Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Records 1 - 29 (of 29 Records) |
| Query Trace: Blood Disorder[original query] |
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| Survival prediction in acute myeloid leukemia using gene expression profiling. BMC medical informatics and decision making 2022 Mar 22 (1): 57. Lai Binbin, Lai Yanli, Zhang Yanli, Zhou Miao, OuYang Guifa |
| Polymorphism analysis in the COLIA1 gene of patients with thalassemia major and intermedia. Haematologia 2002 32 (4): 475-82. Arisal O, Deviren A, Fenerci E Yosunkaya, Hacihanefioglu S, Ulutin T, Erkmen S, Buyru |
| [Prediction of acute GVHD after umbilical cord blood transplantation by HLA three-dimensional structure matching]. Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2004 Jun 12 (3): 282-6. Xu Ri, Yan Wen-Ying, Jiang Xi-Feng, Xie Song-Mei, Zhu Na, Kong Fan-Hua, Pei Xue-T |
| Screening of concurrent alpha-thalassaemia 1 in beta-thalassaemia carriers. The Medical journal of Malaysia 2006 Jun 61 (2): 217-20. Chong Y M, Tan J A M A, Zubaidah Z, Rahimah A, Kuldip K, George |
| DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
| TGF-Beta codon 25 polymorphism and the risk of graft-versus-host disease after allogenic hematopoietic stem cell transplantation. Iranian journal of allergy, asthma, and immunology 2010 Mar 9 (1): 1-6. Rashidi-Nezhad Ali, Azimi Cyrus, Alimoghaddam Kamran, Ghavamzadeh Ardeshir, Hossein-Nezhad Arash, Izadi Pantea, Sobhani Maryam, Noori-Daloii Ali-Reza, Noori-Daloii Mohammad-Re |
| An SP1-binding site polymorphism in the COLIAI gene and osteoporosis in Egyptian patients with thalassemia major. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 Mar 22 (2): 81-5. Hamed Hanan M, Galal Ashraf, Ghamrawy Mona E L, Abd El Azeem Khaled, Hussein Ibtessam Ramzi, Abd-Elgawad Mona Fay |
| Association between clinical expression and molecular heterogeneity in ß-thalassemia Tunisian patients. Molecular biology reports 2013 Nov 40 (11): 6205-12. Jouini L, Sahli C A, Laaouini N, Ouali F, Ben Youssef I, Dakhlaoui B, Othmeni R, Ouennich F, Hadj Fredj S, Siala H, Becher M, Toumi N E, Fattoum S, Hafsia R, Bibi A, Messaoud |
| Specific and straightforward molecular investigation of ß-thalassemia mutations in the Malaysian Malays and Chinese using direct TaqMan genotyping assays. Genetics and molecular research : GMR 2013 12 (3): 2409-15. Kho S L, Chua K H, George E, Tan J A M |
| Molecular Scanning of ß-Thalassemia in the Southern Region of Central Java, Indonesia; a Step Towards a Local Prevention Program. Hemoglobin 2015 Oct 39 (5): 330-3. Rujito Lantip, Basalamah Muhammad, Mulatsih Sri, Sofro Abdul Salam |
| The Spectrum of a-Thalassemia Mutations in Kermanshah Province, West Iran. Hemoglobin 2015 Aug 1-4. Alibakhshi Reza, Mehrabi Masomeh, Omidniakan Leila, Shafieenia Saman |
| Novel ?eta (ß)-Thalassemia Mutation in Turkish Children. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2015 Jun 31 (2): 218-22. Ulasli Mustafa, Oztuzcu Serdar, Kirkbes Sevil, Bay Ali, Igci Yusuf Ziya, Bayraktar Recep, Igci Mehri, Ergun Sercan, Cakmak Ecir Ali, Aytekin Elif, Arslan Ahm |
| Leukemia-associated somatic mutations drive distinct patterns of age-related clonal hemopoiesis. Cell reports 2015 Mar 10 (8): 1239-45. McKerrell Thomas, Park Naomi, Moreno Thaidy, Grove Carolyn S, Ponstingl Hannes, Stephens Jonathan, , Crawley Charles, Craig Jenny, Scott Mike A, Hodkinson Clare, Baxter Joanna, Rad Roland, Forsyth Duncan R, Quail Michael A, Zeggini Eleftheria, Ouwehand Willem, Varela Ignacio, Vassiliou George |
| Sickle cell anemia - Nitric oxide related genetic modifiers of hematological and biochemical parameters. Clinical hemorheology and microcirculation 2016 Oct . Aguiar Laura, Matos Andreia, Gil Ângela, Afonso Conceiçã, Braga Lígia, João Lavinha, Kjollerstrom Paula, Faustino Paula, Bicho Manuel, Inácio Ânge |
| Cross-Sectional Study for the Detection of Mutations in the Beta-Globin Gene Among Patients with Hemoglobinopathies in the Bengali Population. Genetic testing and molecular biomarkers 2016 Nov . Panja Amrita, Chowdhury Prosanto, Chakraborty Sharmistha, Ghosh Tapan Kumar, Basu Anup |
| Serum Soluble Transferrin Receptor Concentrations Are Elevated in Congolese Children with Glucose-6-Phosphate Dehydrogenase Variants, but Not Sickle Cell Variants or ?-Thalassemia. The Journal of nutrition 2017 8 147 (9): 1785-1794. Barker Mikaela K, Henderson Amanda M, Naguib Karimah, Vercauteren Suzanne M, Devlin Angela M, Albert Arianne Y, Bahizire Esto, Tugirimana Pierrot L, Akilimali Pierre Z, Boy Erick, Green Tim J, Karakochuk Crystal |
| Ocular manifestations of sickle cell disease and genetic susceptibility for refractive errors. Taiwan journal of ophthalmology 0 7 (2): 89-93. Shukla Palak, Verma Henu, Patel Santosh, Patra P K, Bhaskar L V K |
| Epidemiological, clinical and genetic characterization of aplastic anemia patients in Pakistan. Annals of hematology 2019 Feb 98 (2): 301-312. Akram Zaineb, Ahmed Parvez, Kajigaya Sachiko, Satti Tariq Mahmood, Satti Humayoon Shafique, Chaudhary Qamar Un Nisa, Gutierrez-Rodrigues Fernanda, Ibanez Pilar F, Feng Xingmin, Mahmood Syed Kamran, Ghafoor Tariq, Shahbaz Nighat, Khan Mehreen Ali, Sultan Anee |
| The Spectrum of ß-Thalassemia Mutations in Siirt Province, Southeastern Turkey. Hemoglobin 2019 Aug 1-8. Yilmaz Sed |
A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A With Implications for Glycemic Status in U.S. Hispanics/Latinos.
Diabetes care 2019 Jun . Moon Jee-Young, Louie Tin L, Jain Deepti, Sofer Tamar, Schurmann Claudia, Below Jennifer E, Lai Chao-Qiang, Aviles-Santa M Larissa, Talavera Gregory A, Smith Caren E, Petty Lauren E, Bottinger Erwin P, Chen Yii-Der Ida, Taylor Kent D, Daviglus Martha L, Cai Jianwen, Wang Tao, Tucker Katherine L, Ordovás José M, Hanis Craig L, Loos Ruth J F, Schneiderman Neil, Rotter Jerome I, Kaplan Robert C, Qi Qib |
| Single tube allele specific PCR: a low cost technique for molecular screening of sickle cell anaemia in Nigeria. African health sciences 2019 2 18 (4): 995-1002. Toye Emuejevoke T, van Marle Guido, Hutchins Wendy, Abgabiaje Olayinka, Okpuzor J |
| Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
| MTHFR C677T, Prothrombin G20210A, and Factor V Leiden (G1691A) Polymorphism and Beta-Thalassemia Risk: A Meta-Analysis. Cureus 2020 11 12 (9): e10743. Nigam Nitu, Singh Prithvi K, Agrawal Monica, Nigam Sanjay, Gupta Harish, Saxena Shailend |
| Genotypic Diversity among Angolan Children with Sickle Cell Anemia. International journal of environmental research and public health 2021 6 18 (10): . Delgadinho Mariana, Ginete Catarina, Santos Brígida, Miranda Armandina, Brito Migu |
| Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and ?-Major Regulatory Element Haplotype Analysis in Iran. Hemoglobin 2021 3 45 (1): 37-40. Alimohammadi-Bidhendi Sara, Azadmehr Sarah, Razipour Masoumeh, Zeinali Sirous, Eslami Maryam, Davoudi-Dehaghani Elh |
| Internalizing Symptoms in Adolescents With Sickle Cell Disease. Journal of pediatric psychology 2022 8 48 (1): 91-103. Heitzer Andrew M, Longoria Jennifer, Porter Jerlym S, MacArthur Erin, Potter Brian, Ding Juan, Gossett Jeffrey, Kang Guolian, Hankins Jane |
| Evaluation of the Association of Transferrin Receptor Type 2 Gene Mutation (Y250X) with Iron Overload in Major ?- Thalassemia. Archives of Razi Institute 2022 3 76 (5): 1551-1554. Abdulmalek Jaafar J, Al-Rashedi N A |
| Role of NKG2D Ligands and Receptor in Haploidentical Related Donor Hematopoietic Cell Transplantation. Blood advances 2023 2 . Petersdorf Effie W, McKallor Caroline, Malkki Mari, He Meilun, Spellman Stephen, Hsu Katharine C, Strong Roland, Gooley Theodore A, Stevenson Phil |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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