نتایج جستجو برای: gene defect

تعداد نتایج: 1219432  

Journal: :Development 1994
D H Castrillon S A Wasserman

We show that the Drosophila gene diaphanous is required for cytokinesis. Males homozygous for the dia1 mutation are sterile due to a defect in cytokinesis in the germline. Females trans-heterozygous for dia1 and a deficiency are sterile and lay eggs with defective eggshells; failure of cytokinesis is observed in the follicle cell layer. Null alleles are lethal. Death occurs at the onset of pupa...

Journal: :Human molecular genetics 1998
D J Kleinjan V van Heyningen

The spatially, temporally and quantitatively correct expression of a gene requires the presence not only of intact coding sequence, free of adverse nucleotide changes, but also correctly functioning regulatory control. With the identification of an increasing number of disease-related genes, the molecular defect in many cases has been defined. It is becoming clear that it is not always the tran...

Journal: :Journal of virology 1989
M Ayata A Hirano T C Wong

Biken strain, a nonproductive measles viruslike agent isolated from a subacute sclerosing panencephalitis (SSPE) patient, contains a posttranscriptional defect affecting matrix (M) protein. A putative M protein was translated in vitro with RNA from Biken strain-infected cells. A similar protein was detected in vivo by an antiserum against a peptide synthesized from the cloned M gene of Edmonsto...

ژورنال: مجله دندانپزشکی 2002
لطفی, رضا , نامجوی نیک, شهرام ,

Nowadays, different materials have been used for regeneration of interosseous defects and Neo-Os is one of them. The objective of this study was to evaluate histologically the influence of Neo-Os® particles on bone regeneration using rabbit caivarias defects with and without protection of Gore-Tex® barrier membrane. A cutaneous- periosteal incision and flap was made on the forehead of 32 rabbit...

Background and purpose: Adipose - drived stem cells are multipotent cells that capable to diffrentiate in to osteogenic cells. On the other hand, the scaffold of chitosan and gelatin are biodegradable and compatible used for tissue repair. This study evaluated the repair of femoral bone defect using adipose-derived stem cells on gelatin – chitosan membrane in adult Albino Wistar rats by radiog...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007
Masahiro Aoyama Toshiro Sugimoto Tomonobu Yokono Masayoshi Sakaguchi Naoko Deji Takashi Uzu Atsunori Kashiwagi

great majority of our patients presented the same 419delG mutation that also produce a truncate protein, and may be comparable with the above defect. Lack of heart defects in the majority of our patients lessens the likelihood of the podocin protein defect being associated with cardiac defects. We suggest re-evaluation of the association, because it cannot be excluded that in the Frishberg stud...

Journal: :American Journal of Medical Genetics 2021

Intellectual disability (ID) has an estimated prevalence of 1.5%–2%. Whole exome sequencing (WES) studies have identified a multitude novel causative gene defects and shown that sporadic ID cases result from de novo mutations in genes associated with ID. Here, we report on 10-year-old girl, who been regularly presented our neuropediatric genetic outpatient clinic. A median cleft palate heart de...

Journal: :Journal of virology 2003
Iglika V Pavlova Herbert W Virgin Samuel H Speck

Gammaherpesvirus pathogenesis is dependent on the ability of these viruses to establish a lifelong latent infection and the ability to reactivate from latency. Immediate-early genes of theses viruses are thought to be critical regulators of lytic replication and reactivation from latency. The gene 50-encoded Rta is the only immediate-early gene product that appears to be conserved among all cha...

In this paper, we improve b-spline collocation method for Benjamin-Bona-Mahony-Burgers (BBMB) by using defect correction principle. The exact finite difference scheme is used to find defect and the defect correction principle is used to improve collocation method. The method is tested on somemodel problems and the numerical results have been obtained and compared.

Journal: :Journal of neurology, neurosurgery, and psychiatry 1995
O Bandmann M B Davis C D Marsden A E Harding

Mutations in the superoxide dismutase 1 (SOD1) gene have been detected in affected members of some families with familial amyotrophic lateral sclerosis. To evaluate the possibility of a shared genetic defect in amyotrophic lateral sclerosis and Parkinson's disease, the SOD1 gene was sequenced in index patients with familial Parkinson's disease from 23 families. No changes were detected.

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