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HBA1 wt Allele

Known as: Hemoglobin Alpha 1 Globin Chain Gene, MGC126895, MGC126897 
Human HBA1 wild-type allele is located in the vicinity of 16p13.3 and is approximately 1 kb in length. This allele, which encodes hemoglobin subunit… Expand
National Institutes of Health

Related topics

Related topics

6 relations
16p13.3CD31 AntigensHomo sapiensLigand Binding
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Papers overview

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2018
2018
Spasticity assessment based on the Hilbert–Huang transform marginal spectrum entropy and the root mean square of surface electromyography signals: a preliminary study
BackgroundMost of the objective and quantitative methods proposed for spasticity measurement are not suitable for clinical… Expand
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2018
2018
A two-stage microbial association mapping framework with advanced FDR control
BackgroundIn microbiome studies, it is important to detect taxa which are associated with pathological outcomes at the lowest… Expand
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2017
2017
Should I Convince My Partner to Go on Pre-Exposure Prophylaxis (PrEP)? The Role of Personal and Relationship Factors on PrEP-Related Social Control among Gay and Bisexual Men
An estimated 35–68% of new HIV infections among gay, bisexual, and other men who have sex with men (GBM) are transmitted through… Expand
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2016
2016
Addressing the High Costs of Pancreaticoduodenectomy at Safety-Net Hospitals.
Importance Safety-net hospitals care for vulnerable patients, providing complex surgery at increased costs. These hospitals are… Expand
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2016
2016
Preclinical animal study and human clinical trial data of co-electrospun poly(l-lactide-co-caprolactone) and fibrinogen mesh for anterior pelvic floor reconstruction
Synthetic and biological materials are commonly used for pelvic floor reconstruction. In this study, host tissue response and… Expand
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2011
2011
Heterogeneity of hemoglobin H disease in childhood.
BACKGROUND Early diagnosis during newborn screening or infancy has enabled the observation of the natural history of hemoglobin H… Expand
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2008
2008
Subtypes of Alpha Thalassemia Diagnosed at a Medical Center in Jordan
BACKGROUND: This retrospective analysis study provides the molecular genetics of α-Thalassemia Mutations and identify the… Expand
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2003
2003
Hb Q-India: an uncommon variant diagnosed in three Punjabi patients with diabetes is identified by a novel DNA analysis test
Aims: An abnormality in the glycated haemoglobin peak (Hb A1c) on Diastat (Bio-Rad) cation exchange low pressure liquid… Expand
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2003
2003
Can defects in transferrin receptor 2 and hereditary hemochromatosis genes account for iron overload in HbH disease?
Iron overload was found to be the major cause of disability in Chinese HbH disease patients although they were not on regular… Expand
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1988
1988
Small cytoplasmic Ro RNA pseudogene and an Alu repeat in the human alpha-1 globin gene.
 
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