| 1 | TNXB, VUR8
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| TNXB mutations can cause vesicoureteral reflux.
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| 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.
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| J Am Soc Nephrol 24(8):1313-22. doi: 10.1681/ASN.2012121148. Epub 2013 Apr 25.
2013
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| 2 | EDSL1, TNXB
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| Phenotypic effects of Ehlers-Danlos syndrome-associated mutation on the FnIII domain of tenascin-X.
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| Zhuang S, Linhananta A, Li H.
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| Protein Sci 19(11):2231-9.
2010
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| 3 | EDSL1, TNXB
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| Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.
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| Huijing PA, Voermans NC, Baan GC, Busé TE, van Engelen BG, de Haan A.
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| J Appl Physiol 109(4):986-95. Epub 2010 Jun 24.
2010
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| 4 | TNXB
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| Tenascin-X increases the stiffness of collagen gels without affecting fibrillogenesis.
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| Margaron Y, Bostan L, Exposito JY, Malbouyres M, Trunfio-Sfarghiu AM, Berthier Y, Lethias C.
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| Biophys Chem 147(1-2):87-91. Epub 2010 Jan 4.
2010
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| 5 | KIF11, TNXB
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| Truncated form of tenascin-X, XB-S, interacts with mitotic motor kinesin Eg5.
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| Endo T, Ariga H, Matsumoto K.
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| Mol Cell Biochem 320(1-2):53-66. Epub 2008 Aug 5.
2009
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| 6 | TNXB
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| Tenascin-X is a novel diagnostic marker of malignant mesothelioma.
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| Yuan Y, Nymoen DA, Stavnes HT, Rosnes AK, Bjørang O, Wu C, Nesland JM, Davidson B.
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| Am J Surg Pathol 33(11):1673-82.
2009
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| 7 | TNXB
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| Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
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| 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.
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| J Hum Genet 53(1):64-73. Epub 2007 Dec 6. 2008
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| 8 | TNXB
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| Novel localization of tenascin-X in adult mouse leptomeninges and choroid plexus.
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| Imura K, Sato I.
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| Ann Anat 190(4):324-8. Epub 2008 May 27.
2008
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| 9 | TNXB
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| Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
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| 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.
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| J Hum Genet Hum Genet. 2008 2008
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| 10 | TNXB
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| Wound healing in tenascin-X deficient mice suggests that tenascin-X is involved in matrix maturation rather than matrix deposition.
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| Egging D, van Vlijmen-Willems I, van Tongeren T, Schalkwijk J, Peeters A.
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| Connect Tissue Res 48(2):93-8.
2007
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| 11 | TNXB
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| Identification and characterization of multiple species of tenascin-X in human serum.
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| Egging DF, Peeters AC, Grebenchtchikov N, Geurts-Moespot A, Sweep CG, den Heijer M, Schalkwijk J.
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| FEBS J 274(5):1280-9. Epub 2007 Jan 29.
2007
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| 12 | TNXB
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| A model of tenascin-X integration within the collagenous network.
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| Lethias C, Carisey A, Comte J, Cluzel C, Exposito JY.
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| FEBS Lett 580(26):6281-5. Epub 2006 Oct 26.
2006
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| 13 | TNXB, EDSL1
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| Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations.
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| Zweers MC, Dean WB, van Kuppevelt TH, Bristow J, Schalkwijk J.
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| Clin Genet 67(4):330-4. 2005
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| 14 | NFKBIL1, TNXB, NOTCH4, MRPL48, PAAF1, UCP2, OPTN, CCDC3, LTB4R2
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| Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.
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| 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.
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| Hum Mol Genet 14(16):2305-21. Epub 2005 Jul 6. 2005
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| 15 | TNXB, EDSL1
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| Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology.
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| Zweers MC, van Vlijmen-Willems IM, van Kuppevelt TH, Mecham RP, Steijlen PM, Bristow J, Schalkwijk J.
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| J Invest Dermatol 122(4):885-91. 2004
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| 16 | EDSL1, TNXB
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| A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.
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| Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J.
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| N Engl J Med 345(16):1167-75. 2001
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| 17 | TNXA, TNXB
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| Allelic polymorphism of two multifunctional regions in the central human MHC: tenascin X, XB-S and YB, and their duplicated fragments XA and YA.
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| Weissensteiner T, Lanchbury JS.
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| Eur J Immunogenet 24(3):201-9. 1997
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| 18 | EDSL1, TNXB
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| Tenascin-X deficiency is associated with Ehlers-Danlos syndrome.
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| Burch GH, Gong Y, Liu W, Dettman RW, Curry CJ, Smith L, Miller WL, Bristow J.
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| Nat Genet 17(1):104-8. 1997
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| 19 | ATF6B, CYP21A1P, TNXB
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| Alternate promoters and alternate splicing of human tenascin-X, a gene with 5' and 3' ends buried in other genes.
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| Speek M, et al.
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| Hum Mol Genet 5 : 1749-1758. 1996
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| 20 | C4A, C4B, TNXA, TNXB
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| 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 ?
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| Tee MK, et al.
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| Hum Mol Genet 4 : 2109-2116. 1995
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| 21 | TNXB
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| 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.
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| Tee MK, et al.
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| Genomics 28 : 171-178. 1995
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| 22 | TNXA, TNXB
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| Tenascin-X : a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B.
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| Bristow J, et al.
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| J Cell Biol 122 : 265-278. 1993
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| 23 | TNXA,TNXB
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| Extracellular matrix protein tenascin-like gene found in human MHC class III region.
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| Matsumoto K, et al.
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| Immunogenetics 36 : 400-403. 1992
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| 24 | TNXA, TNXB
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| 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.
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| Matsumoto K, et al.
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| Genomics 12 : 485-491. 1992
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| 25 | TNXA, TNXB
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| Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus.
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| Morel Y, et al.
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| Proc Natl Acad Sci U S A 86 : 6582-6586. 1989
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