Abnormalities of the Erythrocyte Membrane

Tekijä Gallagher, Patrick G.
Julkaistu 2013

Disorders of erythrocyte hydration

Tekijä Gallagher, Patrick G.
Julkaisussa Blood (2017)

Red cell membrane: past, present, and future

Tekijä Mohandas, Narla, Gallagher, Patrick G.
Julkaistu 2008

Disorders of Erythrocyte Volume Homeostasis

Tekijä Glogowska, Edyta, Gallagher, Patrick G.
Julkaisussa Int J Lab Hematol (2015)

Erythrocyte Disorders in the Perinatal Period in Adverse Pregnancy Outcome and the Fetus/Neonate

Tekijä Steiner, Laurie A., Gallagher, Patrick G.
Julkaistu 2007

Methicillin-Resistant Staphylococcus aureus in the Neonatal Intensive Care Unit

Tekijä Nelson, Melissa U., Gallagher, Patrick G.
Julkaistu 2012

Applications of high-throughput DNA sequencing to benign hematology

Tekijä Sankaran, Vijay G., Gallagher, Patrick G.
Julkaistu 2013

Piezo Proteins: Regulators of Mechanosensation and Other Cellular Processes

Tekijä Bagriantsev, Sviatoslav N., Gracheva, Elena O., Gallagher, Patrick G.
Julkaisussa J Biol Chem (2014)

Human and murine erythropoiesis

Tekijä An, Xiuli, Schulz, Vincent P., Mohandas, Narla, Gallagher, Patrick G.
Julkaisussa Curr Opin Hematol (2015)

A Pediatrician’s Practical Guide to Diagnosing and Treating Hereditary Spherocytosis in Neonates

Tekijä Christensen, Robert D., Yaish, Hassan M., Gallagher, Patrick G.
Julkaisussa Pediatrics (2015)

A novel splicing mutation of the α-spectrin gene in the original hereditary pyropoikilocytosis kindred

Tekijä Costa, Daniel B., Lozovatsky, Larisa, Gallagher, Patrick G., Forget, Bernard G.
Julkaistu 2005

Case‐control analysis of endemic Serratia marcescens bacteremia in a neonatal intensive care unit

Tekijä Bizzarro, Matthew J, Dembry, Louise‐Marie, Baltimore, Robert S, Gallagher, Patrick G
Julkaistu 2007

A complex splicing defect associated with homozygous ankyrin-deficient hereditary spherocytosis

Tekijä Edelman, E. Jennifer, Maksimova, Yelena, Duru, Feride, Altay, Cigdem, Gallagher, Patrick G.
Julkaistu 2007

Structural and functional effects of hereditary hemolytic anemia-associated point mutations in the alpha spectrin tetramer site

Tekijä Gaetani, Massimiliano, Mootien, Sara, Harper, Sandra, Gallagher, Patrick G., Speicher, David W.
Julkaistu 2008

A Fused α-β “Mini-spectrin” Mimics the Intact Erythrocyte Spectrin Head-to-head Tetramer

Tekijä Harper, Sandra L., Li, Donghai, Maksimova, Yelena, Gallagher, Patrick G., Speicher, David W.
Julkaistu 2010

Patterns of Histone H3 Lysine 27 Monomethylation and Erythroid Cell Type-specific Gene Expression

Tekijä Steiner, Laurie A., Schulz, Vincent P., Maksimova, Yelena, Wong, Clara, Gallagher, Patrick G.
Julkaistu 2011

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

Tekijä Glogowska, Edyta, Lezon-Geyda, Kimberly, Maksimova, Yelena, Schulz, Vincent P., Gallagher, Patrick G.
Julkaisussa Blood (2015)

CTCF and Cohesin(SA-1) Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells

Tekijä Steiner, Laurie A., Schulz, Vincent, Makismova, Yelena, Lezon-Geyda, Kimberly, Gallagher, Patrick G.
Julkaisussa PLoS One (2016)

Probing large conformational rearrangements in wild-type and mutant spectrin using structural mass spectrometry

Tekijä Sriswasdi, Sira, Harper, Sandra L., Tang, Hsin-Yao, Gallagher, Patrick G., Speicher, David W.
Julkaistu 2014

Determinants of Erythrocyte Hydration In Current Opinion in Hematology

Tekijä Rinehart, Jesse, Gulcicek, Erol E., Joiner, Clinton H., Lifton, Richard P., Gallagher, Patrick G.
Julkaistu 2010