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Article title matches
- Category:Moco deficiency (46 bytes)
1: List of pages with the keyword Moco deficiency - Category:Ataxia with vitamin e deficiency (63 bytes)
1: ...t of pages with the keyword Ataxia with vitamin e deficiency - Category:Multiple sulfatase deficiency (60 bytes)
1: List of pages with the keyword Multiple sulfatase deficiency - Category:Inosine triphosphatase deficiency (64 bytes)
1: ... of pages with the keyword Inosine triphosphatase deficiency - Category:Pyrimidine 5-prime nucleotidase deficiency (73 bytes)
1: ... with the keyword Pyrimidine 5-prime nucleotidase deficiency - Category:Phosphoglycerate dehydrogenase deficiency (72 bytes)
1: ...s with the keyword Phosphoglycerate dehydrogenase deficiency - Category:Adenylosuccinase deficiency (58 bytes)
1: List of pages with the keyword Adenylosuccinase deficiency - Category:Methylmalonyl coa mutase deficiency (66 bytes)
1: ...f pages with the keyword Methylmalonyl coa mutase deficiency - Category:Coagulation factor deficiency (60 bytes)
1: List of pages with the keyword Coagulation factor deficiency - Category:Aadc deficiency (46 bytes)
1: List of pages with the keyword Aadc deficiency - Image:Pathology of G6PD deficiency.jpg (34 bytes)
1: Pathophysiology of G6PD deficiency - Category:Vitamin e deficiency (51 bytes)
1: List of pages with the keyword Vitamin e deficiency - Category:Cps1 deficiency (46 bytes)
1: List of pages with the keyword Cps1 deficiency - Category:Tap-deficiency (45 bytes)
1: List of pages with the keyword Tap-deficiency - Category:E3 deficiency (44 bytes)
1: List of pages with the keyword E3 deficiency - Category:Pyruvate dehydrogenase deficiency (64 bytes)
1: ... of pages with the keyword Pyruvate dehydrogenase deficiency - Investigating the Mechanisms of Active Site Mutations to the 1T9G WT MCAD Protein to Better Understand Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD) (12,666 bytes)
1: ...er Understand Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)" (2022). Protein Modeling Reports. 7.
5: ...tions contribute to Medium Acyl-CoA Dehydrogenase Deficiency (MCADD)?
9: ...ics/condition/medium-chain-acyl-coa-dehydrogenase-deficiency/</ref> Once mutated, the Acyl-CoA Dehydrogenase M...
13: ... needed to metabolize medium-chain fatty acids, a deficiency of this protein has effects ranging from hypoglyc...
19: ...ity in medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: Are predictions possible? Journal of inherited m... - Category:Deficiency (41 bytes)
1: List of pages with the keyword Deficiency - Image:Pathology of G6PD deficiency.png (106 bytes)
Page text matches
- Acetylcholine (3,078 bytes)
12: ...h various neurological disorders. For instance, a deficiency of acetylcholine is observed in Alzheimer's disea... - 1dan (5,989 bytes)
11: ..._HUMAN] Defects in F7 are the cause of factor VII deficiency (FA7D) [MIM:[https://omim.org/entry/227500 227500... - 2bok (3,718 bytes)
11: ...0_HUMAN] Defects in F10 are the cause of factor X deficiency (FA10D) [MIM:[https://omim.org/entry/227600 22760... - 2boh (5,419 bytes)
11: ...0_HUMAN] Defects in F10 are the cause of factor X deficiency (FA10D) [MIM:[https://omim.org/entry/227600 22760... - 2cn0 (7,541 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 1qrz (5,533 bytes)
10: ... The most common clinical manifestation of type 1 deficiency is ligneous conjunctivitis in which pseudomembran... - 2j2u (4,523 bytes)
11: ...0_HUMAN] Defects in F10 are the cause of factor X deficiency (FA10D) [MIM:[https://omim.org/entry/227600 22760... - 1zsc (3,768 bytes)
11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai... - 1zsb (3,881 bytes)
11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai... - 9k3k (2,250 bytes)
10: ...C4R_HUMAN] Obesity due to melanocortin 4 receptor deficiency. The disease is caused by mutations affecting the... - 1ad8 (7,631 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 2cf9 (7,729 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 2cf8 (7,737 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 2ald (2,878 bytes)
10: ...y/611881 611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased h... - 4ald (3,551 bytes)
11: ...y/611881 611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased h... - 4eca (3,673 bytes)
24: ...ediate. Kinetic analysis confirms the deacylation deficiency, which is also explained on a structural basis. T... - 1awf (7,921 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 1awh (7,597 bytes)
11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679... - 1avn (4,042 bytes)
11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai... - 1hkc (4,708 bytes)
11: ...) [MIM:[https://omim.org/entry/235700 235700]. HK deficiency is a rare autosomal recessive disease with nonsph...
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