CRYM
CRYM (Crystallin mu) هوَ بروتين يُشَفر بواسطة جين CRYM في الإنسان.[1][2]
الوظيفة
الأهمية السريرية
المراجع
- ^ "Entrez Gene: CRYM crystallin, mu". مؤرشف من الأصل في 2010-12-05.
- ^ Chen H، Phillips HA، Callen DF، Kim RY، Wistow GJ، Antonarakis SE (فبراير 1993). "Localization of the human gene for mu-crystallin to chromosome 16p". Genomics. ج. 14 ع. 4: 1115–6. DOI:10.1016/S0888-7543(05)80143-0. PMID:1478656.
قراءة متعمقة
- Kim RY، Gasser R، Wistow GJ (1992). "mu-crystallin is a mammalian homologue of Agrobacterium ornithine cyclodeaminase and is expressed in human retina". Proc. Natl. Acad. Sci. U.S.A. ج. 89 ع. 19: 9292–6. DOI:10.1073/pnas.89.19.9292. PMC:50112. PMID:1384048.
- Vié MP، Blanchet P، Samson M، وآخرون (1996). "High affinity thyroid hormone-binding protein in human kidney: kinetic characterization and identification by photoaffinity labeling". Endocrinology. ج. 137 ع. 11: 4563–70. DOI:10.1210/en.137.11.4563. PMID:8895318.
- Segovia L، Horwitz J، Gasser R، Wistow G (1998). "Two roles for mu-crystallin: a lens structural protein in diurnal marsupials and a possible enzyme in mammalian retinas". Mol. Vis. ج. 3: 9. PMID:9285773.
- Vié MP، Evrard C، Osty J، وآخرون (1998). "Purification, molecular cloning, and functional expression of the human nicodinamide-adenine dinucleotide phosphate-regulated thyroid hormone-binding protein". Mol. Endocrinol. ج. 11 ع. 11: 1728–36. DOI:10.1210/me.11.11.1728. PMID:9328354.
- Loftus BJ، Kim UJ، Sneddon VP، وآخرون (1999). "Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16q". Genomics. ج. 60 ع. 3: 295–308. DOI:10.1006/geno.1999.5927. PMID:10493829.
- Abe S، Katagiri T، Saito-Hisaminato A، وآخرون (2003). "Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissues". Am. J. Hum. Genet. ج. 72 ع. 1: 73–82. DOI:10.1086/345398. PMC:420014. PMID:12471561.
- 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. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- 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.
- Reed PW، Corse AM، Porter NC، وآخرون (2007). "Abnormal expression of mu-crystallin in facioscapulohumeral muscular dystrophy". Exp. Neurol. ج. 205 ع. 2: 583–6. DOI:10.1016/j.expneurol.2007.03.009. PMID:17451686.