Suchergebnisse - Beleford, Daniah

High Temperature Requirement A3 (HtrA3) Promotes Etoposide- and Cisplatin-induced Cytotoxicity in Lung Cancer Cell Lines von Beleford, Daniah, Rattan, Ramandeep, Chien, Jeremy, Shridhar, Viji

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Role of heparan sulfatases in ovarian and breast cancer von Khurana, Ashwani, Beleford, Daniah, He, Xiaoping, Chien, Jeremy, Shridhar, Viji

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Cell Proliferation and Epidermal Growth Factor Signaling in Non-small Cell Lung Adenocarcinoma Cell Lines Are Dependent on Rin1 von Tomshine, Jin C., Severson, Sandra R., Wigle, Dennis A., Sun, Zhifu, Beleford, Daniah A. T., Shridhar, Vijayalakshmi, Horazdovsky, Bruce F.

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Cleavage of PGRP-LC receptor in the Drosophila IMD pathway in response to live bacterial infection in S2 cells von Schmidt, Rebecca L, Rinaldo, Francesca M, Hesse, Shayla E, Hamada, Masakazu, Ortiz, Zachary, Beleford, Daniah T, Page-McCaw, Andrea, Platt, Jeffrey L, Tang, Amy H

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Familial melanoma-astrocytoma syndrome: synchronous diffuse astrocytoma and pleomorphic xanthoastrocytoma in a patient with germline CDKN2A/B deletion and a significant family hist... von Chan, Andrew K., Han, Seunggu J., Choy, Winward, Beleford, Daniah, Aghi, Manish K., Berger, Mitchel S., Shieh, Joseph T., Bollen, Andrew W., Perry, Arie, Phillips, Joanna J., Butowski, Nicholas, Solomon, David A.

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PATH-07. FAMILIAL MELANOMA-ASTROCYTOMA SYNDROME: SYNCHRONOUS DIFFUSE ASTROCYTOMA AND PLEOMORPHIC XANTHOASTROCYTOMA IN A PATIENT WITH GERMLINE CDKN2A/B DELETION AND A SIGNIFICANT FA... von Choy, Winward, Chan, Andrew K, Han, Seunggu J, Beleford, Daniah, Aghi, Manish K, Berger, Mitchel S, Shieh, Joseph T, Bollen, Andrew W, Perry, Arie, Phillips, Joanna J, Butowski, Nicholas, Solomon, David A

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Application of full-genome analysis to diagnose rare monogenic disorders von Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario

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Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders von Shieh, Joseph T., Penon-Portmann, Monica, Wong, Karen H. Y., Levy-Sakin, Michal, Verghese, Michelle, Slavotinek, Anne, Gallagher, Renata C., Mendelsohn, Bryce A., Tenney, Jessica, Beleford, Daniah, Perry, Hazel, Chow, Stephen K., Sharo, Andrew G., Brenner, Steven E., Qi, Zhongxia, Yu, Jingwei, Klein, Ophir D., Martin, David, Kwok, Pui-Yan, Boffelli, Dario

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Extracutaneous Manifestations in Phacomatosis Cesioflammea and Cesiomarmorata: Case Series and Literature Review von Kumar, Akash, Zastrow, Diane B, Kravets, Elijah J, Beleford, Daniah, Ruzhnikov, Maura RZ, Grove, Megan E., Dries, Annika M., Kohler, Jennefer N., Waggott, Daryl M., Yang, Yaping, Huang, Yong, Mackenzie, Katherine M., Eng, Christine M., Fisher, Paul G., Ashley, Euan A, Teng, Joyce M., Stevenson, David A., Shieh, Joseph T., Wheeler, Matthew T., Bernstein, Jonathan A.

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Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness von Slavotinek, Anne, Misceo, Doriana, Htun, Stephanie, Mathisen, Linda, Frengen, Eirik, Foreman, Michelle, Hurtig, Jennifer E, Enyenihi, Liz, Sterrett, Maria C, Leung, Sara W, Schneidman-Duhovny, Dina, Estrada-Veras, Juvianee, Duncan, Jacque L, Haaxma, Charlotte A, Kamsteeg, Erik-Jan, Xia, Vivian, Beleford, Daniah, Si, Yue, Douglas, Ganka, Treidene, Hans Einar, van Hoof, Ambro, Fasken, Milo B, Corbett, Anita H

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