Search results

From Proteopedia

There is no page with the exact title "Deficiency". The search results for "Deficiency" are displayed below. You can create a page titled Deficiency (by clicking on the red link).

For more information about searching Proteopedia, see Help.

Showing below up to 20 results starting with #1.

Article title matches

1. Category:Moco deficiency (46 bytes)
   1: List of pages with the keyword Moco deficiency
2. Category:Ataxia with vitamin e deficiency (63 bytes)
   1: ...t of pages with the keyword Ataxia with vitamin e deficiency
3. Category:Multiple sulfatase deficiency (60 bytes)
   1: List of pages with the keyword Multiple sulfatase deficiency
4. Category:Inosine triphosphatase deficiency (64 bytes)
   1: ... of pages with the keyword Inosine triphosphatase deficiency
5. Category:Pyrimidine 5-prime nucleotidase deficiency (73 bytes)
   1: ... with the keyword Pyrimidine 5-prime nucleotidase deficiency
6. Category:Phosphoglycerate dehydrogenase deficiency (72 bytes)
   1: ...s with the keyword Phosphoglycerate dehydrogenase deficiency
7. Category:Adenylosuccinase deficiency (58 bytes)
   1: List of pages with the keyword Adenylosuccinase deficiency
8. Category:Methylmalonyl coa mutase deficiency (66 bytes)
   1: ...f pages with the keyword Methylmalonyl coa mutase deficiency
9. Category:Coagulation factor deficiency (60 bytes)
   1: List of pages with the keyword Coagulation factor deficiency
10. Insulin Deficiency Syndrome (36 bytes)
11. Category:Aadc deficiency (46 bytes)
    1: List of pages with the keyword Aadc deficiency
12. Image:Pathology of G6PD deficiency.jpg (34 bytes)
    1: Pathophysiology of G6PD deficiency
13. Category:Vitamin e deficiency (51 bytes)
    1: List of pages with the keyword Vitamin e deficiency
14. Category:Cps1 deficiency (46 bytes)
    1: List of pages with the keyword Cps1 deficiency
15. Category:Tap-deficiency (45 bytes)
    1: List of pages with the keyword Tap-deficiency
16. Category:E3 deficiency (44 bytes)
    1: List of pages with the keyword E3 deficiency
17. Category:Pyruvate dehydrogenase deficiency (64 bytes)
    1: ... of pages with the keyword Pyruvate dehydrogenase deficiency
18. 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...
19. Category:Deficiency (41 bytes)
    1: List of pages with the keyword Deficiency
20. Image:Pathology of G6PD deficiency.png (106 bytes)

Page text matches

1. Acetylcholine (3,078 bytes)
   12: ...h various neurological disorders. For instance, a deficiency of acetylcholine is observed in Alzheimer's disea...
2. 1dan (4,927 bytes)
   11: ..._HUMAN] Defects in F7 are the cause of factor VII deficiency (FA7D) [MIM:[https://omim.org/entry/227500 227500...
3. 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...
4. 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...
5. 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...
6. 1qrz (4,330 bytes)
   10: ... The most common clinical manifestation of type 1 deficiency is ligneous conjunctivitis in which pseudomembran...
7. 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...
8. 1zsc (3,768 bytes)
   11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai...
9. 1zsb (3,881 bytes)
   11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai...
10. 1ad8 (5,218 bytes)
    11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679...
11. 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...
12. 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...
13. 2ald (2,878 bytes)
    10: ...y/611881 611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased h...
14. 4ald (3,551 bytes)
    11: ...y/611881 611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased h...
15. 4eca (3,673 bytes)
    24: ...ediate. Kinetic analysis confirms the deacylation deficiency, which is also explained on a structural basis. T...
16. 1awf (5,272 bytes)
    11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679...
17. 1awh (5,017 bytes)
    11: ...B_HUMAN] Defects in F2 are the cause of factor II deficiency (FA2D) [MIM:[https://omim.org/entry/613679 613679...
18. 1avn (4,042 bytes)
    11: ...ith renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brai...
19. 1hkc (4,708 bytes)
    11: ...) [MIM:[https://omim.org/entry/235700 235700]. HK deficiency is a rare autosomal recessive disease with nonsph...
20. 1hkb (2,998 bytes)
    11: ...) [MIM:[https://omim.org/entry/235700 235700]. HK deficiency is a rare autosomal recessive disease with nonsph...

View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)