Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2005 | 1 |
2009 | 1 |
2010 | 2 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
PubMed (cited) for id: 613138
7 results
Results by year
Filters applied: . Clear all
Page 1
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).
Invest Ophthalmol Vis Sci. 2012 May 14;53(6):2873-9. doi: 10.1167/iovs.11-8629.
Invest Ophthalmol Vis Sci. 2012.
PMID: 22427576
Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.
Kondo H, Kusaka S, Yoshinaga A, Uchio E, Tawara A, Hayashi K, Tahira T.
Kondo H, et al.
Am J Ophthalmol. 2011 Jun;151(6):1095-1100.e1. doi: 10.1016/j.ajo.2010.11.026. Epub 2011 Feb 19.
Am J Ophthalmol. 2011.
PMID: 21334594
Item in Clipboard
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C.
Poulter JA, et al.
Am J Hum Genet. 2010 Feb 12;86(2):248-53. doi: 10.1016/j.ajhg.2010.01.012.
Am J Hum Genet. 2010.
PMID: 20159112
Free PMC article.
Item in Clipboard
Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy.
Nikopoulos K, Gilissen C, Hoischen A, van Nouhuys CE, Boonstra FN, Blokland EA, Arts P, Wieskamp N, Strom TM, Ayuso C, Tilanus MA, Bouwhuis S, Mukhopadhyay A, Scheffer H, Hoefsloot LH, Veltman JA, Cremers FP, Collin RW.
Nikopoulos K, et al.
Am J Hum Genet. 2010 Feb 12;86(2):240-7. doi: 10.1016/j.ajhg.2009.12.016.
Am J Hum Genet. 2010.
PMID: 20159111
Free PMC article.
Item in Clipboard
TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling.
Junge HJ, Yang S, Burton JB, Paes K, Shu X, French DM, Costa M, Rice DS, Ye W.
Junge HJ, et al.
Cell. 2009 Oct 16;139(2):299-311. doi: 10.1016/j.cell.2009.07.048.
Cell. 2009.
PMID: 19837033
Free article.
Item in Clipboard
Further evidence of genetic heterogeneity in familial exudative vitreoretinopathy; exclusion of EVR1, EVR3, and EVR4 in a large autosomal dominant pedigree.
Toomes C, Downey LM, Bottomley HM, Mintz-Hittner HA, Inglehearn CF.
Toomes C, et al.
Br J Ophthalmol. 2005 Feb;89(2):194-7. doi: 10.1136/bjo.2004.042507.
Br J Ophthalmol. 2005.
PMID: 15665352
Free PMC article.
Item in Clipboard
Sequence and expression of seven new tetraspans.
Serru V, Dessen P, Boucheix C, Rubinstein E.
Serru V, et al.
Biochim Biophys Acta. 2000 Mar 16;1478(1):159-63. doi: 10.1016/s0167-4838(00)00022-4.
Biochim Biophys Acta. 2000.
PMID: 10719184
Item in Clipboard
Cite
Cite