检索结果 - Prasad, Megana

Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family rais... 由 Goussot, Raphaëlle, Prasad, Megana, Stoetzel, Corinne, Lenormand, Cédric, Dollfus, Hélène, Lipsker, Dan

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Peroxisome-proliferator-activated receptor-binding protein (PBP) is essential for the growth of active Notch4-immortalized mammary epithelial cells by activating SOX10 expression 由 Zhu, Yiwei Tony, Jia, Yuzhi, Hu, Liping, Qi, Chao, Prasad, Megana K., McCallion, Andrew S., Zhu, Yi-Jun

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Close association of olfactory placode precursors and cranial neural crest cells does not predestine cell mixing 由 Harden, Maegan V., Pereiro, Luisa, Ramialison, Mirana, Wittbrodt, Jochen, Prasad, Megana K., McCallion, Andrew S., Whitlock, Kathleen E.

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Allele-specific enhancers mediate associations between LCAT and ABCA1 polymorphisms and HDL metabolism 由 Howard, Alicia D., Wang, Xiaochun, Prasad, Megana, Sahu, Avinash Das, Aniba, Radhouane, Miller, Michael, Hannenhalli, Sridhar, Chang, Yen-Pei Christy

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A Polymorphic 3’UTR Element in ATP1B1 Regulates Alternative Polyadenylation and Is Associated with Blood Pressure 由 Prasad, Megana K., Bhalla, Kavita, Pan, Zhen Hua, O’Connell, Jeffrey R., Weder, Alan B., Chakravarti, Aravinda, Tian, Bin, Chang, Yen-Pei C.

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Insights into Ciliary Genes and Evolution from Multi-Level Phylogenetic Profiling 由 Nevers, Yannis, Prasad, Megana K., Poidevin, Laetitia, Chennen, Kirsley, Allot, Alexis, Kress, Arnaud, Ripp, Raymond, Thompson, Julie D., Dollfus, Hélène, Poch, Olivier, Lecompte, Odile

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SOX10 Regulates Expression of the SH3-Domain Kinase Binding Protein 1 (Sh3kbp1) locus in Schwann Cells via an Alternative Promoter 由 Hodonsky, Chani J., Kleinbrink, Erica L., Charney, Kira N., Prasad, Megana, Bessling, Seneca L., Jones, Erin A., Srinivasan, Rajini, Svaren, John, McCallion, Andrew S., Antonellis, Anthony

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Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta 由 Gasse, Barbara, Prasad, Megana, Delgado, Sidney, Huckert, Mathilde, Kawczynski, Marzena, Garret-Bernardin, Annelyse, Lopez-Cazaux, Serena, Bailleul-Forestier, Isabelle, Manière, Marie-Cécile, Stoetzel, Corinne, Bloch-Zupan, Agnès, Sire, Jean-Yves

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Alzheimer’s Risk Gene TREM2 Determines Functional Properties of New Type of Human iPSC-Derived Microglia 由 Reich, Marvin, Paris, Iñaki, Ebeling, Martin, Dahm, Nadine, Schweitzer, Christophe, Reinhardt, Dieter, Schmucki, Roland, Prasad, Megana, Köchl, Fabian, Leist, Marcel, Cowley, Sally A., Zhang, Jitao David, Patsch, Christoph, Gutbier, Simon, Britschgi, Markus

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SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer 由 Prasad, Megana K, Reed, Xylena, Gorkin, David U, Cronin, Julia C, McAdow, Anthony R, Chain, Kristopher, Hodonsky, Chani J, Jones, Erin A, Svaren, John, Antonellis, Anthony, Johnson, Stephen L, Loftus, Stacie K, Pavan, William J, McCallion, Andrew S

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Gpnmb is a Melanoblast-Expressed, MITF-Dependent Gene 由 Loftus, Stacie K., Antonellis, Anthony, Matera, Ivana, Renaud, Gabriel, Baxter, Laura L., Reid, Duncan, Wolfsberg, Tyra G., Chen, Yidong, Wang, ChenWei, Prasad, Megana K., Bessling, Seneca L., McCallion, Andrew S., Green, Eric D., Bennett, Dorothy C., Pavan, William J.

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Neuropathy target esterase impairments cause Oliver–McFarlane and Laurence–Moon syndromes 由 Hufnagel, Robert B, Arno, Gavin, Hein, Nichole D, Hersheson, Joshua, Prasad, Megana, Anderson, Yvonne, Krueger, Laura A, Gregory, Louise C, Stoetzel, Corinne, Jaworek, Thomas J, Hull, Sarah, Li, Abi, Plagnol, Vincent, Willen, Christi M, Morgan, Thomas M, Prows, Cynthia A, Hegde, Rashmi S, Riazuddin, Saima, Grabowski, Gregory A, Richardson, Rudy J, Dieterich, Klaus, Huang, Taosheng, Revesz, Tamas, Martinez-Barbera, J P, Sisk, Robert A, Jefferies, Craig, Houlden, Henry, Dattani, Mehul T, Fink, John K, Dollfus, Helene, Moore, Anthony T, Ahmed, Zubair M

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Mutations in the latent TGF-beta binding protein 3 (LTBP3) gene cause brachyolmia with amelogenesis imperfecta 由 Huckert, Mathilde, Stoetzel, Corinne, Morkmued, Supawich, Laugel-Haushalter, Virginie, Geoffroy, Véronique, Muller, Jean, Clauss, François, Prasad, Megana K., Obry, Frédéric, Raymond, Jean Louis, Switala, Marzena, Alembik, Yves, Soskin, Sylvie, Mathieu, Eric, Hemmerlé, Joseph, Weickert, Jean-Luc, Dabovic, Branka Brukner, Rifkin, Daniel B., Dheedene, Annelies, Boudin, Eveline, Caluseriu, Oana, Cholette, Marie-Claude, Mcleod, Ross, Antequera, Reynaldo, Gellé, Marie-Paule, Coeuriot, Jean-Louis, Jacquelin, Louis-Frédéric, Bailleul-Forestier, Isabelle, Manière, Marie-Cécile, Van Hul, Wim, Bertola, Debora, Dollé, Pascal, Verloes, Alain, Mortier, Geert, Dollfus, Hélène, Bloch-Zupan, Agnès

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