All Relations between hb and alpha

Publication Sentence Publish Date Extraction Date Species
M Lipshitz, J Visser, R Anderson, D G Nel, T Smit, H C Steel, B L Rapopor. Relationships of emerging biomarkers of cancer cachexia with quality of life, appetite, and cachexia. Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer. vol 32. issue 6. 2024-05-14. PMID:38744744. quality of life (qol), appetite, cachexia, and biomarkers [albumin, hemoglobin (hb), neutrophils, lymphocytes, platelets, c-reactive protein (crp), tumor necrosis factor alpha (tnfα), interleukin 6 (il-6), interleukin 8 (il-8), c-x-c motif chemokine ligand 5 (cxcl5) and citrullinated histoneh3 (h3cit)] were compared for 40 cases with advanced cancer and 40 healthy controls. 2024-05-14 2024-05-27 Not clear
S Anuwutnavin, K Russameecharoen, P Ruangvutilert, S Viboonchard, C Yaiyiam, M Sklansky, G R DeVor. Evaluation of cardiac findings using speckle tracking in fetuses with hemoglobin Bart's disease. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 2024-05-06. PMID:38706423. hemoglobin (hb) bart's disease is a severe manifestation of alpha thalassemia, resulting in fetal tissue hypoxia and severe anemia. 2024-05-06 2024-05-08 Not clear
Mat Jusoh Siti Asmaa, Lee Miin Phoon, Nur Atikah Zakaria, Suryati Hussin, Rosnah Bahar, Mohd Nazri Hassan, Zefarina Zulkafli, Salfarina Iberahim, Marne Abdullah, Noor Haslina Mohd Noor, Shafini Mohamed Yusoff, Marini Raml. Hematological Profile of Hb Adana Among High School Students in Northeast Peninsular Malaysia. Cureus. vol 16. issue 3. 2024-05-02. PMID:38694420. background hb adana is a non-deletional alpha (α)-thalassaemia variant resulting from mutations in α1- or α2-globin codon 59 (α 2024-05-02 2024-05-04 Not clear
Nada Assaf, Roba El Zibaoui, Carla Monsef, Tania Abi Nassif, Miguel Abboud, Soha Yazbe. Severe Transfusion-Dependent Thalassemia in Compound Heterozygote Palestinian Siblings with Two α-Globin Gene Defects, Hb Taybe D Hemoglobin. 2024-04-16. PMID:38626925. severe transfusion-dependent thalassemia in compound heterozygote palestinian siblings with two α-globin gene defects, hb taybe d alpha and beta thalassemia are autosomal recessive anemias that cause significant morbidity and mortality worldwide, especially in the middle east and north africa (mena) region where carrier rates reach up to 50%. 2024-04-16 2024-04-19 Not clear
Bruno Fattizzo, Giacinto Luca Pedone, Caterina Brambilla, Loredana Pettine, Anna Zaninoni, Francesco Passamonti, Wilma Barcellin. Recombinant erythropoietin in autoimmune hemolytic anemia with inadequate bone marrow response: a prospective analysis. Blood advances. vol 8. issue 5. 2024-03-12. PMID:38029356. epoetin alpha 40 000 international units per week were administered subcutaneously until hemoglobin (hb) >11 g/dl and then tapered off. 2024-03-12 2024-03-14 Not clear
Shengmei Zhou, Stephen F Sarabia, Dolores Estrine, Dejerianne Ostrow, Ryan J Schmidt, Mikako Warren, Gordana Raca, Nick Shillingford, Larry Wang, Bruce Pawel, James E Stein, Jaclyn A Biegel, Dolores Lopez-Terrada, Leo Mascarenhas, Jianling J. Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. vol 37. issue 2. 2023-12-10. PMID:37992967. we found that patients with hcn-nos were older (p < .001) and more frequently classified as high risk (p < .01), yet they showed no significant differences in alpha fetoprotein levels or survival outcomes compared with those with hb. 2023-12-10 2023-12-17 Not clear
Shengmei Zhou, Stephen F Sarabia, Dolores Estrine, Dejerianne Ostrow, Ryan J Schmidt, Mikako Warren, Gordana Raca, Nick Shillingford, Larry Wang, Bruce Pawel, James E Stein, Jaclyn A Biegel, Dolores Lopez-Terrada, Leo Mascarenhas, Jianling J. Comparative Clinicopathologic and Genomic Analysis of Hepatocellular Neoplasm, Not Otherwise Specified, and Hepatoblastoma. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. vol 37. issue 2. 2023-12-10. PMID:37992967. however, patients with hcn-nos exhibit comparable alpha fetoprotein levels at diagnosis, ctnnb1 mutation rates, and survival outcomes when subjected to aggressive treatment, as compared with those with hb. 2023-12-10 2023-12-17 Not clear
Thinzar Aung, Bo Ram Kim, Han Sub Kwak, Mi Jeong Ki. Neuroimaging Approach: Effects of Hot and Cold Germinated Wheat Beverages on Electroencephalographic (EEG) Activity of the Human Brain. Foods (Basel, Switzerland). vol 12. issue 18. 2023-09-28. PMID:37761203. significant increases in delta and theta waves were observed as a result of drinking hb, but significant decreases in alpha and beta waves were observed after drinking cb. 2023-09-28 2023-10-07 human
Michael D Diamantidis, Stefania Pitsava, Omar Zayed, Ioanna Argyrakouli, Konstantinos Karapiperis, Christos Chatzoulis, Evangelos Alexiou, Achilles Manafas, Evangelos Tsangalas, Konstantinos Karakoussi. Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review. Hematology reports. vol 15. issue 3. 2023-08-22. PMID:37606495. the clinical manifestations of a carrier of a single hb agrinio mutation (single heterozygosity) depend on the concomitant presence or absence of other mutations or variants in the beta, alpha or other modifying genes. 2023-08-22 2023-09-07 Not clear
Michael D Diamantidis, Stefania Pitsava, Omar Zayed, Ioanna Argyrakouli, Konstantinos Karapiperis, Christos Chatzoulis, Evangelos Alexiou, Achilles Manafas, Evangelos Tsangalas, Konstantinos Karakoussi. Concomitant Presence of Hb Agrinio and - -Med Deletion in a Greek Male Patient with Hemoglobinopathy H: More Severe Phenotype and Literature Review. Hematology reports. vol 15. issue 3. 2023-08-22. PMID:37606495. we present a greek patient harboring a hb agrinio variant plus the - -med alpha deletional allele, having an infrequent severe form of alpha thalassemia, in contrast to the typical alpha thalassemic patient and requiring regular red blood cell (rbc) transfusions and chelation treatment. 2023-08-22 2023-09-07 Not clear
George Chan, Jenna Wong, Tina Tan, Nikhil Ghallyan, Peter Browet. False positive Hb Bart's immunochromatographic strip test for alpha thalassaemia in delta-beta thalassaemia carriers. International journal of laboratory hematology. 2023-06-15. PMID:37317650. false positive hb bart's immunochromatographic strip test for alpha thalassaemia in delta-beta thalassaemia carriers. 2023-06-15 2023-08-14 Not clear
Elio Haroun, Dibyendu Dutta, Seah H Li. Effects of GBT1118, a voxelotor analog, on intestinal pathophysiology in sickle cell disease. British journal of haematology. 2023-04-13. PMID:37052197. voxelotor is an allosteric haemoglobin (hb) modulator that binds covalently and reversibly to hb alpha chain to facilitate improved hb-o 2023-04-13 2023-08-14 Not clear
Sadaf Khan, Aabgeena Naee. Bovine serum albumin prevents human hemoglobin aggregation and retains its chaperone-like activity. Journal of biomolecular structure & dynamics. 2023-03-28. PMID:36974939. the results showed that bsa has the potential to inhibit hb's dissociation into alpha and beta subunits and protein aggregation by inhibiting secondary nucleation. 2023-03-28 2023-08-14 human
Thu Thi Minh Vo, Gianluca Amoroso, Tomer Ventura, Abigail Elizu. Histological and transcriptomic analysis of muscular atrophy associated with depleted flesh pigmentation in Atlantic salmon (Salmo salar) exposed to elevated seawater temperatures. Scientific reports. vol 13. issue 1. 2023-03-15. PMID:36918611. when comparing the back central region of the three phenotypes, actin alpha skeletal muscle and myosin genes were upregulated in the hn and hb fish, while tropomyosin genes were upregulated in the pale fish. 2023-03-15 2023-08-14 Not clear
Estefanía Rossetti, Silvia Eandi Eberle, Fernando Aguirre, Carolina Pepe, Lilian Díaz, Verónica Harris, Vanesa Ávalo. Hemoglobin Denver, a cause of desaturated pulse oximetry. A pediatric case report. Archivos argentinos de pediatria. 2023-03-01. PMID:36857142. mutations in the alpha or beta chains altering the hb tetramer may modify the molecule's oxygen-binding capacity. 2023-03-01 2023-08-14 Not clear
Anthony Pasquarella, Erin Miller, Edward C C Wong, Masamichi Ito, Marc J Braunstei. Hemoglobin Alpha Chain Variant Zara Associated With Familial Asymptomatic Hypoxemia. Journal of hematology. vol 11. issue 5. 2022-11-21. PMID:36406831. further sequencing of the alpha globin locus showed both individuals to be heterozygous for the hb zara c.274c>a (p.leu92ile) variant of unknown significance in the alpha2-globin gene. 2022-11-21 2023-08-14 Not clear
Husen Qiu, Jieyun Liu, Mohammad Reza Boorboori, Li De, Sheng Chen, Xun Ma, Peng Cheng, Haiyang Zhan. Effect of biochar application rate on changes in soil labile organic carbon fractions and the association between bacterial community assembly and carbon metabolism with time. The Science of the total environment. 2022-09-24. PMID:36152866. furthermore, lb and hb stabilized the bacterial alpha diversities with time. 2022-09-24 2023-08-14 Not clear
Mohammad Hamid, Bijan Keikhaei, Hamid Galehdari, Alihossein Saberi, Alireza Sedaghat, Gholamreza Shariati, Marziye Mohammadi-Anae. Alpha-globin gene triplication and its effect in beta-thalassemia carrier, sickle cell trait, and healthy individual. EJHaem. vol 2. issue 3. 2022-07-18. PMID:35844714. therefore, not every individual with triplicated alpha globin coinherited with beta-thalassemia trait will have a significantly lower hb than normal, and it is highly likely that none of them will need transfusion. 2022-07-18 2023-08-14 Not clear
Manisha Ramani Daruwalla, Amar Das Gupta, Ravikiran Pawa. Screening of Dry Blood Spots from Newborns by Two High Performance Liquid Chromatography (HPLC) Systems: A Comparison of Their Ability to Diagnose Both Sickle and Non-sickle Hemoglobinopathies. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. vol 37. issue 3. 2021-07-17. PMID:34267462. newborns with hbq india showed an additional hb peak in hplc resulting from combination of the abnormal alpha globin chain of hbq india with the normal gamma chain of hbf-'hbf q india'. 2021-07-17 2023-08-13 Not clear
Hanna Perez-Chrzanowska, Ana Cruz Pardos, Maria Dolores Burgueño Gonzalez, Enrique Gomez Barren. Preoperative Correction of Anemia to Allow a 3000 ml Blood Loss Without Transfusion in a Jehovah's Witness Presenting for Explantation of an Infected Hip Joint Prosthesis: A Case Report. A&A practice. vol 14. issue 6. 2021-06-29. PMID:32784312. a 70-year-old jehovah's witness was treated with iron carboxymaltose intravenously, recombinant human erythropoietin alpha subcutaneously, and vitamin b12 and folate orally for 9 weeks to raise hemoglobin (hb) from 10.8 to 17.0 g/dl before explantation of an infected hip joint prosthesis. 2021-06-29 2023-08-13 human