Results 11 to 20 of about 1,717,353 (273)
الحذف في المتلازمات النحوية من منظور الدراسات الأسلوبية "المجموعة القصصية (Beyaz Türkü) الأنشودة البيضاء لـ بكير يلدز أنموذجا" [PDF]
يعد الحذف ظاهرة لغويّة لها فوائد دلاليّة، وأغراض بلاغيّة كثيرة، يتناول هذا البحث ظاهرة الحذف في المتلازمات النحوية بوصفها إحدى الوسائل الأسلوبية البارزة التي تسهم في تكثيف المعنى وتحقيق الإيجاز، وذلك من خلال تطبيقها على المجموعة القصصية (Beyaz Türkü ...
سعد على عبده أحمد
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Although several studies have shown the correlation between chromosomal rearrangements and the risk of developing psychotic disorders, such as schizophrenia, little attention has been given to identifying the genetic basis of pre-disposing personality so
Cecilia Maria Esposito +9 more
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Structural and dynamic changes associated with beneficial engineered single-amino-acid deletion mutations in enhanced green fluorescent protein. [PDF]
Single-amino-acid deletions are a common part of the natural evolutionary landscape but are rarely sampled during protein engineering owing to limited and prejudiced molecular understanding of mutations that shorten the protein backbone.
Arpino, JA, Jones, DD, Rizkallah, PJ
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Artistic and Aesthetic Functions of "Tanazo" in Poetry [PDF]
The Tanazo is one of the disciplines of grammar, according to which, part of the sentence takes several different syntactic roles simultaneously. The purpose of this paper is to determine the aesthetic roles of this language preparation in poetry.
Mehdi Dehrami
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A polynomial kernel for Block Graph Deletion [PDF]
In the Block Graph Deletion problem, we are given a graph $G$ on $n$ vertices and a positive integer $k$, and the objective is to check whether it is possible to delete at most $k$ vertices from $G$ to make it a block graph, i.e., a graph in which each ...
Kim, Eun Jung, Kwon, O-joung
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Key Clinical Message I report a novel BCR‐ABL point mutation c.844G>C p.E282Q and a case of combination of two BCR‐ABL point mutations (p.E282Q and p.L298R) and exon 7 deletion (del. c.1086‐1270) in TKI‐resistant patient.
Ilya Mikhailov
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Defects in FARS2 are associated with either epileptic phenotypes or a spastic paraplegia subtype known as SPG77. Here, we describe an 8-year-old patient with severe and complicated spastic paraplegia, carrying a missense variant (p.Pro361Leu) and a novel
Elena Panzeri +5 more
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Evolutionary and functional features of copy number variation in the cattle genome
Genomic structural variations are an important source of genetic diversity. Copy number variations (CNVs), gains and losses of large regions of genomic sequence between individuals of a species, have been associated with a wide variety of phenotypic ...
Brittney N Keel +2 more
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Identification of genomic indels and structural variations using split reads
Background Recent studies have demonstrated the genetic significance of insertions, deletions, and other more complex structural variants (SVs) in the human population.
Urban Alexander E +6 more
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