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Inositol pyrophosphates promote the interaction of SPX domains with the coiled-coil motif of PHR transcription factors to regulate plant phosphate homeostasis Ried, Martina; Wild, Rebekka; Zhu, Jinsheng; Pipercevic, Joka; ... Hothorn, Michael 2021
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Molecular motion and tridimensional nanoscale localization of kindlin control integrin activation in focal adhesions Orré, Thomas; Joly, Adrien; Karatas, Zeynep; Kastberger, Birgit; ... Giannone, Grégory 2021
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A connexin/ifi30 pathway bridges HSCs with their niche to dampen oxidative stress Cacialli, Pietro; Mahony, Christopher; Petzold, Tim; Bordignon, Patrizia; ... Bertrand, Julien 2021
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The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice Bagheri-Fam, Stefan; Chen, Huijun; Wilson, Sean; Ayers, Katie; ... Wilhelm, Dagmar 2020
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Investigating and modulating the regulation of fibrinogen production Ferreira Vilar Da Silva, Rui Filipe 2020
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Putting some context to the aerosolization debate around SARS-CoV-2 Peters, Alexandra; Parneix, P.; Otter, J.; Pittet, Didier 2020
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Genetic T-cell receptor diversity at 1 year following allogeneic hematopoietic stem cell transplantation Buhler, Stéphane; Bettens, Florence; Dantin, Carole Alice; Ferrari-Lacraz, Sylvie; ... Villard, Jean 2020
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MCF2 is linked to a complex perisylvian syndrome and affects cortical lamination Molinard-Chenu, Aude; Fluss, Joël Victor; Laurent, Sacha; Laurent, Meryle; ... Dayer, Alexandre 2020
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Adult T-cell acute lymphoblastic leukemias with IL7R pathway mutations are slow-responders who do not benefit from allogeneic stem-cell transplantation Kim, Rathana; Boissel, Nicolas; Touzart, Aurore; Leguay, Thibaut; ... Lhermitte, Ludovic 2020
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SCN8A heterozygous variants are associated with anoxic-epileptic seizures Ranza, Emmanuelle Nathalie; Z'Graggen, Werner; Lidgren, Mathias; Beghetti, Maurice; ... Korff, Christian 2020
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Révolution dans le traitement de la mucoviscidose Sauty, Alain; Plojoux, Jérôme Pierre Olivier; Mornand, Anne; Blanchon, Sylvain; Koutsokera, Angela 2020
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Compartmentalization of a Multidrug-Resistant Cytomegalovirus UL54 Mutant in a Stem Cell Transplant Recipient with Encephalitis Piret, Jocelyne; Schibler, Manuel; Pham, Van Dung; Hantz, Sébastien; ... Boivin, Guy 2019
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PAX5 P80R mutation identifies a novel subtype of B-cell precursor acute lymphoblastic leukemia with favorable outcome Passet, Marie; Boissel, Nicolas; Sigaux, François; Saillard, Colombe; ... Clappier, Emmanuelle 2019
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Polyamine uptake transporter 2 (put2) and decaying seeds enhance phyA-mediated germination by overcoming PIF1 repression of germination Kim, Woohyun; Zeljković, Sanja Ćavar; Piskurewicz, Urszula; Megies, Christian; ... Lopez Molina, Luis 2019
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Usefulness of genetic testing in sudden cardiac arrest survivors with or without previous clinical evidence of heart disease Asatryan, Babken; Schaller, André; Seiler, Jens; Servatius, Helge; ... Medeiros-Domingo, Argelia 2019
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RINT1 Bi-allelic variations cause infantile-onset recurrent acute liver failure and skeletal abnormalities Cousin, Margot A; Conboy, Erin; Wang, Jian-She; Lenz, Dominic; ... Klee, Eric W 2019
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The spectrum of intermediate SCN8A-related epilepsy Johannesen, Katrine M; Gardella, Elena; Encinas, Alejandra C; Lehesjoki, Anna-Elina; ... Møller, Rikke S 2019
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Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation Zimmern, Vincent; Riant, Florence; Roze, Emmanuel; Ranza, Emmanuelle Nathalie; ... Korff, Christian 2019
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Cerebral perfusion changes in presymptomatic genetic frontotemporal dementia: a GENFI study Mutsaerts, Henri J M M; Mirza, Saira S; Petr, Jan; Thomas, David L; ... Masellis, Mario 2019
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A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIII Dorgalaleh, Akbar; Tabibian, Shadi; Shams, Mahmood; Majid, Golbahar; ... Safa, Majid 2019
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