Serum alkaline phosphatase of intestinal origin in patients with cancer and with cirrhosis of the liver

Fishman, William H.; Inglis, Norma I.; Krant, Melvin J.

doi:10.1016/0009-8981(65)90049-5

Cited by 89 publications

(10 citation statements)

References 9 publications

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“…Langman et al [36] found similar results but not as high a percentage of inhibition as Fishman, Inglis and Krant [23]. Langman et al [36] classified individual sera as p°, p+, p++, and found the mean percent age of inhibition by L-phenylalanine in each to be 15.4%, 22.9% and 28.6%, respectively.…”

Section: Intestinal Phosphatase : L-phenylalanine Inhibitionsupporting

confidence: 60%

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Genetically Determined Variants of Serum Alkaline Phosphatase: A Review

Robinson¹,

Goldsmith²

1967

Vox Sanguinis

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Section: Intestinal Phosphatase : L-phenylalanine Inhibitionsupporting

confidence: 60%

“…Fishman, Inglis and Krant [23] found that 20-65% of the alkaline phosphatase in normal sera was inhibited by L-phenylalanine. Langman et al [36] found similar results but not as high a percentage of inhibition as Fishman, Inglis and Krant [23].…”

Section: Intestinal Phosphatase : L-phenylalanine Inhibitionmentioning

confidence: 99%

Genetically Determined Variants of Serum Alkaline Phosphatase: A Review

Robinson¹,

Goldsmith²

1967

Vox Sanguinis

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“…The first report of the intestinal band in cirrhosis was by Fishman, Inglis, and Krant (1965). Their patients were of blood groups B and 0: other series (Kaplan and Rogers, 1969) have confirmed their finding.…”

Section: Methodsmentioning

confidence: 81%

Plasma alkaline phosphatase isoenzymes in hepatobiliary disease

Afonja

Baron

1974

J Clin Pathol

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By cellulose acetate or acrylamide gel electrophoresis it is possible to separate these alkaline phosphatase isoenzymes from serum: [anode] fast liver, slow liver, placenta/Regan, bone, intestine, bile [cathode]. Heat or chemical inhibition can confirm the differentiation.Normal adult serum always contains slow-liver isoenzyme, and sometimes bone isoenzyme: the latter is always present in serum of children. In hepatobiliary disease slow-liver isoenzyme was always increased: intestinal isoenzyme appeared in many cases of cirrhosis (of blood groups B and 0) but fast-liver and bile isoenzymes were occasionally seen in miscellaneous cases. The findings in other diseases included Regan isoenzyme in six out of 45 cases of malignant disease.

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“…Increased serum intestinal alkaline phosphatase levels have been noted in hepatic cirrhosis and in cancer patients (Fishman et al, 1965).…”

Section: Enzyme Polymorpffismsmentioning

confidence: 99%

Recent Advances in Clinical Enzymology

Rosalki

1970

Ann Clin Biochem

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The past year has seen a wider application of knowledge originating over the last decade rather than startling new developments. For brevity, only serum enzymes will be considered and the points at which progress is being made are indicated by the sectional headings which follow. ENZYME METHODOLOGY Considerable change is taking place in established enzyme methods and new forms of methodology are being developed. Colorimetric kinetic assays

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Serum alkaline phosphatase of intestinal origin in patients with cancer and with cirrhosis of the liver

Cited by 89 publications

References 9 publications

Genetically Determined Variants of Serum Alkaline Phosphatase: A Review

Genetically Determined Variants of Serum Alkaline Phosphatase: A Review

Plasma alkaline phosphatase isoenzymes in hepatobiliary disease

Recent Advances in Clinical Enzymology

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