WordNet

deeply affected by a strong feeling; "sat completely still, sick with envy"; "she was sick with longing"
people who are sick; "they devote their lives to caring for the sick"
a hemoprotein composed of globin and heme that gives red blood cells their characteristic color; function primarily to transport oxygen from the lungs to the body tissues; "fish have simpler hemoglobin than mammals" (同)haemoglobin, Hb
an edge tool for cutting grass or crops; has a curved blade and a short handle (同)reaping_hook, reap hook

PrepTutorEJDIC

(人が)『病気の』;(部屋などが)病人の[ための];(顔色などが)病気を示す(思わせる) / 《名詞的に》《the ~;複数扱い》病人 / 《補語にのみ用いて》《おもに英》(…で)むかついて,吐き気を催して,気分が悪い《+『at(『with』,『from』+『名』(do『ing』)》 / 《補語にのみ用いて》(…に)『うんざりして』,あきあきして,いや気がさして;(…に)しゃくにさわって,腹が立って《+『of』+『名』(do『ing』)》 / 《補語にのみ用いて》(…に)『がっかりして』,落胆して《+『at』(『about』)+『名』(do『ing』)》 / 《補語にのみ用いて》(…を)熱望して,こがれて《+『for』+『名』》 / 病的な,異常心理の;気味の悪い
ヘモグロビン,血色素
(麦刈り用の三日月形の)小がま

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1. 鎌状赤血球形質 sickle cell trait
2. 鎌状ヘモグロビン多量体：構造と機能特性 sickle hemoglobin polymer structure and functional properties
3. 鎌状赤血球障害の診断 diagnosis of sickle cell disorders
4. 異常ヘモグロビン症の検査室診断 laboratory diagnosis of the hemoglobinopathies
5. 異型鎌状赤血球症候群 variant sickle cell syndromes

Mechanisms of haptoglobin protection against hemoglobin peroxidation triggered endothelial damage.

Schaer CA, Deuel JW, Bittermann AG, Rubio IG, Schoedon G, Spahn DR, Wepf RA, Vallelian F, Schaer DJ.SourceInstitute of Anesthesiology, University Hospital, Zurich, Switzerland.
Cell death and differentiation.Cell Death Differ.2013 Nov;20(11):1569-79. doi: 10.1038/cdd.2013.113. Epub 2013 Aug 30.
Extracellular hemoglobin (Hb) has been recognized as a disease trigger in hemolytic conditions such as sickle cell disease, malaria, and blood transfusion. In vivo, many of the adverse effects of free Hb can be attenuated by the Hb scavenger acute-phase protein haptoglobin (Hp). The primary physiolo
PMID 23995229

Intraday blood rheological changes induced by ramadan fasting in sickle cell trait carriers.

Diaw M, Connes P, Samb A, Sow AK, Sall ND, Sar FB, Ba A, Diop S, Niang MN, Tripette J.SourceLaboratoire de physiologie et explorations fonctionnelles, FMPOS, UCAD , Dakar , Senegal .
Chronobiology international.Chronobiol Int.2013 Nov;30(9):1116-22. doi: 10.3109/07420528.2013.804083. Epub 2013 Aug 5.
The goal of the present study was to test whether fasting during the holy period of Ramadan may disturb blood rheology in sickle cell trait (SCT) carriers more than in a group of subjects with normal hemoglobin. Twenty African male students participated in the study: 10 SCT carriers and 10 subjects
PMID 23915011

Madu AJ, Ubesie A, Madu KA, Okwor B, Anigbo C.SourceDepartment of Haematology & Immunology, University of Nigeria Enugu Campus, Enugu, Nigeria; Department of Haematology & Immunology, University of Nigeria Teaching Hospital, Enugu, Nigeria.
Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.Wound Repair Regen.2013 Oct 17. doi: 10.1111/wrr.12100. [Epub ahead of print]
The exact mechanism for the occurrence of sickle leg ulcers (SLUs) has not been fully explained, although, popular opinion supports a multifactorial etio-pathogenetic process. Leg ulceration in sickle cell is a chronic and debilitating condition which is difficult to treat and may worsen the psychos
PMID 24134724

和田芳直
Journal of the Mass Spectrometry Society of Japan = 質量分析 61(4), 35-41, 2013
… In 1949, Linus Pauling coined this term in his report on the discovery of an electrophoretic change indicating the existence of a structural abnormality in hemoglobin derived from patients with sickle cell anemia. …
NAID 130003366692

Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients

BHATNAGAR Pallav,PURVIS Shirley,BARRON-CASELLA Emily,DEBAUN Michael R,CASELLA James F,ARKING Dan E,KEEFER Jeffrey R
Journal of human genetics 56(4), 316-323, 2011-04-01
NAID 10030658973