The role of globins in cardiovascular physiology

TCS Keller 4th, C Lechauve, AS Keller… - Physiological …, 2022 - journals.physiology.org
Globin proteins exist in every cell type of the vasculature, from erythrocytes to endothelial
cells, vascular smooth muscle cells, and peripheral nerve cells. Many globin subtypes are …

Thalassemia: impact of consanguineous marriages on most prevalent monogenic disorders of humans

U Saeed, ZZ Piracha - Asian Pacific Journal of Tropical Disease, 2016 - Elsevier
Thalassaemia is an inherited autosomal recessive disorder closely associated with
consanguineous marriages. A literature search was conducted with an aim to investigate …

Selection of highly specific and sensitive mRNA biomarkers for the identification of blood

C Haas, E Hanson, A Kratzer, W Bär… - Forensic Science …, 2011 - Elsevier
In the present work, we have evaluated eight reportedly blood-specific mRNA markers (HBB,
HBA, ALAS2, CD3G, ANK1, PBGD, SPTB, AQP9) in an attempt to determine the most …

Successful mRNA profiling of 23 years old blood stains

F Kohlmeier, PM Schneider - Forensic science international: Genetics, 2012 - Elsevier
In this study, 23 years old human blood stains on different and problematic carrier materials,
such as jeans, leather, wood, wallpaper, carpet, wool, and nylon fabric, were investigated by …

[HTML][HTML] Hematologic features of alpha thalassemia carriers

H Akhavan-Niaki, RY Kamangari… - … journal of molecular …, 2012 - ncbi.nlm.nih.gov
Alpha thalassemia (α-thal) is relatively common worldwide. Most carriers are defective in
either one or two alpha globin genes out of four functional ones, with deletions being more …

[HTML][HTML] Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR

RM Grimholt, P Urdal, O Klingenberg, AP Piehler - BMC hematology, 2014 - Springer
Background Alpha-thalassemia is the most common human genetic disease worldwide.
Copy number variations in the form of deletions of α-globin genes lead to α-thalassemia …

Alpha thalassemia gene mutations in neonates from Mazandaran, Iran, 2012

H Jalali, MR Mahdavi, P Roshan, M Kosaryan… - …, 2014 - Taylor & Francis
Aim Alpha thalassemia is one of the most prevalent disorders worldwide and carrier
frequency of the disease is varied in different parts of the world. Although different studies in …

[HTML][HTML] Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening

I Lachover-Roth, S Peretz, H Zoabi, E Harel… - International Journal of …, 2024 - mdpi.com
The blood counts of α thalassemia carriers (α-thal) are similar to those of β thalassemia
carriers, except for Hemoglobin A2 (Hb A2), which is not elevated. The objective of this study …

[HTML][HTML] miR-338 inhibits the metastasis of lung cancer by targeting integrin β3

X Chen, L Wei, S Zhao - Oncology reports, 2016 - spandidos-publications.com
Abstract miR-338 as an intronic miRNA from apoptosis-associated tyrosine kinase (AATK) is
involved in tumor proliferation and apoptosis, but its function and regulatory mechanism in …

Hydrops fetalis in the stillborn: a series from the central region of Thailand

M Taweevisit, PS Thorner - Pediatric and Developmental …, 2010 - journals.sagepub.com
The purpose of this study was to analyze the cause of hydrops fetalis (HF) among fetal
deaths in the central region of Thailand. Autopsy reports diagnosed as HF from 1999 to …