loss-of-function SAMD9 and SAMD9L alterations in adult myelodysplastic syndromes 由 Nagata, Yasunobu, Narumi, Satoshi, Guan, Yihong, Przychodzen, Bartlomiej P., Hirsch, Cassandra M., Makishima, Hideki, Shima, Hirohito, Aly, Mai, Pastor, Victor, Kuzmanovic, Teodora, Radivoyevitch, Tomas, Adema, Vera, Awada, Hassan, Yoshida, Kenichi, Li, Samuel, Sole, Francesc, Hanna, Rabi, Jha, Babal K., LaFramboise, Thomas, Ogawa, Seishi, Sekeres, Mikkael A., Wlodarski, Marcin W., Cammenga, Jörg, Maciejewski, Jaroslaw P.

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Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong 由 Chung, Claudia Ching Yan, Chan, Kelvin Yuen Kwong, Hui, Pui Wah, Au, Patrick Kwok Cheung, Tam, Wai Keung, Li, Samuel Kai Man, Leung, Gordon Ka Chun, Fung, Jasmine Lee Fong, Chan, Marcus Chun Yin, Luk, Ho Ming, Mak, Annisa Shui Lam, Leung, Kwok Yin, Tang, Mary Hoi Yin, Chung, Brian Hon Yin, Kan, Anita Sik Yau

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