A mixed function oxidase enzyme which during hemoglobin catabolism catalyzes the degradation of heme to ferrous iron, carbon monoxide and biliverdin in the presence of molecular oxygen and reduced NADPH. The enzyme is induced by metals, particularly cobalt
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Heme oxygenase. : Heme oxygenase and the kidney / David E. Stec
2011
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Proteins that contain an iron-porphyrin, or heme, prosthetic group resembling that of hemoglobin. (From Lehninger, Principles of Biochemistry, 1982, p480)
Proteins that contain an iron-porphyrin, or heme, prosthetic group resembling that of hemoglobin. (From Lehninger, Principles of Biochemistry, 1982, p480)
A transferase that catalyzes the addition of aliphatic, aromatic, or heterocyclic FREE RADICALS as well as EPOXIDES and arene oxides to GLUTATHIONE. Addition takes place at the SULFUR. It also catalyzes the reduction of polyol nitrate by glutathione to polyol and nitrite
Hemensley, Kris. : Christopher / by Kris Hemensley ; illustrated by Jiri Tibor Novak
1987
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Hemenway Southwestern Archaeological Expedition (1886-1894) / http://id.loc.gov/authorities/names/n50056417 : The Southwest in the American imagination : the writings of Sylvester Baxter, 1881-1889 / edited by Curtis M. Hinsley and David R. Wilcox
Hemer <2010> : Burgen in Westfalen : Wehranlagen, Herrschaftssitze, Wirtschaftskerne (12.-14. Jahrhundert) : Beiträge der Tagung am 10. und 11. September 2010 in Hemer / Werner Freitag, Wilfried Reininghaus (Hg.)
Visual impairments limiting one or more of the basic functions of the eye: visual acuity, dark adaptation, color vision, or peripheral vision. These may result from EYE DISEASES; OPTIC NERVE DISEASES; VISUAL PATHWAY diseases; OCCIPITAL LOBE diseases; OCULAR MOTILITY DISORDERS; and other conditions (From Newell, Ophthalmology: Principles and Concepts, 7th ed, p132)
Visual impairments limiting one or more of the basic functions of the eye: visual acuity, dark adaptation, color vision, or peripheral vision. These may result from EYE DISEASES; OPTIC NERVE DISEASES; VISUAL PATHWAY diseases; OCCIPITAL LOBE diseases; OCULAR MOTILITY DISORDERS; and other conditions (From Newell, Ophthalmology: Principles and Concepts, 7th ed, p132)
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Hemerologion : Books of Fate and Popular Culture in Early China : the Daybook Manuscripts of the Warring States, Qin, and Han / edited by Donald Harper and Marc Kalinowski
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
Organs involved in the production of BLOOD, including the cellular and the molecular components essential in providing defense against foreign organisms or substances
Hemicellulose -- Industrial applications : Hemicellulose biorefinery : a sustainable solution for value addition to bio-based products and bioenergy / Michel Brienzo, editor
A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
A class of disabling primary headache disorders, characterized by recurrent unilateral pulsatile headaches. The two major subtypes are common migraine (without aura) and classic migraine (with aura or neurological symptoms). (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
Hemifacial microsomia. : Craniofacial microsomia and Treacher Collins syndrome : comprehensive treatment of associated facial deformities / David M. Yates, Michael R. Markiewicz, editors
