about
DNA Methylation of PITX2 and PANCR Is Prognostic for Overall Survival in Patients with Resected Adenocarcinomas of the Biliary TractThe transcription factor Foxc1 is necessary for Ihh-Gli2-regulated endochondral ossificationPediatric glaucoma suspects.Clinical performance validation of PITX2 DNA methylation as prognostic biomarker in patients with head and neck squamous cell carcinoma.Unilateral foveal hypoplasia in a child with bilateral anterior segment dysgenesisGenetic Analysis of 'PAX6-Negative' Individuals with Aniridia or Gillespie SyndromeFoxC1-dependent regulation of vascular endothelial growth factor signaling in corneal avascularity.A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.Novel c.300_301delinsT mutation in PITX2 in a Korean family with Axenfeld-Rieger syndrome.Heterozygous Pitx2 Null Mice Accurately Recapitulate the Ocular Features of Axenfeld-Rieger Syndrome and Congenital Glaucoma.Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome.Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.Malformation syndromes associated with disorders of sex development.The 6p25 deletion syndrome: An update on a rare neurocristopathy.Unclassified Axenfeld-Rieger Syndrome: A CASE SERIES and Review of Literature.Mutations in zebrafish pitx2 model congenital malformations in Axenfeld-Rieger syndrome but do not disrupt left-right placement of visceral organs.Axenfeld-Rieger syndrome associated with severe maxillofacial and skeletal anomalies.Surgical management in primary congenital glaucoma: four debates.OLOGEN(®) implant in the management of glaucoma in an unusual case of Axenfeld-Rieger syndrome.A Novel Mutation in PITX2 in a Patient with Axenfeld-Rieger Syndrome.Development and clinical validation of a real-time PCR assay for PITX2 DNA methylation to predict prostate-specific antigen recurrence in prostate cancer patients following radical prostatectomy.Mutations of conserved non-coding elements of PITX2 in patients with ocular dysgenesis and developmental glaucoma.PITX2-related Axenfeld-Rieger Syndrome with a Novel Pathogenic Variant (c.475_476delCT).Novel de novo FOXC1 nonsense mutation in an Axenfeld-Rieger syndrome patient
P2860
Q28109676-AD130CE4-EFED-4CD6-8F7F-3EF9B6BE3B84Q28910226-D3FC77D2-94AC-49D2-8820-8646D4E4E4A5Q33783782-B0D2CC3C-646C-4DBD-9DD4-B64FFCCD1191Q33803297-03CDE02A-11E6-4F5E-8685-695FA3B04D08Q35924922-B66EAFB3-6296-4749-89D3-F257D872A852Q36001944-672CF1FF-1C3B-4ABE-86D0-B63D30B201B2Q36476460-E02A6ED0-7E83-402E-9555-D5CCA98E4987Q36891473-7F719979-7BDC-4075-86FD-3858A3FA36E4Q37129451-2D52540B-FC05-419C-87BF-C7745468F747Q37292402-6CA2E3A9-1A57-4589-B3E3-039DC03EC10DQ37476047-54749E15-C5CD-4551-B3A2-A414753CA6F2Q37715257-6EAFB8F7-8DDC-401B-A8B0-244CD3A66E8AQ38218950-A1B619BA-AA0C-41BA-A913-8E89BEAA91A5Q38806126-B37D21CC-CD8D-447A-BA3F-702BBBADE905Q39032796-AF464F5D-719E-4DFC-8F80-195A033AEBA5Q41190613-E6676765-710A-4083-8224-F98408765C2FQ41528245-232B2510-3172-4628-A657-69E15D8A35EEQ42018059-807ED44C-D9A5-430C-9F17-D6E53FC5BD61Q42155281-2212A500-AA9A-4B13-A557-31B3C3576265Q42211114-21BD3A6B-95D2-4A85-AE0D-04F5B97F9CE9Q44019552-31FD1427-93EC-4F42-AAE3-D6042AF90776Q46445385-899DC1B7-A1D6-4AF3-ADB9-EA0E065B3EA4Q52699553-8DB7E509-6698-48F7-B9F3-44E8C8DF2097Q59257860-5AC6E07B-E7A7-4BC2-BEB5-2A3C6341B4CB
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Axenfeld-Rieger syndrome: new perspectives.
@en
Axenfeld-Rieger syndrome: new perspectives.
@nl
type
label
Axenfeld-Rieger syndrome: new perspectives.
@en
Axenfeld-Rieger syndrome: new perspectives.
@nl
prefLabel
Axenfeld-Rieger syndrome: new perspectives.
@en
Axenfeld-Rieger syndrome: new perspectives.
@nl
P2093
P1476
Axenfeld-Rieger syndrome: new perspectives
@en
P2093
Alana L Grajewski
C Gail Summers
Ta C Chang
P304
P356
10.1136/BJOPHTHALMOL-2011-300801
P407
P577
2011-12-23T00:00:00Z