FXR1
المظهر
FXR1 (FMR1 autosomal homolog 1) هوَ بروتين يُشَفر بواسطة جين FXR1 في الإنسان.[1][2][3][3]
الوظيفة
[عدل]هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
[عدل]هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
[عدل]- ^ Bolivar J، Guelman S، Iglesias C، Ortiz M، Valdivia MM (أغسطس 1998). "The fragile-X-related gene FXR1 is a human autoantigen processed during apoptosis". J Biol Chem. ج. 273 ع. 27: 17122–7. DOI:10.1074/jbc.273.27.17122. PMID:9642279.
{{استشهاد بدورية محكمة}}
: صيانة الاستشهاد: دوي مجاني غير معلم (link) - ^ Siomi MC، Siomi H، Sauer WH، Srinivasan S، Nussbaum RL، Dreyfuss G (يوليو 1995). "FXR1, an autosomal homolog of the fragile X mental retardation gene". EMBO J. ج. 14 ع. 11: 2401–8. PMC:398353. PMID:7781595.
- ^ ا ب "Entrez Gene: FXR1 fragile X mental retardation, autosomal homolog 1". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
[عدل]- Zhang Y، O'Connor JP، Siomi MC، وآخرون (1996). "The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2". EMBO J. ج. 14 ع. 21: 5358–66. PMC:394645. PMID:7489725.
- Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
- Coy JF، Sedlacek Z، Bächner D، وآخرون (1996). "Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1". Hum. Mol. Genet. ج. 4 ع. 12: 2209–18. DOI:10.1093/hmg/4.12.2209. PMID:8634689.
- Siomi MC، Zhang Y، Siomi H، Dreyfuss G (1996). "Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them". Mol. Cell. Biol. ج. 16 ع. 7: 3825–32. DOI:10.1128/mcb.16.7.3825. PMC:231379. PMID:8668200.
- Tamanini F، Willemsen R، van Unen L، وآخرون (1997). "Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis". Hum. Mol. Genet. ج. 6 ع. 8: 1315–22. DOI:10.1093/hmg/6.8.1315. PMID:9259278.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
- Khandjian EW، Bardoni B، Corbin F، وآخرون (1999). "Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis". Hum. Mol. Genet. ج. 7 ع. 13: 2121–8. DOI:10.1093/hmg/7.13.2121. PMID:9817930.
- Tamanini F، Bontekoe C، Bakker CE، وآخرون (1999). "Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations". Hum. Mol. Genet. ج. 8 ع. 5: 863–9. DOI:10.1093/hmg/8.5.863. PMID:10196376.
- Tamanini F، Van Unen L، Bakker C، وآخرون (2000). "Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P". Biochem. J. ج. 343 ع. 3: 517–23. DOI:10.1042/0264-6021:3430517. PMC:1220581. PMID:10527928.
- Bardoni B، Schenck A، Mandel JL (2000). "A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein". Hum. Mol. Genet. ج. 8 ع. 13: 2557–66. DOI:10.1093/hmg/8.13.2557. PMID:10556305.
- Ceman S، Brown V، Warren ST (2000). "Isolation of an FMRP-Associated Messenger Ribonucleoprotein Particle and Identification of Nucleolin and the Fragile X-Related Proteins as Components of the Complex". Mol. Cell. Biol. ج. 19 ع. 12: 7925–32. DOI:10.1128/mcb.19.12.7925. PMC:84877. PMID:10567518.
- Tamanini F، Kirkpatrick LL، Schonkeren J، وآخرون (2000). "The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins". Hum. Mol. Genet. ج. 9 ع. 10: 1487–93. DOI:10.1093/hmg/9.10.1487. PMID:10888599.
- Hartley JL، Temple GF، Brasch MA (2001). "DNA Cloning Using In Vitro Site-Specific Recombination". Genome Res. ج. 10 ع. 11: 1788–95. DOI:10.1101/gr.143000. PMC:310948. PMID:11076863.
- Schenck A، Bardoni B، Moro A، وآخرون (2001). "A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P". Proc. Natl. Acad. Sci. U.S.A. ج. 98 ع. 15: 8844–9. Bibcode:2001PNAS...98.8844S. DOI:10.1073/pnas.151231598. PMC:37523. PMID:11438699.
- Kirkpatrick LL، McIlwain KA، Nelson DL (2002). "Comparative genomic sequence analysis of the FXR gene family: FMR1, FXR1, and FXR2". Genomics. ج. 78 ع. 3: 169–77. DOI:10.1006/geno.2001.6667. PMID:11735223.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Imabayashi H، Mori T، Gojo S، وآخرون (2003). "Redifferentiation of dedifferentiated chondrocytes and chondrogenesis of human bone marrow stromal cells via chondrosphere formation with expression profiling by large-scale cDNA analysis". Exp. Cell Res. ج. 288 ع. 1: 35–50. DOI:10.1016/S0014-4827(03)00130-7. PMID:12878157.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.