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Found 65 matches. Displaying 1 - 10

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1. Knight JS, Caricchio R, Casanova JL, Combes AJ, Diamond B, Fox SE, Hanauer DA, James JA, Kanthi Y, Ladd V, Mehta P, Ring AM, Sanz I, Selmi C, Tracy RP, Utz PJ, Wagner CA, Wang JY, McCune WJ   The intersection of COVID-19 and autoimmunity   JOURNAL OF CLINICAL INVESTIGATION 2021 DEC 15; 131(24):? Article e154886 Full Text | PMID/PMCID

2. Hogg SJ, Motorna O, Cluse LA, Johanson TM, Coughlan HD, Raviram R, Myers RM, Costacurta M, Todorovski I, Pijpers L, Bjelosevic S, Williams T, Huskins SN, Kearney CJ, Devlin JR, Fan Z, Jabbari JS, Martin BP, Fareh M, Kelly MJ, Dupere-Richer D, Sandow JJ, Feran B, Knight D, Khong T   Targeting histone acetylation dynamics and oncogenic transcription by catalytic P300/CBP inhibition   MOLECULAR CELL 2021 MAY 20; 81(10):2183-2200.e13 Full Text | PMID/PMCID

3. Dong WL, Jin SC, Allocco A, Zeng X, Sheth AH, Panchagnula S, Castonguay A, Lorenzo LE, Islam B, Brindle G, Bachand K, Hu J, Sularz A, Gaillard J, Choi J, Dunbar A, Nelson-Williams C, Kiziltug E, Furey CG, Conine S, Duy PQ, Kundishora AJ, Loring E, Li BY, Lu QS   Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal Neuralgia   ISCIENCE 2020 OCT 23; 23(10):? Article 101552 Full Text | PMID/PMCID

4. Jin SC, Lewis SA, Bakhtiari S, Zeng X, Sierant MC, Shetty S, Nordlie SM, Elie A, Corbett MA, Norton BY, van Eyk CL, Haider S, Guida BS, Magee H, Liu JM, Pastore S, Vincent JB, Brunstrom-Hernandez J, Papavasileiou A, Fahey MC, Berry JG, Harper K, Zhou CC, Zhang JH, Li BY   Mutations disrupting neuritogenesis genes confer risk for cerebral palsy   NATURE GENETICS 2020 OCT; 52(10):1046-1056 Full Text | PMID/PMCID

5. Callewaert C, Nakatsuji T, Knight R, Kosciolek T, Vrbanac A, Kotol P, Ardeleanu M, Hultsch T, Guttman-Yassky E, Bissonnette R, Silverberg JI, Krueger J, Menter A, Graham NMH, Pirozzi G, Hamilton JD, Gallo RL   IL-4R alpha Blockade by Dupilumab Decreases Staphylococcus aureus Colonization and Increases Microbial Diversity in Atopic Dermatitis   JOURNAL OF INVESTIGATIVE DERMATOLOGY 2020 JAN; 140(1):191-202.e7 Full Text | PMID/PMCID

6. Duran D, Zeng X, Jin SC, Choi J, Nelson-Williams C, Yatsula B, Gaillard J, Furey CG, Lu QS, Timberlake AT, Dong WL, Sorscher MA, Loring E, Klein J, Allocco A, Hunt A, Conine S, Karimy JK, Youngblood MW, Zhang JW, DiLuna ML, Matouk CC, Mane S, Tikhonova IR, Castaldi C   Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation   NEURON 2019 FEB 6; 101(3):429-443.e4 Full Text | PMID/PMCID

7. Furey CG, Choi J, Jin SC, Zeng X, Timberlake AT, Nelson-Williams C, Mansuri MS, Lu QS, Duran D, Panchagnula S, Allocco A, Karimy JK, Khanna A, Gaillard JR, DeSpenza T, Antwi P, Loring E, Butler WE, Smith ER, Warf BC, Strahle JM, Limbrick DD, Storm PB, Heuer G, Jackson EM   De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus   NEURON 2018 JUL 25; 99(2):302-314.e4 Full Text | PMID/PMCID

8. Dobenecker MW, Park JS, Marcello J, McCabe MT, Gregory R, Knight SD, Rioja I, Bassil AK, Prinjha RK, Tarakhovsky A   Signaling function of PRC2 is essential for TCR-driven T cell responses   JOURNAL OF EXPERIMENTAL MEDICINE 2018 APR; 215(4):1101-1113 Full Text | PMID/PMCID

9. Galluzzi L, Vitale I, Aaronson SA, Abrams JM, Adam D, Agostinis P, Alnemri ES, Altucci L, Amelio I, Andrews DW, Annicchiarico-Petruzzelli M, Antonov AV, Arama E, Baehrecke EH, Barlev NA, Bazan NG, Bernassola F, Bertrand MJM, Bianchi K, Blagosklonny MV, Blomgren K, Borner C, Boya P, Brenner C, Campanella M   Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018   CELL DEATH AND DIFFERENTIATION 2018 MAR; 25(3):486-541 Full Text | PMID/PMCID

10. Jin SC, Homsy J, Zaidi S, Lu QS, Morton S, DePalma SR, Zeng X, Qi HJ, Chang WI, Sierant MC, Hung WC, Haider S, Zhang JH, Knight J, Bjornson RD, Castaldi C, Tikhonoa IR, Bilguvar K, Mane SM, Sanders SJ, Mital S, Russell MW, Gaynor JW, Deanfield J, Giardini A   Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands   NATURE GENETICS 2017 NOV; 49(11):1593-1601 Full Text | PMID/PMCID

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