Ad
related to: human molecular geneticsebay.com has been visited by 1M+ users in the past month
Search results
Results from the WOW.Com Content Network
Human Molecular Genetics is a semimonthly peer-reviewed scientific journal published by Oxford University Press. It covers all topics related to human molecular genetics. In addition, two "special review" issues are published each year. The editor-in-chief is Charis Eng (Case Western Reserve University). The journal was established in 1992.
Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics , cytogenetics , molecular genetics , biochemical genetics , genomics , population genetics , developmental genetics , clinical genetics , and genetic counseling .
Molecular genetics is a branch of biology that addresses how differences in the structures or expression of DNA molecules manifests as variation among organisms. Molecular genetics often applies an "investigative approach" to determine the structure and/or function of genes in an organism's genome using genetic screens.
Genetic disorders can be caused by any or all known types of sequence variation. To molecularly characterize a new genetic disorder, it is necessary to establish a causal link between a particular genomic sequence variant and the clinical disease under investigation. Such studies constitute the realm of human molecular genetics.
The human BMAL1 gene has a predicted 24 exons, located on the p15 band of the 11th chromosome. [4] The BMAL1 protein is 626 amino acids long and plays a key role as one of the positive elements in the mammalian auto-regulatory transcription-translation negative feedback loop (TTFL), which is responsible for generating molecular circadian rhythms.
Molecular anthropology, also known as genetic anthropology, is the study of how molecular biology has contributed to the understanding of human evolution. [1] This field of anthropology examines evolutionary links between ancient and modern human populations, as well as between contemporary species.
Human MBNL1 is a 370 amino acid protein [13] composed of four Zinc Finger protein domains of the CCCH type linked in tandem. [10] The MBNL1 protein specifically binds to double stranded CUG RNA expansions. [14] The Zinc Finger domains play a role in both protein:protein contacts as well as RNA:protein contacts when bound to an oligonucleotide. [10]
It has a molecular weight of 427 kDa [5] [6] Dystrophin is coded for by the DMD gene – the largest known human gene, covering 2.4 megabases (0.08% of the human genome) at locus Xp21. The primary transcript in muscle measures about 2,100 kilobases and takes 16 hours to transcribe; [7] the mature mRNA measures 14.0 kilobases. [8]
Ad
related to: human molecular geneticsebay.com has been visited by 1M+ users in the past month