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Gastrointestinal Mucosal Lymphoid Hyperplasia: Mutation in PIK3CD Gene.

07:00 EST 6th November 2019 | BioPortfolio

Summary of "Gastrointestinal Mucosal Lymphoid Hyperplasia: Mutation in PIK3CD Gene."

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Name: Journal of pediatric gastroenterology and nutrition
ISSN: 1536-4801
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Medical and Biotech [MESH] Definitions

An autosomal dominant disorder that is manifested by thickened spongiform ORAL MUCOSA with a white opalescent tint. Other MUCOSAL TISSUE may also be involved mucosa found in the VAGINA; RECTUM, and NASAL CAVITY may be similarly involved. This form of LEUKOKERATOSIS can be caused by a mutation in the gene for KERATIN 4 and is not considered a PRENEOPLASTIC CONDITION.

Mutation process that restores the wild-type PHENOTYPE in an organism possessing a mutationally altered GENOTYPE. The second "suppressor" mutation may be on a different gene, on the same gene but located at a distance from the site of the primary mutation, or in extrachromosomal genes (EXTRACHROMOSOMAL INHERITANCE).

Leukemia associated with HYPERPLASIA of the lymphoid tissues and increased numbers of circulating malignant LYMPHOCYTES and lymphoblasts.

A mutation that results in an increase in a gene's activity or in acquiring a new molecular function or a new pattern of gene expression.

Myeloid-lymphoid leukemia protein is a transcription factor that maintains high levels of HOMEOTIC GENE expression during development. The GENE for myeloid-lymphoid leukemia protein is commonly disrupted in LEUKEMIA and combines with over 40 partner genes to form FUSION ONCOGENE PROTEINS.

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