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Wyszukujesz frazę ""Anemia, Hypochromic"" wg kryterium: Temat


Tytuł:
The activation of iron deficiency responses of grapevine rootstocks is dependent to the availability of the nitrogen forms.
Autorzy:
Khalil S; University of Natural Resources and Life Sciences, Vienna, Department of Crop Sciences, Institute of Viticulture and Pomology, Tulln an der Donau, Austria. .
Strah R; National Institute of Biology, Department of Biotechnology and Systems Biology, Ljubljana,, Slovenia.; Jožef Stefan International Postgraduate School, Ljubljana, Slovenia.
Lodovici A; University of Udine, Department of Agricultural, Food, Environmental, and Animal Sciences, Udine, Italy.
Vojta P; University of Natural Resources and Life Sciences, Vienna, Department of Biotechnology, Institute of Computational Biology, Vienna, Austria.
Berardinis F; University of Natural Resources and Life Sciences, Vienna, Department of Crop Sciences, Institute of Viticulture and Pomology, Tulln an der Donau, Austria.
Ziegler J; Leibniz Institute of Plant Biochemistry, Department Molecular Signal Processing, Halle (Saale), Germany.
Pompe Novak M; National Institute of Biology, Department of Biotechnology and Systems Biology, Ljubljana,, Slovenia.; University of Nova Gorica, Faculty of Viticulture and Enology, Vipava, Slovenia.
Zanin L; University of Udine, Department of Agricultural, Food, Environmental, and Animal Sciences, Udine, Italy.
Tomasi N; University of Udine, Department of Agricultural, Food, Environmental, and Animal Sciences, Udine, Italy.
Forneck A; University of Natural Resources and Life Sciences, Vienna, Department of Crop Sciences, Institute of Viticulture and Pomology, Tulln an der Donau, Austria.
Griesser M; University of Natural Resources and Life Sciences, Vienna, Department of Crop Sciences, Institute of Viticulture and Pomology, Tulln an der Donau, Austria. .
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Źródło:
BMC plant biology [BMC Plant Biol] 2024 Mar 26; Vol. 24 (1), pp. 218. Date of Electronic Publication: 2024 Mar 26.
Typ publikacji:
Journal Article
MeSH Terms:
Iron Deficiencies*
Anemia, Hypochromic*/metabolism
Vitis*/genetics
Ammonium Compounds*/metabolism
Nitrogen/metabolism ; Nitrates/metabolism ; Plant Roots/metabolism
Czasopismo naukowe
Tytuł:
Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran.
Autorzy:
Mousavi SS; Novin Genetic Diagnostic Laboratory, Farah Abad Boulevard, Sari, Iran.
Karami H; Department of Pediatrics Hematology & Oncology, Thalassemia Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Tamadoni A; Non-Communicable Pediatric Diseases Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
Mahmoudi H; The Clinical Research Development Unit of Amirkola Children's Hospital, Babol University of Medical Sciences, Babol, Iran.
Shekarriz R; Department of Hematology and Oncology, Gastrointestinal Cancer Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Siami R; Ghaemshahr Health Center, Mazandaran University of Medical Sciences, Sari, Mazandaran, Iran.
Hashemi-Soteh MB; Immunogenetic Research Center, Molecular and Cell Biology Research Center, Biochemistry and Genetic Department, Medical Faculty, Mazandaran University of Medical Sciences, Sari, Iran.
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Źródło:
BioMed research international [Biomed Res Int] 2024 Jan 30; Vol. 2024, pp. 8664803. Date of Electronic Publication: 2024 Jan 30 (Print Publication: 2024).
Typ publikacji:
Journal Article
MeSH Terms:
beta-Thalassemia*/genetics
Anemia, Hypochromic*
Humans ; Iran ; Cadmium ; Mutation
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
A Turkish Patient with Aceruloplasminemia Found to Have a Novel Pathogenic Variant Presenting with High Ferritin Level and Microcytic Anemia
Autorzy:
Özkalaycı H; Bolu Abant İzzet Baysal Training and Research Hospital, Department of Medical Genetics, Bolu, Türkiye
Uluköylü Mengüç M; Bolu Abant İzzet Baysal Training and Research Hospital, Department of Hematology, Bolu, Türkiye
Güleray Lafcı N; Hacettepe University Faculty of Medicine, Department of Medical Genetics, Ankara, Türkiye
Öztürk Kaymak A; Düzen Laboratory, Department of Medical Genetics, Ankara, Türkiye
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Źródło:
Turkish journal of haematology : official journal of Turkish Society of Haematology [Turk J Haematol] 2023 Dec 05; Vol. 40 (4), pp. 288-290. Date of Electronic Publication: 2023 Sep 12.
Typ publikacji:
Journal Article
MeSH Terms:
Iron Metabolism Disorders*/diagnosis
Iron Metabolism Disorders*/genetics
Anemia, Hypochromic*
Humans ; Ceruloplasmin/genetics ; Ferritins
SCR Disease Name:
Familial apoceruloplasmin deficiency; Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Identification of double heterozygous -α using third-generation sequencing.
Autorzy:
Liang L; Center for Medical Genetics and Prenatal Diagnosis, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
Xiao Y; Department of clinical laboratory, The Second Nanning People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
Guo W; Yaneng Biotechnology Corporation, Shenzhen, People's Republic of China.
Xie T; Berry Genomics Corporation, Beijing, People's Republic of China.
Zheng L; Center for Medical Genetics and Prenatal Diagnosis, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
Li Y; Center for Medical Genetics and Prenatal Diagnosis, People's Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
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Źródło:
Hematology (Amsterdam, Netherlands) [Hematology] 2023 Dec; Vol. 28 (1), pp. 2250646.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Anemia, Hypochromic*/genetics
Humans ; Asian People ; Electrophoresis, Capillary ; Heterozygote ; Homozygote ; Sequence Analysis, DNA
Czasopismo naukowe
Tytuł:
Identification of a c-type heme oxygenase and its function during acclimation of cyanobacteria to nitrogen fluctuations.
Autorzy:
Ran Z; School of Ecological and Environmental Sciences, East China Normal University, 200241, Shanghai, China.; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Du Z; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Miao G; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Zheng M; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Luo L; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Pang X; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China.
Wei L; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China. .
Li D; School of Ecological and Environmental Sciences, East China Normal University, 200241, Shanghai, China. .; Key Laboratory of Urbanization and Ecological Restoration of Shanghai, 200241, Shanghai, China. .; Institute of Eco-Chongming (IEC), 20 Cuiniao Rd, Chenjia Zhen, Chongming, 202162, Shanghai, China. .; Technology Innovation Center for Land Spatial Eco-restoration in Metropolitan Area, Ministry of Natural Resources, 3663 N. Zhongshan Road, 200062, Shanghai, China. .
Ma W; College of Life Sciences, Shanghai Normal University, 200234, Shanghai, China. .
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Źródło:
Communications biology [Commun Biol] 2023 Sep 15; Vol. 6 (1), pp. 944. Date of Electronic Publication: 2023 Sep 15.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cyanobacteria*
Anemia, Hypochromic*
Humans ; Heme Oxygenase (Decyclizing) ; Acclimatization ; Nitrogen ; Phycobiliproteins
Czasopismo naukowe
Tytuł:
Prevalence of anemia and associated factors in a Moroccan population from the Northwestern region of Morocco (M'diq-Fnideq-Martil Prefecture).
Autorzy:
Bakrim S; Geo-Bio-Environment Engineering and Innovation Laboratory, Molecular Engineering, Biotechnology and Innovation Team, Polydisciplinary Faculty of Taroudant, Ibn Zohr University, Agadir, Morocco.; Hematology Laboratory, Faculty of Medicine and Pharmacy, Mohammed V University, Central Hematology Laboratory, Ibn Sina University Hospital, Rabat, Morocco.
Hichou NE; Department of Biology, Faculty of Sciences, Abdelmalek Essaâdi University, Tetouan, Morocco.
Driss EKB; Department of Biology, Faculty of Sciences, Abdelmalek Essaâdi University, Tetouan, Morocco.
Aboulaghras S; Physiology and Physiopathology Team, Faculty of Sciences, Genomic of Human Pathologies Research, Mohammed V University in Rabat, Rabat, Morocco.
Balahbib A; Laboratory of Biodiversity, Ecology and Genome, Faculty of Sciences, Mohammed V University, Rabat 10106, Rabat, Morocco.
Bouyahya A; Laboratory of Human Pathologies Biology, Department of Biology, Faculty of Sciences, Mohammed V University in Rabat, Rabat, Morocco.
Masrar A; Hematology Laboratory, Faculty of Medicine and Pharmacy, Mohammed V University, Central Hematology Laboratory, Ibn Sina University Hospital, Rabat, Morocco.
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Źródło:
The Pan African medical journal [Pan Afr Med J] 2023 Mar 15; Vol. 44, pp. 131. Date of Electronic Publication: 2023 Mar 15 (Print Publication: 2023).
Typ publikacji:
Journal Article
MeSH Terms:
Anemia*/epidemiology
Anemia, Hypochromic*
Adult ; Child ; Female ; Humans ; Pregnancy ; Prevalence ; Morocco/epidemiology ; Pregnant Women ; Risk Factors ; Socioeconomic Factors
Czasopismo naukowe
Tytuł:
Z score analysis: A novel approach to interpretation of an erythrogram.
Autorzy:
Chauhan K; Department of Pathology, Polo Labs, Mohali, Punjab, India.
Bisht B; Department of Pathology, Polo Labs, Ivy Hospital, Mohali, Punjab, India.
Kathuria K; Department of Pathology, Polo Labs, Mohali, Punjab, India.
Bisht R; Department of Pathology, Dr. Ahujas' Pathology and Radiology Collection Centre, Dehradun, Uttarakhand, India.
Hatwal V; Department of Pathology, Polo Labs, Mohali, Punjab, India.
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Źródło:
Indian journal of pathology & microbiology [Indian J Pathol Microbiol] 2023 Jan-Mar; Vol. 66 (1), pp. 85-90.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*/diagnosis
Anemia, Iron-Deficiency*/diagnosis
beta-Thalassemia*/diagnosis
Humans ; Retrospective Studies ; Erythrocyte Indices
Czasopismo naukowe
Tytuł:
Identification of effector CEP112 that promotes the infection of necrotrophic Alternaria solani.
Autorzy:
Wang C; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Zhang D; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Cheng J; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Zhao D; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Pan Y; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Li Q; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China.
Zhu J; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China. .; Technological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, Baoding, 071001, People's Republic of China. .
Yang Z; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China. .; Technological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, Baoding, 071001, People's Republic of China. .
Wang J; College of Plant Protection, Hebei Agricultural University, Baoding, 071001, People's Republic of China. .; Technological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, Baoding, 071001, People's Republic of China. .
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Źródło:
BMC plant biology [BMC Plant Biol] 2022 Sep 29; Vol. 22 (1), pp. 466. Date of Electronic Publication: 2022 Sep 29.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*
Plant Diseases*/genetics
Alternaria/physiology ; Melanins
SCR Organism:
Alternaria solani
Czasopismo naukowe
Tytuł:
Alleviation of iron deficiency in pear by ammonium nitrate and nitric oxide.
Autorzy:
Liu J; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Wang J; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Wang Z; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Li M; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Liang C; Haidu College, Qingdao Agricultural University, Laiyang, 265200, China.
Yang Y; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Li D; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China.
Wang R; College of Horticulture, Qingdao Agricultural University, Qingdao, 266109, China. .
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Źródło:
BMC plant biology [BMC Plant Biol] 2022 Sep 12; Vol. 22 (1), pp. 434. Date of Electronic Publication: 2022 Sep 12.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*
Iron Deficiencies*
Pyrus*/metabolism
Iron/metabolism ; Nitrates/metabolism ; Nitric Oxide ; Nitrogen/metabolism ; Plants/metabolism
Czasopismo naukowe
Tytuł:
Physiological and Transcriptome Analyses Revealed the Mechanism by Which Deferoxamine Promotes Iron Absorption in Cinnamomum camphora .
Autorzy:
Kong WL; Co-Innovation Center for Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.; Jiangsu Key Laboratory for Prevention and Management of Invasive Species, Nanjing Forestry University, Nanjing 210037, China.
Wen TY; Co-Innovation Center for Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.; Jiangsu Key Laboratory for Prevention and Management of Invasive Species, Nanjing Forestry University, Nanjing 210037, China.
Wang YH; Co-Innovation Center for Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.; Jiangsu Key Laboratory for Prevention and Management of Invasive Species, Nanjing Forestry University, Nanjing 210037, China.
Wu XQ; Co-Innovation Center for Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.; Jiangsu Key Laboratory for Prevention and Management of Invasive Species, Nanjing Forestry University, Nanjing 210037, China.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Aug 30; Vol. 23 (17). Date of Electronic Publication: 2022 Aug 30.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*
Cinnamomum camphora*
Deferoxamine/pharmacology ; Gene Expression Profiling ; Iron/metabolism ; Siderophores/metabolism
Czasopismo naukowe
Tytuł:
Discovery and Characterization of a Novel Umbravirus from Paederia scandens Plants Showing Leaf Chlorosis and Yellowing Symptoms.
Autorzy:
Zheng L; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.; Hainan Institute, Zhejiang University, Sanya 572025, China.
Fu S; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.
Xie Y; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.
Han Y; Beijing Institute of Genomics, Chinese Academy of Sciences, China National Center for Bioinformation, Beijing 100101, China.
Zhou X; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.; State Key Laboratory for Biology of Plant Diseases and Insect Pests, Institute of Plant Protection, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Wu J; State Key Laboratory of Rice Biology, Institute of Biotechnology, Zhejiang University, Hangzhou 310058, China.; Hainan Institute, Zhejiang University, Sanya 572025, China.
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Źródło:
Viruses [Viruses] 2022 Aug 19; Vol. 14 (8). Date of Electronic Publication: 2022 Aug 19.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Anemia, Hypochromic*/genetics
Tombusviridae*/genetics
Genome, Viral ; Open Reading Frames ; Phylogeny ; Plant Diseases ; Plant Leaves ; RNA, Viral/genetics ; RNA-Dependent RNA Polymerase ; Viral Proteins/genetics
Czasopismo naukowe
Tytuł:
36-year-old male with X-linked congenital sideroblastic anemia presenting as chronic microcytic anemia with iron overload.
Autorzy:
Simpson SJ; Department of Pathology, University of Utah Health, Salt Lake City, Utah, USA.
Lim MY; Division of Hematology and Hematologic Malignancy, Department of Internal Medicine, University of Utah, Salt Lake City, Utah, USA.
George TI; Department of Pathology, University of Utah Health, Salt Lake City, Utah, USA.; ARUP Laboratories Inc., Salt Lake City, Utah, USA.
Rets A; Department of Pathology, University of Utah Health, Salt Lake City, Utah, USA.; ARUP Laboratories Inc., Salt Lake City, Utah, USA.
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Źródło:
International journal of laboratory hematology [Int J Lab Hematol] 2022 Feb; Vol. 44 (1), pp. 69-71. Date of Electronic Publication: 2021 Nov 15.
Typ publikacji:
Case Reports
MeSH Terms:
Anemia, Hypochromic*/blood
Anemia, Hypochromic*/diagnosis
Anemia, Hypochromic*/genetics
Anemia, Sideroblastic*/blood
Anemia, Sideroblastic*/diagnosis
Anemia, Sideroblastic*/genetics
Genetic Diseases, X-Linked*/blood
Genetic Diseases, X-Linked*/diagnosis
Genetic Diseases, X-Linked*/genetics
Iron Overload*/blood
Iron Overload*/diagnosis
Iron Overload*/genetics
Adult ; Diagnosis, Differential ; Humans ; Male
SCR Disease Name:
Anemia, hypochromic microcytic; X-linked sideroblastic anemia
Raport
Tytuł:
Transcriptome and metabolome analyses reveal new insights into chlorophyll, photosynthesis, metal ion and phenylpropanoids related pathways during sugarcane ratoon chlorosis.
Autorzy:
Luo T; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Zhou Z; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Deng Y; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Fan Y; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Qiu L; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Chen R; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Yan H; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Zhou H; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China.; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China.; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China.
Lakshmanan P; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China.; Interdisciplinary Research Center for Agriculture Green Development in Yangtze River Basin, College of Resources and Environment, Southwest University, Chongqing, 400716, China.; Queensland Alliance for Agriculture and Food Innovation, University of Queensland, QLD, St Lucia, 4067, Australia.
Wu J; Sugarcane Research Institute, Guangxi Academy of Agricultural Sciences, Nanning, Guangxi, China. .; Sugarcane Research Center, Chinese Academy of Agricultural Sciences, Nanning, Guangxi, China. .; Key Laboratory of Sugarcane Biotechnology and Genetic Improvement (Guangxi), Ministry of Agriculture, Nanning, Guangxi, China. .; Guangxi Key Laboratory of Sugarcane Genetic Improvement, Nanning, Guangxi, China. .
Chen Q; Nanning New Technology Entrepreneur Center, Nanning, Guangxi, China.
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Źródło:
BMC plant biology [BMC Plant Biol] 2022 Apr 29; Vol. 22 (1), pp. 222. Date of Electronic Publication: 2022 Apr 29.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*
Saccharum*/genetics
Saccharum*/metabolism
Chlorophyll/metabolism ; Gene Expression Regulation, Plant ; Metabolome ; Photosynthesis/genetics ; Transcriptome
Czasopismo naukowe
Tytuł:
New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation.
Autorzy:
Romero-Cortadellas L; Iron Metabolism: Regulation and Diseases, Department of Basic Sciences, Universitat Internacional de Catalunya (UIC), 08195 Sant Cugat del Vallès, Spain.
Hernández G; Iron Metabolism: Regulation and Diseases, Department of Basic Sciences, Universitat Internacional de Catalunya (UIC), 08195 Sant Cugat del Vallès, Spain.; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
Ferrer-Cortès X; Iron Metabolism: Regulation and Diseases, Department of Basic Sciences, Universitat Internacional de Catalunya (UIC), 08195 Sant Cugat del Vallès, Spain.; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
Zalba-Jadraque L; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
Fuster JL; Pediatric OncoHematology Service, Clinic University Hospital Virgen de la Arrixaca, Instituto Murciano de Investigación Biosanitaria (IMIB), 30120 Murcia, Spain.
Bermúdez-Cortés M; Pediatric OncoHematology Service, Clinic University Hospital Virgen de la Arrixaca, Instituto Murciano de Investigación Biosanitaria (IMIB), 30120 Murcia, Spain.
Galera-Miñarro AM; Pediatric OncoHematology Service, Clinic University Hospital Virgen de la Arrixaca, Instituto Murciano de Investigación Biosanitaria (IMIB), 30120 Murcia, Spain.
Pérez-Montero S; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
Tornador C; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
Sánchez M; Iron Metabolism: Regulation and Diseases, Department of Basic Sciences, Universitat Internacional de Catalunya (UIC), 08195 Sant Cugat del Vallès, Spain.; BloodGenetics S.L. Diagnostics in Inherited Blood Diseases, 08950 Esplugues de Llobregat, Spain.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Apr 15; Vol. 23 (8). Date of Electronic Publication: 2022 Apr 15.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Anemia*/genetics
Anemia, Hypochromic*/genetics
Iron Overload*/metabolism
Animals ; Humans ; Iron/metabolism ; Mammals/metabolism ; Mutation
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Associations between Serum Aflatoxin-B1 and Anemia in Pregnant Women: Evidence from Guangxi Zhuang Birth Cohort in China.
Autorzy:
Lei L; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Liu S; Department of Maternal, Child and Adolescent Health, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Ye Y; Center for Disease Control and Prevention, Guangxi Liuzhou Iron & Steel Group Co., Ltd., Liuzhou 545002, China.
Qiu X; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Huang D; Department of Sanitary Chemistry, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Pan D; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Chen J; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Qian Z; Department of Epidemiology and Biostatistics, College for Public Health & Social Justice, Saint Louis University, St. Louis, MO 63103, USA.
McMillin SE; School of Social Work, College for Public Health & Social Justice, Saint Louis University, St. Louis, MO 63103, USA.
Vaughn MG; School of Social Work, College for Public Health & Social Justice, Saint Louis University, St. Louis, MO 63103, USA.
Luo X; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Wu K; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Xiao S; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Li J; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Liu M; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Yang Y; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Lai M; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
Dong G; Department of Environmental and Occupational Health, School of Public Health, Sun Yat-sen University, Guangzhou 510080, China.
Zeng X; Department of Epidemiology and Health Statistics, School of Public Health, Guangxi Medical University, Nanning 530021, China.
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Źródło:
Toxins [Toxins (Basel)] 2021 Nov 15; Vol. 13 (11). Date of Electronic Publication: 2021 Nov 15.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Aflatoxin B1/*blood
Anemia/*epidemiology
Anemia, Hypochromic/*epidemiology
Pregnancy Complications, Hematologic/*epidemiology
Adult ; Anemia/etiology ; Anemia, Hypochromic/etiology ; China ; Cohort Studies ; Erythrocyte Indices/physiology ; Female ; Hemoglobins/metabolism ; Humans ; Infant, Newborn ; Male ; Maternal Exposure/adverse effects ; Pregnancy ; Pregnancy Complications, Hematologic/etiology ; Pregnancy Trimesters ; Prospective Studies ; Young Adult
Czasopismo naukowe
Tytuł:
Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran.
Autorzy:
Alimohammadi-Bidhendi S; Department of Genetics, Faculty of Advanced Technologies in Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Azadmehr S; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.; Department of Genetics, Faculty of Basic Sciences, Shahr-e Rey, Payame Noor University, Tehran, Iran.
Razipour M; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.; Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Zeinali S; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.; Medical Genetics Laboratory of Dr. Zeinali, Kawsar Human Genetics Research Center, Tehran, Iran.
Eslami M; Departments of Genetics, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.; Applied Biotechnology Research Center, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Davoudi-Dehaghani E; Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Jan; Vol. 45 (1), pp. 37-40. Date of Electronic Publication: 2021 Mar 27.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Hypochromic*
Iron Deficiencies*
alpha-Thalassemia*
Haplotypes ; Humans ; Iran ; Mutation
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Application of HbA 2 levels and red cell indices-based new model in the differentiation of thalassemia traits from iron deficiency in hypochromic microcytic anemia Cases.
Autorzy:
Zhou Y; The First People's Hospital of Changde, Changde, China.
Zhang J; The First People's Hospital of Changde, Changde, China.
Wang C; The First People's Hospital of Changde, Changde, China.
Zhou L; The First People's Hospital of Changde, Changde, China.
Zhou L; The First People's Hospital of Changde, Changde, China.
Ou D; Changde Hospital of University of South China, Changde, China.
Peng D; The First People's Hospital of Changde, Changde, China.; Changde Hospital of University of South China, Changde, China.
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Źródło:
International journal of laboratory hematology [Int J Lab Hematol] 2020 Oct; Vol. 42 (5), pp. 526-532. Date of Electronic Publication: 2020 Jun 21.
Typ publikacji:
Journal Article
MeSH Terms:
Hemoglobin A2*/genetics
Anemia, Hypochromic/*blood
Anemia, Hypochromic/*diagnosis
Anemia, Iron-Deficiency/*blood
Anemia, Iron-Deficiency/*diagnosis
Thalassemia/*blood
Thalassemia/*diagnosis
Adolescent ; Adult ; Alleles ; Anemia, Hypochromic/etiology ; Diagnosis, Differential ; Erythrocyte Indices ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Mutation ; ROC Curve ; Sensitivity and Specificity ; Young Adult
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene.
Autorzy:
Ropero P; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.; Instituto de Investigación Sanitaria, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
Arbeteta J; Servicio de Hematología, Hospital Universitario de Guadalajara, Guadalajara, Spain.
Nieto JM; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.; Instituto de Investigación Sanitaria, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
González FA; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
González B; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.; Instituto de Investigación Sanitaria, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
Villegas A; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
Benavente C; Servicio de Hematología, Hospital Clínico San Carlos de Madrid, Madrid, Spain.
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Źródło:
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 17-19. Date of Electronic Publication: 2020 Jan 31.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Frameshift Mutation*
Anemia, Hypochromic/*genetics
Hemoglobin A2/*genetics
Hemoglobin H/*genetics
alpha-Globins/*genetics
alpha-Thalassemia/*genetics
Adult ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/pathology ; Base Sequence ; Codon ; Female ; Gene Expression ; Genotype ; Humans ; Male ; Phenotype ; Sequence Analysis, DNA ; Severity of Illness Index ; alpha-Thalassemia/diagnosis ; alpha-Thalassemia/pathology
Czasopismo naukowe
Tytuł:
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
Autorzy:
Sajadpour Z; Genetic Division, Biology Department, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Amini-Farsani Z; Young Researchers and Elites Club, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Motovali-Bashi M; Genetic Division, Biology Department, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Yadollahi M; Department of Operative Dentistry, School of Dentistry, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Khosravi-Farsani N; Department of Biology, University of Kharazmi, Tehran, Iran.
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Źródło:
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 27-30. Date of Electronic Publication: 2020 Jan 03.
Typ publikacji:
Journal Article
MeSH Terms:
Mutation*
Anemia, Hypochromic/*genetics
Fetal Hemoglobin/*genetics
Hemoglobins, Abnormal/*genetics
alpha-Globins/*genetics
beta-Globins/*genetics
beta-Thalassemia/*genetics
Adult ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/pathology ; Female ; Gene Expression ; Haplotypes ; Hepatomegaly/diagnosis ; Hepatomegaly/genetics ; Hepatomegaly/pathology ; Humans ; Iran ; Linkage Disequilibrium ; Male ; Phenotype ; Polymorphism, Restriction Fragment Length ; Sequence Analysis, DNA ; Splenomegaly/diagnosis ; Splenomegaly/genetics ; Splenomegaly/pathology ; alpha-Globins/deficiency ; beta-Globins/deficiency ; beta-Thalassemia/diagnosis ; beta-Thalassemia/pathology
Czasopismo naukowe
Tytuł:
A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB : c.92+6T>G] in a Chinese Family.
Autorzy:
Luo H; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
Zou Y; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
Liu Y; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
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Źródło:
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 55-57. Date of Electronic Publication: 2020 Jan 15.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Mutation*
Anemia, Hypochromic/*genetics
Hemoglobins, Abnormal/*genetics
beta-Globins/*genetics
beta-Thalassemia/*genetics
Adult ; Alleles ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/ethnology ; Asian People ; Child ; Family ; Female ; Gene Expression ; Genotype ; Hemoglobin A2/genetics ; Humans ; Middle Aged ; Pedigree ; Phenotype ; Polymerase Chain Reaction ; Sequence Analysis, DNA ; beta-Globins/deficiency ; beta-Thalassemia/diagnosis ; beta-Thalassemia/ethnology
Czasopismo naukowe
Tytuł:
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
Autorzy:
Al-Riyami AZ; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
Daar S; Department of Hematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Kindi SA; Department of Hematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Madhani AA; Department of Medicine, Sohar Hospital, Ministry of Health, Muscat, Oman.
Wali Y; Department of Child Health, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Rawahi MA; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
Zadjali SA; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
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Źródło:
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 20-26. Date of Electronic Publication: 2020 Feb 05.
Typ publikacji:
Journal Article
MeSH Terms:
Mutation*
Anemia, Hypochromic/*genetics
Hemoglobin A2/*genetics
Hemoglobin H/*genetics
Hemoglobin, Sickle/*genetics
alpha-Globins/*genetics
alpha-Thalassemia/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/pathology ; Child ; Child, Preschool ; Erythrocyte Indices ; Female ; Gene Expression ; Genotype ; Humans ; Infant ; Male ; Mediterranean Region ; Middle Aged ; Oman ; Phenotype ; Retrospective Studies ; Sequence Analysis, DNA ; alpha-Globins/deficiency ; alpha-Thalassemia/diagnosis ; alpha-Thalassemia/pathology
Czasopismo naukowe
Tytuł:
Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis.
Autorzy:
Osman HA; Department of Biotechnology, School of Pharmacy, Ahafad University for Women, Omdurman, Sudan. .
Hamid MMA; Institute of Endemic Diseases, Medical Campus, University of Khartoum, Khartoum, Sudan.
Ahmad RB; Hematology Unit, Cancer Research Centre Institute for Medical Research Jalan Pahang, 50588, Kuala Lumpur, Malaysia.
Saleem M; Advanced Genomics SDN BHD (GenomixLAB), Kota Damansara, Malaysia.
Abdallah SA; Department of Pathology, Faculty of Medicine, Alneelain University, Khartoum, Sudan.
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Źródło:
BMC research notes [BMC Res Notes] 2020 Feb 10; Vol. 13 (1), pp. 65. Date of Electronic Publication: 2020 Feb 10.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Testing*
Anemia, Hypochromic/*genetics
Chromosomes, Human, Pair 3/*genetics
Chromosomes, Human, Pair 4/*genetics
alpha-Thalassemia/*diagnosis
alpha-Thalassemia/*genetics
Adolescent ; Adult ; Anemia, Hypochromic/epidemiology ; Child ; Female ; Humans ; Male ; Middle Aged ; Prevalence ; Sequence Deletion ; Sudan/epidemiology ; Young Adult ; alpha-Thalassemia/epidemiology
Czasopismo naukowe
Tytuł:
An Unusual Compound Heterozygosity for Hb O-Arab ( HBB : c.364G>A) and Hb D-Los Angeles ( HBB : c.364G>C).
Autorzy:
van Gammeren AJ; Department of Clinical Chemistry and Hematology, Amphia Hospital, Breda, The Netherlands.
Pelkmans L; Department of Clinical Chemistry and Hematology, Amphia Hospital, Breda, The Netherlands.
Endschot CCWV; Department of Clinical Chemistry and Hematology, Amphia Hospital, Breda, The Netherlands.
Roelofsen-de Beer RJAC; Department of Clinical Chemistry and Hematology, Amphia Hospital, Breda, The Netherlands.
Harteveld CL; The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
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Źródło:
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 61-63. Date of Electronic Publication: 2020 Jan 23.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Mutation*
Anemia, Hypochromic/*genetics
Hemoglobins, Abnormal/*genetics
beta-Globins/*genetics
beta-Thalassemia/*genetics
Anemia, Hypochromic/diagnosis ; Chromatography, High Pressure Liquid ; Consanguinity ; Electrophoresis, Capillary ; Female ; Gene Expression ; Heterozygote ; Humans ; Infant, Newborn ; Sequence Analysis, DNA ; beta-Globins/deficiency ; beta-Thalassemia/diagnosis
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Anemia among pregnant women in internally displaced camps in Mogadishu, Somalia: a cross-sectional study on prevalence, severity and associated risk factors.
Autorzy:
Ahmed RH; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia.
Yussuf AA; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia.
Ali AA; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia.
Iyow SN; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia.
Abdulahi M; Obstetrics and Gynaecology Department, Dr Sumait Hospital, Mogadishu, Somalia.; Faculty of Medicine & Health Sciences, SIMAD University, Mogadishu, Somalia.
Mohamed LM; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia.; Paediatric Department, Jazeera University Hospital, Mogadishu, Somalia.
Mohamud MHT; Faculty of Medicine & Surgery, Jazeera University, Mogadishu, Somalia. .; Research Unit, Jazeera University, Mogadishu, Somalia. .
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Źródło:
BMC pregnancy and childbirth [BMC Pregnancy Childbirth] 2021 Dec 14; Vol. 21 (1), pp. 832. Date of Electronic Publication: 2021 Dec 14.
Typ publikacji:
Journal Article
MeSH Terms:
Refugee Camps*
Refugees*
Anemia/*epidemiology
Pregnancy Complications, Hematologic/*epidemiology
Pregnant Women/*ethnology
Adolescent ; Adult ; Anemia, Hypochromic/epidemiology ; Cross-Sectional Studies ; Female ; Humans ; Patient Acuity ; Pregnancy ; Prevalence ; Risk Factors ; Somalia/epidemiology ; Young Adult
SCR Disease Name:
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł:
Diagnosis and molecular characterization of a novel α -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia.
Autorzy:
Makis A; Child Health Department, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
Georgiou I; Genetics and IVF Unit, Department of Obstetrics and Gynecology, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
Traeger-Synodinos J; Laboratory of Medical Genetics, National and Kapodistrian University of Athens, Athens, Greece.
Chaliasos N; Child Health Department, Faculty of Medicine, University of Ioannina, Ioannina, Greece.
Grosso M; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, CEINGE- Advanced Biotechnologies, Italy.
Gambale A; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, CEINGE- Advanced Biotechnologies, Italy.
Iolascon A; Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, CEINGE- Advanced Biotechnologies, Italy.
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Źródło:
International journal of laboratory hematology [Int J Lab Hematol] 2017 Oct; Vol. 39 (5), pp. e124-e126. Date of Electronic Publication: 2017 Jun 12.
Typ publikacji:
Case Reports; Letter
MeSH Terms:
Base Sequence*
Sequence Deletion*
Anemia, Hypochromic/*genetics
Hemoglobins, Abnormal/*genetics
alpha-Thalassemia/*genetics
Anemia, Hypochromic/pathology ; Child, Preschool ; Female ; Glycated Hemoglobin/genetics ; Greece ; Hemoglobin A2/genetics ; Humans ; alpha-Thalassemia/pathology ; beta-Globins/genetics
Raport

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