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2025
2024
Kim JK, Tierney BT, Overbey EG, Dantas E, Fuentealba M, Park J, S Narayanan A, Wu F, Najjar D, Chin CR et al. .
2024. Single-cell multi-ome and immune profiles of the Inspiration4 crew reveal conserved, cell-type, and sex-specific responses to spaceflight. . Nat Commun. 15(1):4954.
2023
2022
Strillacci A, Sansone P, Rajasekhar VK, Turkekul M, Boyko V, Meng F, Houck-Loomis B, Brown D, Berger MF, Hendrickson RC et al. .
2022. ERα-LBD, an isoform of estrogen receptor alpha, promotes breast cancer proliferation and endocrine resistance. . NPJ Breast Cancer. 8(1):96.
Li L, Changrob S, Fu Y, Stovicek O, Guthmiller JJ, McGrath JJC, Dugan HL, Stamper CT, Zheng N-Y, Huang M et al. .
2022. Librator: a platform for the optimized analysis, design, and expression of mutable influenza viral antigens. . Brief Bioinform. 23(2)
Lyden D, Ghajar CM, Correia ALuísa, Aguirre-Ghiso JA, Cai S, Rescigno M, Zhang P, Hu G, Fendt S-M, Boire A et al. .
2022. Metastasis. . Cancer Cell. 40(8):787-791.
2021
Bojmar L, Kim HSang, Tobias GC, Vatter FAPelissie, Lucotti S, Gyan KEnnu, Kenific CM, Wan Z, Kim K-A, Kim DA et al. .
2021. Extracellular vesicle and particle isolation from human and murine cell lines, tissues, and bodily fluids. . STAR Protoc. 2(1):100225.
2020
2019
2018
2017
Arostegui JI, Anton J, Calvo I, Robles A, Iglesias E, López-Montesinos B, Banchereau R, Hong S, Joubert Y, Junge G et al. .
2017. Open-Label, Phase II Study to Assess the Efficacy and Safety of Canakinumab Treatment in Active Hyperimmunoglobulinemia D With Periodic Fever Syndrome. . Arthritis Rheumatol. 69(8):1679-1688.
2016
Kaya N, Alsagob M, D'Adamo MCristina, Al-Bakheet A, Hasan S, Muccioli M, Almutairi FB, Almass R, Aldosary M, Monies D et al. .
2016. deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability. . J Med Genet. 53(11):786-792.
Shaheen R, Anazi S, Ben-Omran T, Seidahmed MZain, L Caddle B, Palmer K, Ali R, Alshidi T, Hagos S, Goodwin L et al. .
2016. Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. . Am J Hum Genet. 98(4):643-52.
Al-Hassnan ZN, Shinwari ZMa, Wakil SM, Tulbah S, Mohammed S, Rahbeeni Z, Alghamdi M, Rababh M, Colak D, Kaya N et al. .
2016. A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy. . BMC Med Genet. 17:3.
2015
Anandasabapathy N, Breton G, Hurley A, Caskey M, Trumpfheller C, Sarma P, Pring J, Pack M, Buckley N, Matei I et al. .
2015. Efficacy and safety of CDX-301, recombinant human Flt3L, at expanding dendritic cells and hematopoietic stem cells in healthy human volunteers. . Bone Marrow Transplant. 50(7):924-30.