Citations for
1TNXB, VUR8
TNXB mutations can cause vesicoureteral reflux.
Gbadegesin RA, Brophy PD, Adeyemo A, Hall G, Gupta IR, Hains D, Bartkowiak B, Rabinovich CE, Chandrasekharappa S, Homstad A, Westreich K, Wu G, Liu Y, Holanda D, Clarke J, Lavin P, Selim A, Miller S, Wiener JS, Ross SS, Foreman J, Rotimi C, Winn MP.
J Am Soc Nephrol 24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25. 2013
2EDSL1, TNXB
Phenotypic effects of Ehlers-Danlos syndrome-associated mutation on the FnIII domain of tenascin-X.
Zhuang S, Linhananta A, Li H.
Protein Sci 19(11):2231-9. 2010
3EDSL1, TNXB
Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.
Huijing PA, Voermans NC, Baan GC, BusÚ TE, van Engelen BG, de Haan A.
J Appl Physiol 109(4):986-95. Epub 2010 Jun 24. 2010
4TNXB
Tenascin-X increases the stiffness of collagen gels without affecting fibrillogenesis.
Margaron Y, Bostan L, Exposito JY, Malbouyres M, Trunfio-Sfarghiu AM, Berthier Y, Lethias C.
Biophys Chem 147(1-2):87-91. Epub 2010 Jan 4. 2010
5KIF11, TNXB
Truncated form of tenascin-X, XB-S, interacts with mitotic motor kinesin Eg5.
Endo T, Ariga H, Matsumoto K.
Mol Cell Biochem 320(1-2):53-66. Epub 2008 Aug 5. 2009
6TNXB
Tenascin-X is a novel diagnostic marker of malignant mesothelioma.
Yuan Y, Nymoen DA, Stavnes HT, Rosnes AK, Bj°rang O, Wu C, Nesland JM, Davidson B.
Am J Surg Pathol 33(11):1673-82. 2009
7TNXB
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
Kamatani Y, Matsuda K, Ohishi T, Ohtsubo S, Yamazaki K, Iida A, Hosono N, Kubo M, Yumura W, Nitta K, Katagiri T, Kawaguchi Y, Kamatani N, Nakamura Y.
J Hum Genet 53(1):64-73. Epub 2007 Dec 6. 2008
8TNXB
Novel localization of tenascin-X in adult mouse leptomeninges and choroid plexus.
Imura K, Sato I.
Ann Anat 190(4):324-8. Epub 2008 May 27. 2008
9TNXB
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
Kamatani Y, Matsuda K, Ohishi T, Ohtsubo S, Yamazaki K, Iida A, Hosono N, Kubo M, Yumura W, Nitta K, Katagiri T, Kawaguchi Y, Kamatani N, Nakamura Y.
J Hum Genet Hum Genet. 2008 2008
10TNXB
Wound healing in tenascin-X deficient mice suggests that tenascin-X is involved in matrix maturation rather than matrix deposition.
Egging D, van Vlijmen-Willems I, van Tongeren T, Schalkwijk J, Peeters A.
Connect Tissue Res 48(2):93-8. 2007
11TNXB
Identification and characterization of multiple species of tenascin-X in human serum.
Egging DF, Peeters AC, Grebenchtchikov N, Geurts-Moespot A, Sweep CG, den Heijer M, Schalkwijk J.
FEBS J 274(5):1280-9. Epub 2007 Jan 29. 2007
12TNXB
A model of tenascin-X integration within the collagenous network.
Lethias C, Carisey A, Comte J, Cluzel C, Exposito JY.
FEBS Lett 580(26):6281-5. Epub 2006 Oct 26. 2006
13TNXB, EDSL1
Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations.
Zweers MC, Dean WB, van Kuppevelt TH, Bristow J, Schalkwijk J.
Clin Genet 67(4):330-4. 2005
14NFKBIL1, TNXB, NOTCH4, MRPL48, PAAF1, UCP2, OPTN, CCDC3, LTB4R2
Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.
Tamiya G, Shinya M, Imanishi T, Ikuta T, Makino S, Okamoto K, Furugaki K, Matsumoto T, Mano S, Ando S, Nozaki Y, Yukawa W, Nakashige R, Yamaguchi D, Ishibashi H, Yonekura M, Nakami Y, Takayama S, Endo T, Saruwatari T, Yagura M, Yoshikawa Y, Fujimoto K, Oka A, Chiku S, Linsen SE, Giphart MJ, Kulski JK, Fukazawa T, Hashimoto H, Kimura M, Hoshina Y, Suzuki Y, Hotta T, Mochida J, Minezaki T, Komai K, Shiozawa S, Taniguchi A, Yamanaka H, Kamatani N, Gojobori T, Bahram S, Inoko H.
Hum Mol Genet 14(16):2305-21. Epub 2005 Jul 6. 2005
15TNXB, EDSL1
Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.
Zweers MC, van Vlijmen-Willems IM, van Kuppevelt TH, Mecham RP, Steijlen PM, Bristow J, Schalkwijk J.
J Invest Dermatol 122(4):885-91. 2004
16EDSL1, TNXB
A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J.
N Engl J Med 345(16):1167-75. 2001
17TNXA, TNXB
Allelic polymorphism of two multifunctional regions in the central human MHC: tenascin X, XB-S and YB, and their duplicated fragments XA and YA.
Weissensteiner T, Lanchbury JS.
Eur J Immunogenet 24(3):201-9. 1997
18EDSL1, TNXB
Tenascin-X deficiency is associated with Ehlers-Danlos syndrome.
Burch GH, Gong Y, Liu W, Dettman RW, Curry CJ, Smith L, Miller WL, Bristow J.
Nat Genet 17(1):104-8. 1997
19ATF6B, CYP21A1P, TNXB
Alternate promoters and alternate splicing of human tenascin-X, a gene with 5' and 3' ends buried in other genes.
Speek M, et al.
Hum Mol Genet 5 : 1749-1758. 1996
20C4A, C4B, TNXA, TNXB
A promoter within intron 35 of the human C4A gene initiates abundant adrenal-specific transcription of a 1 kb RNA : location of a cryptic CYP21 promoter element ?
Tee MK, et al.
Hum Mol Genet 4 : 2109-2116. 1995
21TNXB
Sequences promoting the transcription of the human XA gene overlapping P450c21A correctly predict the presence of a novel, adrenal-specific, truncated form of tenascin-X.
Tee MK, et al.
Genomics 28 : 171-178. 1995
22TNXA, TNXB
Tenascin-X : a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B.
Bristow J, et al.
J Cell Biol 122 : 265-278. 1993
23TNXA,TNXB
Extracellular matrix protein tenascin-like gene found in human MHC class III region.
Matsumoto K, et al.
Immunogenetics 36 : 400-403. 1992
24TNXA, TNXB
Cluster of fibronectin type III repeats found in the human major histocompatibility complex class III region shows the highest homology with repeats in an extracellular matrix protein tenascin.
Matsumoto K, et al.
Genomics 12 : 485-491. 1992
25TNXA, TNXB
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.
Morel Y, et al.
Proc Natl Acad Sci U S A 86 : 6582-6586. 1989