fmr1 gene - Axtarish в Google
FMR1 Ген FMR1
FMR1 — это человеческий ген, который кодирует белок, называемый хрупким рибонуклеопротеином-мессенджером X, или FMRP. Этот белок, чаще всего встречающийся в головном мозге, необходим для нормального когнитивного развития и женской репродуктивной... Википедия (Английский язык)
FMR1 (Fragile X Messenger Ribonucleoprotein 1) is a human gene that codes for a protein called fragile X messenger ribonucleoprotein, or FMRP. ... This protein, ... Function · Gene expression · Related conditions
6 дней назад · The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from ...
FMR1 (Fragile X Messenger Ribonucleoprotein 1) is a Protein Coding gene. Diseases associated with FMR1 include Fragile X Syndrome and Premature Ovarian Failure ...
16 мая 2024 г. · FMR1 related disorders are caused by CGG trinucleotide repeat expansion in the 5' UTR of FMR1 with abnormal gene methylation for most alleles ...
1 апр. 2020 г. · The FMR1 gene provides instructions for making a protein called FMRP. This protein is present in many tissues, including the brain, testes, ...
... FMR1 gene to form an RNA/DNA duplex. Disrupting the interaction of the mRNA with the CGG-repeat portion of the FMR1 gene prevents promoter silencing. Colak ...
15 мая 2024 г. · FXS is caused by a change (mutation) in the fragile X messenger ribonucleoprotein 1 (FMR1) gene. The FMR1 gene makes a protein called FMRP that ...
FMR1 is a cause of fragile X syndrome and is the most common genetic linkage associated with autism spectrum disorders (Kaufmann et al., 2017). FMR1 is located ...
The FMR1 gene is responsible for the production of the FMR1 protein (FMRP), which is an mRNA-binding and -carrier protein that stabilizes mRNAs but also ...
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