| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Félix de la Fuente-Gonzalo, Jorge M Nieto, Lara Vinuesa, Julián Sevilla, Joaquín Díaz-Mediavilla, Ana Villegas, Fernando A González, Paloma Roper. Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia. International journal of hematology. vol 100. issue 6. 2015-08-18. PMID:25212678. |
hb cibeles [α2 cd25(b6) (gly → asp)]: a novel alpha chain variant causing alpha-thalassemia. |
2015-08-18 |
2023-08-13 |
Not clear |
| Félix de la Fuente-Gonzalo, Jorge M Nieto, Lara Vinuesa, Julián Sevilla, Joaquín Díaz-Mediavilla, Ana Villegas, Fernando A González, Paloma Roper. Hb Cibeles [α2 CD25(B6) (Gly → Asp)]: a novel alpha chain variant causing alpha-thalassemia. International journal of hematology. vol 100. issue 6. 2015-08-18. PMID:25212678. |
in this study we show a new structural variant of α-chain, hb cibeles [alpha 25(b6) gly → asp], in heterozygous state, which was undetectable by electrophoretic or chromatographic methods. |
2015-08-18 |
2023-08-13 |
Not clear |
| Quentin A Hill, Lisa Farrar, Jim Lordan, Alice Gallienne, Shirley Henderso. A combination of two novel alpha globin variants Hb Bridlington (HBA1) and Hb Taybe (HBA2) resulting in severe hemolysis, pulmonary hypertension, and death. Hematology (Amsterdam, Netherlands). vol 20. issue 1. 2015-07-28. PMID:24716903. |
a combination of two novel alpha globin variants hb bridlington (hba1) and hb taybe (hba2) resulting in severe hemolysis, pulmonary hypertension, and death. |
2015-07-28 |
2023-08-13 |
Not clear |
| S M Hassan, M Al Muslahi, M Al Riyami, E Bakker, C L Harteveld, P C Giordan. Sickle cell anemia and α-thalassemia: a modulating factor in homozygous HbS/S patients in Oman. European journal of medical genetics. vol 57. issue 11-12. 2015-07-24. PMID:25266642. |
no clear general phenotype correlation was found when patients were compared regardless of the haplotype but overall, patients with homozygous alpha thalassemia (α-/α-) had the highest hb, hct, rbc and the lowest mcv, mch and mchc levels. |
2015-07-24 |
2023-08-13 |
Not clear |
| Pranee Winichagoon, Pornnapa Kumpan, Paula Holmes, Jill Finlayson, Christopher Newbound, Arnold Kabral, Benjamin Li, Manit Nuinoon, Terry Fawcett, Chatchai Tayapiwatana, Watchara Kasinrerk, Suthat Fucharoe. Validation of the immunochromatographic strip for α-thalassemia screening: a multicenter study. Translational research : the journal of laboratory and clinical medicine. vol 165. issue 6. 2015-07-23. PMID:25450870. |
the alpha thal ic strip also has the potential to replace testing for hb h inclusion bodies, as it appears to be more sensitive, specific, and less labor intensive. |
2015-07-23 |
2023-08-13 |
Not clear |
| 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 |