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Items: 1 to 20 of 41

1.

Sex, Scavengers, and Chaperones: Transcriptome Secrets of Divergent Symbiodinium Thermal Tolerances.

Levin RA, Beltran VH, Hill R, Kjelleberg S, McDougald D, Steinberg PD, van Oppen MJ.

Mol Biol Evol. 2016 Sep;33(9):2201-15. doi: 10.1093/molbev/msw119. Erratum in: Mol Biol Evol. 2016 Nov;33(11):3032.

2.

Proteomic Analysis Reveals a Novel Mutator S (MutS) Partner Involved in Mismatch Repair Pathway.

Chen Z, Tran M, Tang M, Wang W, Gong Z, Chen J.

Mol Cell Proteomics. 2016 Apr;15(4):1299-308. doi: 10.1074/mcp.M115.056093 .

PMID:
27037360
3.

Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.

Keller MD, Pandey R, Li D, Glessner J, Tian L, Henrickson SE, Chinn IK, Monaco-Shawver L, Heimall J, Hou C, Otieno FG, Jyonouchi S, Calabrese L, van Montfrans J, Orange JS, Hakonarson H.

J Allergy Clin Immunol. 2016 Aug;138(2):544-550.e4. doi: 10.1016/j.jaci.2016.01.018.

PMID:
27016798
4.

Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.

Kelsen JR, Dawany N, Moran CJ, Petersen BS, Sarmady M, Sasson A, Pauly-Hubbard H, Martinez A, Maurer K, Soong J, Rappaport E, Franke A, Keller A, Winter HS, Mamula P, Piccoli D, Artis D, Sonnenberg GF, Daly M, Sullivan KE, Baldassano RN, Devoto M.

Gastroenterology. 2015 Nov;149(6):1415-24. doi: 10.1053/j.gastro.2015.07.006.

5.

Bone marrow transcriptome and epigenome profiles of equine common variable immunodeficiency patients unveil block of B lymphocyte differentiation.

Tallmadge RL, Shen L, Tseng CT, Miller SC, Barry J, Felippe MJ.

Clin Immunol. 2015 Oct;160(2):261-76. doi: 10.1016/j.clim.2015.05.005.

6.

Rare variants at 16p11.2 are associated with common variable immunodeficiency.

Maggadottir SM, Li J, Glessner JT, Li YR, Wei Z, Chang X, Mentch FD, Thomas KA, Kim CE, Zhao Y, Hou C, Wang F, Jørgensen SF, Perez EE, Sullivan KE, Orange JS, Karlsen TH, Chapel H, Cunningham-Rundles C, Hakonarson H.

J Allergy Clin Immunol. 2015 Jun;135(6):1569-77. doi: 10.1016/j.jaci.2014.12.1939.

7.

Comparison of diagnostic criteria for common variable immunodeficiency disorder.

Ameratunga R, Brewerton M, Slade C, Jordan A, Gillis D, Steele R, Koopmans W, Woon ST.

Front Immunol. 2014 Sep 15;5:415. doi: 10.3389/fimmu.2014.00415. Review.

9.

Genetic defects and the role of helper T-cells in the pathogenesis of common variable immunodeficiency.

Yazdani R, Hakemi MG, Sherkat R, Homayouni V, Farahani R.

Adv Biomed Res. 2014 Jan 9;3:2. doi: 10.4103/2277-9175.124627. Review.

10.

Expression of activation-induced cytidine deaminase gene in B lymphocytes of patients with common variable immunodeficiency.

Abolhassani H, Farrokhi AS, Pourhamdi S, Mohammadinejad P, Sadeghi B, Moazzeni SM, Aghamohammadi A.

Iran J Pediatr. 2013 Aug;23(4):451-7.

11.

MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human Diseases.

Clark N, Wu X, Her C.

Curr Genomics. 2013 Apr;14(2):81-90. doi: 10.2174/1389202911314020002.

12.

MutS homologue hMSH5: recombinational DSB repair and non-synonymous polymorphic variants.

Wu X, Xu Y, Feng K, Tompkins JD, Her C.

PLoS One. 2013 Sep 4;8(9):e73284. doi: 10.1371/journal.pone.0073284.

13.

Common variable immunodeficiency.

Tam JS, Routes JM.

Am J Rhinol Allergy. 2013 Jul-Aug;27(4):260-5. doi: 10.2500/ajra.2013.27.3899.

14.

New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin.

Ameratunga R, Woon ST, Gillis D, Koopmans W, Steele R.

Clin Exp Immunol. 2013 Nov;174(2):203-11. doi: 10.1111/cei.12178. Review.

15.

Chipping away at a mountain: genomic studies in common variable immunodeficiency.

Keller MD, Jyonouchi S.

Autoimmun Rev. 2013 Apr;12(6):687-9. doi: 10.1016/j.autrev.2012.10.017. Review.

16.

Autoimmune cytopenias in common variable immunodeficiency.

Podjasek JC, Abraham RS.

Front Immunol. 2012 Jul 24;3:189. doi: 10.3389/fimmu.2012.00189.

17.

Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing.

Connolly JJ, Hakonarson H.

J Biomed Biotechnol. 2012;2012:798924. doi: 10.1155/2012/798924. Review.

18.

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.

Lopez-Herrera G, Tampella G, Pan-Hammarström Q, Herholz P, Trujillo-Vargas CM, Phadwal K, Simon AK, Moutschen M, Etzioni A, Mory A, Srugo I, Melamed D, Hultenby K, Liu C, Baronio M, Vitali M, Philippet P, Dideberg V, Aghamohammadi A, Rezaei N, Enright V, Du L, Salzer U, Eibel H, Pfeifer D, Veelken H, Stauss H, Lougaris V, Plebani A, Gertz EM, Schäffer AA, Hammarström L, Grimbacher B.

Am J Hum Genet. 2012 Jun 8;90(6):986-1001. doi: 10.1016/j.ajhg.2012.04.015.

19.

Expression of essential B cell development genes in horses with common variable immunodeficiency.

Tallmadge RL, Such KA, Miller KC, Matychak MB, Felippe MJ.

Mol Immunol. 2012 Jun;51(2):169-76. doi: 10.1016/j.molimm.2012.03.018.

20.

MutS homologue hMSH5: role in cisplatin-induced DNA damage response.

Tompkins JD, Wu X, Her C.

Mol Cancer. 2012 Mar 8;11:10. doi: 10.1186/1476-4598-11-10.

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