Suchergebnisse - Rice, Gillian

My Student Elective: By brigantine across the Pacific von Rice, Gillian

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Enhancing a primary care environment: a case study of effects on patients and staff in a single general practice von Rice, Gillian, Ingram, Jenny, Mizan, Jacques

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MDA5-Associated Neuroinflammation and the Singleton–Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum von Buers, Insa, Rice, Gillian I., Crow, Yanick J., Rutsch, Frank

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Evaluation of angiotensin-converting enzyme (ACE), its homologue ACE2 and neprilysin in angiotensin peptide metabolism von Rice, Gillian I., Thomas, Daniel A., Grant, Peter J., Turner, Anthony J., Hooper, Nigel M.

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SAMHD1 restricts HIV-1 reverse transcription in quiescent CD4(+) T-cells von Descours, Benjamin, Cribier, Alexandra, Chable-Bessia, Christine, Ayinde, Diana, Rice, Gillian, Crow, Yanick, Yatim, Ahmad, Schwartz, Olivier, Laguette, Nadine, Benkirane, Monsef

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The SKIV2L RNA exosome limits activation of the RIG-I-like receptors von Eckard, Sterling C., Rice, Gillian I., Fabre, Alexandre, Badens, Catherine, Gray, Elizabeth E., Hartley, Jane L., Crow, Yanick J., Stetson, Daniel B.

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Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKD von Ibrahim, Sara T., Chinnadurai, Rajkumar, Ali, Ibrahim, Payne, Debbie, Rice, Gillian I., Newman, William G., Algohary, Eman, Adam, Ahmed G., Kalra, Philip A.

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Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case von Haskell, Gloria T., Mori, Mari, Powell, Cynthia, Amrhein, Timothy J., Rice, Gillian I., Bailey, Lauren, Strande, Natasha, Weck, Karen E., Evans, James P., Berg, Jonathan S., Kishnani, Priya

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Analysis of U8 snoRNA Variants in Zebrafish Reveals How Bi-allelic Variants Cause Leukoencephalopathy with Calcifications and Cysts von Badrock, Andrew P., Uggenti, Carolina, Wacheul, Ludivine, Crilly, Siobhan, Jenkinson, Emma M., Rice, Gillian I., Kasher, Paul R., Lafontaine, Denis L.J., Crow, Yanick J., O’Keefe, Raymond T.

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Elevation of proinflammatory cytokines in patients with Aicardi-Goutières syndrome von Takanohashi, Asako, Prust, Morgan, Wang, Jichuan, Gordish-Dressman, Heather, Bloom, Miriam, Rice, Gillian I., Schmidt, Johanna L., Crow, Yanick J., Lebon, Pierre, Kuijpers, Taco W., Nagaraju, Kanneboyina, Vanderver, Adeline

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Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease von Rice, Gillian I., Melki, Isabelle, Frémond, Marie-Louise, Briggs, Tracy A., Rodero, Mathieu P., Kitabayashi, Naoki, Oojageer, Anthony, Bader-Meunier, Brigitte, Belot, Alexandre, Bodemer, Christine, Quartier, Pierre, Crow, Yanick J.

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Neprilysin, obesity and the metabolic syndrome von Standeven, Kristina F., Hess, Katharina, Carter, Angela M., Rice, Gillian I., Cordell, Paul A., Balmforth, Anthony J., Lu, Bao, Scott, D. Julian, Turner, Anthony J., Hooper, Nigel M., Grant, Peter J.

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Bloom syndrome protein restrains innate immune sensing of micronuclei by cGAS von Gratia, Matthieu, Rodero, Mathieu P., Conrad, Cécile, Bou Samra, Elias, Maurin, Mathieu, Rice, Gillian I., Duffy, Darragh, Revy, Patrick, Petit, Florence, Dale, Russell C., Crow, Yanick J., Amor-Gueret, Mounira, Manel, Nicolas

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Complexity in unclassified auto-inflammatory disease: a case report illustrating the potential for disease arising from the allelic burden of multiple variants von Tucker, Lori B., Lamot, Lovro, Niemietz, Iwona, Chung, Brian K., Cabral, David A., Houghton, Kristin, Petty, Ross E., Morishita, Kimberly A., Rice, Gillian I., Turvey, Stuart E., Gibson, William T., Brown, Kelly L.

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A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome von Rutsch, Frank, MacDougall, Mary, Lu, Changming, Buers, Insa, Mamaeva, Olga, Nitschke, Yvonne, Rice, Gillian I., Erlandsen, Heidi, Kehl, Hans Gerd, Thiele, Holger, Nürnberg, Peter, Höhne, Wolfgang, Crow, Yanick J., Feigenbaum, Annette, Hennekam, Raoul C.

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MRSD: A quantitative approach for assessing suitability of RNA-seq in the investigation of mis-splicing in Mendelian disease von Rowlands, Charlie F., Taylor, Algy, Rice, Gillian, Whiffin, Nicola, Hall, Hildegard Nikki, Newman, William G., Black, Graeme C.M., O’Keefe, Raymond T., Hubbard, Simon, Douglas, Andrew G.L., Baralle, Diana, Briggs, Tracy A., Ellingford, Jamie M.

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Heterozygous Mutations in TREX1 Cause Familial Chilblain Lupus and Dominant Aicardi-Goutières Syndrome von Rice, Gillian, Newman, William G., Dean, John, Patrick, Teresa, Parmar, Rekha, Flintoff, Kim, Robins, Peter, Harvey, Scott, Hollis, Thomas, O’Hara, Ann, Herrick, Ariane L., Bowden, Andrew P., Perrino, Fred W., Lindahl, Tomas, Barnes, Deborah E., Crow, Yanick J.

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Type I interferon in patients with systemic autoimmune rheumatic disease is associated with haematological abnormalities and specific autoantibody profiles von Reynolds, John A., Briggs, Tracy A., Rice, Gillian I., Darmalinggam, Sathya, Bondet, Vincent, Bruce, Ellen, Khan, Mumtaz, Haque, Sahena, Chinoy, Hector, Herrick, Ariane L., McCarthy, Eoghan M., Zeef, Leo, Hayes, Andrew, Duffy, Darragh, Parker, Ben, Bruce, Ian N.

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Mutations in CECR1 associated with a neutrophil signature in peripheral blood von Belot, Alexandre, Wassmer, Evangeline, Twilt, Marinka, Lega, Jean-Christophe, Zeef, Leo AH, Oojageer, Anthony, Kasher, Paul R, Mathieu, Anne-Laure, Malcus, Christophe, Demaret, Julie, Fabien, Nicole, Collardeau-Frachon, Sophie, Mechtouff, Laura, Derex, Laurent, Walzer, Thierry, Rice, Gillian I, Durieu, Isabelle, Crow, Yanick J

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Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations von Jeremiah, Nadia, Neven, Bénédicte, Gentili, Matteo, Callebaut, Isabelle, Maschalidi, Sophia, Stolzenberg, Marie-Claude, Goudin, Nicolas, Frémond, Marie-Louis, Nitschke, Patrick, Molina, Thierry J., Blanche, Stéphane, Picard, Capucine, Rice, Gillian I., Crow, Yanick J., Manel, Nicolas, Fischer, Alain, Bader-Meunier, Brigitte, Rieux-Laucat, Frédéric

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