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ACE is expressed in osteoblasts and hypertrophic chondrocytes in the periosteal callus during fracture healing, accompanied by expression of the angiotensin type-1 and type-2 receptors
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high ACE peptidase activity coincides with every transition state, from embryo to larva, from larva to larva and from larva to pupa
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at 11-13 weeks of gestation ACE-positive cells are observed in the primitive epidermis, as the fetuses develops ACE-positive cells appear in all the epidermal layers, and from 21 weeks of gestation ACE expression is largely restricted to the basal layer of the fetal epidermis, while ACE-positive cells are found only in the adult skin basal layer which harbours epidermal stem cells
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brush border of absorptive epithelia on the small intestine and the renal convoluted tubule
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weak activity
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of the last larval stage
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cultured, corneal
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ischemic and contralateral non-ischemic legs
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stably transfected with full-length ACE2
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of the last larval stage
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endogenously expressing ACE2
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intestinal mucosa and arteries
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dorsomedial medulla
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PBMC
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high ACE peptidase activity coincides with every transition state, from embryo to larva, from larva to larva and from larva to pupa. pupa. A peak value in activity occurs during the early pupal stage
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from aorta, extracellular ACE binds to smooth muscle cells, overview
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spermatogonial, somatic ACE (sACE), but not testicular ACE (tACE), is expressed in mouse cultured spermatogonial stem cells (SSCs)
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stably overexpressing human somatic ACE
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the direct antioxidative and anti-inflammatory effects of peroxisome proliferator-activated receptors ligands are associated with the inhibition of angiotensin converting enzyme expression in streptozotocin-induced diabetic rat aorta
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soluble form
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no significant difference between enzyme activity in peripheral and left spermatic vein blood sample from the varicocele and control group. The somatic ACE has no causative role in pathophysiology of varicocele and varicocels related infertility
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corpus striatum
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of the last larval stage
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striatum, 2 enzyme forms: MW 170000 Da and MW 180000 Da
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707653, 707697, 707763, 707764, 707811, 708825, 708837, 708857, 709304, 710252, 710591 brenda
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type VI-S
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from lung with 98% purity
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membrane-bound form
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vascular
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membrane-bound form, surface of epithelial cells of epididymis and prostate
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cultured, corneal
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of pulmonary capillaries
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high activity
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high activity
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of the last larval stage
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high activity
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mice with angiotensin converting enzyme expression only in the heart show atria enlargement and electrical conduction defects but normal ventricular function
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heart membrane, ACE activity is significantly higher in hearts of young Zucker rats than in those of Sprague-Dawley rats
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81211, 81212, 81213, 81217, 81225, 81236, 81237, 81238, 81240, 81241, 81249, 81278, 81288, 681545, 707029, 708183, 708199, 708800 brenda
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cortex
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activity is not correlated with the annual reproductive cycle phases
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ACE mRNA in the kidney is significantoly higher in the exercise rats than in the control rats
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highly expressed in the kidney
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proximal tubules
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cortex
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one enzyme form of 180000 Da
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high activity
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high ACE peptidase activity coincides with every transition state, from embryo to larva, from larva to larva and from larva to pupa
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weak activity
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angiotensin-converting enzyme inhibitor enhances the liver regeneration in rats after partial hepatectomy
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81209, 81211, 81213, 81225, 81231, 81236, 81238, 81241, 81248, 81249, 81256, 81282, 81288, 707147 brenda
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3 different enzyme forms: I, II, and III
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81209, 81211, 81214, 81218, 81221, 81222, 81226, 81227, 81230, 81256, 81257, 81258, 81259, 81276, 81281, 81287, 651263, 651335, 652613, 652614, 653414, 668985, 669020, 669023, 669026, 669033, 670519, 670730, 678863, 678955, 679858, 679936, 680284, 680295, 680316, 680317, 680328, 681097, 681160, 681163, 681344, 681562, 682248, 682306, 695571, 695798, 697524, 698406, 698416, 698423, 698425, 698426, 698430, 700690, 701430, 707653, 707697, 707764, 707811, 708537, 708825, 708837, 708857, 709304, 710252, 710591, 731965 brenda
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acetone powder
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activity is not correlated with the annual reproductive cycle phases
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81211, 81219, 81220, 81241, 81251, 81254, 81255, 81283, 668009, 695446, 699747 brenda
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81209, 81211, 81260, 81262, 81282, 652617, 669015, 669028, 680284, 707126, 710213 brenda
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high activity
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mice with expression of angiotensin convertzing enzyme only in monocytes and macrophages have a marked resistance to the growth of melanoma due to an enhanced immune response
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primary
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primary
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classical, CD14++CD16- cells
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mice with expression of angiotensin convertzing enzyme only in monocytes and macrophages have a marked resistance to the growth of melanoma due to an enhanced immune response
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weak activity
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weak activity
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activity shows the highest value among the different tissues with a significant peak in late-winter-early spring
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follicular granulosa cells, corpora lutea, germinal epithelium, ovarian blood vessels, high levels of activity on the surface of granulosa cells
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weak activity
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weak activity
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two distinct enzyme forms
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seminal plasma
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soluble form
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a peak of activity is present in the post-reproductive period both in male and female frogs
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from hind limb
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fetal skin
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weak activity
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weak activity
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immunolocalized in the acrosome
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testicular ACE is located in the plasma membrane of the post-acrosomal region, the neck and midpiece of normal spermatozoa, but shows a variable distribution on the defective cells
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germinal isozyme
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spermatogonial, somatic ACE (sACE), but not testicular ACE (tACE), is expressed in mouse testis before postpartum day 7
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activity follows a significant seasonal cycle, increasing from September to peak in April and then decreases in the post-reproductive period
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additional information
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expressed in all presumptive and developing bloodforming tissues of the human embryo and fetus: para-aortic splanchnopleura, yolk sac, aorta-gonad-mesonephros, liver, and bone marrow
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additional information
angiotensin-converting enzyme (ACE) is expressed as a type-1 membrane glycoprotein on the surface of endothelial and epithelial cells. ACE is also presents as a soluble form in biological fluids, among which seminal fluid being the richest in ACE content with 50fold higher content compared to blood
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additional information
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angiotensin-converting enzyme (ACE) is expressed as a type-1 membrane glycoprotein on the surface of endothelial and epithelial cells. ACE is also presents as a soluble form in biological fluids, among which seminal fluid being the richest in ACE content with 50fold higher content compared to blood
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additional information
highest relative level of ACE1 mRNA expression is observed in CD14++CD16- (classical) monocytes. In peripheral blood mononuclear cells (PBMC), monocytes and classical monocytes, ACE1 protein expression is stronger compared to other monocyte subpopulations. ACE1 expression is slightly more diverse than ACE2 (EC 3.4.17.23) levels, imune cell expression analysis
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additional information
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highest relative level of ACE1 mRNA expression is observed in CD14++CD16- (classical) monocytes. In peripheral blood mononuclear cells (PBMC), monocytes and classical monocytes, ACE1 protein expression is stronger compared to other monocyte subpopulations. ACE1 expression is slightly more diverse than ACE2 (EC 3.4.17.23) levels, imune cell expression analysis
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additional information
ACE colocalizes with beta-arrestin1
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additional information
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ACE colocalizes with beta-arrestin1
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additional information
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ACE colocalizes with beta-arrestin1
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additional information
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no enzyme detected in erythrocytes
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