Výsledky vyhledávání - Quintana, Anita M

The necessity for in vivo functional analysis in human medical genetics Autor Quintana, Anita M.

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Leading by example: developing mentoring strategies to promote diversity and student success Autor Quintana, Anita M.

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The role of HCFC1 in syndromic and non-syndromic intellectual disability. Autor Castro, Victoria L., Quintana, Anita M.

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Functional analysis of the zebrafish ortholog of HMGCS1 reveals independent functions for cholesterol and isoprenoids in craniofacial development Autor Quintana, Anita M., Hernandez, Jose A., Gonzalez, Cesar G.

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Knockdown of hspg2 is associated with abnormal mandibular joint formation and neural crest cell dysfunction in zebrafish Autor Castellanos, Barbara S., Reyes-Nava, Nayeli G., Quintana, Anita M.

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Identification and Regulation of c-Myb Target Genes in MCF-7 Cells Autor Quintana, Anita M, Liu, Fan, O'Rourke, John P, Ness, Scott A

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Zebrafish etv7 regulates red blood cell development through the cholesterol synthesis pathway Autor Quintana, Anita M., Picchione, Fabrizio, Klein Geltink, Ramon I., Taylor, Michael R., Grosveld, Gerard C.

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Mutations in the zebrafish hmgcs1 gene reveal a novel function for isoprenoids during red blood cell development Autor Hernandez, Jose A., Castro, Victoria L., Reyes-Nava, Nayeli, Montes, Laura P., Quintana, Anita M.

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Hcfc1a regulates neural precursor proliferation and asxl1 expression in the developing brain Autor Castro, Victoria L., Reyes, Joel F., Reyes-Nava, Nayeli G., Paz, David, Quintana, Anita M.

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Dramatic Repositioning of c-Myb to Different Promoters during the Cell Cycle Observed by Combining Cell Sorting with Chromatin Immunoprecipitation Autor Quintana, Anita M., Zhou, Ye E., Pena, Janeth J., O'Rourke, John P., Ness, Scott A.

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Abnormal expression of GABA(A) receptor subunits and hypomotility upon loss of gabra1 in zebrafish Autor Reyes-Nava, Nayeli G., Yu, Hung-Chun, Coughlin, Curtis R., Shaikh, Tamim H., Quintana, Anita M.

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Activation of WNT signaling restores the facial deficits in a zebrafish with defects in cholesterol metabolism Autor Castro, Victoria L., Reyes‐Nava, Nayeli G., Sanchez, Brianna B., Gonzalez, Cesar G., Paz, David, Quintana, Anita M.

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Hcfc1b, a zebrafish ortholog of HCFC1, regulates craniofacial development by modulating mmachc expression Autor Quintana, Anita M., Geiger, Elizabeth A., Achilly, Nate, Rosenblatt, David S., Maclean, Kenneth N., Stabler, Sally P., Artinger, Kristin B., Appel, Bruce, Shaikh, Tamim H.

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Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K Autor Conley, Mary Ellen, Dobbs, A. Kerry, Quintana, Anita M., Bosompem, Amma, Wang, Yong-Dong, Coustan-Smith, Elaine, Smith, Amber M., Perez, Elena E., Murray, Peter J.

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Kabuki syndrome genes KMT2D and KDM6A: functional analyses demonstrate critical roles in craniofacial, heart and brain development Autor Van Laarhoven, Peter M., Neitzel, Leif R., Quintana, Anita M, Geiger, Elizabeth A., Zackai, Elaine H., Clouthier, David E., Artinger, Kristin B., Ming, Jeffrey E., Shaikh, Tamim H.

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Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities Autor Quintana, Anita M., Yu, Hung-Chun, Brebner, Alison, Pupavac, Mihaela, Geiger, Elizabeth A., Watson, Abigail, Castro, Victoria L., Cheung, Warren, Chen, Shu-Huang, Watkins, David, Pastinen, Tomi, Skovby, Flemming, Appel, Bruce, Rosenblatt, David S., Shaikh, Tamim H.

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An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1 Autor Yu, Hung-Chun, Sloan, Jennifer L., Scharer, Gunter, Brebner, Alison, Quintana, Anita M., Achilly, Nathan P., Manoli, Irini, Coughlin, Curtis R., Geiger, Elizabeth A., Schneck, Una, Watkins, David, Suormala, Terttu, Van Hove, Johan L.K., Fowler, Brian, Baumgartner, Matthias R., Rosenblatt, David S., Venditti, Charles P., Shaikh, Tamim H.

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