FOXE1

Forkhead box E1
معرفات
أسماء بديلة	forkhead box protein E2, forkhead box protein E1, forkhead-related protein FKHL15, HFKL5, thyroid transcription factor 2, HFKH4, TTF-2, forkhead, drosophila, homolog-like 15, HNF-3/fork head-like protein 5, FOXE1
معرفات خارجية
تماثلات متسلسلة
	n/a
	n/a
	n/a
	n/a
	n/a
	n/a
	ويكي بيانات
اعرض/عدّل إنسان

FOXE1‏ (Forkhead box E1) هوَ بروتين يُشَفر بواسطة جين FOXE1 في الإنسان.^[1]^[2]^[3]

الوظيفة

الأهمية السريرية

المراجع

↑ Chadwick BP، Obermayr F، Frischauf AM (يوليو 1997). "FKHL15, a new human member of the forkhead gene family located on chromosome 9q22". Genomics. ج. 41 ع. 3: 390–6. DOI:10.1006/geno.1997.4692. PMID:9169137.
↑ Clifton-Bligh RJ، Wentworth JM، Heinz P، Crisp MS، John R، Lazarus JH، Ludgate M، Chatterjee VK (سبتمبر 1998). "Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia". Nat Genet. ج. 19 ع. 4: 399–401. DOI:10.1038/1294. PMID:9697705.
↑ "Entrez Gene: FOXE1 forkhead box E1 (thyroid transcription factor 2)". مؤرشف من الأصل في 2010-12-05.

قراءة متعمقة

Wiese S، Emmerich D، Schröder B، وآخرون (1997). "The novel human HNF-3/fork head-like 5 gene: chromosomal localization and expression pattern". DNA Cell Biol. ج. 16 ع. 2: 165–71. DOI:10.1089/dna.1997.16.165. PMID:9052737.
Zannini M، Avantaggiato V، Biffali E، وآخرون (1997). "TTF-2, a new forkhead protein, shows a temporal expression in the developing thyroid which is consistent with a role in controlling the onset of differentiation". EMBO J. ج. 16 ع. 11: 3185–97. DOI:10.1093/emboj/16.11.3185. PMC:1169936. PMID:9214635.
Macchia PE، Mattei MG، Lapi P، وآخرون (1999). "Cloning, chromosomal localization and identification of polymorphisms in the human thyroid transcription factor 2 gene (TITF2)". Biochimie. ج. 81 ع. 5: 433–40. DOI:10.1016/S0300-9084(99)80092-3. PMID:10403172.
Wang JC، Waltner-Law M، Yamada K، وآخرون (2000). "Transducin-like enhancer of split proteins, the human homologs of Drosophila groucho, interact with hepatic nuclear factor 3beta". J. Biol. Chem. ج. 275 ع. 24: 18418–23. DOI:10.1074/jbc.M910211199. PMID:10748198.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
Sequeira MJ، Morgan JM، Fuhrer D، وآخرون (2002). "Thyroid transcription factor-2 gene expression in benign and malignant thyroid lesions". Thyroid. ج. 11 ع. 11: 995–1001. DOI:10.1089/105072501753271662. PMID:11762722.
Castanet M، Park SM، Smith A، وآخرون (2003). "A novel loss-of-function mutation in TTF-2 is associated with congenital hypothyroidism, thyroid agenesis and cleft palate". Hum. Mol. Genet. ج. 11 ع. 17: 2051–9. DOI:10.1093/hmg/11.17.2051. PMID:12165566.
Sequeira M، Al-Khafaji F، Park S، وآخرون (2004). "Production and application of polyclonal antibody to human thyroid transcription factor 2 reveals thyroid transcription factor 2 protein expression in adult thyroid and hair follicles and prepubertal testis". Thyroid. ج. 13 ع. 10: 927–32. DOI:10.1089/105072503322511328. PMID:14611701.
Romanelli MG، Tato' L، Lorenzi P، Morandi C (2004). "Nuclear localization domains in human thyroid transcription factor 2". Biochim. Biophys. Acta. ج. 1643 ع. 1–3: 55–64. DOI:10.1016/j.bbamcr.2003.09.002. PMID:14654228.
Eichberger T، Regl G، Ikram MS، وآخرون (2004). "FOXE1, a new transcriptional target of GLI2 is expressed in human epidermis and basal cell carcinoma". J. Invest. Dermatol. ج. 122 ع. 5: 1180–7. DOI:10.1111/j.0022-202X.2004.22505.x. PMID:15140221.
Tonacchera M، Banco M، Lapi P، وآخرون (2005). "Genetic analysis of TTF-2 gene in children with congenital hypothyroidism and cleft palate, congenital hypothyroidism, or isolated cleft palate". Thyroid. ج. 14 ع. 8: 584–8. DOI:10.1089/1050725041692864. PMID:15320969.
Brancaccio A، Minichiello A، Grachtchouk M، وآخرون (2005). "Requirement of the forkhead gene Foxe1, a target of sonic hedgehog signaling, in hair follicle morphogenesis". Hum. Mol. Genet. ج. 13 ع. 21: 2595–606. DOI:10.1093/hmg/ddh292. PMID:15367491.
Watkins WJ، Harris SE، Craven MJ، وآخرون (2006). "An investigation into FOXE1 polyalanine tract length in premature ovarian failure". Mol. Hum. Reprod. ج. 12 ع. 3: 145–9. DOI:10.1093/molehr/gal017. PMID:16481406.
Baris I، Arisoy AE، Smith A، وآخرون (2006). "A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis". J. Clin. Endocrinol. Metab. ج. 91 ع. 10: 4183–7. DOI:10.1210/jc.2006-0405. PMID:16882747.

[pmid9169137-1] Chadwick BP، Obermayr F، Frischauf AM (يوليو 1997). "FKHL15, a new human member of the forkhead gene family located on chromosome 9q22". Genomics. ج. 41 ع. 3: 390–6. DOI:10.1006/geno.1997.4692. PMID:9169137.

[pmid9697705-2] Clifton-Bligh RJ، Wentworth JM، Heinz P، Crisp MS، John R، Lazarus JH، Ludgate M، Chatterjee VK (سبتمبر 1998). "Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia". Nat Genet. ج. 19 ع. 4: 399–401. DOI:10.1038/1294. PMID:9697705.

[entrez-3] "Entrez Gene: FOXE1 forkhead box E1 (thyroid transcription factor 2)". مؤرشف من الأصل في 2010-12-05.

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