| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Berndt Zur, Michael Ludwig, Birgit Stoffel-Wagne. Hemoglobin Hasharon and hemoglobin NYU in subjects of German origin. Biochemia medica. vol 21. issue 3. 2012-04-09. PMID:22420247. |
we coincidentally detected two cases of hb hasharon, an alpha globin gene mutation, in two heterozygous patients and one case of hb nyu, a delta globin gene mutation, in another patient. |
2012-04-09 |
2023-08-12 |
human |
| Jesús M Planesas, Rosa M Claramunt, Jordi Teixidó, José I Borrell, Violeta I Pérez-Nuen. Improving VEGFR-2 docking-based screening by pharmacophore postfiltering and similarity search postprocessing. Journal of chemical information and modeling. vol 51. issue 4. 2011-09-30. PMID:21417262. |
the resulting docking poses calculated using the alpha hb scoring function implemented in moe are postfiltered according to defined pharmacophore interactions (structure based). |
2011-09-30 |
2023-08-12 |
Not clear |
| Fuanglada Tongprasert, Chanane Wanapirak, Theera Tongson. Maternal serum hCG, PAPP-A and AFP as predictors of hemoglobin Bart disease at mid-pregnancy. Prenatal diagnosis. vol 31. issue 5. 2011-09-22. PMID:21312197. |
to evaluate the ability of maternal serum-free β-human chorionic gonadotrophin (β-hcg), pregnancy-associated plasma protein-a (papp-a), and alpha fetoprotein (afp) levels in the screening of fetuses with hemoglobin (hb) bart's disease among pregnancies at risk. |
2011-09-22 |
2023-08-12 |
Not clear |
| Snehal O Kulkarni, Pradnya P Kanekar, Jyoti P Jog, Prashant A Patil, Smita S Nilegaonkar, Seema S Sarnaik, Pranav R Kshirsaga. Characterisation of copolymer, poly (hydroxybutyrate-co-hydroxyvalerate) (PHB-co-PHV) produced by Halomonas campisalis (MCM B-1027), its biodegradability and potential application. Bioresource technology. vol 102. issue 11. 2011-08-16. PMID:21481588. |
characterisation of polyhydroxyalkanoate (pha) film produced by haloalkalitolerant halomonas campisalis (mcm b-1027) in 14l ss fermenter revealed it to have composition of monomer units, hb:hv as 96:4 as analysed by (1)h nmr indicating the pha as a co-polymer of phb-co-phv, molecular weight by gel permeation chromatography as 2.08 × 10(6), melting temperature 166.51°c, tensile strength 18.8 mpa; two relaxations namely beta transition corresponding to the glass rubber transition and alpha transition corresponding to crystalline relaxation by dynamic mechanical thermal analysis and only one relaxation corresponding to mws interfacial polarisation with activation energy of 129 kj/mol by broadband dielectric spectroscopy. |
2011-08-16 |
2023-08-12 |
Not clear |
| Min Lin, Yue Huang, Li-Ye Yang, Qian Wang, Lei Zhen. Hb Stanleyville II [alpha 78(EF7) Asn→Lys] occurrence in combination with Hb Constant Spring. Blood cells, molecules & diseases. vol 46. issue 2. 2011-06-29. PMID:21093326. |
hb stanleyville ii [alpha 78(ef7) asn→lys] occurrence in combination with hb constant spring. |
2011-06-29 |
2023-08-12 |
Not clear |
| Martin Hergersberg, Saskia Brunner-Agten, Thomas Kühne, Michael Paulussen, Andreas R Hube. A new stable alpha chain variant: Hb Basel [alpha14(A12)Trp-->Leu (alpha1)]. Hemoglobin. vol 34. issue 3. 2011-02-09. PMID:20524822. |
a new stable alpha chain variant: hb basel [alpha14(a12)trp-->leu (alpha1)]. |
2011-02-09 |
2023-08-12 |
Not clear |
| F Xiong, M Sun, X Zhang, R Cai, Y Zhou, J Lou, L Zeng, Q Sun, Q Xiao, X Shang, X Wei, T Zhang, P Chen, X X. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China. Clinical genetics. vol 78. issue 2. 2010-12-07. PMID:20412082. |
the mutational spectrum among the local population for each type of disorder was described, including the first report on the true prevalence of three silent alpha thalassemia defects, -alpha(3.7)/(4.78%), -alpha(4.2)/(1.61%) and hb westmead (alpha(ws)alpha/) (1.57%) and of delta-thalassemia resulting from five novel and two rare mutations never before identified in chinese individuals. |
2010-12-07 |
2023-08-12 |
human |
| Marion Phylipsen, Ingrid P Vogelaar, Rianne A C Schaap, Sandra G J Arkesteijn, George L Boxma, Willem C H van Helden, Irene C M Wildschut, Andrea C de Bruin-Roest, Piero C Giordano, Cornelis L Hartevel. A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW)). Blood cells, molecules & diseases. vol 45. issue 2. 2010-12-07. PMID:20682466. |
because of a 25% risk of hb bart's with hydrops foetalis in the offspring when in combination with another alpha(0)-thalassemia allele, it is important to diagnose this deletion. |
2010-12-07 |
2023-08-12 |
human |
| Raymond M Esquerra, Ignacio López-Peña, Pooncharas Tipgunlakant, Ivan Birukou, Rosa L Nguyen, Jayashree Soman, John S Olson, David S Kliger, Robert A Goldbec. Kinetic spectroscopy of heme hydration and ligand binding in myoglobin and isolated hemoglobin chains: an optical window into heme pocket water dynamics. Physical chemistry chemical physics : PCCP. vol 12. issue 35. 2010-12-03. PMID:20668762. |
internal hydration is higher in the native alpha chains than in the beta chains, in agreement with previous crystallographic results for the subunits within hb tetramers. |
2010-12-03 |
2023-08-12 |
Not clear |
| E George, Tan Jama, A S Nor Azian, A Rahimah, Z Zubaida. A rare case of alpha-thalassaemia intermedia in a Malay patient double heterozygous for alpha(+)-thalassaemia and a mutation in alpha1 globin gene CD59 (GGC --> GAC). The Medical journal of Malaysia. vol 64. issue 4. 2010-11-09. PMID:20954559. |
a rare case of thalassaemia-intermedia involving a non-deletion alpha thalassemia point mutation in the alpha1-globin gene cd59 (ggc --> gac) and a deletion alpha+ (-alpha(3.7)) thalassaemia in which use of high performance liquid chromatography (hplc) c-gram hb subtype profile and dna molecular analysis helped establish the diagnosis. |
2010-11-09 |
2023-08-12 |
Not clear |
| Piero C Giordano, Marjon H Cnossen, Annemarie M S Joosten, Cees A M Jansen, Tineke E Hakvoort, Margreet Bakker-Verweij, Sandra G J Arkesteijn, Peter van Delft, John S Waye, Marelle J Bouva, Cornelis L Hartevel. Codon 24 (TAT>TAG) and codon 32 (ATG>AGG) (Hb Rotterdam): two novel alpha2 gene mutations associated with mild alpha-thalassemia found in the same family after newborn screening. Hemoglobin. vol 34. issue 4. 2010-10-29. PMID:20642333. |
shortly thereafter, hb rotterdam was again found in two unrelated adult females and in a canadian newborn, all of african origin, suggesting that hb rotterdam could be a frequently occurring alpha(t) determinant in the black population. |
2010-10-29 |
2023-08-12 |
Not clear |
| Philippe Joly, Anton Szymanowicz, Marie-Jeanne Neyron, Abdellah Zine, Henri Wajcman, Alain Francin. Hb Charlieu [alpha106(G13)Leu-->Pro (alpha1)]: a new phenotypically silent hemoglobin variant associated with a mild alpha-thalassemia phenotype. Hemoglobin. vol 34. issue 4. 2010-10-29. PMID:20642334. |
as the alpha/beta mrna ratios, determined by reverse-transcriptase real-time quantitative polymerase chain reaction (pcr), are not concordant with an alpha-thalassemia (alpha-thal) state, we hypothesize that the underlying physiopathologic mechanism is an assembling defect of the hb charlieu molecule, rather than an instability of the alpha(charlieu) mrna. |
2010-10-29 |
2023-08-12 |
Not clear |
| Vassiliki Kalotychou, Revekka Tzanetea, Kostas Konstantopoulos, Ioannis Papassotiriou, Ioannis Rombo. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature. Hemoglobin. vol 34. issue 4. 2010-10-29. PMID:20642336. |
this hemoglobin (hb) variant was found in combination with two thalassemia-type globin gene defects, namely beta(0)-thalassemia (beta(0)-thal), hbb:c.118c>t and alpha(0)-thal (- -(med)). |
2010-10-29 |
2023-08-12 |
Not clear |
| Stephen O Brennan, Sheila Ryken, Tim Cha. Hb Koya Dora [alpha142, Term-->Ser (TAA>TCA in alpha2)]: a rare mutation of the alpha2 gene stop codon associated with alpha-thalassemia. Hemoglobin. vol 34. issue 4. 2010-10-29. PMID:20642339. |
here we identify a homozygous case of hb koya dora and confirm the structure of the 31 residue alpha chain extension. |
2010-10-29 |
2023-08-12 |
Not clear |
| Shruti Trivedi, Naved I Malek, Kamalakanta Behera, Siddharth Pande. Temperature-dependent solvatochromic probe behavior within ionic liquids and (ionic liquid + water) mixtures. The journal of physical chemistry. B. vol 114. issue 24. 2010-09-14. PMID:20518546. |
changes in kamlet-taft parameters dipolarity/polarizability (pi*), hbd acidity (alpha), and hb accepting (hba) basicity (beta) with temperature show interesting trends. |
2010-09-14 |
2023-08-12 |
Not clear |
| Jochen S Hub, Marcus B Kubitzki, Bert L de Groo. Spontaneous quaternary and tertiary T-R transitions of human hemoglobin in molecular dynamics simulation. PLoS computational biology. vol 6. issue 5. 2010-08-26. PMID:20463873. |
we observe spontaneous and reproducible t-->r quaternary transitions of the hb tetramer and tertiary transitions of the alpha and beta subunits, as detected from principal component projections, from an rmsd measure, and from rigid body rotation analysis. |
2010-08-26 |
2023-08-12 |
human |
| Jochen S Hub, Marcus B Kubitzki, Bert L de Groo. Spontaneous quaternary and tertiary T-R transitions of human hemoglobin in molecular dynamics simulation. PLoS computational biology. vol 6. issue 5. 2010-08-26. PMID:20463873. |
in addition, the tertiary populations of the alpha and beta subunits differ substantially, with the beta subunits showing a tendency towards r, and the alpha subunits showing a tendency towards t. based on the simulation results, we present a transition pathway for coupled quaternary and tertiary transitions between the r and t conformations of hb. |
2010-08-26 |
2023-08-12 |
human |
| Yu Yang, Dong-Zhi L. Detection of uncommon deletions in alpha-thalassemia using the pcr-reverse dot-blot method for prenatal diagnosis of nondeletional hemoglobin H disease. Acta haematologica. vol 124. issue 1. 2010-08-17. PMID:20516677. |
nondeletional hemoglobin (hb) h disease is caused by a deletion of both alpha-globin genes on one chromosome 16 and of an alpha(+)-thalassemia point mutation on the other chromosome 16. |
2010-08-17 |
2023-08-12 |
Not clear |
| Weidong Zheng, Yanhui Liu, Dong Chen, Kabin Rong, Yanfen Ge, Caiping Gong, Heping Che. Complex interaction of Hb Q-Thailand and Hb E with alpha(0)-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family. Annals of hematology. vol 89. issue 9. 2010-08-16. PMID:20333523. |
complex interaction of hb q-thailand and hb e with alpha(0)-thalassemia and hereditary persistence of fetal hemoglobin in a chinese family. |
2010-08-16 |
2023-08-12 |
Not clear |
| Weidong Zheng, Yanhui Liu, Dong Chen, Kabin Rong, Yanfen Ge, Caiping Gong, Heping Che. Complex interaction of Hb Q-Thailand and Hb E with alpha(0)-thalassemia and hereditary persistence of fetal hemoglobin in a Chinese family. Annals of hematology. vol 89. issue 9. 2010-08-16. PMID:20333523. |
dna analysis demonstrated that the proband was a double heterozygote of hb q-thailand and hb e in combination with alpha(0)-thalassemia and southeast asian-type hereditary persistence of fetal hemoglobin (sea-hpfh). |
2010-08-16 |
2023-08-12 |
Not clear |