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2024年12月25日 · NFIX (Nuclear Factor I X) is a Protein Coding gene. Diseases associated with NFIX include Malan Syndrome and Marshall-Smith Syndrome. Among its related pathways are …

Nuclear factor 1 X-type is a protein that in humans is encoded by the NFIX gene. [5] [6] [7] NFI-X3, a splice variant of NFIX, regulates Glial fibrillary acidic protein and YKL-40 in astrocytes. [8]

2023年8月23日 · Nfix deficiency results in a loss of long-term hematopoietic stem cells and an accumulation of megakaryocyte and myelo-erythroid progenitors. NFIX interacts with PU.1 at …

NFIX provides a selection of phone cases and covers designed to protect your device from scratches, drops, and other forms of damage. They may offer a variety of styles, materials, …

Pathogenic variant in NFIX gene affecting three sisters due to paternal mosaicism. Excess of de novo variants in genes involved in chromatin remodelling in patients with marfanoid habitus …