نتایج جستجو برای: microphthalmia

تعداد نتایج: 1639  

Journal: :Clinical and Experimental Dermatology 2018

Journal: :Investigative ophthalmology & visual science 2011
Zhengmao Hu Changhong Yu Jingzhi Li Yiqiang Wang Deyuan Liu Xinying Xiang Wei Su Qian Pan Lixin Xie Kun Xia

PURPOSE To investigate the etiology in a family with autosomal-dominant congenital simple microphthalmia of Chinese origin. METHODS A whole-genome scan was performed by using 382 microsatellite DNA markers after the exclusion of reported candidates linked to microphthalmia. Additional fluorescent markers were genotyped for fine mapping. To find out the novel predisposing gene, 14 candidate ge...

Journal: :Genetics 2009
Jack Favor Alan Bradley Nathalie Conte Dirk Janik Walter Pretsch Peter Reitmeir Michael Rosemann Wolfgang Schmahl Johannes Wienberg Irmgard Zaus

In the mouse Pax6 function is critical in a dose-dependent manner for proper eye development. Pax6 contiguous gene deletions were shown to be homozygous lethal at an early embryonic stage. Heterozygotes express belly spotting and extreme microphthalmia. The eye phenotype is more severe than in heterozygous Pax6 intragenic null mutants, raising the possibility that deletions are functionally dif...

2009
Jack Favor Alan Bradley Nathalie Conte Dirk Janik Walter Pretsch Peter Reitmeir Michael Rosemann Wolfgang Schmahl Johannes Wienberg Irmgard Zaus

In the mouse Pax6 function is critical in a dose-dependent manner for proper eye development. Pax6 contiguous gene deletions were previously shown to be homozygous lethal at an early embryonic stage. Heterozygotes express belly spotting and extreme microphthalmia. The eye phenotype is more severe than in heterozygous Pax6 intragenic null mutants, raising the possibility that deletions are funct...

2016
Jing Li Shusheng Wang Chastain Anderson Fangkun Zhao Yu Qin Di Wu Xinwei Wu Jia Liu Xuefei He Jiangyue Zhao Jinsong Zhang

Microphthalmia is characterized by abnormally small eyes and usually retinal dysplasia, accounting for up to 11% of the blindness in children. Right now there is no effective treatment for the disease, and the underlying mechanisms, especially how retinal dysplasia develops from microphthalmia and whether it depends on the signals from lens ectoderm are still unclear. Mutations in genes of the ...

Journal: :BMJ 1998
H Dolk A Busby B G Armstrong P H Walls

OBJECTIVE To investigate the geographical variation and clustering of congenital anophthalmia and microphthalmia in England, in response to media reports of clusters. DESIGN Comparison of pattern of residence at birth of cases of anophthalmia and microphthalmia in England in 1988-94, notified to a special register, with pattern of residence of all births. Three groups studied included all cas...

Journal: :The Journal of biological chemistry 1998
E Aberdam C Bertolotto E V Sviderskaya V de Thillot T J Hemesath D E Fisher D C Bennett J P Ortonne R Ballotti

In mouse follicular melanocytes, production of eumelanins (brown-black pigments) and pheomelanins (yellow-brownish pigments) is under the control of two intercellular signaling molecules that exert opposite actions, alpha-melanocyte-stimulating hormone (alphaMSH) which preferentially increases the synthesis of eumelanins, and agouti signal protein (ASP) whose expression favors the production of...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2013

Journal: :Archives of disease in childhood. Fetal and neonatal edition 1998
A Busby H Dolk R Collin R B Jones R Winter

AIM To describe the prevalence of anophthalmia/microphthalmia in babies born in England 1988-94, as well as their overall survival, and the incidence of associated eye and non-eye malformations; to determine the usefulness of different sources of medical and health service information for establishing a retrospective register of anophthalmia/microphthalmia. METHODS Multiple sources for initia...

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