P. Gallagher

J. Copel, P. Gallagher, M. Reyes-Múgica, 2001, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Human and murine erythropoiesis

N. Mohandas, X. An, V. Schulz, 2015, Current opinion in hematology.

Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype.

P. Sebastiani, L. Farrer, C. Baldwin, 2013, Blood cells, molecules & diseases.

Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E.

N. Mohandas, X. An, J. Hale, 2014, Blood.

Multiple isoforms of the KC1 cotransporter are expressed in sickle and normal erythroid cells.

S. Hammond, P. Gallagher, C. Joiner, 2005, Experimental hematology.

Failure of Terminal Erythroid Differentiation in EKLF-Deficient Mice Is Associated with Cell Cycle Perturbation and Reduced Expression of E2F2

H. Dressman, M. Arcasoy, D. Bodine, 2008, Molecular and Cellular Biology.

Concurrent bloodstream infections in infants with necrotizing enterocolitis.

R. Ehrenkranz, P. Gallagher, M. Bizzarro, 2014, The Journal of pediatrics.

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.

Brian E. Smith, D. S. Houston, R. Zarychanski, 2012, Blood.

Substitution of the Human β-Spectrin Promoter for the Human Aγ-Globin Promoter Prevents Silencing of a Linked Human β-Globin Gene in Transgenic Mice

G. Stamatoyannopoulos, D. Bodine, B. Forget, 1998, Molecular and Cellular Biology.

Long-term expression of gamma-globin mRNA in mouse erythrocytes from retrovirus vectors containing the human gamma-globin gene fused to the ankyrin-1 promoter.

D. Bodine, S. Anderson, D. Sabatino, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Global transcriptome analyses of human and murine terminal erythroid differentiation.

Jie Li, Jing Liu, Fumin Xue, 2014, Blood.

A New Case of KLF1 G973A Mutation and Congenital Dyserythropoeitic Anemia (CDA)- Further Definition of Emerging New Syndrome and Possible Association with Gonadal Dysgenesis

A. Dombkowski, Y. Ravindranath, Robert M. Johnson, 2011 .

Ankyrin‐linked hereditary spherocytosis in an African–American kindred

J. Sangerman, B. Forget, P. Gallagher, 2008, American journal of hematology.

Applications of high-throughput DNA sequencing to benign hematology.

V. Sankaran, P. Gallagher, 2013, Blood.

MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activation

Christopher W Carroll, Abhishek Kumar, Mei Zhong, 2019, Nature Communications.

Structure and Organization of the Human Ankyrin-1 Gene

B. Forget, P. Gallagher, S. Lux, 1997, The Journal of Biological Chemistry.

An insulator with barrier-element activity promotes alpha-spectrin gene expression in erythroid cells.

D. Bodine, P. Gallagher, Laurie A. Steiner, 2009, Blood.

Nonstochastic Reprogramming from a Privileged Somatic Cell State

Rong Fan, Shangqin Guo, Sherman M. Weissman, 2014, Cell.

Identification of Biologically Relevant Enhancers in Human Erythroid Cells*

Ross C Hardison, Tejaswini Mishra, R. Hardison, 2013, The Journal of Biological Chemistry.

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

V. Schulz, P. Gallagher, Laurie A. Steiner, 2011, The Journal of Biological Chemistry.

The human ankyrin-1 gene is selectively transcribed in erythroid cell lines despite the presence of a housekeeping-like promoter.

B. Forget, P. Gallagher, S. Lux, 2000, Blood.

Aberrant splicing contributes to severe α-spectrin-linked congenital hemolytic anemia.

P. Newburger, D. Speicher, S. Israels, 2019, The Journal of clinical investigation.

Mutation in a Highly Conserved COOH-Terminal Residue of Krüppel-Like Factor 1 Associated with Elevated Hb F in a Compound Heterozygous β-Thalassemia Patient with a Nontransfusion-Dependent Thalassemia Phenotype

B. Forget, V. Schulz, P. Gallagher, 2016, Hemoglobin.

Aberrant splicing contributes to severe alpha-spectrin-linked congenital hemolytic anemia

P. Newburger, D. Speicher, S. Israels, 2022 .

Pklr Intron Splicing-Associated Mutations and Alternate Diagnoses Are Common in Pyruvate Kinase Deficient Patients with Single or No Pklr Coding Mutations

B. Glader, P. Bianchi, H. Yaish, 2018, Blood.

MKL1 and MKL2 play redundant and crucial roles in megakaryocyte maturation and platelet formation.

S. Halene, Elenoe C Smith, J. Italiano, 2012, Blood.

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

Hongyu Zhao, V. Schulz, P. Gallagher, 2014, Molecular Cytogenetics.

Human Extrafollicular CD4+ Th Cells Help Memory B Cells Produce Igs

D. Karas, Jin-Young Choi, Sang Taek Kim, 2018, The Journal of Immunology.

CTCF and CohesinSA-1 Mark Active Promoters and Boundaries of Repressive Chromatin Domains in Primary Human Erythroid Cells

Kimberly Lezon-Geyda, V. Schulz, K. Lezon-Geyda, 2016, PloS one.

Long noncoding RNAs in erythropoiesis.

P. Gallagher, 2014, Blood.

Development of a Stable Retrovirus Vector Capable of Long‐Term Expression of γ‐Globin mRNA in Mouse Erythrocytes

D. Bodine, S. Anderson, D. Sabatino, 2001, Annals of the New York Academy of Sciences.

Pseudoexstrophy of the bladder: case report and literature review.

R. Weiss, P. Gallagher, H. Swana, 1997, Journal of pediatric surgery.

Hematologically important mutations: spectrin and ankyrin variants in hereditary spherocytosis.

B. Forget, P. Gallagher, 1998, Blood cells, molecules & diseases.

Severe nondominant hereditary spherocytosis in an infant with coinheritance of three rare alpha‐spectrin gene defects

N. Mittal, P. Gallagher, J. Loew, 2018, Pediatric blood & cancer.

Molecular mechanisms in the inherited red cell membrane disorders

P. Gallagher, R. Liem, 2005 .

Amino‐acid substitution in α‐spectrin commonly coinherited with nondominant hereditary spherocytosis

D. Speicher, P. Agre, B. Forget, 1997, American journal of hematology.

Spectrin genes in health and disease.

B. Forget, P. Gallagher, 1993, Seminars in hematology.

Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis.

B. Forget, P. Gallagher, 1997, Blood cells, molecules & diseases.

Spectrin St Louis and the alpha LELY allele.

B. Forget, P. Gallagher, 1994, Blood.

USF1 and hSET1A Mediated Epigenetic Modifications Regulate Lineage Differentiation and HoxB4 Transcription

Kairong Cui, K. Zhao, Y. Li, 2013, PLoS genetics.

USF 1 and hSET 1 A Mediated Epigenetic Modifications Regulate Lineage Differentiation and HoxB 4 Transcription

Kairong Cui, K. Zhao, R. Roeder, 2013 .

A Decline in the Frequency of Neonatal Exchange Transfusions and Its Effect on Exchange-Related Morbidity and Mortality

R. Ehrenkranz, P. Gallagher, M. Bizzarro, 2007, Pediatrics.

Adult human megakaryocyte-erythroid progenitors are in the CD34+CD38mid fraction.

Gazelle Zerafati, P. Gallagher, D. Krause, 2016, Blood.

Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitro.

M. Debatis, B. Forget, P. Gallagher, 2000, Experimental hematology.

An 11-amino acid β-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes

P. Low, D. Bodine, P. Gallagher, 2007, Proceedings of the National Academy of Sciences.

Seventy-Five Years of Neonatal Sepsis at Yale: 1928–2003

R. Baltimore, P. Gallagher, M. Bizzarro, 2005, Pediatrics.

Diaphragmatic plication in the extremely low birth weight infant.

P. Gallagher, R. Touloukian, J. Seashore, 2000, Journal of pediatric surgery.

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.

E. R. Schneider, R. Altura, John Wu, 2017, Blood.

RED CELLS , IRON , AND ERYTHROPOIESIS Novel mechanisms of PIEZO 1 dysfunction in hereditary xerocytosis

E. R. Schneider, R. Altura, John Wu, 2017 .

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

V. Schulz, K. Lezon-Geyda, P. Gallagher, 2015, Blood.

Mutation of a barrier insulator in the human ankyrin-1 gene is associated with hereditary spherocytosis.

D. Bodine, P. Gallagher, L. Garrett, 2010, The Journal of clinical investigation.

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

H. Yaish, P. Gallagher, R. Christensen, 2015, Pediatrics.

Congenital chylothorax

I. N. King, P. J. Dubin, P. Gallagher, 2000, Current opinion in pediatrics.

Molecular diagnosis of hemoglobinopathies and other red blood cell disorders.

M. Arcasoy, P. Gallagher, 1999, Seminars in hematology (Print).

GATA-1 and Oct-1 Are Required for Expression of the Human α-Hemoglobin-stabilizing Protein Gene*

M. Weiss, D. Bodine, P. Gallagher, 2005, Journal of Biological Chemistry.

Genotype‐phenotype correlation and molecular heterogeneity in pyruvate kinase deficiency

P. Newburger, D. Morton, M. Wlodarski, 2020, American journal of hematology.

Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study.

P. Newburger, D. Morton, E. Neufeld, 2018, Blood.

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function

R. Secolin, Xiaomei Wang, M. Weiss, 2008, American journal of hematology/oncology.

GATA-1 and Oct-1 are required for expression of the human alpha-hemoglobin-stabilizing protein gene.

M. Weiss, D. Bodine, P. Gallagher, 2005, The Journal of biological chemistry.

Changing Patterns in Neonatal Escherichia coli Sepsis and Ampicillin Resistance in the Era of Intrapartum Antibiotic Prophylaxis

R. Baltimore, P. Gallagher, L. Dembry, 2008, Pediatrics.

Clinical and Laboratory Factors That Predict Death in Very Low Birth Weight Infants Presenting With Late-onset Sepsis

V. Bhandari, P. Gallagher, V. Shabanova, 2014, The Pediatric infectious disease journal.

A dinucleotide deletion in the ankyrin promoter alters gene expression, transcription initiation and TFIID complex formation in hereditary spherocytosis.

D. Bodine, P. Gallagher, L. Garrett-Beal, 2005, Human molecular genetics.

Antibiotic-resistant organisms in the neonatal intensive care unit.

P. Gallagher, M. Bizzarro, 2007, Seminars in perinatology.

Partial exchange transfusion for polycythemia hyperviscosity syndrome.

R. Ehrenkranz, P. Gallagher, M. Bizzarro, 2011, American journal of perinatology.

Hepatic Malignancy in an Infant with Wolf–Hirschhorn Syndrome

P. Gallagher, S. Peterec, S. Rutter, 2017, Fetal and pediatric pathology.

Hereditary xerocytosis: Diagnostic considerations

C. Quinn, Kejian Zhang, P. Gallagher, 2018, American journal of hematology.

Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptide.

L. Valentino, B. Forget, P. Gallagher, 1991, Blood.

Spectrin Rouen (beta 220-218), a novel shortened beta-chain variant in a kindred with hereditary elliptocytosis. Characterization of the molecular defect as exon skipping due to a splice site mutation.

F. Galibert, B. Forget, P. Gallagher, 1991, The Journal of clinical investigation.

Erythrocyte disorders in the perinatal period.

P. Gallagher, Laurie A. Steiner, 2007, Seminars in perinatology.

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

P. Gallagher, Laurie A. Steiner, 2007 .

Osteomyelitis of the Skull after Varicella Infection

P. Gallagher, 1990, Clinical pediatrics.

Recommendations for diagnosis and treatment of methemoglobinemia

A. Iolascon, A. Kulozik, R. Russo, 2021, American journal of hematology.

Diagnosis of Pyruvate Kinase Deficiency

B. Glader, P. Gallagher, 2016, Pediatric blood & cancer.

Diagnosis and management of rare congenital nonimmune hemolytic disease.

P. Gallagher, 2015, Hematology. American Society of Hematology. Education Program.

Molecular Characterization of 140 Patients in the Pyruvate Kinase Deficiency (PKD) Natural History Study (NHS): Report of 20 New Variants

P. Newburger, D. Morton, M. Wlodarski, 2015 .

Update on the clinical spectrum and genetics of red blood cell membrane disorders.

P. Gallagher, Patrick G Gallagher, 2004, Current hematology reports.

A recurrent frameshift mutation of the ankyrin gene associated with severe hereditary spherocytosis

F. Costa, B. Forget, S. Saad, 2000, British journal of haematology.

Altered subcellular localization of transcription factor TEAD4 regulates first mammalian cell lineage commitment

Barry Behr, Soumen Paul, Byunggil Yoo, 2012, Proceedings of the National Academy of Sciences.

Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.

S. Weed, N. Mohandas, B. Forget, 1997, The Journal of clinical investigation.

Erythropoietin therapy for anemia of prematurity.

R. Ehrenkranz, P. Gallagher, 1993, Clinics in perinatology.

Genome-wide ChIP-Seq reveals a dramatic shift in the binding of the transcription factor erythroid Kruppel-like factor during erythrocyte differentiation.

S. S. Ajay, E. H. Margulies, J. Mullikin, 2011, Blood.

HbA(2): at the borderline of the KLF.

P. Gallagher, 2011, Blood.

Neonatal sepsis due to echovirus 18 infection

Samir S. Shah, P. Gallagher, Samir S Shah, 1997, Journal of perinatal medicine.

Comprehensive proteomic analysis of murine terminal erythroid differentiation.

C. Hillyer, N. Mohandas, C. Lacombe, 2020, Blood advances.

Spectrin oligomerization is cooperatively coupled to membrane assembly: a linkage targeted by many hereditary hemolytic anemias?

M. Giorgi, P. Gallagher, J. Morrow, 2001, Experimental and molecular pathology.

Molecular basis of erythrocyte membrane disorders

P. Gallagher, Jovino D.S. Ferriera, 1997, Current opinion in hematology.

HEMOLYTIC ANEMIAS : RED BLOOD CELL MEMBRANE AND METABOLIC DEFECTS

P. Gallagher, 2015 .

Abnormalities of the erythrocyte membrane.

P. Gallagher, 2013, Pediatric clinics of North America.

Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred.

S. Israels, R. Zarychanski, P. Gallagher, 2011, Blood cells, molecules & diseases.

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

D. Speicher, P. Gallagher, S. Harper, 2008, Blood.

Pathogenic proline mutation in the linker between spectrin repeats: disease caused by spectrin unfolding.

D. Speicher, V. Ortiz, D. Discher, 2007, Blood.

Hereditary pyropoikilocytosis and the spectrinSt. Claude allele

P. Gallagher, S. Mootien, 2004, British journal of haematology.

Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene.

N. Mohandas, B. Forget, P. Gallagher, 1995, The Journal of clinical investigation.

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

P. Gallagher, J. Edelman, F. Duru, 2010 .

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

P. Gallagher, F. Duru, E. Edelman, 2007, Blood.

Regulation of erythrocyte membrane protein gene expression.

P. Gallagher, 2003, Current opinion in hematology.

Functional Analysis of a Novel cis-Acting Regulatory Region within the Human Ankyrin Gene (ANK-1) Promoter

Mary Yang, D. Bodine, P. Gallagher, 2010, Molecular and Cellular Biology.

Bacteremia, Meningitis, and Brain Abscesses in a Hospitalized Infant: Complications of Pseudomonas aeruginosa Conjunctivitis

Samir S. Shah, P. Gallagher, Samir S Shah, 1999, Journal of Perinatology.

A Comprehensive Model of the Spectrin Divalent Tetramer Binding Region Deduced Using Homology Modeling and Chemical Cross-linking of a Mini-spectrin*

David W Speicher, D. Speicher, Hsin-Yao Tang, 2010, Journal of Biological Chemistry.

A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chain.

F. Costa, B. Forget, P. Gallagher, 1991, The Journal of biological chemistry.

A Minimal Ankyrin Promoter Linked to a Human γ-Globin Gene Demonstrates Erythroid Specific Copy Number Dependent Expression with Minimal Position or Enhancer Dependence in Transgenic Mice*

D. Bodine, D. Sabatino, P. Gallagher, 2000, The Journal of Biological Chemistry.

Novel role for EKLF in megakaryocyte lineage commitment.

J. Bieker, D. Manwani, H. Karsunky, 2007, Blood.

Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo.

A. Hadjantonakis, D. Tuck, M. Baron, 2011, Blood.

The Human Alpha Hemoglobin Stabilizing Protein (AHSP) Gene Locus in EKLF-Deficient Erythroid Cells.

M. Weiss, D. Bodine, T. Townes, 2005 .

Canine elliptocytosis due to a mutant beta-spectrin.

N. Mohandas, S. Stockham, P. Gallagher, 2009, Veterinary clinical pathology.

Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion

D. Speicher, B. Forget, P. Gallagher, 1993 .

The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.

D. Speicher, S. Sriswasdi, Hsin-Yao Tang, 2013, Blood.

RED CELLS , IRON , AND ERYTHROPOIESIS The common hereditary elliptocytosis-associated a-spectrin L 260 P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation

D. Speicher, S. Sriswasdi, Hsin-Yao Tang, 2013 .

Human potassium chloride cotransporter 1 (SLC12A4) promoter is regulated by AP-2 and contains a functional downstream promoter element.

P. Gallagher, Guo-Ping Zhou, K. Anderson, 2004, Blood.

Preterm Infants with Paroxysmal Supraventricular Tachycardia: Presentation, Response to Therapy, and Outcome

P. Gallagher, R. Nehgme, N. Boramanand, 2001, Journal of Interventional Cardiac Electrophysiology.

Aplastic Crisis Revealing the Diagnosis of Hb Evans [α62(E11)Val→Met, GTG→ATG (α2)] in a Hispanic Kindred: Case Report and Review

P. Gallagher, J. van Hoff, Laurie A. Steiner, 2007 .

Perinatal aspects on the covid-19 pandemic: a practical resource for perinatal–neonatal specialists

T. Raju, F. Mimouni, P. Gallagher, 2020, Journal of Perinatology.

Proton Block and Voltage Gating Are Potassium-dependent in the Cardiac Leak Channel Kcnk3*

M. Butler, M. E. Buck, S. Goldstein, 2000, The Journal of Biological Chemistry.

Hematologically important mutations: ankyrin variants in hereditary spherocytosis.

P. Gallagher, 2005, Blood cells, molecules & diseases.

Nutritional anemias in infancy.

R. Ehrenkranz, P. Gallagher, 1995, Clinics in perinatology.

Maternal and Infant Characteristics Associated With Perinatal Arterial Stroke in the Preterm Infant

P. Gallagher, 2008 .

Characterization of circulating and cultured Tfh-like cells in sickle cell disease in relation to red blood cell alloimmunization status.

L. Devine, P. Gallagher, Jason S. Weinstein, 2020, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

MRTFA augments megakaryocyte maturation by enhancing the SRF regulatory axis.

V. Schulz, P. Gallagher, D. Krause, 2018, Blood advances.

Radiological case of the month. Mesenteric cyst with hemorrhage.

P. Gallagher, D. Kirks, B. Wood, 1990, American journal of diseases of children.

Gender analysis of Journal of Perinatology authorship during COVID-19

P. Gallagher, K. Machut, Leonardo Barrera, 2022, Journal of Perinatology.

Critical disparities in perinatal health—understanding risks and changing the outcomes

L. Harris, P. Gallagher, Zaneta Forson-Dare, 2021, Journal of Perinatology.

Neonatal sepsis 2004-2013: the rise and fall of coagulase-negative staphylococci.

R. Ehrenkranz, R. Baltimore, P. Gallagher, 2015, The Journal of pediatrics.

Perinatal Onset Mevalonate Kinase Deficiency

R. Ehrenkranz, R. Steiner, P. Gallagher, 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Picture of the month. Blueberry muffin baby (extramedullary hematopoiesis) due to congenital cytomegalovirus infection.

P. Gallagher, J. Gaffin, 2007, Archives of Pediatrics & Adolescent Medicine.

Summary of Joint European Hematology Association (EHA) and EuroBloodNet Recommendations on Diagnosis and Treatment of Methemoglobinemia

A. Iolascon, A. Kulozik, R. Russo, 2021, HemaSphere.

An Initiative to Decrease Laboratory Testing in a NICU

P. Gallagher, M. Bizzarro, S. Peterec, 2021, Pediatrics.

Matched Case-Control Analysis of Polymicrobial Bloodstream Infection In A Neonatal Intensive Care Unit

R. Baltimore, P. Gallagher, L. Dembry, 2008, Infection Control & Hospital Epidemiology.

Clinical and Molecular Epidemiology of Methicillin-Resistant Staphylococcus aureus in a Neonatal Intensive Care Unit in the Decade following Implementation of an Active Detection and Isolation Program

R. Baltimore, P. Gallagher, L. Dembry, 2015, Journal of Clinical Microbiology.

MKL1-actin pathway restricts chromatin accessibility and prevents mature pluripotency activation

Christopher W Carroll, Mei Zhong, Zongzhi Z. Liu, 2019, Nature Communications.

Increasing incidence of gram-negative rod bacteremia in a newborn intensive care unit.

R. Ehrenkranz, P. Gallagher, S. Shah, 1999, The Pediatric infectious disease journal.

Bi‐allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemia

P. Gallagher, D. Krause, R. Bajaj, 2011, Pediatric blood & cancer.

A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis.

J. Casey, R. Reithmeier, K. Lezon-Geyda, 2018, Blood.

Analysis of a Pst I polymorphism of the human erythrocyte band 3 gene (EPB3)

B. Forget, P. Gallagher, P. B. Jenkins, 1993, British journal of haematology.

Exclusion of the stomatin, α‐adducin and β‐adducin loci in a large kindred with dehydrated hereditary stomatocytosis

J. Sinard, L. Snyder, P. Gallagher, 1999 .

Staphylococcus aureus: impact on care in the neonatal unit

P. Gallagher, M. Bizzarro, M. Nelson, 2014 .

Methicillin-resistant Staphylococcus aureus in the neonatal intensive care unit.

P. Gallagher, M. Nelson, 2012, Seminars in perinatology.

Why so little progress in regionalization of perinatal care when transport of high-risk neonates remains a substantial risk?

P. Gallagher, M. Bizzarro, 2020, Journal of Perinatology.

A de novo band 3 mutation in hereditary spherocytosis

B. Forget, P. Gallagher, Y. Maksimova, 2012, Pediatric blood & cancer.

D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia

Preti Jain, S. Ferdinandusse, W. Ji, 2021, American journal of medical genetics. Part A.

Erythroid Expression of the Human α-Spectrin Gene Promoter Is Mediated by GATA-1- and NF-E2-binding Proteins*

D. Bodine, D. Sabatino, P. Gallagher, 2002, The Journal of Biological Chemistry.

cDNA structure, tissue-specific expression, and chromosomal localization of the murine band 7.2b gene.

D. Ward, P. Gallagher, M. Romana, 1995, Blood.

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

D. Speicher, S. Sriswasdi, Hsin-Yao Tang, 2014, Proceedings of the National Academy of Sciences.

A common type of the spectrin alpha I 46-50a-kD peptide abnormality in hereditary elliptocytosis and pyropoikilocytosis is associated with a mutation distant from the proteolytic cleavage site. Evidence for the functional importance of the triple helical model of spectrin.

A. Baruchel, B. Forget, S. Ballas, 1992, The Journal of clinical investigation.

Dynamic CO-Localization of GATA1, NFE2, and EKLF and Changes in Gene Expression During Hematopoiesis

M. Mahajan, D. Bodine, V. Schulz, 2010 .

Glucose Phosphate Isomerase Deficiency In 2 Patients With Novel Mutations Presenting As Severe Neurologic Abnormalities and Transfusion Dependent Hemolytic Anemia

T. Coates, B. Glader, P. Gallagher, 2013 .

Genomic organization and chromosomal localization of the murine 2 P domain potassium channel gene Kcnk8: conservation of gene structure in 2 P domain potassium channels.

D. Ward, D. Bockenhauer, S. Goldstein, 2000, Gene.

Molecular basis and haplotyping of the alphaII domain polymorphisms of spectrin: application to the study of hereditary elliptocytosis and pyropoikilocytosis.

D. Speicher, B. Forget, P. Gallagher, 1996, American journal of human genetics.

Clinical and molecular aspects of disorders of the erythrocyte membrane skeleton.

B. Forget, P. Gallagher, W. Tse, 1990, Seminars in perinatology.

An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).

F. Costa, B. Forget, P. Gallagher, 1991, Blood.

A Human β-Spectrin Gene Promoter Directs High Level Expression in Erythroid but Not Muscle or Neural Cells*

D. Bodine, B. Forget, D. Sabatino, 1999, The Journal of Biological Chemistry.

Chromatin Remodeling of the Mouse AHSP Gene Requires EKLF.

M. Weiss, D. Bodine, P. Gallagher, 2004 .

Vancomycin-resistant enterococcal bacteremia and necrotizing enterocolitis in a preterm neonate.

P. Gallagher, L. Dembry, Craig H Raskind, 2005, The Pediatric infectious disease journal.

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

D. Speicher, P. Gallagher, S. Harper, 2010, The Journal of Biological Chemistry.

Determinants of erythrocyte hydration

R. Lifton, J. Rinehart, E. Gulcicek, 2010, Current opinion in hematology.

Genetic basis of the polymorphisms of the alphaI domain of spectrin.

B. Forget, P. Gallagher, C. Wong, 1997, American journal of hematology/oncology.

Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the αβ spectrin self-association binding site

B. Forget, P. Gallagher, J. Morrow, 2004, Laboratory Investigation.

Location and PCR‐based detection of three polymorphisms of the human erythrocyte β‐spectrin gene (SPTB)

B. Forget, P. Gallagher, M. Lecomte, 1994, British journal of haematology.

Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletion.

D. Speicher, B. Forget, P. Gallagher, 1993, Blood.

UKCCCR guidelines for the use of cell lines in cancer research

T. Thangarajah, M. Hattori, N. Saitou, 1999, Cytogenetic and Genome Research.

A tissue-specific chromatin loop activates the erythroid ankyrin-1 promoter.

D. Bodine, P. Gallagher, L. Garrett, 2012, Blood.

Erythrocyte Ankyrin Promoter Mutations Associated with Recessive Hereditary Spherocytosis Cause Significant Abnormalities in Ankyrin Expression*

D. Bodine, D. S. Bassères, D. Sabatino, 2001, The Journal of Biological Chemistry.

promoter ankyrin-1 A tissue-specific chromatin loop activates the erythroid

D. Bodine, P. Gallagher, L. Garrett, 2013 .

Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene [letter]

B. Forget, P. Gallagher, W. Tse, 1992 .

Polymerase chain reaction analysis of an NcoI polymorphism of the human erythrocyte ankyrin gene.

B. Forget, P. Gallagher, W. Tse, 1992, Blood.

Group B streptococcal meningitis in adults.

P. Gallagher, C. Watanakunakorn, 1985, Archives of neurology.

Hereditary spherocytosis

S. Perrotta, N. Mohandas, P. Gallagher, 2008, The Lancet.

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

V. Schulz, P. Gallagher, Fang Xu, 2014, Molecular Cytogenetics.

Hereditary elliptocytosis: spectrin and protein 4.1R.

P. Gallagher, A. G. Gallagher, 2004, Seminars in hematology.

Conjunctival Colonization of Infants Hospitalized in a Neonatal Intensive Care Unit: A Longitudinal Analysis

P. Gallagher, L. Dembry, P. Farrel, 2004, Infection Control & Hospital Epidemiology.

Assignment1 of the 2P domain, acid-sensitive potassium channel OAT1 gene KCNK3 to human chromosome bands 2p24.1→p23.3 and murine 5B by in situ hybridization

P. Bray-Ward, P. Gallagher, N. Manjunath, 1999, Cytogenetic and Genome Research.

Transporting down the road to dehydration.

P. Gallagher, 2015, Blood.

Dehydrated hereditary stomatocytosis is not linked to the hlK1 locus, a Gardos channel candidate, on chromosome 19q13.2.

P. Gallagher, B. D. Smith, 1999, Blood.

Red Cells Red Cell Membrane Disorders

H. Bonkovsky, E. Beutler, P. Gallagher, 2005 .

Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X linked contiguous gene deletion syndrome?

A Ballabio, A. Ballabio, F. Vitelli, 1998, Journal of medical genetics.

Picture of the month. Blueberry muffin baby (extramedullary hematopoiesis) due to congenital cytomegalovirus infection.

P. Gallagher, J. Gaffin, 2007, Archives of pediatrics & adolescent medicine.

Global transcriptome analyses of human and murine terminal erythroid differentiation.

J. Li, N. Mohandas, X. An, 2014, Blood.

Clinical and Laboratory Factors That Predict Death in Very Low Birth Weight Infants Presenting With Late-onset Sepsis

V. Bhandari, P. Gallagher, V. Shabanova, 2014, The Pediatric infectious disease journal.

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

D. Speicher, S. Sriswasdi, Hsin-Yao Tang, 2014, Proceedings of the National Academy of Sciences.

The common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.

D. Speicher, S. Sriswasdi, Hsin-Yao Tang, 2013, Blood.

Regulation of RNA Polymerase II Activity is Essential for Terminal Erythroid Maturation.

K. Lezon-Geyda, P. Gallagher, M. Narla, 2021, Blood.

Large numbers of alternatively spliced isoforms of the regulatory region of human erythrocyte ankyrin.

B. Forget, P. Gallagher, S. Lux, 1992, Transactions of the Association of American Physicians.