نتایج جستجو برای: fish finger
تعداد نتایج: 136966 فیلتر نتایج به سال:
This paper describes the automation of a forearm prosthesis using signal collected by Fiber Bragg Grating (FBG) sensor. The FBG sensor is applied to one subject's measure deformation as result index and middle fingers when moved individually. It possible control joint model allied compliant hand mechanism through analyses. Each finger movement has its features, such amplitude, which opens possi...
In this case report we present an 11-year-old boy with a history of trauma to distal phalanx of the forth finger of his left hand from three years ago. This trauma led to a lesion which was resistant to antibiotic therapy. Underline bone and nail of finger have been destructed by tumor. Microscopic examination revealed plump spindle cells arranged in sheets with paralleled orientati...
Introduction: Onycholemmal carcinoma is a rare slow-growing malignant epithelial neoplasm originating from nail bed epithelium. Clinical presentations are nonspecific and include warty mass, ulceration, and crust, onycholysis, periungual erythema, edema, and pain. Case Report: Herein, we report a 65-year-old woman with a mass lesion in the second finger of right hand that lasted for 3 years,...
Myotonic dystrophy type 2 (DM2) is a dominantly inherited disorder with multisystemic clinical features, caused by a CCTG repeat expansion in intron 1 of the zinc finger protein 9 (ZNF9) gene. The mutant transcripts are retained in the nucleus forming multiple discrete foci also called ribonuclear inclusions. The size and the somatic instability of DM2 expansion complicate the molecular diagnos...
We identified a novel 6.33 Mb deletion of 1q21.3q23.3 (hg18; chr1: 153035245-159367106) in two siblings presenting with blepharophimosis, ptosis, microbrachycephaly, severe psychomotor, and intellectual disability. Additional common features include small corpus callosum, normal birth length and head circumference, postnatal growth restriction, low anterior hairline, upturned nose, bilateral pr...
Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish
KDM2A is a histone demethylase associated with transcriptional silencing, however very little is known about its in vivo role in development and disease. Here we demonstrate that loss of the orthologue kdm2aa in zebrafish causes widespread transcriptional disruption and leads to spontaneous melanomas at a high frequency. Fish homozygous for two independent premature stop codon alleles show redu...
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