| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| 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 |
| Wenhui Gao, Ke Gao, Zonghao Guo, Yuan Liu, Li Jiang, Cheng Liu, Xiaoyu Liu, Guangli Wan. Different Responses of Soil Bacterial and Fungal Communities to 3 Years of Biochar Amendment in an Alkaline Soybean Soil. Frontiers in microbiology. vol 12. 2021-06-15. PMID:34122356. |
lb treatment significantly increased the fungal alpha diversity, while there was no significant change under hb. |
2021-06-15 |
2023-08-13 |
Not clear |
| Carlo Cafiero, Gianrico Spagnuolo, Gaetano Marenzi, Ranieri Martuscelli, Michele Colamaio, Stefania Leuc. Predictive Periodontitis: The Most Promising Salivary Biomarkers for Early Diagnosis of Periodontitis. Journal of clinical medicine. vol 10. issue 7. 2021-05-02. PMID:33916672. |
recent paper reviews and meta-analyses have focused on five promising host derived biomarkers as candidate for early diagnosis of periodontitis: mmp-8 (metalloproteinase-8), mip-1α (macrophage inflammatory protein-1 alpha), il-1 β (interleukin-1 beta), il-6 (interleukin-6), and hb (hemoglobin), and their combinations. |
2021-05-02 |
2023-08-13 |
Not clear |
| Lucky Poh Wah Goh, Eric Tzyy Jiann Chong, Ping-Chin Le. Prevalence of Alpha(α)-Thalassemia in Southeast Asia (2010-2020): A Meta-Analysis Involving 83,674 Subjects. International journal of environmental research and public health. vol 17. issue 20. 2021-01-14. PMID:33050119. |
alpha(α)-thalassemia is a blood disorder caused by many types of inheritable α-globin gene mutations which causes no-to-severe clinical symptoms, such as hb bart's hydrops fetalis that leads to early foetal death. |
2021-01-14 |
2023-08-13 |
human |
| Amit S Mutha, Kalpana U Shah, Aarti A Kinikar, Balasaheb B Ghongan. Efficacy and Safety of Wheat Grass in Thalassemic Children on Regular Blood Transfusion. Cureus. vol 10. issue 3. 2020-10-01. PMID:29755902. |
in thalassemia, mutations either in alpha or beta chain synthesis results in low hemoglobin (hb). |
2020-10-01 |
2023-08-13 |
Not clear |
| Omnia Ahmed Mohamed Abdel El-Gaphar, Amira Mourad Abo-Youssef, Ali Ahmed Abo-Sai. Effect of Losartan in Complete Freund's Adjuvant -Induced Arthritis in Rats. Iranian journal of pharmaceutical research : IJPR. vol 17. issue 4. 2020-09-29. PMID:30568700. |
our results revealed that losartan significantly reduced serum levels of tumor necrosis factor alpha (tnfα), interleukin-6 (il-6) , rheumatoid factor (rf), and erythrocytes sedimentation rate (esr).it significantly decreased serum malondialdehyde and increased blood glutathione .losartan exhibited significant decrease in serum level of total cholesterol (tc), triglycerides (tg) and low density lipoprotein (ldl) coupled with marked increase in high density lipoprotein (hdl).furthermore, losartan decreased white blood cell cells (wbc's) count and increased red blood cells (rbc's) , hemoglobin (hb) , platelets, and hematocrit (hct) counts. |
2020-09-29 |
2023-08-13 |
rat |
| Ganesh Kasinatha. Prolonged Pyrexia: Kikuchi-Fujimoto Disease in a Patient With Hb H-Constant Spring Thalassemia. Clinical medicine insights. Case reports. vol 13. 2020-09-28. PMID:32636691. |
haemoglobin h (hb h) disease is an alpha thalassemia characterised by either 3 alpha-globin gene deletions (deletional type) or 2 alpha-globin gene deletions with 1-point mutation (nondeletional type). |
2020-09-28 |
2023-08-13 |
Not clear |
| Nur Suraya Che Yaacob, Md Asiful Islam, Heba Alsaleh, Ibrahim Khidir Ibrahim, Rosline Hassa. Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia. International journal of hematology. vol 111. issue 3. 2020-09-01. PMID:31894534. |
among the different variants of hb, hba1 is the most common and is composed of two alpha (αhb) and two beta globin chains (βhb) constructing a heterotetrameric protein complex (α |
2020-09-01 |
2023-08-13 |
human |
| Hailong Huang, Meihuan Chen, Xuemei Chen, Yan Wang, Na Lin, Deqin He, Ying Li, Yuan Lin, Liangpu X. A rare α-thalassemia deletion, -α International journal of clinical and experimental pathology. vol 11. issue 8. 2020-01-21. PMID:31949790. |
a rare α-thalassemia deletion, -α alpha (α)-thalassemia (thal) is a common single-gene genetic disease in southern china, which may cause hb bart's hydrops fetalis and hb h disease. |
2020-01-21 |
2023-08-13 |
Not clear |
| Xie Yingjun, Xie Yuhuan, Chen Yuchang, Li Dongzhi, Wang Ding, Song Bing, Yang Yi, Lu Dian, Xue Yanting, Xiong Zeyu, Liu Nengqing, Chen Diyu, Sun Xiaofan. CRISPR/Cas9 gene correction of HbH-CS thalassemia-induced pluripotent stem cells. Annals of hematology. vol 98. issue 12. 2019-12-17. PMID:31495903. |
haemoglobin (hb) h-constant spring (cs) alpha thalassaemia (- -/-α |
2019-12-17 |
2023-08-13 |
Not clear |
| H. V. Rasika Dias, Wiechang Jin, Hyoung-Juhn Kim, Hui-Ling L. Polyfluorinated Tris(pyrazolyl)borates. Syntheses and Spectroscopic and Structural Characterization of Group 1 and Group 11 Metal Complexes of [HB(3,5-(CF(3))(2)Pz)(3)](-) and [HB(3-(CF(3))Pz)(3)](-). Inorganic chemistry. vol 35. issue 8. 2019-11-20. PMID:11666431. |
crystal data with mo kalpha (lambda = 0.710 73 Å) at 193 k: [hb(3,5-(cf(3))(2)pz)(3)]na(h(2)o), c(15)h(6)bf(18)n(6)nao, a = 7.992(2) Å, b = 15.049(2) Å, c = 9.934(2) Å, beta = 101.16(2) degrees, monoclinic, p2(1)/m, z = 2; [{hb(3-(cf(3))pz)(3)}na(thf)](2), c(32)h(30)b(2)f(18)n(12)na(2)o(2), a = 9.063(3) Å, b = 10.183(2) Å, c = 12.129(2) Å, alpha = 94.61(1) degrees, beta = 101.16(2) degrees, gamma = 95.66(2) degrees, triclinic, &pmacr;1, z = 1; [hb(3,5-(cf(3))(2)pz)(3)]cu(dmac), c(19)h(13)bcuf(18)n(7)o, a = 15.124(4) Å, b = 8.833(2) Å, c = 21.637(6) Å, beta = 105.291(14) degrees, monoclinic, p2(1)/n, z = 4; [hb(3,5-(cf(3))(2)pz)(3)]cupph(3), c(33)h(19)bcuf(18)n(6)p, a = 9.1671(8) Å, b = 14.908(2) Å, c = 26.764(3) Å, beta = 94.891(1) degrees, monoclinic, p2(1)/c, z = 4; [hb(3,5-(cf(3))(2)pz)(3)]agpph(3).0.5c(6)h(14), c(36)h(26)agbf(18)n(6)p, a = 13.929(2) Å, b = 16.498(2) Å, c = 18.752(2) Å, beta = 111.439(6) degrees, monoclinic, p2(1)/c, z = 4; [et(4)n][hb(3,5-(cf(3))(2)pz)(3)], c(23)h(24)bf(18)n(7), a = 10.155(2) Å, b = 18.580(4) Å, c = 16.875(5) Å, beta = 99.01(2) degrees, monoclinic, p2(1)/n, z = 4. |
2019-11-20 |
2023-08-12 |
Not clear |
| Ferida S. McQuillan, Hongli Chen, Thomas A. Hamor, Christopher J. Jones, Keith Paxto. Hydrogen Bonding of CHCl(3) to Coordinated Nitric Oxide in a Binuclear Metallomacrocycle and the Crystal Structures of anti-[Mo(NO){HB(3,5-Me(2)C(3)HN(2))(3)}(2,7-O(2)C(10)H(6))](2).2CHCl(3).CH(2)Cl(2), syn-[Mo(NO){HB(3,5-Me(2)C(3)HN(2))(3)}(2,7-O(2)C(10)H(6))](2).0.67CHCl(3).2.7H(2)O, and syn-[Mo(NO){HB(3,5-Me(2)C(3)HN(2))(3)}(2,7-O(2)C(10)H(6))](2).3(CH(3))(2)CO. Inorganic chemistry. vol 36. issue 20. 2019-11-20. PMID:11670108. |
the molecular structures of anti-[mo(no){hb(3,5-me(2)c(3)hn(2))(3)}(2,7-o(2)c(10)h(6))](2).2chcl(3).ch(2)cl(2) (1)(,) syn-[mo(no){hb(3,5-me(2)c(3)hn(2))(3)}(2,7-o(2)c(10)h(6))](2).0.67chcl(3).2.7h(2)o (2) and syn-[mo(no){hb(3,5-me(2)c(3)hn(2))(3)}(2,7-o(2)c(10)h(6))](2).3(ch(3))(2)co (3) have been determined crystallographically: (1) c(50)h(56)b(2)n(14)o(6)mo(2).2chcl(3).ch(2)cl(2), triclinic, space group p&onemacr;, a = 11.535(2) Å, b = 14.032(3) Å, c = 11.247(3) Å, alpha = 94.70(1) degrees, beta = 102.30(2) degrees, gamma = 110.31(2) degrees, z = 1; (2) c(50)h(56)b(2)n(14)o(6)mo(2).0.67chcl(3).2.7h(2)o, monoclinic space group p2(1)/m, a = 23.770(7) Å, b = 26.600(10) Å, c = 11.334(4) Å, beta = 99.86(2) degrees, z = 4; (3) c(50)h(56)b(2)n(14)o(6)mo(2).3c(3)h(6)o, triclinic, space group p&onemacr;, a = 16.929(3) Å, b = 17.465(4) Å, c = 12.739(2) Å, alpha = 100.06(1) degrees, beta = 94.93(2) degrees, gamma = 114.13(1) degrees, z = 2. |
2019-11-20 |
2023-08-12 |
Not clear |
| Osamu Saitoh, Kazunori Sugi, Keishi Lojima, Hisashi Matsumoto, Ken Nakagawa, Masanobu Kayazawa, Seigou Tanaka, Tsutomu Teranishi, Ichiro Hirata, Ken-ichi Katsu K. Increased prevalence of intestinal inflammation in patients with liver cirrhosis. World journal of gastroenterology. vol 5. issue 5. 2019-11-20. PMID:11819475. |
aim:to investigate the pathophysiology of the digestive tract in patients with liver cirrhosis.methods:in 42 cirrhotic patients and 20 control subjects, the following fecal proteins were measured by enzyme-linked immunosorbent assay: albumin (alb), transferrin (tf), and alpha(1)antitrypsin (alpha(1)-at) as a marker for intestinal protein loss, hemoglobin (hb) for bleeding, pmn-elastase for intestinal inflammation, and secretory iga for intestinal immunity.results:the fecal concentrations of hb, alb, tf,alpha(1)-at, and pmn-elastase were increased in 13 (31%), 8(19%), 10(24%), 6(14%), and 11 (26%) cases among 42 patients, respectively. |
2019-11-20 |
2023-08-12 |
human |
| Fatemeh Kazemi, Adeleh Divsalar, Ali Akbar Saboury, Arefeh Seyedarab. Propolis nanoparticles prevent structural changes in human hemoglobin during glycation and fructation. Colloids and surfaces. B, Biointerfaces. vol 177. 2019-09-09. PMID:30738325. |
cd results revealed that pnp caused an increase in hb beta-sheet content while decreasing the alpha helical content. |
2019-09-09 |
2023-08-13 |
human |
| J A Ruiz-Roca, R E Oñate-Sánchez, I Urrutia-Rodríguez, A Martínez-Izquierdo, D Mengual-Pujante, F J Rodríguez-Lozan. Clinical management of the homozygous α-thalassemia with unusual mandibular manifestation of hematopoiesis. Journal of stomatology, oral and maxillofacial surgery. vol 118. issue 1. 2019-08-26. PMID:28330575. |
alpha (α)-thalassemias are the most common genetic disorder of hemoglobin (hb) synthesis, affecting up to 5% of the world's population. |
2019-08-26 |
2023-08-13 |
Not clear |
| Kainaz Sidhwa, Manisha Ramani Daruwalla, Ravikiran Pawar, Anita Nadkarni, Priya Hariharan, Pallavi Mehta, Amar Das Gupt. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband. Indian journal of pathology & microbiology. vol 62. issue 2. 2019-08-02. PMID:30971568. |
diagnostic challenges posed by a rare alpha globin chain variant hb fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband. |
2019-08-02 |
2023-08-13 |
Not clear |
| Kainaz Sidhwa, Manisha Ramani Daruwalla, Ravikiran Pawar, Anita Nadkarni, Priya Hariharan, Pallavi Mehta, Amar Das Gupt. Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband. Indian journal of pathology & microbiology. vol 62. issue 2. 2019-08-02. PMID:30971568. |
hemoglobin (hb) fontainebleau is a rare alpha globin chain variant [alpha 21(b2) ala→pro], of which only three families have been reported from india in the past. |
2019-08-02 |
2023-08-13 |
Not clear |
| Xi Li, Chao Yuan, Licong Xing, Philippe Humber. Topographical diversity of common skin microflora and its association with skin environment type: An observational study in Chinese women. Scientific reports. vol 7. issue 1. 2019-07-17. PMID:29273721. |
bacterial alpha diversity was higher in exposed (hb, is, and gl) compared with unexposed sites (ba, af and vf). |
2019-07-17 |
2023-08-13 |
Not clear |