Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 270

Similar articles for PubMed (Select 19509472)


Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-beta2 signaling.

Iwao K, Inatani M, Matsumoto Y, Ogata-Iwao M, Takihara Y, Irie F, Yamaguchi Y, Okinami S, Tanihara H.

J Clin Invest. 2009 Jul;119(7):1997-2008. doi: 10.1172/JCI38519. Epub 2009 Jun 8.


Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells.

Ittner LM, Wurdak H, Schwerdtfeger K, Kunz T, Ille F, Leveen P, Hjalt TA, Suter U, Karlsson S, Hafezi F, Born W, Sommer L.

J Biol. 2005;4(3):11. Epub 2005 Dec 14.


[Exploration of the molecular mechanism of ocular development and the creation of animal models for ocular diseases].

Inatani M.

Nihon Ganka Gakkai Zasshi. 2010 Mar;114(3):280-96; discussion 297. Review. Japanese.


Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma.

Kroeber M, Davis N, Holzmann S, Kritzenberger M, Shelah-Goraly M, Ofri R, Ashery-Padan R, Tamm ER.

Hum Mol Genet. 2010 Sep 1;19(17):3332-42. doi: 10.1093/hmg/ddq237. Epub 2010 Jun 10.


Anterior segment development relevant to glaucoma.

Gould DB, Smith RS, John SW.

Int J Dev Biol. 2004;48(8-9):1015-29. Review.


Heparan sulfate deficiency in periocular mesenchyme causes microphthalmia and ciliary body dysgenesis.

Iwao K, Inatani M, Ogata-Iwao M, Yamaguchi Y, Okinami S, Tanihara H.

Exp Eye Res. 2010 Jan;90(1):81-8. doi: 10.1016/j.exer.2009.09.017. Epub 2009 Sep 24.


Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.

Berry FB, Lines MA, Oas JM, Footz T, Underhill DA, Gage PJ, Walter MA.

Hum Mol Genet. 2006 Mar 15;15(6):905-19. Epub 2006 Jan 31.


Transforming growth factor beta-SMAD2 signaling regulates aortic arch innervation and development.

Molin DG, Poelmann RE, DeRuiter MC, Azhar M, Doetschman T, Gittenberger-de Groot AC.

Circ Res. 2004 Nov 26;95(11):1109-17. Epub 2004 Nov 4.


Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.

Smith RS, Zabaleta A, Kume T, Savinova OV, Kidson SH, Martin JE, Nishimura DY, Alward WL, Hogan BL, John SW.

Hum Mol Genet. 2000 Apr 12;9(7):1021-32.


Molecular and developmental mechanisms of anterior segment dysgenesis.

Sowden JC.

Eye (Lond). 2007 Oct;21(10):1310-8. Review.


Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M.

Mol Vis. 2006 Dec 1;12:1448-60.


Targeted overexpression of TGF-α in the corneal epithelium of adult transgenic mice induces changes in anterior segment morphology and activates noncanonical Wnt signaling.

Yuan Y, Yeh LK, Liu H, Yamanaka O, Hardie WD, Kao WW, Liu CY.

Invest Ophthalmol Vis Sci. 2013 Mar 11;54(3):1829-37. doi: 10.1167/iovs.12-11477.


Abnormal migration and distribution of neural crest cells in Pax6 heterozygous mutant eye, a model for human eye diseases.

Kanakubo S, Nomura T, Yamamura K, Miyazaki J, Tamai M, Osumi N.

Genes Cells. 2006 Aug;11(8):919-33.


Msx2 is an immediate downstream effector of Pax3 in the development of the murine cardiac neural crest.

Kwang SJ, Brugger SM, Lazik A, Merrill AE, Wu LY, Liu YH, Ishii M, Sangiorgi FO, Rauchman M, Sucov HM, Maas RL, Maxson RE Jr.

Development. 2002 Jan;129(2):527-38.


Fate maps of neural crest and mesoderm in the mammalian eye.

Gage PJ, Rhoades W, Prucka SK, Hjalt T.

Invest Ophthalmol Vis Sci. 2005 Nov;46(11):4200-8.


Cerebral hypoplasia and craniofacial defects in mice lacking heparan sulfate Ndst1 gene function.

Grobe K, Inatani M, Pallerla SR, Castagnola J, Yamaguchi Y, Esko JD.

Development. 2005 Aug;132(16):3777-86. Epub 2005 Jul 14.


Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.

Strungaru MH, Dinu I, Walter MA.

Invest Ophthalmol Vis Sci. 2007 Jan;48(1):228-37.


Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.

Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS.

Ophthalmic Genet. 2007 Jun;28(2):57-67.

Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk