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  2. Chromogranin-A - Wikipedia

    en.wikipedia.org/wiki/Chromogranin-A

    Chromogranin-A (CgA) or parathyroid secretory protein 1 is encoded in the human by the gene CHGA. Cga is a member of the granin family of neuroendocrine secretory proteins. As such, it is located in secretory vesicles of neurons and endocrine cells such as islet beta cell secretory granules in the pancreas.

  3. Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

    en.wikipedia.org/wiki/Diffuse_idiopathic...

    High-resolution CT scan: diffuse pulmonary nodules 4–10 mm, greater than 20 nodules, mosaic attenuation or air trapping in greater than 50% of the lung; Transbronchial biopsy: proliferation of pulmonary neuroendocrine cells; Serum markers: elevated serum chromogranin A levels

  4. Pheochromocytoma - Wikipedia

    en.wikipedia.org/wiki/Pheochromocytoma

    In comparison to the specificity of elevated catecholamines in the pheochromocytoma patient, chromogranin A is a non-specific polypeptide that is high in a variety of neuroendocrine tumors. [72] However, a 2006 report from Italy found that over 90% of studied pheochromocytoma patients demonstrated elevated chromogranin A levels. [73]

  5. Doctors Say This Is How You Can Loosen and Clear Mucus From ...

    www.aol.com/doctors-loosen-clear-mucus-chest...

    If your symptoms persist for more than 10 days If you experience difficulty breathing, develop a severe cough, notice thick green or yellow mucus, run a fever, and/or feel extremely fatigued

  6. Pancreatic neuroendocrine tumor - Wikipedia

    en.wikipedia.org/wiki/Pancreatic_neuroendocrine...

    Up to 90% [12] of PanNETs are nonsecretory or nonfunctional, in which there is no secretion, or the quantity or type of products, such as pancreatic polypeptide (PPoma), chromogranin A, and neurotensin, do not cause a clinical syndrome although blood levels may be elevated. [13] In total, 85% of PanNETs have an elevated blood marker. [2]

  7. Carcinoid syndrome - Wikipedia

    en.wikipedia.org/wiki/Carcinoid_syndrome

    Carcinoid syndrome is a paraneoplastic syndrome comprising the signs and symptoms that occur secondary to neuroendocrine tumors (formerly known as carcinoid tumors). [1] The syndrome is caused by neuroendocrine tumors most often found in the gut releasing biologically active substances into the blood causing symptoms such as flushing and diarrhea, and less frequently, heart failure, vomiting ...

  8. Neuroendocrine tumor - Wikipedia

    en.wikipedia.org/wiki/Neuroendocrine_tumor

    High levels of CDX2, a homeobox gene product essential for intestinal development and differentiation, are seen in intestinal NETs. Neuroendocrine secretory protein-55, a member of the chromogranin family, is seen in pancreatic endocrine tumors but not intestinal NETs. [62]

  9. Granin - Wikipedia

    en.wikipedia.org/wiki/Granin

    Granin (chromogranin and secretogranin) is a protein family of regulated secretory proteins ubiquitously found in the cores of amine and peptide hormone and neurotransmitter dense-core secretory vesicles.

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