Molecular Genetics
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Recent papers in Molecular Genetics
The mechanisms that drive normal B cell differentiation and activation are frequently subverted by B cell lymphomas for their unlimited growth and survival. B cells are particularly prone to malignant transformation because the machinery... more
Terpenes and sterols are complex molecules synthesized by equally complex biosynthetic pathways. Recent progress in using the tools of genetics, molecular genetics and genetic engineering to dissect triterpene metabolism in the cytosol,... more
Cystic fibrosis is the most common autosomal recessive potentially lethal hereditary disease. The disease is caused by mutations in the CFTR gene of the transmembrane peptide. CFTR, functioning as a cAMP-dependent chlorine channel,... more
Plant seeds that have high phytate content are used as animal feed. Phytases, enzymes that catalyze the breakdown of phytate into inorganic phosphorus and myoinositol phosphate derivatives, have been intensively studied in recent years... more
Recent enhancement of the pool of known molecular markers for avocado has allowed the construction of the first moderately dense genetic map for this species. Over 300 SSR markers have been characterized and 163 of these were used to... more
Advances in molecular genetics have opened opportunities to enhance strategies for genetic improvement of pigs by directly selecting on genes or chromosomal regions that harbor genes that affect traits of interest. In this paper, we... more
Cancer develops secondary to genetic and epigenetic changes of multiple genes. The overall 5 year survival rate of cancer is less than 50%. The main reason of this poor outcome lies in the technical limitations of the methods used for... more
The present review summarizes the current state of knowledge about the genetics of pain-related phenomena and illustrates the scope and power of genetic approaches to the study of pain. We focus on work performed in our laboratories in... more
In 2003, an international working group last reported on recommendations for diagnosis, response assessment, and treatment outcomes in acute myeloid leukemia (AML). Since that time, considerable progress has been made in elucidating the... more
Substrate reduction therapy (SRT) is considered to be a potential therapeutic option for juvenile GM2 gangliosidosis (jGM2g). We evaluated the efficacy of SRT in jGM2g, assessing neurological, neuropsychological and brain magnetic... more
Urogenital birth defects are one of the common phenotypes observed in hereditary human disorders. In particular, limb malformations are often associated with urogenital developmental abnormalities, as the case for Hand-foot-genital... more
Eight isolates of Sclerotium rolfsii from four strategically geographical sites of Bangladesh were characterized and their cultural properties like average linear mycelial growth, colony colour, colony consistency, growth pattern and... more
A joint evaluation of all animals, uses all additive genetic relationships uses all data on all animal jointly It works as a linear model (correcting different effects for each other), jointly estimates animal effects and fixed effects... more
New insights into the phenomenon of systemic acquired resistance have been gained in recent years, by the use of techniques in molecular genetics and biology that have replaced the largely descriptive approach of earlier work. The... more
Introduction Mowat–Wilson syndrome is a congenital syndrome caused by a defect of the transcriptional repressor ZFHX1B (SIP1) gene on the chromosome 2q22–q23. The genotype–phenotype analysis confirmed that ZFHX1B deletions and mutations... more
KEYWORDS Recurrent pregnancy loss; immunity; pro-inflammatory cytokines; homogenous samples ... ABSTRACT It is a well-known fact that pro-inflammatory cytokines exert an adverse effect on conceptus and result in pregnancy failure and... more
Currently, molecular diagnosis of haemophilia A and B (HA and HB) highlights the excess risk-inhibitor development associated with specific mutations, and enables carrier testing of female relatives and prenatal or preimplantation genetic... more
Рассмотрены концептуальные положения молекулярной биологии, важнейшие признаки формирования индивидуальных признаков живого организма, молекулярные процессы, лежащие в основе функционирования нервной системы человека, его психики,а также... more