| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Mario C Foti, Salvatore Sortino, K U Ingol. New insight into solvent effects on the formal HOO. + HOO. reaction. Chemistry (Weinheim an der Bergstrasse, Germany). vol 11. issue 6. 2006-07-28. PMID:15685709. |
we find that it can be quantitatively accounted for by using abraham's hb acceptor parameter, beta(2)(h), for water of 0.38 and an estimated hb donor parameter, alpha(2)(h), for hoo. |
2006-07-28 |
2023-08-12 |
Not clear |
| Heather Imrie, Freya J I Fowkes, Pascal Michon, Livingstone Tavul, Jennifer C C Hume, Karen P Piper, John C Reeder, Karen P Da. Haptoglobin levels are associated with haptoglobin genotype and alpha+ -Thalassemia in a malaria-endemic area. The American journal of tropical medicine and hygiene. vol 74. issue 6. 2006-07-20. PMID:16760505. |
hp levels were related to age, hp genotype, hb levels, parasitemia, splenomegaly, and alpha(+)-thalassemia genotype. |
2006-07-20 |
2023-08-12 |
Not clear |
| Heather Imrie, Freya J I Fowkes, Pascal Michon, Livingstone Tavul, Jennifer C C Hume, Karen P Piper, John C Reeder, Karen P Da. Haptoglobin levels are associated with haptoglobin genotype and alpha+ -Thalassemia in a malaria-endemic area. The American journal of tropical medicine and hygiene. vol 74. issue 6. 2006-07-20. PMID:16760505. |
we suggest that this is the result of either reduced mean cell hb associated with alpha(+) -thalassemia homozygosity or an elevated il-6-dependent acute phase response. |
2006-07-20 |
2023-08-12 |
Not clear |
| Mitchell J Weiss, Suiping Zhou, Liang Feng, David A Gell, Joel P Mackay, Yigong Shi, Andrew J Go. Role of alpha-hemoglobin-stabilizing protein in normal erythropoiesis and beta-thalassemia. Annals of the New York Academy of Sciences. vol 1054. 2006-07-13. PMID:16339656. |
hemoglobin (hb) synthesis is coordinated by homeostatic mechanisms to limit the accumulation of free alpha or beta subunits, which are cytotoxic. |
2006-07-13 |
2023-08-12 |
mouse |
| Raveen K Basran, Margie Patterson, Lynda Walker, Lisa M Nakamura, Barry Eng, David H K Chui, John S Way. Prenatal diagnosis of hemoglobinopathies in Ontario, Canada. Annals of the New York Academy of Sciences. vol 1054. 2006-07-13. PMID:16339708. |
over the past 15 years, the laboratory has provided prenatal diagnosis for 672 pregnancies at-risk for severe hemoglobinopathies: 276 (41%) for homozygous beta-thalassemia or hemoglobin (hb) e/beta-thalassemia, 211 (31%) for homozygous alpha 0-thalassemia (hb bart's hydrops fetalis), and/or hb h disease, and 185 (28%) for various sickling disorders (hb ss, hb sc, hb s/beta-thalassemia). |
2006-07-13 |
2023-08-12 |
Not clear |
| Rupert Bartsch, Catharina Wenzel, Ursula Sevelda, Dagmar Hussian, Ursula Pluschnig, Gottfried J Locker, Robert Mader, Christoph C Zielinski, Guenther G Stege. Darbepoetin alpha as treatment for anemia in patients receiving chemotherapy: a single-center experience. Anti-cancer drugs. vol 16. issue 6. 2006-07-06. PMID:15930888. |
if no increase in hb was seen after 4 weeks, the dose of darbepoetin alpha was increased to 300 microg. |
2006-07-06 |
2023-08-12 |
Not clear |
| Cornelis L Harteveld, Gerard Steen, L Thomas Vlasveld, Peter van Delft, Piero C Giordan. Hb Bronovo, a new globin gene mutation at alpha2 103 (His->Leu) associated with an alpha thalassemia phenotype. Haematologica. vol 91. issue 4. 2006-06-12. PMID:16533721. |
hb bronovo, a new globin gene mutation at alpha2 103 (his->leu) associated with an alpha thalassemia phenotype. |
2006-06-12 |
2023-08-12 |
Not clear |
| Kris T Huang, Ivan Azarov, Swati Basu, Jinming Huang, Daniel B Kim-Shapir. Lack of allosterically controlled intramolecular transfer of nitric oxide from the heme to cysteine in the beta subunit of hemoglobin. Blood. vol 107. issue 7. 2006-05-08. PMID:16339397. |
electron paramagnetic resonance (epr) spectroscopy was used to (1) determine the concentration of iron nitrosyl hb (fe-no hb), (2) show that the no is evenly distributed among alpha and beta subunits, and (3) show that the hb undergoes a change in its quaternary state (t to r) upon oxygenation. |
2006-05-08 |
2023-08-12 |
Not clear |
| Sammy Wambua, Jedidah Mwacharo, Sophie Uyoga, Alexander Macharia, Thomas N William. Co-inheritance of alpha+-thalassaemia and sickle trait results in specific effects on haematological parameters. British journal of haematology. vol 133. issue 2. 2006-05-03. PMID:16611313. |
overall, the difference in hb concentrations between non-thalassaemics (alphaalpha/alphaalpha) and alpha(+)-thalassaemia homozygotes (-alpha/-alpha) was greater in non-hbas (hbaa) (0.63 g/dl) than in hbas children (0.25 g/dl). |
2006-05-03 |
2023-08-12 |
Not clear |
| Fuyu Guan, Cornelius Uboh, Lawrence Soma, Yi Luo, Bernd Driesse. Unique tryptic peptides specific for bovine and human hemoglobin in the detection and confirmation of hemoglobin-based oxygen carriers. Analytical chemistry. vol 76. issue 17. 2006-05-02. PMID:15373451. |
the peptides specific for bovine hb and oxy are related to bovine hb alpha chain residues 69-90 and beta chain residues 40-58. |
2006-05-02 |
2023-08-12 |
human |
| Fuyu Guan, Cornelius Uboh, Lawrence Soma, Yi Luo, Bernd Driesse. Unique tryptic peptides specific for bovine and human hemoglobin in the detection and confirmation of hemoglobin-based oxygen carriers. Analytical chemistry. vol 76. issue 17. 2006-05-02. PMID:15373451. |
the peptides specific for human hb are related to human hb alpha chain residues 63-91 and beta chain residues 42-60 and 68-83. |
2006-05-02 |
2023-08-12 |
human |
| Fuyu Guan, Cornelius E Uboh, Lawrence R Soma, Yi Luo, Jonathan S Jahr, Bernd Driesse. Confirmation and quantification of hemoglobin-based oxygen carriers in equine and human plasma by hyphenated liquid chromatography tandem mass spectrometry. Analytical chemistry. vol 76. issue 17. 2006-05-02. PMID:15373452. |
oxy and hmp were detected, quantified, and confirmed using the y14 ion and b8 ion of the tryptic peptide from bovine hb alpha chain residues 69-90, and hml was quantified using the tryptic peptide from human hb alpha chain residues 63-91. |
2006-05-02 |
2023-08-12 |
human |
| Gunçag Dinçol, Serkan Güvenç, Dedrey Elam, Abdullah Kutlar, Ferdane Kutla. Hb J- Meerut [alpha 120 (H3) Ala ->Glu (alpha1)] in a Turkish male. International journal of medical sciences. vol 3. issue 1. 2006-04-26. PMID:16575421. |
hb j- meerut [alpha 120 (h3) ala ->glu (alpha1)] in a turkish male. |
2006-04-26 |
2023-08-12 |
Not clear |
| Reena Das, Gurjeewan Garewal, R V Shaji, Jasmina Ahluwalia, H K Bali, S Varm. Investigation of persistent hypochromic microcytosis unmasks hemoglobin Evanston [alpha 14 (A12) Try--> Arg] in a patient of cyclic thrombocytopenia preceding Takayasu's disease. Hematology (Amsterdam, Netherlands). vol 10. issue 5. 2006-03-23. PMID:16273737. |
to the best of our knowledge our patient is the first report of hb evanston from the indigenous population of india and highlights the need to look for point mutations in the alpha globin gene, which may interact with thalassemia or other hemoglobinopathies, in atypical cases. |
2006-03-23 |
2023-08-12 |
Not clear |
| Vip Viprakasit, Worrawut Chinchang, Pipat Chotimara. Hb Woodville, a rare alpha-globin variant, caused by codon 6 mutation of the alpha1 gene. European journal of haematology. vol 76. issue 1. 2006-03-01. PMID:16343275. |
subsequent analyses demonstrated that observed atypical 'hba2' was, in fact, a rare innocuous alpha-globin variant, called hb woodville [alpha 2 6(a4); asp --> tyr]. |
2006-03-01 |
2023-08-12 |
Not clear |
| Cornelis L Harteveld, Mark Vervloet, Sonja Zweegman, Peter van Delft, Nicole Akkermans, Sandra Arkestijn, Piero C Giordan. Hb Amsterdam [alpha32(B13)Met--Ile (alpha2)]: a new unstable variant associated with an alpha-thalassemia phenotype and a new African polymorphism. Hemoglobin. vol 29. issue 4. 2006-02-27. PMID:16370485. |
both hb amsterdam and the--alpha(-3.7) allele were found in association with a new polymorphism, ivs-i-39 (c-->t), previously observed in our laboratory in seven patients of african origin, on both the alpha1 and alpha2 genes. |
2006-02-27 |
2023-08-12 |
Not clear |
| Barry Eng, Robert Walsh, Lynda Walker, Margie Patterson, John S Way. Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H disease. Hemoglobin. vol 29. issue 4. 2006-02-27. PMID:16370493. |
a chinese patient with hb h (beta4) disease was found to be a compound heterozygote for a 2.4 kb alpha(+)-thalassemia (thal) deletion and the common southeast asian alpha0-thal deletion. |
2006-02-27 |
2023-08-12 |
Not clear |
| Eric Pujade-Lauraine, Alain J Richard, Claudine Sapède, Colin Haywar. Erythropoietic agents in anaemic patients with cancer: a retrospective observational survey of epoetin alpha, epoetin beta and darbepoetin alpha use in routine clinical practice. Oncology reports. vol 14. issue 4. 2006-02-03. PMID:16142369. |
the mean changes in maximum hb level during treatment were 2.8 g/dl (epoetin alpha), 3.3 g/dl (epoetin beta) and 2.1 g/dl (darbepoetin alpha) (p=0.02, epoetin beta versus darbepoetin alpha). |
2006-02-03 |
2023-08-12 |
Not clear |
| Eric Pujade-Lauraine, Alain J Richard, Claudine Sapède, Colin Haywar. Erythropoietic agents in anaemic patients with cancer: a retrospective observational survey of epoetin alpha, epoetin beta and darbepoetin alpha use in routine clinical practice. Oncology reports. vol 14. issue 4. 2006-02-03. PMID:16142369. |
the proportions of patients achieving > or =1 g/ dl hb increases were 85.7% (epoetin alpha), 87.5% (epoetin beta) and 79.1% (darbepoetin alpha). |
2006-02-03 |
2023-08-12 |
Not clear |
| Eric Pujade-Lauraine, Alain J Richard, Claudine Sapède, Colin Haywar. Erythropoietic agents in anaemic patients with cancer: a retrospective observational survey of epoetin alpha, epoetin beta and darbepoetin alpha use in routine clinical practice. Oncology reports. vol 14. issue 4. 2006-02-03. PMID:16142369. |
the proportions of patients achieving > or =2 g/dl hb increases were 66.7% (epoetin alpha), 77.5% (epoetin beta) and 58.1% (darbepoetin alpha). |
2006-02-03 |
2023-08-12 |
Not clear |