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Create the page "1-pyrroline-4-hydroxy-2-carboxylate deaminase" on this wiki! See also the search results found.
Page title matches
- ...minase deficiency; MMDD; Adenosine monophosphate deaminase deficiency; AMP deaminase deficiency Adenosine monophosphate deaminase 1 (AMPD1) deficiency is an inherited condition that can affect the muscles4 KB (649 words) - 12:18, 27 November 2020
- ...iciency specifically involves a lack of the enzyme adenosine monophosphate deaminase, which plays a crucial role in the [[adenosine triphosphate]] (ATP) regener ...ations in the AMPD1 gene, which encodes the enzyme adenosine monophosphate deaminase. These genetic mutations lead to reduced activity or complete absence of th3 KB (351 words) - 04:06, 30 March 2024
- ...ations in the AMPD1 gene, which encodes the enzyme adenosine monophosphate deaminase 1, crucial for the [[adenosine triphosphate]] (ATP) regeneration process in ...ead to reduced activity or complete absence of the adenosine monophosphate deaminase enzyme, which plays a critical role in the purine nucleotide cycle, essenti3 KB (363 words) - 16:40, 24 April 2024
Page text matches
- ...ro-9-(2-'''h'''ydroxy-3-'''n'''onyl)'''a'''denine) is a potent [[adenosine deaminase]] inhibitor,<ref>{{cite web|title=Sigma Aldrich|url=http://www.sigmaaldrich1 KB (155 words) - 05:41, 26 September 2023
- ...It is characterized by the absence or mutation of the enzyme myoadenylate deaminase, which plays a crucial role in the [[adenosine triphosphate]] (ATP) regener The primary symptoms associated with Myoadenylate Deaminase Deficiency include muscle pain, weakness, fatigue, and sometimes muscle cra3 KB (372 words) - 05:35, 28 March 2024
- ...minase deficiency; MMDD; Adenosine monophosphate deaminase deficiency; AMP deaminase deficiency Adenosine monophosphate deaminase 1 (AMPD1) deficiency is an inherited condition that can affect the muscles4 KB (649 words) - 12:18, 27 November 2020
- '''Dipeptidyl peptidase 4''' (DPP-4), also known as '''adenosine deaminase complexing protein 2''' or '''CD26''', is a [[protein]] that in humans is e2 KB (308 words) - 04:28, 30 March 2024
- ...to [[deoxyuridine]]. Cytidine deaminase is part of the larger family of [[deaminase]] enzymes, which are involved in removing [[amine]] groups from molecules. Cytidine deaminase catalyzes the hydrolytic deamination of cytidine and deoxycytidine to uridi3 KB (356 words) - 02:46, 28 March 2024
- ...nd [[DNA methyltransferase inhibitor]], and [[cedazuridine]], a [[cytidine deaminase inhibitor]]. Following oral administration, cedazuridine inhibits the action of cytidine deaminase in the gut and liver, allowing more decitabine to reach the systemic circul2 KB (244 words) - 13:36, 8 March 2024
- * '''[[Adenosine Deaminase 2 deficiency]]''' * '''[[Adenosine deaminase deficiency]]'''7 KB (911 words) - 22:53, 18 September 2019
- * '''[[Adenosine Deaminase 2 deficiency]]''' * '''[[Adenosine deaminase deficiency]]'''7 KB (908 words) - 15:26, 21 June 2020
- ...problems. For example, an excess of deoxyadenosine can lead to [[adenosine deaminase deficiency]], a genetic disorder that results in [[immunodeficiency]]. On t * [[Adenosine deaminase deficiency]]2 KB (206 words) - 15:53, 22 February 2024
- ...ations in the AMPD1 gene, which encodes the enzyme adenosine monophosphate deaminase 1, crucial for the [[adenosine triphosphate]] (ATP) regeneration process in ...ead to reduced activity or complete absence of the adenosine monophosphate deaminase enzyme, which plays a critical role in the purine nucleotide cycle, essenti3 KB (363 words) - 16:40, 24 April 2024
- | name = Adenosine deaminase deficiency ...=Hirschhorn R, Vawter GF, ((Kirkpatrick JA Jr)), Rosen FS |title=Adenosine deaminase deficiency: frequency and comparative pathology in autosomally recessive se9 KB (1,109 words) - 18:01, 20 February 2024
- ...iciency specifically involves a lack of the enzyme adenosine monophosphate deaminase, which plays a crucial role in the [[adenosine triphosphate]] (ATP) regener ...ations in the AMPD1 gene, which encodes the enzyme adenosine monophosphate deaminase. These genetic mutations lead to reduced activity or complete absence of th3 KB (351 words) - 04:06, 30 March 2024
- '''Other Names:''' AIP; Porphobilinogen deaminase deficiency; PBGD deficiency; Uroporphyrinogen synthase deficiency; UPS defi ...(hepatic) [[porphyrias]]. AIP is caused by low levels of [[porphobilinogen deaminase]] (PBGD), an enzyme also often called [[hydroxymethylbilane synthase]]. The4 KB (502 words) - 16:17, 23 June 2020
- ...''a nucleoside metabolic inhibitor''', and [[cedazuridine]], '''a cytidine deaminase inhibitor''' used to treat adults with [[myelodysplastic syndromes]] (MDS), Inqovi is a type of antimetabolite and a type of''' cytidine deaminase inhibitor'''.6 KB (861 words) - 07:52, 22 June 2022
- * [[Adenosine deaminase deficiency]] | Pegademase || Adagen || Adenosine Deaminase || 2000 || ADA Deficiency5 KB (542 words) - 03:19, 4 September 2023
- Adenosine Deaminase 2 deficiency is an inherited disorder causing [[inflammation]] in the body, Adenosine deaminase 2 (ADA2) deficiency is a disorder characterized by abnormal inflammation of9 KB (1,132 words) - 10:09, 3 August 2020
- * '''[[Adenosine deaminase deficiency]]''' * '''[[Adenosine monophosphate deaminase 1 deficiency]]'''22 KB (2,804 words) - 22:50, 18 September 2019
- * '''[[Adenosine Deaminase 2 deficiency]]'''14 KB (1,803 words) - 22:13, 18 September 2019
- * '''[[Adenosine Deaminase 2 deficiency]]'''15 KB (1,827 words) - 14:57, 21 June 2020
- * [[Adenosine deaminase 2 deficiency]]4 KB (399 words) - 20:46, 11 November 2023