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Selection of housekeeping genes for gene expression studies in human reticulocytes using real-time PCR

BMC molecular biology, 2006-10, Vol.7 (1), p.33-33, Article 33

2006

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HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers

The Journal of clinical investigation, 2014-04, Vol.124 (4), p.1699-1710

2014

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A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

Nature genetics, 2007-10, Vol.39 (10), p.1197-1199

2007

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Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing Fetal Hemoglobin Levels in Adults

Proceedings of the National Academy of Sciences - PNAS, 2007-07, Vol.104 (27), p.11346-11351

2007

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Binding patterns of BCL11A in the globin and GATA1 loci and characterization of the BCL11A fetal hemoglobin locus

Blood cells, molecules, & diseases, 2010-08, Vol.45 (2), p.140-146

2010

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cMYB is involved in the regulation of fetal hemoglobin production in adults

Blood, 2006-08, Vol.108 (3), p.1077-1083

2006

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Treatment of post-anesthesia dementia with perispinal etanercept injection and hyperbaric oxygen therapy: a case report

Journal of medical case reports, 2017-04, Vol.11 (1), p.105-105, Article 105

2017

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Class II Cytokine Receptor Gene Cluster Is a Major Locus for Hepatitis B Persistence

Proceedings of the National Academy of Sciences - PNAS, 2006-06, Vol.103 (24), p.9148-9153

2006

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Long-Term Efficacy of Combination Therapy of Transcranial Magnetic Stimulation with Ketamine for Patients with Treatment-Resistant Depression

CNS spectrums, 2021-04, Vol.26 (2), p.171-171

2021

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Germ line DDX41 mutations define a unique subtype of myeloid neoplasms

Blood, 2023-02, Vol.141 (5), p.534-549

2023

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A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Twin research and human genetics, 2010-12, Vol.13 (6), p.567-572

2010

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Structure and Expression of the Hairless Gene of Mice

Proceedings of the National Academy of Sciences - PNAS, 1994-08, Vol.91 (16), p.7717-7721

1994

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The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

Blood, 2009-08, Vol.114 (6), p.1254-1262

2009

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Update on collagen receptor interactions in platelets: is the two-state model still valid?

Platelets (Edinburgh), 2000, Vol.11 (5), p.252-258

Watson, Oscar Berlanga, Denise Best, Jon Frampton, Steve

2000

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A novel 506kb deletion causing εγδβ thalassemia

Blood cells, molecules, & diseases, 2012-10, Vol.49 (3-4), p.121-127

2012

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Positional cloning of the mouse retrovirus restriction gene Fv1

Nature (London), 1996-08, Vol.382 (6594), p.826-829

1996

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α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

British journal of haematology, 2006-06, Vol.133 (6), p.675-682

2006

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Bio-electrospraying whole human blood: analysing cellular viability at a molecular level

Journal of tissue engineering and regenerative medicine, 2009-10, Vol.3 (7), p.562-566

2009

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Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobin

Blood, 2004-10, Vol.104 (7), p.2184-2186

2004

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Lamin B‐receptor mutations in Pelger–Huët anomaly

British journal of haematology, 2003-11, Vol.123 (3), p.542-544

2003

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Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin

American journal of human genetics, 2002-03, Vol.70 (3), p.793-799

2002

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Detection of prothrombin gene polymorphism at position 20209 (PT20209C/T): pilot study in a black population in the United Kingdom

Thrombosis and haemostasis, 2005-01, Vol.93 (1), p.179-180

Arya, Roopen

2005

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Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin

European journal of human genetics : EJHG, 2006-01, Vol.14 (1), p.101-108

2006

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Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletions

British journal of haematology, 2005-03, Vol.128 (5), p.722

2005

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Suicidal ideation among outpatients at general neurology clinics: prospective study

BMJ (Online), 2000-05, Vol.320 (7245), p.1311-1312

International edition, 2000

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Selection of housekeeping genes for gene expression studies in human reticulocytes using real-time PCR

HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15

Intergenic Variants of HBS1L-MYB Are Responsible for a Major Quantitative Trait Locus on Chromosome 6q23 Influencing Fetal Hemoglobin Levels in Adults

Binding patterns of BCL11A in the globin and GATA1 loci and characterization of the BCL11A fetal hemoglobin locus

cMYB is involved in the regulation of fetal hemoglobin production in adults

Treatment of post-anesthesia dementia with perispinal etanercept injection and hyperbaric oxygen therapy: a case report

Class II Cytokine Receptor Gene Cluster Is a Major Locus for Hepatitis B Persistence

Long-Term Efficacy of Combination Therapy of Transcranial Magnetic Stimulation with Ketamine for Patients with Treatment-Resistant Depression

Germ line DDX41 mutations define a unique subtype of myeloid neoplasms

A Twins Heritability Study on Alpha Hemoglobin Stabilizing Protein (AHSP) Expression Variability

Structure and Expression of the Hairless Gene of Mice

The HBS1L-MYB intergenic interval associated with elevated HbF levels shows characteristics of a distal regulatory region in erythroid cells

Update on collagen receptor interactions in platelets: is the two-state model still valid?

A novel 506kb deletion causing εγδβ thalassemia

Positional cloning of the mouse retrovirus restriction gene Fv1

α‐Haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β‐thalassaemia

Bio-electrospraying whole human blood: analysing cellular viability at a molecular level

Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobin

Lamin B‐receptor mutations in Pelger–Huët anomaly

Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin

Detection of prothrombin gene polymorphism at position 20209 (PT20209C/T): pilot study in a black population in the United Kingdom

Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin

Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletions

Suicidal ideation among outpatients at general neurology clinics: prospective study

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