Long-Term Delivery of an Anti-SIV Monoclonal Antibody With AAV von Martinez-Navio, José M, Fuchs, Sebastian P, Mendes, Desiree E, Rakasz, Eva G, Gao, Guangping, Lifson, Jeffrey D, Desrosiers, Ronald C

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Definition of functionally and structurally distinct repressive states in the nuclear receptor PPARγ von Heidari, Zahra, Chrisman, Ian M., Nemetchek, Michelle D., Novick, Scott J., Blayo, Anne-Laure, Patton, Trey, Mendes, Desiree E., Diaz, Philippe, Kamenecka, Theodore M., Griffin, Patrick R., Hughes, Travis S.

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High concordance of ELISA and neutralization assays allows for the detection of antibodies to individual AAV serotypes von Gardner, Matthew R., Mendes, Desiree E., Muniz, Claudia P., Martinez-Navio, José M., Fuchs, Sebastian P., Gao, Guangping, Desrosiers, Ronald C.

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Functional prostate-specific membrane antigen is enriched in exosomes from prostate cancer cells von LIU, TIANCHENG, MENDES, DESIREE E, BERKMAN, CLIFFORD E

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From AR to c-Met: Androgen deprivation leads to a signaling pathway switch in prostate cancer cells von LIU, TIANCHENG, MENDES, DESIREE E, BERKMAN, CLIFFORD E

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Prolonged androgen deprivation leads to overexpression of calpain 2: Implications for prostate cancer progression von LIU, TIANCHENG, MENDES, DESIREE E, BERKMAN, CLIFFORD E

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Phosphoramidate-based peptidomimetic inhibitors of membrane type-1 matrix metalloproteinase von Mendes, Desiree E., Wong-On-Wing, Annie, Berkman, Clifford E.

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Citrus Peel Additives for One-Pot Triazole Formation by Decarboxylation, Nucleophilic Substitution, and Azide–Alkyne Cycloaddition Reactions von Mendes, Desiree E, Schoffstall, Allen M

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Biochemical characterization of prostate-specific membrane antigen from canine prostate carcinoma cells von Wu, Lisa Y., Johnson, Jacqueline M., Simmons, Jessica K., Mendes, Desiree E., Geruntho, Jonathan J., Liu, Tiancheng, Dirksen, Wessel P., Rosol, Thomas J., Davis, William C., Berkman, Clifford E.

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Biochemical characterization of prostate-specific membrane antigen from canine prostate carcinoma cells: PSMA Expression in Canine Prostate Cancer von Wu, Lisa Y., Johnson, Jacqueline M., Simmons, Jessica K., Mendes, Desiree E., Geruntho, Jonathan J., Liu, Tiancheng, Dirksen, Wessel P., Rosol, Thomas J., Davis, William C., Berkman, Clifford E.

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Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly von Wang, Lu, Li, Zhen, Sievert, David, Smith, Desirée E. C., Mendes, Marisa I., Chen, Dillon Y., Stanley, Valentina, Ghosh, Shereen, Wang, Yulu, Kara, Majdi, Aslanger, Ayca Dilruba, Rosti, Rasim O., Houlden, Henry, Salomons, Gajja S., Gleeson, Joseph G.

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Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy von Botta, Elena, Theil, Arjan F, Raams, Anja, Caligiuri, Giuseppina, Giachetti, Sarah, Bione, Silvia, Accadia, Maria, Lombardi, Anita, Smith, Desiree E C, Mendes, Marisa I, Swagemakers, Sigrid M A, van der Spek, Peter J, Salomons, Gajja S, Hoeijmakers, Jan H J, Yesodharan, Dhanya, Nampoothiri, Sheela, Ogi, Tomoo, Lehmann, Alan R, Orioli, Donata, Vermeulen, Wim

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Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype von Theil, Arjan F., Botta, Elena, Raams, Anja, Smith, Desiree E.C., Mendes, Marisa I., Caligiuri, Giuseppina, Giachetti, Sarah, Bione, Silvia, Carriero, Roberta, Liberi, Giordano, Zardoni, Luca, Swagemakers, Sigrid M.A., Salomons, Gajja S., Sarasin, Alain, Lehmann, Alan, van der Spek, Peter J., Ogi, Tomoo, Hoeijmakers, Jan H.J., Vermeulen, Wim, Orioli, Donata

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Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy von van der Knaap, Marjo S, Bugiani, Marianna, Mendes, Marisa I, Riley, Lisa G, Smith, Desiree E.C, Rudinger-Thirion, Joëlle, Frugier, Magali, Breur, Marjolein, Crawford, Joanna, van Gaalen, Judith, Schouten, Meyke, Willems, Marjolaine, Waisfisz, Quinten, Mau-Them, Frederic Tran, Rodenburg, Richard J, Taft, Ryan J, Keren, Boris, Christodoulou, John, Depienne, Christel, Simons, Cas, Salomons, Gajja S, Mochel, Fanny

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Cysteinyl-tRNA Synthetase Mutations Cause a Multi-System, Recessive Disease That Includes Microcephaly, Developmental Delay, and Brittle Hair and Nails von Kuo, Molly E., Theil, Arjan F., Kievit, Anneke, Malicdan, May Christine, Introne, Wendy J., Christian, Thomas, Verheijen, Frans W., Smith, Desiree E.C., Mendes, Marisa I., Hussaarts-Odijk, Lidia, van der Meijden, Eric, van Slegtenhorst, Marjon, Wilke, Martina, Vermeulen, Wim, Raams, Anja, Groden, Catherine, Shimada, Shino, Meyer-Schuman, Rebecca, Hou, Ya Ming, Gahl, William A., Antonellis, Anthony, Salomons, Gajja S., Mancini, Grazia M.S.

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Treatment of ARS deficiencies with specific amino acids von Kok, Gautam, Tseng, Laura, Schene, Imre F., Dijsselhof, Monique E., Salomons, Gajja, Mendes, Marisa I., Smith, Desiree E. C., Wiedemann, Arnaud, Canton, Marie, Feillet, François, de Koning, Tom J., Boothe, Megan, Dean, Joy, Kassel, Rachel, Ferreira, Elise A., van den Born, Margreet, Nieuwenhuis, Edward E. S., Rehmann, Holger, Terheggen-Lagro, Suzanne W. J., van Karnebeek, Clara D. M., Fuchs, Sabine A.

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FARS1‐related disorders caused by bi‐allelic mutations in cytosolic phenylalanyl‐tRNA synthetase genes: Look beyond the lungs von Schuch, Luise A., Forstner, Maria, Rapp, Christina K., Li, Yang, Smith, Desiree E. C., Mendes, Marisa I., Delhommel, Florent, Sattler, Michael, Emiralioğlu, Nagehan, Taskiran, Ekim Z., Orhan, Diclehan, Kiper, Nural, Rohlfs, Meino, Jeske, Tim, Hastreiter, Maximilian, Gerstlauer, Michael, Torrent‐Vernetta, Alba, Moreno‐Galdó, Antonio, Kammer, Birgit, Brasch, Frank, Reu‐Hofer, Simone, Griese, Matthias

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WARS1 and SARS1: Two tRNA synthetases implicated in autosomal recessive microcephaly von Bögershausen, Nina, Krawczyk, Hannah E., Jamra, Rami A., Lin, Sheng‐Jia, Yigit, Gökhan, Hüning, Irina, Polo, Anna M., Vona, Barbara, Huang, Kevin, Schmidt, Julia, Altmüller, Janine, Luppe, Johannes, Platzer, Konrad, Dörgeloh, Beate B., Busche, Andreas, Biskup, Saskia, Mendes, Marisa I., Smith, Desiree E. C., Salomons, Gajja S., Zibat, Arne, Bültmann, Eva, Nürnberg, Peter, Spielmann, Malte, Lemke, Johannes R., Li, Yun, Zenker, Martin, Varshney, Gaurav K., Hillen, Hauke S., Kratz, Christian P., Wollnik, Bernd

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Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy von Mendes, Marisa I., Gutierrez Salazar, Mariana, Guerrero, Kether, Thiffault, Isabelle, Salomons, Gajja S., Gauquelin, Laurence, Tran, Luan T., Forget, Diane, Gauthier, Marie-Soleil, Waisfisz, Quinten, Smith, Desiree E.C., Simons, Cas, van der Knaap, Marjo S., Marquardt, Iris, Lemes, Aida, Mierzewska, Hanna, Weschke, Bernhard, Koehler, Wolfgang, Coulombe, Benoit, Wolf, Nicole I., Bernard, Geneviève

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Expanded phenotype of AARS1-related white matter disease von Helman, Guy, Mendes, Marisa I., Nicita, Francesco, Darbelli, Lama, Sherbini, Omar, Moore, Travis, Derksen, Alexa, Amy Pizzino, Carrozzo, Rosalba, Torraco, Alessandra, Catteruccia, Michela, Aiello, Chiara, Goffrini, Paola, Figuccia, Sonia, Smith, Desiree E. C., Hadzsiev, Kinga, Hahn, Andreas, Biskup, Saskia, Brösse, Ines, Kotzaeridou, Urania, Gauck, Darja, Grebe, Theresa A., Elmslie, Frances, Stals, Karen, Gupta, Rajat, Bertini, Enrico, Thiffault, Isabelle, Taft, Ryan J., Schiffmann, Raphael, Brandl, Ulrich, Haack, Tobias B., Salomons, Gajja S., Simons, Cas, Bernard, Geneviève, van der Knaap, Marjo S., Vanderver, Adeline, Husain, Ralf A.

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