Found 10 results
Filters: Keyword is Genetic Predisposition to Disease  [Clear All Filters]
2017
Holland SM, Pierce VM, Shailam R, Glomski K, Farmer JR.  2017.  Case 28-2017. A 13-Month-Old Girl with Pneumonia and a 33-Year-Old Woman with Hip Pain.. N Engl J Med. 377(11):1077-1091.
Morton LM, Sampson JN, Armstrong GT, Chen T-H, Hudson MM, Karlins E, Dagnall CL, Li SAlfred, Wilson CL, Srivastava DKumar et al..  2017.  Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.. J Natl Cancer Inst. 109(11)
DeBerge M, Yeap XYi, Dehn S, Zhang S, Grigoryeva L, Misener S, Procissi D, Zhou X, Lee DC, Muller WA et al..  2017.  MerTK Cleavage on Resident Cardiac Macrophages Compromises Repair After Myocardial Ischemia Reperfusion Injury.. Circ Res. 121(8):930-940.
Hosono N, Makishima H, Mahfouz R, Przychodzen B, Yoshida K, Jerez A, LaFramboise T, Polprasert C, Clemente MJ, Shiraishi Y et al..  2017.  Recurrent genetic defects on chromosome 5q in myeloid neoplasms.. Oncotarget. 8(4):6483-6495.
2016
Simsek S, Zhou T, Robinson CL, Tsai S-Y, Crespo M, Amin S, Lin X, Hon J, Evans T, Chen S.  2016.  Modeling Cystic Fibrosis Using Pluripotent Stem Cell-Derived Human Pancreatic Ductal Epithelial Cells.. Stem Cells Transl Med. 5(5):572-9.
Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EMarisa, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G et al..  2016.  Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.. Acta Neuropathol Commun. 4(1):98.
2015
Ross JB, Huh D, Noble LB, Tavazoie SF.  2015.  Identification of molecular determinants of primary and metastatic tumour re-initiation in breast cancer.. Nat Cell Biol. 17(5):651-64.
2014
Weyn-Vanhentenryck SM, Mele A, Yan Q, Sun S, Farny N, Zhang Z, Xue C, Herre M, Silver PA, Zhang MQ et al..  2014.  HITS-CLIP and integrative modeling define the Rbfox splicing-regulatory network linked to brain development and autism.. Cell Rep. 6(6):1139-1152.
Harp JL, Kinnebrew MA, Shinkai K.  2014.  Severe cutaneous adverse reactions: impact of immunology, genetics, and pharmacology.. Semin Cutan Med Surg. 33(1):17-27.
2013
Wang H-Y, Ma CA, Zhao Y, Fan X, Zhou Q, Edmonds P, Uzel G, Oliveira JBosco, Orange J, Jain A.  2013.  Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAK.. Proc Natl Acad Sci U S A. 110(13):5127-32.