ヘモグロビンM
WordNet
- 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
- the 13th letter of the Roman alphabet (同)m
- the imperial dynasty of China from 1368 to 1644 (同)Ming dynasty
- a form of address for a woman (同)Ms.
PrepTutorEJDIC
- ヘモグロビン,血色素
- Mach number / mark[s] / Monsieur
- (中国の)明,明朝(1368‐1644)
- mendeleviumの化学記号
UpToDate Contents
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English Journal
- Hb M-Iwate in an Indian family.
- Kumar GV1, Sharma P1, Chhabra S1, Hira JK1, Trehan A2, Das R3.
- Clinica chimica acta; international journal of clinical chemistry.Clin Chim Acta.2015 Jun 15;446:192-4. doi: 10.1016/j.cca.2015.04.031. Epub 2015 Apr 27.
- BACKGROUND: High performance liquid chromatography in a newborn girl with congenital cyanosis and a unilateral cleft palate revealed a variant hemoglobin with retention time of 4.8 min, similar to hemoglobin Q-India. Since hemoglobin Q-India did not explain the cyanosis, further investigations were
- PMID 25931326
- An unusual cause of neonatal cyanosis….
- Carreira R1, Palaré MJ2, Prior AR3, Garcia P4, Abrantes M2.
- BMJ case reports.BMJ Case Rep.2015 Mar 9;2015. pii: bcr2014208371. doi: 10.1136/bcr-2014-208371.
- We report a case of a female neonate whose pulse oximetry screening for congenital heart disease at 40 h of life was positive. The pregnancy was uneventful with no relevant family history. The neonate presented with bluish discolouration of the skin lasting until day 15. Cardiovascular examination
- PMID 25754164
- De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth.
- Viana MB1, Belisário AR2.
- Revista brasileira de hematologia e hemoterapia.Rev Bras Hematol Hemoter.2014 May-Jun;36(3):230-4. doi: 10.1016/j.bjhh.2014.03.020. Epub 2014 Mar 29.
- Cyanosis in an apparently healthy newborn baby may be caused by hemoglobin variants associated with the formation of methemoglobin, collectively known as M hemoglobins. They should not be confused with genetic alterations in methemoglobin reductase enzyme systems of red cells since treatment and pro
- PMID 25031065
Japanese Journal
- 非侵襲的ヘモグロビン測定器を用いた妊娠貧血検査の可能性
- Use of Proton Pump Inhibitors Is Associated With Anemia in Cardiovascular Outpatients
- Shikata Toshiyuki,Sasaki Naoko,Ueda Masahiro [他]
- Circulation journal : official journal of the Japanese Circulation Society 79(1), 193-200, 2015-01
- NAID 40020311976
- SGLT2阻害薬の有効性と今後の課題 (糖尿病) -- (臨床分野での進歩)
Related Links
- hemoglobin M n. Abbr. Hb M A group of abnormal hemoglobins in which a single amino acid substitution favors the formation of methemoglobin and is thus associated with methemoglobinemia. hemoglobin M, any of several abnormal ...
- hemoglobin M n. Abbr. Hb M A group of abnormal hemoglobins in which a single amino acid substitution favors the formation of methemoglobin and is thus associated with methemoglobinemia.
Related Pictures
★リンクテーブル★
[★]
- 英
- hemoglobin M, Hb M
- 同
- M型血色素
- 関
- ヘモグロビン、メトヘモグロビン
[★]
メンデレビウム mendelevium
[★]
メチオニン methionine
[★]
ヘモグロビン