renal type H⁺/peptide symporter PEPT2: structure-affinity relationships von Biegel, A, Knütter, I, Hartrodt, B, Gebauer, S, Theis, S, Luckner, P, Kottra, G, Rastetter, M, Zebisch, K, Thondorf, I, Daniel, H, Neubert, K, Brandsch, M

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CpG island methylation and expression of tumour-associated genes in lung carcinoma von Dammann, Reinhard, Strunnikova, Maria, Schagdarsurengin, Undraga, Rastetter, Matthias, Papritz, Mirko, Hattenhorst, Uwe E., Hofmann, Hans-Stefan, Silber, Rolf-Edgar, Burdach, Stefan, Hansen, Gesine

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Alterations of cancer‐related genes in soft tissue sarcomas: Hypermethylation of RASSF1A is frequently detected in leiomyosarcoma and associated with poor prognosis in sarcoma von Seidel, Claudia, Bartel, Frank, Rastetter, Matthias, Bluemke, Karen, Wurl, Peter, Taubert, Helge, Dammann, Reinhard

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Microanalysis of complex tissue lipids by high-performance thin-layer chromatography von Yao, Jeffrey K., Rastetter, Gregory M.

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Analysis of the transport properties of side chain modified dipeptides at the mammalian peptide transporter PEPT1 von Knütter, Ilka, Hartrodt, Bianka, Theis, Stephan, Foltz, Martin, Rastetter, Matthias, Daniel, Hannelore, Neubert, Klaus, Brandsch, Matthias

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Rapid Diagnosis of Cytomegaloviral Pneumonia by Tissue Immunofluorescence with a Murine Monoclonal Antibody von Hackman, Robert C., Myerson, David, Meyers, Joel D., Shulman, Howard M., Sale, George E., Goldstein, Lynn C., Rastetter, Mary, Flournoy, Nancy, Thomas, E. Donnall

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The renal type H super(+)/peptide symporter PEPT2: structure-affinity relationships von Biegel, A, Knuetter, I, Hartrodt, B, Gebauer, S, Theis, S, Luckner, P, Kottra, G, Rastetter, M, Zebisch, K, Thondorf, I, Daniel, H, Neubert, K, Brandsch, M

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A model of multiple-element limitation for acclimating vegetation von Rastetter, Edward B., Shaver, Gaius R.

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Ranunculus auricomus L

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Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments von Leblond, Claire S, Nava, Caroline, Polge, Anne, Gauthier, Julie, Huguet, Guillaume, Lumbroso, Serge, Giuliano, Fabienne, Stordeur, Coline, Depienne, Christel, Mouzat, Kevin, Pinto, Dalila, Howe, Jennifer, Lemière, Nathalie, Durand, Christelle M, Guibert, Jessica, Ey, Elodie, Toro, Roberto, Peyre, Hugo, Mathieu, Alexandre, Amsellem, Frédérique, Rastam, Maria, Gillberg, I Carina, Rappold, Gudrun A, Holt, Richard, Monaco, Anthony P, Maestrini, Elena, Galan, Pilar, Heron, Delphine, Jacquette, Aurélia, Afenjar, Alexandra, Rastetter, Agnès, Brice, Alexis, Devillard, Françoise, Assouline, Brigitte, Laffargue, Fanny, Lespinasse, James, Chiesa, Jean, Rivier, François, Bonneau, Dominique, Regnault, Beatrice, Zelenika, Diana, Delepine, Marc, Lathrop, Mark, Sanlaville, Damien, Schluth-Bolard, Caroline, Edery, Patrick, Perrin, Laurence, Tabet, Anne Claude, Schmeisser, Michael J, Boeckers, Tobias M, Coleman, Mary, Sato, Daisuke, Szatmari, Peter, Scherer, Stephen W, Rouleau, Guy A, Betancur, Catalina, Leboyer, Marion, Gillberg, Christopher, Delorme, Richard, Bourgeron, Thomas

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Mailbox tray insert von RASTETTER JEAN M

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Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity von Asselin, Laure, Rivera Alvarez, José, Heide, Solveig, Bonnet, Camille S., Tilly, Peggy, Vitet, Hélène, Weber, Chantal, Bacino, Carlos A., Baranaño, Kristin, Chassevent, Anna, Dameron, Amy, Faivre, Laurence, Hanchard, Neil A., Mahida, Sonal, McWalter, Kirsty, Mignot, Cyril, Nava, Caroline, Rastetter, Agnès, Streff, Haley, Thauvin-Robinet, Christel, Weiss, Marjan M., Zapata, Gladys, Zwijnenburg, Petra J. G., Saudou, Frédéric, Depienne, Christel, Golzio, Christelle, Héron, Delphine, Godin, Juliette D.

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Dynamic expression patterns of Irx3 and Irx5 during germline nest breakdown and primordial follicle formation promote follicle survival in mouse ovaries von Fu, Anqi, Oberholtzer, Sydney M, Bagheri-Fam, Stefan, Rastetter, Raphael H, Holdreith, Claire, Caceres, Valeria L, John, Steven V, Shaw, Sarah A, Krentz, Kathleen J, Zhang, Xiaoyun, Hui, Chi-Chung, Wilhelm, Dagmar, Jorgensen, Joan S

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Controls on Nitrogen Cycling in Terrestrial Ecosystems: A Synthetic Analysis of Literature Data von Booth, Mary S., Stark, John M., Rastetter, Edward

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Microanalysis of complex tissue lipids by high-performance thin-layer chromatoraphy von YAO, J. K, RASTETTER, G. M

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Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X von Leitão, Elsa, Schröder, Christopher, Parenti, Ilaria, Dalle, Carine, Rastetter, Agnès, Kühnel, Theresa, Kuechler, Alma, Kaya, Sabine, Gérard, Bénédicte, Schaefer, Elise, Nava, Caroline, Drouot, Nathalie, Engel, Camille, Piard, Juliette, Duban-Bedu, Bénédicte, Villard, Laurent, Stegmann, Alexander P. A., Vanhoutte, Els K., Verdonschot, Job A. J., Kaiser, Frank J., Tran Mau-Them, Frédéric, Scala, Marcello, Striano, Pasquale, Frints, Suzanna G. M., Argilli, Emanuela, Sherr, Elliott H., Elder, Fikret, Buratti, Julien, Keren, Boris, Mignot, Cyril, Héron, Delphine, Mandel, Jean-Louis, Gecz, Jozef, Kalscheuer, Vera M., Horsthemke, Bernhard, Piton, Amélie, Depienne, Christel

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De novo mutations in HCN1 cause early infantile epileptic encephalopathy von Nava, Caroline, Dalle, Carine, Rastetter, Agnès, Striano, Pasquale, de Kovel, Carolien G F, Nabbout, Rima, Cancès, Claude, Ville, Dorothée, Brilstra, Eva H, Gobbi, Giuseppe, Raffo, Emmanuel, Bouteiller, Delphine, Marie, Yannick, Trouillard, Oriane, Robbiano, Angela, Keren, Boris, Agher, Dahbia, Roze, Emmanuel, Lesage, Suzanne, Nicolas, Aude, Brice, Alexis, Baulac, Michel, Vogt, Cornelia, El Hajj, Nady, Schneider, Eberhard, Suls, Arvid, Weckhuysen, Sarah, Gormley, Padhraig, Lehesjoki, Anna-Elina, De Jonghe, Peter, Helbig, Ingo, Baulac, Stéphanie, Zara, Federico, Koeleman, Bobby P C, Haaf, Thomas, LeGuern, Eric, Depienne, Christel

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Functional convergence in regulation of net CO₂ flux in heterogeneous tundra landscapes in Alaska and Sweden von SHAVER, G.R, STREET, L.E, RASTETTER, E.B, VAN WIJK, M.T, WILLIAMS, M

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Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders von Mochel, Fanny, Rastetter, Agnès, Ceulemans, Berten, Platzer, Konrad, Yang, Sandra, Shinde, Deepali N, Helbig, Katherine L, Lopergolo, Diego, Mari, Francesca, Renieri, Alessandra, Benetti, Elisa, Canitano, Roberto, Waisfisz, Quinten, Plomp, Astrid S, Huisman, Sylvia A, Wilson, Golder N, Cathey, Sara S, Louie, Raymond J, Gaudio, Daniela Del, Waggoner, Darrel, Kacker, Shawn, Nugent, Kimberly M, Roeder, Elizabeth R, Bruel, Ange-Line, Thevenon, Julien, Ehmke, Nadja, Horn, Denise, Holtgrewe, Manuel, Kaiser, Frank J, Kamphausen, Susanne B, Abou Jamra, Rami, Weckhuysen, Sarah, Dalle, Carine, Depienne, Christel

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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU von Depienne, Christel, Nava, Caroline, Keren, Boris, Heide, Solveig, Rastetter, Agnès, Passemard, Sandrine, Chantot-Bastaraud, Sandra, Moutard, Marie-Laure, Agrawal, Pankaj B., VanNoy, Grace, Stoler, Joan M., Amor, David J., Billette de Villemeur, Thierry, Doummar, Diane, Alby, Caroline, Cormier-Daire, Valérie, Garel, Catherine, Marzin, Pauline, Scheidecker, Sophie, de Saint-Martin, Anne, Hirsch, Edouard, Korff, Christian, Bottani, Armand, Faivre, Laurence, Verloes, Alain, Orzechowski, Christine, Burglen, Lydie, Leheup, Bruno, Roume, Joelle, Andrieux, Joris, Sheth, Frenny, Datar, Chaitanya, Parker, Michael J., Pasquier, Laurent, Odent, Sylvie, Naudion, Sophie, Delrue, Marie-Ange, Le Caignec, Cédric, Vincent, Marie, Isidor, Bertrand, Renaldo, Florence, Stewart, Fiona, Toutain, Annick, Koehler, Udo, Häckl, Birgit, von Stülpnagel, Celina, Kluger, Gerhard, Møller, Rikke S., Pal, Deb, Jonson, Tord, Soller, Maria, Verbeek, Nienke E., van Haelst, Mieke M., de Kovel, Carolien, Koeleman, Bobby, Monroe, Glen, van Haaften, Gijs, Attié-Bitach, Tania, Boutaud, Lucile, Héron, Delphine, Mignot, Cyril

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