Gallagher, Patrick G - Yale University - Biological & Biomedical Sciences

个人简介

MD Northeastern Ohio University (1985) Fellow Yale University School of Medicine Chief Resident Children's Hospital Medical Center, University of Cincinnati Intern & Resident Children's Hospital Medical Center, University of Cincinnati Board Certification AB of Pediatrics, Neonatal-Perinatal Medicine (1993, recertified: 2016)

研究领域

Anemia, Sickle Cell; Elliptocytosis, Hereditary; Erythropoiesis; Genetics; Neonatology; Pathology; Pediatrics; Spherocytosis, Hereditary

近期论文

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Identification of Biologically Relevant Enhancers in Human Erythroid Cells Su MY, Steiner LA, Bogardus H, Mishra T, Schulz VP, Hardison RC, Gallagher PG. (2013). Identification of Biologically Relevant Enhancers in Human Erythroid Cells. J Biol Chem 2013; 288:8433-44.PMID: 23341446 The common hereditary elliptocytosis-associated a-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation Harper SL, Sriswasdi S, Tang HY, Gaetani M, Gallagher PG, Speicher DW. The common hereditary elliptocytosis-associated a-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation. Blood. 2013; In press. PMID: 23974198 A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter Yocum, AO, Steiner, LA, Seidel, NE, Cline, AP, Rout, ED, Lin, JY, Wong, C, Garrett, LJ, Gallagher, PG, Bodine, DM. (2012). A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter. Blood, 120, 3586-3593. PMCID: 3482866 Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis Zarychanski R, Schulz VP, Houston BL, Maksimova Y, Houston DS, Smith B, Rinehart J, Gallagher PG: Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis. Blood 2012; 120:1908-15. PMCID: PMC3448561. Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing Walker RH, Schulz VP, Tikhonova IR, Mahajan MC, Mane S, Arroyo Muniz M, Gallagher PG: Genetic diagnosis of neuroacanthocytosis disorders using exome sequencing. Mov Disord 2012; 27:539-43. PMID: 22038564. PMCID: PMC Journal - In Process. Patterns of histone H3 lysine 27 mono-methylation and erythroid cell-type specific gene expression Steiner LA, Schulz VP, Maksimova Y, Wong C, Gallagher PG: Patterns of histone H3 lysine 27 mono-methylation and erythroid cell-type specific gene expression. J Biol Chem 2011; 286:39453-65. PMCID: PMC3234769. Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S Stewart AK, Shmukler BE, Vandorpe DH, Rivera A, Li X, Hsu A, Karpatkin M, O'Neill A, Bauer DE, Heeney M, John K, Kuypers FA, Gallagher PG, Lux SE, Brugnara C, Westhoff CM, Alper SL: Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S. Am J Physiol Cell Physiol 2011; 301:C1325-43. PMCID: PMC3233792. Identification of Biologically Relevant Enhancers in Human Erythroid Cells Su MY, Steiner LA, Bogardus H, Mishra T, Schulz VP, Hardison RC, Gallagher PG. (2013). Identification of Biologically Relevant Enhancers in Human Erythroid Cells. J Biol Chem 2013; 288:8433-44.PMID: 23341446