When.com Web Search

  1. Ad

    related to: clinical significance of acid phosphatase therapy

Search results

  1. Results From The WOW.Com Content Network
  2. PPAP2B - Wikipedia

    en.wikipedia.org/wiki/PPAP2B

    Lipid phosphate phosphohydrolase 3 (LPP3), also known as phospholipid phosphatase 3 (PLPP3) and phosphatidic acid phosphatase type 2B (PAP-2b or PPAP2B), is an enzyme that in humans is encoded by the PPAP2B gene on chromosome 1. [5] [6] [7] It is ubiquitously expressed in many tissues and cell types. [8]

  3. ACP1 - Wikipedia

    en.wikipedia.org/wiki/ACP1

    Clinical significance [ edit ] Clinically, increased expression of ACP1 is a biomarker for poor prognosis in prostate cancer has been linked to worse clinical behaviour of prostate cancer, possibly outperforming the widely used Gleason grading system with respect to this important parameter. [ 6 ]

  4. Acid phosphatase - Wikipedia

    en.wikipedia.org/wiki/Acid_phosphatase

    Acid phosphatase (EC 3.1.3.2, systematic name phosphate-monoester phosphohydrolase (acid optimum)) is an enzyme that frees attached phosphoryl groups from other molecules during digestion. It can be further classified as a phosphomonoesterase .

  5. PTEN (gene) - Wikipedia

    en.wikipedia.org/wiki/PTEN_(gene)

    PTEN acts as a tumor suppressor gene through the action of its phosphatase protein product. This phosphatase is involved in the regulation of the cell cycle, preventing cells from growing and dividing too rapidly. [8] It is a target of many anticancer drugs. The protein encoded by this gene is a phosphatidylinositol-3,4,5-trisphosphate 3 ...

  6. PTPN1 - Wikipedia

    en.wikipedia.org/wiki/PTPN1

    Tyrosine-protein phosphatase non-receptor type 1 also known as protein-tyrosine phosphatase 1B (PTP1B) is an enzyme that is the founding member of the protein tyrosine phosphatase (PTP) family. In humans it is encoded by the PTPN1 gene . [ 5 ]

  7. ALPL - Wikipedia

    en.wikipedia.org/wiki/ALPL

    The severity of symptoms ranges from premature loss of deciduous teeth with no bone abnormalities to stillbirth [18] depending upon which amino acid [19] [20] is changed in the ALPL gene. Mutations in the ALPL gene lead to varying low activity of the enzyme tissue-nonspecific alkaline phosphatase (TNSALP or TNAP) resulting in hypophosphatasia ...

  8. Alkaline phosphatase, placental type - Wikipedia

    en.wikipedia.org/wiki/Alkaline_phosphatase...

    The coding sequence for this form of alkaline phosphatase is unique in that the 3' untranslated region contains multiple copies of an Alu family repeat. In addition, this gene is polymorphic and three common alleles (type 1, type 2, and type 3) for this form of alkaline phosphatase have been well-characterized.

  9. Phosphoglycerate mutase - Wikipedia

    en.wikipedia.org/wiki/Phosphoglycerate_mutase

    PGM is an isomerase enzyme, effectively transferring a phosphate group (PO 4 3−) from the C-3 carbon of 3-phosphoglycerate to the C-2 carbon forming 2-phosphoglycerate.There are a total of three reactions dPGM can catalyze: a mutase reaction resulting in the conversion of 3PG to 2PG and vice versa, [4] [5] a phosphatase reaction creating phosphoglycerate from 2,3-bisphosphoglycerate, [6] [7 ...