Literature DB >> 15733276

Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.

M L E MacDonald, Y P Goldberg, J Macfarlane, M E Samuels, M T Trese, B S Shastry.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2005        PMID： 15733276     DOI： 10.1111/j.1399-0004.2005.00408.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  22 in total

1.  [Mutations of the frizzled-4 gene. Their impact on medical care of patients with autosomal dominant exudative vitreoretinopathy].

Authors:  M Müller; C Kusserow; U Orth; U Klär-Dissars; H Laqua; A Gal
Journal:  Ophthalmologe       Date:  2008-03       Impact factor: 1.059

Review 2.  Genomics in the neonatal nursery: Focus on ROP.

Authors:  Mary Elizabeth Hartnett; C Michael Cotten
Journal:  Semin Perinatol       Date:  2015-10-23       Impact factor: 3.300

Review 3.  Retinopathy of prematurity: a review of risk factors and their clinical significance.

Authors:  Sang Jin Kim; Alexander D Port; Ryan Swan; J Peter Campbell; R V Paul Chan; Michael F Chiang
Journal:  Surv Ophthalmol       Date:  2018-04-19       Impact factor: 6.048

Review 4.  Current update on retinopathy of prematurity: screening and treatment.

Authors:  Jing Chen; Andreas Stahl; Ann Hellstrom; Lois E Smith
Journal:  Curr Opin Pediatr       Date:  2011-04       Impact factor: 2.856

5.  Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.

Authors:  Jason Salvo; Vera Lyubasyuk; Mingchu Xu; Hui Wang; Feng Wang; Duy Nguyen; Keqing Wang; Hongrong Luo; Cindy Wen; Catherine Shi; Danni Lin; Kang Zhang; Rui Chen
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-02-24       Impact factor: 4.799

Review 6.  Impact of GPCRs in clinical medicine: monogenic diseases, genetic variants and drug targets.

Authors:  Paul A Insel; Chih-Min Tang; Ines Hahntow; Martin C Michel
Journal:  Biochim Biophys Acta       Date:  2006-10-05

7.  Retinopathy of prematurity and maternal age.

Authors:  Wei-Chi Wu; Frank Shih-Chang Ong; Jane Zea-Chin Kuo; Chi-Chun Lai; Ning-Chia Wang; Kuan-Jen Chen; Yih-Shiou Hwang; Tun-Lu Chen; Chia-Pang Shih
Journal:  Retina       Date:  2010-02       Impact factor: 4.256

8.  Genetic contributions to the development of retinopathy of prematurity.

Authors:  Shakir Mohamed; Kendra Schaa; Margaret E Cooper; Elise Ahrens; Ana Alvarado; Tarah Colaizy; Mary L Marazita; Jeffrey C Murray; John M Dagle
Journal:  Pediatr Res       Date:  2009-02       Impact factor: 3.756

9.  Whole exome sequencing in patients with Williams-Beuren syndrome followed by disease modeling in mice points to four novel pathways that may modify stenosis risk.

Authors:  Phoebe C R Parrish; Delong Liu; Russell H Knutsen; Charles J Billington; Robert P Mecham; Yi-Ping Fu; Beth A Kozel
Journal:  Hum Mol Genet       Date:  2020-07-29       Impact factor: 6.150

10.  Genetic variants associated with severe retinopathy of prematurity in extremely low birth weight infants.

Authors:  M Elizabeth Hartnett; Margaux A Morrison; Silvia Smith; Tammy L Yanovitch; Terri L Young; Tarah Colaizy; Allison Momany; John Dagle; Waldemar A Carlo; Erin A S Clark; Grier Page; Jeff Murray; Margaret M DeAngelis; C Michael Cotten
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-08-12       Impact factor: 4.799
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.