| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Sushama Parab, Suhas Sakhare, Caesar Sengupta, Arokiaswamy Veluman. Diagnosis of a rare double heterozygous Hb D Punjab/Hb Q India hemoglobinopathy using Sebia capillary zone electrophoresis. Indian journal of pathology & microbiology. vol 57. issue 4. 2015-04-19. PMID:25308024. |
small peak in z1 zone indicated the presence of alpha chain variant hb q india. |
2015-04-19 |
2023-08-13 |
Not clear |
| Sitthichai Panyasai, Sakorn Pornpraser. Hemoglobin Q-Thailand and its combinations with other forms of thalassemia or hemoglobinopathies in northern Thailand. Clinical laboratory. vol 60. issue 7. 2014-09-15. PMID:25134377. |
there have been no reports for the frequency of hb q-thailand [alpha 74(ef3)asp --> his, gac > cac] and its combinations either with other forms of thalassemia or hemoglobinopathies in northern thailand. |
2014-09-15 |
2023-08-13 |
Not clear |
| Raja Zahratul Azma, Othman Ainoon, Alauddin Hafiza, Ithnin Azlin, Abudul Razak Noor Farisah, Sardi Nor Hidayati, Hussin Noor Hamida. Molecular characteristic of alpha thalassaemia among patients diagnosed in UKM Medical Centre. The Malaysian journal of pathology. vol 36. issue 1. 2014-08-21. PMID:24763232. |
full blood count (fbc) and haemoglobin (hb) analysis using either gel electrophoresis, high performance liquid chromatography (hplc) or capillary zone electrophoresis (ce) are unable to detect definitively alpha thalassaemia carriers. |
2014-08-21 |
2023-08-13 |
Not clear |
| Abhishek Purohit, Mukul Aggarwal, Roshan B Colah, Anita H Nadkarni, Hara P Pat. A Case of Iron Deficiency Anemia with Co-existing Hb Fontainebleau. Mediterranean journal of hematology and infectious diseases. vol 6. issue 1. 2014-07-21. PMID:25045459. |
hb fontainebleau is a rare alpha chain variant in the indian population which generates an unknown peak on hemoglobin hplc study and does cause diagnostic difficulty to those who are not acquainted with this entity. |
2014-07-21 |
2023-08-13 |
Not clear |
| Prasanta Purohit, Snehadhini Dehury, Siris Patel, Dilip Kumar Pate. Prevalence of deletional alpha thalassemia and sickle gene in a tribal dominated malaria endemic area of eastern India. ISRN hematology. vol 2014. 2014-05-08. PMID:24808962. |
sickling test, hb electrophoresis, hplc, and molecular studies were undertaken to diagnose the prevalence of sickle allele, β -thalassemia allele, and deletional alpha thalassemia. |
2014-05-08 |
2023-08-13 |
human |
| Ranjeet Singh Mashon, Sona Nair, Pratibha Sawant, Roshan B Colah, Kanjaksha Ghosh, Sheila Da. Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India. Indian journal of human genetics. vol 19. issue 3. 2013-12-16. PMID:24339552. |
here, we report a rare alpha globin gene variant hb fontainebleau [a21(b2)ala>pro] detected in the heterozygous condition in a 35-year-old pregnant lady screened during this program. |
2013-12-16 |
2023-08-12 |
Not clear |
| Sanjay Pandey, Rahasya Mani Mishra, Sweta Pandey, Vineet Shah, Renu Saxen. Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients. Sao Paulo medical journal = Revista paulista de medicina. vol 130. issue 4. 2013-06-06. PMID:22965366. |
thus, our aim was to molecularly characterize the hb d trait among individuals who were clinically symptomatic because of co-inheritance of alpha deletions or any beta-globin gene mutations. |
2013-06-06 |
2023-08-12 |
Not clear |
| Kolattukudy P Santo, Mark Berjanskii, David S Wishart, Maria Stepanov. Comparative analysis of essential collective dynamics and NMR-derived flexibility profiles in evolutionarily diverse prion proteins. Prion. vol 5. issue 3. 2013-04-11. PMID:21869604. |
interestingly, flexibility differences in the loop between second beta strand (s2) and the second alpha helix (hb) appear to distinguish prion proteins from species that are susceptible to prion disease and those that are resistant. |
2013-04-11 |
2023-08-12 |
human |
| Zongping Mo, Changshun Yu, Zhaohui Hu, Wenli Fen. A novel deletion of -2.8 kb removing the entire alpha 2-globin gene observed in a Chinese patient with Hb H. Clinical laboratory. vol 58. issue 11-12. 2013-02-04. PMID:23289204. |
a novel deletion of -2.8 kb removing the entire alpha 2-globin gene observed in a chinese patient with hb h. most of recognized alpha-thalassemia mutations include deletions of one or both alpha-globin genes. |
2013-02-04 |
2023-08-12 |
human |
| Rodrigo Belmonte, Carlos E Cruz, José R Pires, Sirlei Daffr. Purification and characterization of Hb 98-114: a novel hemoglobin-derived antimicrobial peptide from the midgut of Rhipicephalus (Boophilus) microplus. Peptides. vol 37. issue 1. 2013-01-07. PMID:22749988. |
microplus females, which comprises the amino acids 98-114 of the alpha subunit of bovine hemoglobin, and was designated hb 98-114. |
2013-01-07 |
2023-08-12 |
cattle |
| Eliana Litsuko Tomimatsu Shimauti, Paula Juliana Antoniato Zamaro, Claudia Regina Bonini-Domingo. Interaction between Hb SS and alpha thalassemia (3.7 kb deletion): a familial study. Revista brasileira de hematologia e hemoterapia. vol 33. issue 3. 2012-10-10. PMID:23049305. |
interaction between hb ss and alpha thalassemia (3.7 kb deletion): a familial study. |
2012-10-10 |
2023-08-12 |
Not clear |
| Yuan-Di Zhao, Yan-Hua Bi, Wei-De Zhang, Qing-Ming Lu. The interface behavior of hemoglobin at carbon nanotube and the detection for H(2)O(2). Talanta. vol 65. issue 2. 2012-10-02. PMID:18969824. |
the heterogeneous electron transfer rate constant k of hb can be calculated as 0.062s(-1), the transfer coefficient alpha is 0.21 and the average surface coverage of hb on cnt surface is 3.58 x 10(-9) +/- 2.7 x 10(-10)mol/cm(2). |
2012-10-02 |
2023-08-12 |
Not clear |
| Renzo Galanell. Recent advances in the molecular understanding of non-transfusion-dependent thalassemia. Blood reviews. vol 26 Suppl 1. 2012-09-27. PMID:22631043. |
thalassemias are a group of inherited autosomal recessive hematologic disorders that occur because of defects in the alpha (α)- and beta (β)-globin genes of adult hemoglobin (hb). |
2012-09-27 |
2023-08-12 |
Not clear |
| Raja Zahratul Azma, Ainoon Othman, Norazlina Azman, Hafiza Alauddin, Azlin Ithnin, Nurasyikin Yusof, Noor Farisah Razak, Nor Hidayati Sardi, Noor Hamidah Hussi. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge. The Malaysian journal of pathology. vol 34. issue 1. 2012-08-23. PMID:22870600. |
haemoglobin constant spring (hb cs) mutation and single gene deletions are common underlying genetic abnormalities for alpha thalassaemias. |
2012-08-23 |
2023-08-12 |
Not clear |
| Raja Zahratul Azma, Ainoon Othman, Norazlina Azman, Hafiza Alauddin, Azlin Ithnin, Nurasyikin Yusof, Noor Farisah Razak, Nor Hidayati Sardi, Noor Hamidah Hussi. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge. The Malaysian journal of pathology. vol 34. issue 1. 2012-08-23. PMID:22870600. |
dna analysis for alpha globin gene mutations showed a single -alpha(-3.7) deletion and hb cs mutation. |
2012-08-23 |
2023-08-12 |
Not clear |
| Raja Zahratul Azma, Ainoon Othman, Norazlina Azman, Hafiza Alauddin, Azlin Ithnin, Nurasyikin Yusof, Noor Farisah Razak, Nor Hidayati Sardi, Noor Hamidah Hussi. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge. The Malaysian journal of pathology. vol 34. issue 1. 2012-08-23. PMID:22870600. |
co-inheritance of hb cs and a single -alpha(-3.7) deletion is expected to result at the very least in a clinical phenotype similar to that of two alpha genes deletion. |
2012-08-23 |
2023-08-12 |
Not clear |
| Raja Zahratul Azma, Ainoon Othman, Norazlina Azman, Hafiza Alauddin, Azlin Ithnin, Nurasyikin Yusof, Noor Farisah Razak, Nor Hidayati Sardi, Noor Hamidah Hussi. Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge. The Malaysian journal of pathology. vol 34. issue 1. 2012-08-23. PMID:22870600. |
however we demonstrate here a phenotypic modification of alpha thalassemia presumptively as a result of co-inheritance with deltabeta chain abnormality as suggested by the high hb f level. |
2012-08-23 |
2023-08-12 |
Not clear |
| Jan Simoni, Grace Simoni, John F Moeller, Mario Feola, John A Griswold, Donald E Wesso. Adenosine-5'-triphosphate-adenosine-glutathione cross-linked hemoglobin as erythropoiesis-stimulating agent. Artificial organs. vol 36. issue 2. 2012-06-05. PMID:22339724. |
cross-linked hb accelerates erythropoiesis by downregulating nf-kappa b, stabilizing and facilitating hif-1 alpha binding to the epo gene, under both oxygen conditions. |
2012-06-05 |
2023-08-12 |
Not clear |
| Sukanya Sriiam, Amporn Leecharoenkiat, Pathrapol Lithanatudom, Tirawat Wannatung, Saovaros Svasti, Suthat Fucharoen, Jisnuson Svasti, Daranee Chokchaichamnankit, Chantragan Srisomsap, Duncan R Smit. Proteomic analysis of hemoglobin H-constant spring (Hb H-CS) erythroblasts. Blood cells, molecules & diseases. vol 48. issue 2. 2012-06-01. PMID:22154201. |
hemoglobin h disease (hb h) arises through the loss or dysfunction of three of the four alpha globin genes through the co-inheritance of either gross gene deletions or an abnormal hemoglobin which causes a non-deletional loss of α-globin expression. |
2012-06-01 |
2023-08-12 |
Not clear |
| Sukanya Sriiam, Amporn Leecharoenkiat, Pathrapol Lithanatudom, Tirawat Wannatung, Saovaros Svasti, Suthat Fucharoen, Jisnuson Svasti, Daranee Chokchaichamnankit, Chantragan Srisomsap, Duncan R Smit. Proteomic analysis of hemoglobin H-constant spring (Hb H-CS) erythroblasts. Blood cells, molecules & diseases. vol 48. issue 2. 2012-06-01. PMID:22154201. |
this study sought to investigate erythropoiesis in hb h-constant spring (hb h-cs) disease, a common form of hb h disease in southeast asia, caused by the inheritance of the constant spring variant hemoglobin together with deletion of two of the alpha globin genes. |
2012-06-01 |
2023-08-12 |
Not clear |