منابع مشابه
Sex-determining Region Y in Mammals
The Sex-determining Region Y (Sry in mammals but SRY in humans [4]) is a gene found on Y chromosomes that leads to the development of male phenotypes, such as testes [5]. The Sry gene, located on the short branch of the Y chromosome, initiates male embryonic development in the XY sex determination [6] system. The Sry gene follows the central dogma of molecular biology; the DNA encoding the gene...
متن کاملextremal region detection guided by maxima of gradient magnitude
a problem of computer vision applications is to detect regions of interest under dif- ferent imaging conditions. the state-of-the-art maximally stable extremal regions (mser) detects affine covariant regions by applying all possible thresholds on the input image, and through three main steps including: 1) making a component tree of extremal regions’ evolution (enumeration), 2) obtaining region ...
Epigenetic profile of the euchromatic region of human Y chromosome
The genome of a multi-cellular organism acquires various functional capabilities in different cell types by means of distinct chromatin modifications and packaging states. Acquired during early development, the cell type-specific epigenotype is maintained by cellular memory mechanisms that involve epigenetic modifications. Here we present the epigenetic status of the euchromatic region of the h...
متن کاملComparative In silico Study of Sex-Determining Region Y (SRY) Protein Sequences Involved in Sex-Determining
Background: The SRY gene (SRY) provides instructions for making a transcription factor called the sex-determining region Y protein. The sex-determining region Y protein causes a fetus to develop as a male. In this study, SRY of 15 spices included of human, chimpanzee, dog, pig, rat, cattle, buffalo, goat, sheep, horse, zebra, frog, urial, dolphin and killer whale were used for determine of bioi...
متن کاملMolecular Study of Partial Deletions of AZFc Region of the Y Chromosome in Infertile Men
Background & Aims: The most significant cause of infertility in men is the genetic deletion in the azoospermia factor (AZF) region that is caused by the process of intra- and inter-chromosomal homologous recombination in amplicons. Homologous recombination could also result in partial deletions in AZF region. The aim of this research was to determine the association between the partial AZFc del...
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ژورنال
عنوان ژورنال: Revista de Estudios de la Administración Local y Autonómica
سال: 1976
ISSN: 1989-8975,1699-7476
DOI: 10.24965/reala.vi191.7974