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TSPAN12 gene
Known as:
NET2
, NET-2
, TETRASPANIN 12
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National Institutes of Health
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Related topics
Related topics
1 relation
TSPAN2 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
TSPAN12 Is a Norrin Co-receptor that Amplifies Frizzled4 Ligand Selectivity and Signaling.
M. Lai
,
C. Zhang
,
+6 authors
H. Junge
Cell reports
2017
Corpus ID: 5004680
Accessory proteins in Frizzled (FZD) receptor complexes are thought to determine ligand selectivity and signaling amplitude…
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2017
2017
Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Feng-Qin Rao
,
Xue-Bi Cai
,
+6 authors
Zi-Bing Jin
Investigative ophthalmology & visual science
2017
Corpus ID: 2214358
Purpose Familial exudative vitreoretinopathy (FEVR) is a severe hereditary retinal disorder characterized by defects in retinal…
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2015
2015
Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.
S. Seo
,
Y. Yu
,
+8 authors
J. Kim
Investigative ophthalmology & visual science
2015
Corpus ID: 8935363
PURPOSE Familial exudative vitreoretinopathy (FEVR) is a rare hereditary disorder characterized by the failure of peripheral…
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2014
2014
TSPAN12 is a critical factor for cancer–fibroblast cell contact-mediated cancer invasion
Ryo Otomo
,
Chihiro Otsubo
,
+9 authors
M. Enari
Proceedings of the National Academy of Sciences
2014
Corpus ID: 7183691
Significance Cancer-associated fibroblasts (CAFs) are abundant and promote cancer proliferation, invasion, and metastasis…
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2014
2014
Functionalized styryl iridium(III) complexes as active second-order NLO chromophores and building blocks for SHG polymeric films
C. Dragonetti
,
A. Colombo
,
+8 authors
C. Latouche
2014
Corpus ID: 44606826
Abstract We studied the second-order NLO properties in solution of various Ir(III) acetylacetonate complexes bearing a…
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Highly Cited
2012
Highly Cited
2012
Recessive mutations in TSPAN12 cause retinal dysplasia and severe familial exudative vitreoretinopathy (FEVR).
James A. Poulter
,
A. Davidson
,
+14 authors
C. Toomes
Investigative ophthalmology & visual science
2012
Corpus ID: 24265074
PURPOSE Familial exudative vitreoretinopathy (FEVR) is an inherited disorder that disrupts the development of the retinal…
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2011
2011
Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes
H. Yang
,
X. Xiao
,
S. Li
,
Guiying Mai
,
Q. Zhang
Molecular vision
2011
Corpus ID: 2096213
Purpose Mutations in tetraspanin 12 (TSPAN12) have recently been identified as a cause of autosomal dominant familial exudative…
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Highly Cited
2010
Highly Cited
2010
Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.
J. Poulter
,
M. Ali
,
+13 authors
C. Toomes
American journal of human genetics
2010
Corpus ID: 12399375
Familial exudative vitreoretinopathy (FEVR) is an inherited blinding disorder of the retinal vascular system. Although mutations…
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Highly Cited
2009
Highly Cited
2009
TSPAN12 Regulates Retinal Vascular Development by Promoting Norrin- but Not Wnt-Induced FZD4/β-Catenin Signaling
H. Junge
,
S. Yang
,
+6 authors
W. Ye
Cell
2009
Corpus ID: 2276711
Mutations in the genes encoding the Wnt receptor Frizzled-4 (FZD4), coreceptor LRP5, or the ligand Norrin disrupt retinal…
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Highly Cited
2009
Highly Cited
2009
Tetraspanin12 regulates ADAM10‐dependent cleavage of amyloid precursor protein
Daosong Xu
,
Chandan Sharma
,
M. Hemler
FASEB journal : official publication of the…
2009
Corpus ID: 22263978
Using mass spectrometry, we identified ADAM10 (a membrane‐associated metalloproteinase) as a partner for TSPAN12, a tetraspanin…
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