Treffer 1 - 20 von 27 für Suche 'Jones, Linda Lea', Suchdauer: 1,77s Treffer weiter einschränken
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    The Tabula Sapiens: A multiple-organ, single-cell transcriptomic atlas of humans von Jones, Robert C, Karkanias, Jim, Krasnow, Mark A, Pisco, Angela Oliveira, Quake, Stephen R, Salzman, Julia, Yosef, Nir, Bulthaup, Bryan, Brown, Phillip, Harper, William, Hemenez, Marisa, Ponnusamy, Ravikumar, Salehi, Ahmad, Sanagavarapu, Bhavani A, Spallino, Eileen, Aaron, Ksenia A, Concepcion, Waldo, Gardner, James M, Kelly, Burnett, Neidlinger, Nikole, Wang, Zifa, Crasta, Sheela, Kolluru, Saroja, Morri, Maurizio, Tan, Serena Y, Travaglini, Kyle J, Xu, Chenling, Alcántara-Hernández, Marcela, Almanzar, Nicole, Antony, Jane, Beyersdorf, Benjamin, Burhan, Deviana, Calcuttawala, Kruti, Carter, Matthew M, Chan, Charles K F, Chang, Charles A, Chang, Stephen, Colville, Alex, Culver, Rebecca N, Cvijović, Ivana, D'Amato, Gaetano, Ezran, Camille, Galdos, Francisco X, Gillich, Astrid, Goodyer, William R, Hang, Yan, Hayashi, Alyssa, Houshdaran, Sahar, Huang, Xianxi, Irwin, Juan C, Jang, SoRi, Juanico, Julia Vallve, Kershner, Aaron M, Kim, Soochi, Kiss, Bernhard, Kong, William, Kumar, Maya E, Kuo, Angera H, Leylek, Rebecca, Li, Baoxiang, Loeb, Gabriel B, Lu, Wan-Jin, Mantri, Sruthi, Markovic, Maxim, McAlpine, Patrick L, de Morree, Antoine, Mrouj, Karim, Mukherjee, Shravani, Muser, Tyler, Neuhöfer, Patrick, Nguyen, Thi D, Perez, Kimberly, Phansalkar, Ragini, Puluca, Nazan, Qi, Zhen, Rao, Poorvi, Raquer-McKay, Hayley, Schaum, Nicholas, Scott, Bronwyn, Seddighzadeh, Bobak, Segal, Joe, Sen, Sushmita, Sikandar, Shaheen, Spencer, Sean P, Steffes, Lea C, Subramaniam, Varun R, Swarup, Aditi, Swift, Michael, Van Treuren, Will, Trimm, Emily, Veizades, Stefan, Vijayakumar, Sivakamasundari, Vo, Kim Chi, Vorperian, Sevahn K, Wang, Wanxin


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    Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT): a multicentre, randomised, placebo-controlled, phase 3 trial von Karam, Chafic, Murai, Hiroyuki, Smilowski, Marek, Guglietta, Antonio, Utsugisawa, Kimiaki, Mantegazza, Renato, De Mey, Katrien, De Pue, Annelien, Mercelis, Rudolf, Daniyal, Lubna, Mannan, Shabber, Katzberg, Hans D., Siddiqi, Zaeem, Junkerová, Jana, Reguliova, Katerina, Jurajdova, Ivana, Vohanka, Stanislav, Havelkova, Katerina, Horak, Tomas, Horakova, Mageda, Kohler, Siegfried, Gerischer, Lea, Stascheit, Frauke, Autzen, Anne, Andersen, Henning, Salort-Campana, Emmanuelle, Delmont, Emilien, Tsiskaridze, Alexander, Rózsa, Csilla, Toth, Szilvia, Szabo, Gyorgyi, Szabo, Eniko, Campanella, Angela, Vanoli, Fiammetta, Puorro, Giorgia, Reia, Antonio, Antonini, Giovanni, Garibaldi, Matteo, Uzawa, Akiyuki, Sakuma, Kaoru, Yasuda, Manato, Onishi, Yosuke, Ishida, Sayaka, Watanabe, Genya, Takahashi, Masanori, Sugano, Erina, Kubota, Tomoya, Imai, Tomihiro, Suzuki, Mari, Mori, Ayako, Yamamoto, Daisuke, Ikeda, Kazuna, Hisahara, Shin, Minemoto, Kanako, Ido, Nobuhiro, Takematsu, Yuka, Shimizu, Mihiro, Nomura, Eiichi, Van Heur, Marjolein, Tannemaat, Martijn, Ruiter, Annabel, Halas, Marek, Szczudlik, Andrzej, Pinkosz, Marta, Frasinska, Monika, Urtaeva, Lubov, Romanova, Tatiana, Lapochka, Elena, Korobko, Denis, Vergunova, Ilona, Bulatova, Ekaterina, Basta, Ivana, Akhter, Salma, Malekniazi, Ali, Darki, Leila, Cannon, Victoria, Chopra, Manisha, Traub, Rebecca, Habib, Ali, Goyal, Namita, Jones, Sarah, Wagoner, Mary, Benzel, Cindy, Jackson, Carlayne, Dimitrova, Diana, Chahin, Nizar, Levine, Todd, Lisak, Robert, Jia, Kelly, Roath, Katherine, Barohn, Richard, Dimachkie, Mazen, Li, Yuebing, Caristo, Irys, Hastings, Debbie, Muppidi, Srikanth, Welsh, Lesly, Quraishi, Zubair, Berger, Alan, Frishberg, Benjamin

    Veröffentlicht in Lancet neurology

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    SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile von Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

    Veröffentlicht in Genetics in medicine

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