نتایج جستجو برای: deletion

تعداد نتایج: 79449  

Journal: :Journal of East Asian Linguistics 2023

Abstract Japanese has a deletion operation, called argument ellipsis, that targets arguments (Oku in A theory of selection and reconstruction the minimalist program, 1998). The operation does not apply to adjuncts, thus, adjuncts are unelidable. Funakoshi (J East Asian Linguist 25(2):113–42, 2016), following footsteps Otani Whitman (Linguist Inquiry 22:345–58, 1991), argues can be elided when V...

Journal: :Applied Mathematics and Computation 2021

A well-known problem in data science and machine learning is linear regression, which recently extended to dynamic graphs. Existing exact algorithms for updating the solution of graph regression require at least a time (in terms n: size graph). However, this complexity might be intractable practice. In current paper, we utilize subsampled randomized Hadamard transformand CountSketchto propose f...

Journal: :Journal of Medical Genetics 1990

Journal: :Sultan Qaboos University Journal for Science [SQUJS] 2002

Journal: :Genome Biology 2002

Journal: :Archives of Pediatrics & Adolescent Medicine 1998

Journal: :genetics in the 3rd millennium 0
حسین نجم ابادی hossein najmabadi welfare & rehabilitation university of medical sciences, tehran, irankariminejad-najmabadi pathology & genetics centetel: +98218836952-5 r ماندانا حسن زاد mandana hasanzad genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran.tehran medical unit, islamic azad university, tehran, iran مریم آزاد maryam azad kariminejad-najmabadi pathology & genetics center, tehran, iran کیمیا کهریزی kimia kahrizi genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran واله هادوی valeh hadavi kariminejad-najmabadi pathology & genetics center, tehran, iran بهاره شجاع صفار bahareh shoja saffar genetics research center, university of social welfare & rehabilitation, sciences, tehran, iran شهریار نفیسی

spinal muscular atrophy (sma) is a common autosomal recessive neuromuscular disorder caused by the loss of α-motor neurons in the spinal cord. the survival motor neuron (smn) protein is encoded by 2 genes, smn1 and smn2. the most frequent mutation is the biallelic deletion of exon 7 of the smn1 gene. smn2 cannot compensate for the loss of smn1, due to the exclusion of exon 7. carrier frequency ...

Journal: :Emerging Infectious Diseases 2021

Abstract Deletion of histidine-rich protein genes pfhrp2/3 in Plasmodium falciparum causes infections to go undetected by HRP2-based malaria rapid diagnostic tests. We analyzed P. cases imported Australia (n = 210, collected 2010–2018) for their status. detected gene deletions patients from 12 25 countries. found >10% pfhrp2-deletion levels those Nigeria (13.3%, n 30), Sudan (11.2%, 39), and So...

Journal: :Microorganisms 2023

Next-generation sequencing (NGS) from SARS-CoV-2-positive swabs collected during the last months of 2022 revealed a large deletion spanning ORF7b and ORF8 (426 nt) in six patients infected with BA.5.1 Omicron variant. This extensive genome loss removed part these two genes, maintaining frame first 22 aminoacids three ORF8. Interestingly, deleted region was flanked by small repeats, which were l...

Telomerase and systems controlling their activity have been of great attention. There are controversies regarding the role of the alternative splicing forms of the human telomerase reverse transcriptase (hTERT), the catalytic subunit of telomerase. Therefore, the correlation between telomerase enzyme activity, the abundance of alternatively spliced variants of hTERT and doubling time of a seri...

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