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The Clinical and Laboratory Spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] Disease

Hemoglobin, 2013-01, Vol.37 (1), p.16-25

2013

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Inherited Hemoglobin Disorders in Guinea-Bissau, West Africa: A Population Study

Hemoglobin, 2006, Vol.30 (3), p.355-364

2006

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Haemoglobin c in arabs in kuwait

Acta haematologica, 1973-01, Vol.50 (2), p.112-115

1973

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Crucial involvement of the CCL3‐CCR5 axis‐mediated fibroblast accumulation in colitis‐associated carcinogenesis in mice

International journal of cancer, 2014-09, Vol.135 (6), p.1297-1306

2014

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Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India

Hemoglobin, 2021-11, Vol.45 (6), p.380-386

2021

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Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations

Hemoglobin, 2023-03, Vol.47 (2), p.52-55

2023

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β-Catenin mutations as determinants of hepatoblastoma phenotypes in mice

The Journal of biological chemistry, 2019-11, Vol.294 (46), p.17524-17542

2019

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Longitudinal progression of diabetes mellitus in Wolfram syndrome: The Washington University Wolfram Research Clinic experience

Pediatric diabetes, 2022-03, Vol.23 (2), p.212-218

2022

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mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)]

Biomedicines, 2021-10, Vol.9 (10), p.1390

2021

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A novel quantification-driven proteomic strategy identifies an endogenous peptide of pleiotrophin as a new biomarker of Alzheimer's disease

Scientific reports, 2017-10, Vol.7 (1), p.13333-12, Article 13333

2017

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Engulfment of Hb‐activated platelets differentiates monocytes into pro‐inflammatory macrophages in PNH patients

European journal of immunology, 2018-08, Vol.48 (8), p.1285-1294

2018

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HEMOGLOBIN C TRAIT PRESENTING WITH BILATERAL CENTRAL RETINAL VEIN OCCLUSION

Retinal cases & brief reports, 2023-01, Vol.17 (1), p.44-46

2023

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Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant

Hemoglobin, 2017-11, Vol.41 (4-6), p.317-320

2017

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Predictive Power of Tissue and Circulating Biomarkers for the Severity of Biopsy-Validated Chronic Liver Diseases

Journal of clinical medicine, 2022-10, Vol.11 (20), p.5985

2022

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Renal anemia and hydration status in non-dialysis chronic kidney disease: Is there a link?

Journal of medicine and life, 2018-10, Vol.11 (4), p.293-298

2018

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Prediction of development and maintenance of high albuminuria during chronic renin–angiotensin suppression by plasma proteomics

International journal of cardiology, 2015-10, Vol.196, p.170-177

2015

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Are Red Blood Cell Distribution Width and RDW / Hemoglobin Ratio Predictable in Mortality Among Patients with Chronic Obstructive Pulmonary Disease?

Erciyes Medical Journal, 2019-12

organ, nalan

2019

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Blood Typing Profile of a School-Aged Population of a North Togo Township

Hemoglobin, 2014-10, Vol.38 (5), p.316-318

2014

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Non-alcoholic fatty liver disease: An emerging liver disease in Taiwan

Journal of the Formosan Medical Association, 2012-10, Vol.111 (10), p.527-535

2012

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Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease

Hemoglobin, 2016-01, Vol.40 (1), p.64-65

2016

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Pathophysiology and biochemistry of cardiovascular disease

Current opinion in genetics & development, 2004-06, Vol.14 (3), p.271-279

Scott, James

2004

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The placental-umbilical unit in sickle cell disease pregnancy: A model for studying in vivo functional adjustments to hypoxia in humans

Human pathology, 2004-11, Vol.35 (11), p.1353-1359

2004

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Metabolic Pathways Related to Oxidative Stress in Patients With Hemoglobin H Disease and Iron Overload

Journal of clinical laboratory analysis, 2014-07, Vol.28 (4), p.261-268

2014

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HB-EGF Protects the Lungs after Intestinal Ischemia/Reperfusion Injury

The Journal of surgical research, 2010-09, Vol.163 (1), p.86-95

2010

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A Possible Clinical Adaptation of CRM197 in Combination with Conventional Chemotherapeutic Agents for Ovarian Cancer

Anticancer research, 2011-07, Vol.31 (7), p.2461-2465

2011

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The Clinical and Laboratory Spectrum of Hb C [β6(A3)Glu→Lys, GAG>AAG] Disease

Inherited Hemoglobin Disorders in Guinea-Bissau, West Africa: A Population Study

Haemoglobin c in arabs in kuwait

Crucial involvement of the CCL3‐CCR5 axis‐mediated fibroblast accumulation in colitis‐associated carcinogenesis in mice

Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India

Molecular Basis and Hematologic Phenotype of Hemoglobin H Disease Combined with Two Rare β-Globin Mutations

β-Catenin mutations as determinants of hepatoblastoma phenotypes in mice

Longitudinal progression of diabetes mellitus in Wolfram syndrome: The Washington University Wolfram Research Clinic experience

mRNA Analysis of Frameshift Mutations with Stop Codon in the Last Exon: The Case of Hemoglobins Campania [α1 cod95 (−C)] and Sciacca [α1 cod109 (−C)]

A novel quantification-driven proteomic strategy identifies an endogenous peptide of pleiotrophin as a new biomarker of Alzheimer's disease

Engulfment of Hb‐activated platelets differentiates monocytes into pro‐inflammatory macrophages in PNH patients

HEMOGLOBIN C TRAIT PRESENTING WITH BILATERAL CENTRAL RETINAL VEIN OCCLUSION

Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant

Predictive Power of Tissue and Circulating Biomarkers for the Severity of Biopsy-Validated Chronic Liver Diseases

Renal anemia and hydration status in non-dialysis chronic kidney disease: Is there a link?

Prediction of development and maintenance of high albuminuria during chronic renin–angiotensin suppression by plasma proteomics

Are Red Blood Cell Distribution Width and RDW / Hemoglobin Ratio Predictable in Mortality Among Patients with Chronic Obstructive Pulmonary Disease?

Blood Typing Profile of a School-Aged Population of a North Togo Township

Non-alcoholic fatty liver disease: An emerging liver disease in Taiwan

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease

Pathophysiology and biochemistry of cardiovascular disease

The placental-umbilical unit in sickle cell disease pregnancy: A model for studying in vivo functional adjustments to hypoxia in humans

Metabolic Pathways Related to Oxidative Stress in Patients With Hemoglobin H Disease and Iron Overload

HB-EGF Protects the Lungs after Intestinal Ischemia/Reperfusion Injury

A Possible Clinical Adaptation of CRM197 in Combination with Conventional Chemotherapeutic Agents for Ovarian Cancer

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