FOXE1

Forkhead box E1
المعرفات
الأسماء المستعارة	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
أورثولوج
	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]

المراجع

Chadwick BP, Obermayr F, Frischauf AM (يوليو 1997)، "FKHL15, a new human member of the forkhead gene family located on chromosome 9q22"، Genomics، 41 (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، 19 (4): 399–401، doi:10.1038/1294، PMID 9697705.
"Entrez Gene: FOXE1 forkhead box E1 (thyroid transcription factor 2)"، مؤرشف من الأصل في 05 ديسمبر 2010.

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.، 16 (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.، 16 (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، 81 (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.، 275 (24): 18418–23، doi:10.1074/jbc.M910211199، PMID 10748198.
Sequeira MJ, Morgan JM, Fuhrer D, وآخرون (2002)، "Thyroid transcription factor-2 gene expression in benign and malignant thyroid lesions."، Thyroid، 11 (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.، 11 (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، 13 (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، 1643 (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.، 122 (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، 14 (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.، 13 (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.، 12 (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.، 91 (10): 4183–7، doi:10.1210/jc.2006-0405، PMID 16882747.

بوابة علم الأحياء الخلوي والجزيئي
بوابة الكيمياء الحيوية
بوابة طب

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[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، 41 (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، 19 (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 05 ديسمبر 2010.