نتایج جستجو برای: oca1a albinism

تعداد نتایج: 7091  

Journal: :Evolution; international journal of organic evolution 2001
A P Møller T A Mousseau

The effects of mutation on phenotypic expression are supposed to be mainly deleterious because mutations disrupt the expression of genes that function relatively well under current environmental conditions. Thus, mutations are assumed to give rise to deviant phenotypes that are generally selected against. Radioactive contamination in the Chernobyl region of Ukraine is associated with a signific...

Journal: :Journal of medical genetics 1991
I R Walpole M T Mulcahy

A subject with clinical and biochemical tyrosinase positive oculocutaneous albinism (OCA) also had a balanced translocation, 46,XY,t(2;4)(q31.2;q31.22). This observation provides evidence for a possible gene locus in the q31 region of chromosome 2 or 4.

Journal: :Investigative ophthalmology & visual science 2008
Elisabeth A H von dem Hagen Michael B Hoffmann Antony B Morland

PURPOSE To compare VEP and fMRI as a means of detecting the abnormal visual projections in albinism in different stimulation conditions. METHODS Cortical response to monocular full-field pattern-onset and hemifield pattern-onset and -reversal stimulation of 18 subjects with a known diagnosis of albinism, 17 control subjects, and 6 control subjects with infantile nystagmus syndrome (INS) was d...

Journal: :Japanese Journal of Ornithology 1968

Journal: :Proceedings of the Royal Society of Medicine 1961

Journal: :The British journal of ophthalmology 1990
I Russell-Eggitt A Kriss D S Taylor

Flash visual evoked potentials (F. VEPs) and electroretinograms (ERGs) were recorded in a total of 20 young children with albinism (age range 5 months to 11 years, mean 4 years). All recordings were made without sedation. There were 13 oculocutaneous cases (one with Hermansky-Pudlak syndrome) and seven ocular albinos. Monocular flash stimulation commonly elicited an asymmetrical occipital VEP d...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Stacie K Loftus Denise M Larson Laura L Baxter Anthony Antonellis Yidong Chen Xufeng Wu Yuan Jiang Michael Bittner John A Hammer William J Pavan

Mutations of genes needed for melanocyte function can result in oculocutaneous albinism. Examination of similarities in human gene expression patterns by using microarray analysis reveals that RAB38, a small GTP binding protein, demonstrates a similar expression profile to melanocytic genes. Comparative genomic analysis localizes human RAB38 to the mouse chocolate (cht) locus. A G146T mutation ...

2011
Neil Hamilton Wood Razia Khammissa Robin Meyerov Johan Lemmer Liviu Feller

In actinic cheilitis, the current view is that the keratinocytes have undergone transformation forming a field of epithelium with the potential for neoplastic transformation. Clinical features include diffuse and poorly demarcated atrophic, erosive or keratotic plaques that may affect some parts of, or the entire vermilion border. Fair-complexioned people, those with albinism and people with ev...

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