Introduction to Gene Within

What is/are Gene Within?

Gene Within - The positioning of a gene within the nuclear space has been implicated in gene regulation. ^[1] Although the signal was not of genome-wide significance due to the small number of cases, the SBF2 (also known as MTMR13) gene within the region of shared case homozygosity was a strong positional candidate, as 22 genetic variants in the gene have been associated with demyelinating forms of Charcot-Marie-Tooth disease in humans. ^[2] The purpose of the work is to characterize the conditions for the distribution of the soils of the Kharkov suite of Paleogene within the southeast of Belarus and to study the characteristics of their composition and structure. ^[3] A high-fat diet (HFD) induces an increase in arterial pressure and a decrease in baroreflex function, which may be associated with increased expression of angiotensin type 1 receptor (AT1R) and pro-inflammatory cytokine genes and reduced expression of the angiotensin type 2 receptor (AT2R) gene within the nucleus of the solitary tract (NTS), a key area of the brainstem involved in cardiovascular control. ^[4] These exertions delineated natural alleles and superior haplotypes from a CabHLH121 transcription factor (TF) gene within the major QTL governing PW, PH and SAM morphometric traits. ^[5] The protein sequence of a gene within this cluster contained the GTA_TIM domain that is present in bacteria with GTA. ^[6] One additional patient from each cohort showed the emergence of a mutation in an oncogene within the MAPK pathway. ^[7] To do this, we have cloned and overexpressed each gene within the colanic acid biosynthesis operon. ^[8] In addition, we identified a gene within an mQTL in a module conserved in humans that may be targeted to promote resilience to memory decline during aging. ^[9] Delivery using a lentiviral vector is particularly attractive due to the ability to encode the gene within the viral genome, as well as the ability to limit off-target effects by using cell type-specific glycoproteins. ^[10] The lncRNA Jpx, Xist activator, is a nonprotein-coding RNA transcribed from a gene within the X-inactivation center and acts as a numerator element to control X-chromosome number and activate Xist transcription by interacting with CCCTC-binding factor. ^[11] We estimated nucleotide diversity and Tajima’s D for each gene within each population and calculated the strength of correlations between nucleotide diversity and environmental variables. ^[12] A gene within this locus, encoding the Cgr2 enzyme, was sufficient to increase Th17 cells. ^[13]

Target Gene Within

The LAMP assay can efficiently amplify the target gene within 60 min at 63 °C. ^[1] The ability to selectively regulate expression of any target gene within a genome provides a means to address a variety of diseases and disorders. ^[2] The REMOTE-control system employs enhanced lac repression and tet activation systems to achieve down- or upregulation of a target gene within a single biological system. ^[3]

Candidate Gene Within

Three-week-old mice heterozygous for a loss-of-function mutation in FOXI3, a candidate gene within the common deleted region found in patients, were compared to wild-type littermates. ^[1] Population effects, sire effects, and narrow‐sense heritability (h2) were calculated for each candidate gene within each treatment group. ^[2] Importantly, while we identified Actin, a commonly used HK gene, as a candidate gene within our RNAseq analyses, our qPCR results did not demonstrate stable expression throughout the nematode life cycle of this gene. ^[3]

Nra Gene Within

The paper provides a clinical description and analysis of two melanoma cases with mutations in the BRAF and NRAS gene within one tumor. ^[1] The paper provides a clinical description and analysis of two melanoma cases with mutations in the BRAF and NRAS gene within one tumor. ^[2]

Specific Gene Within

Consistent with historical reports in which overlapping deletions defined a minimal critical region in WHS patients, recent reports from exome sequence analysis have provided further evidence that haploinsufficiency of a specific gene within this critical region, NSD2 (WHSC1), is causal for many features of the syndrome. ^[1] The ability to edit a specific gene within our genomes using guided-nucleases (Cas9/ZFN/TALEN - CaZiTa) presents huge opportunities for curing many genetic disorders. ^[2]

One Gene Within

1, and one gene within this locus, PPP1R3B, is related to glycogenesis and has been associated with an increased risk of type 2 diabetes and obesity. ^[1] Here, we focus on one gene within this interval, PPP2R3B, which encodes a protein phosphatase 2A regulatory subunit that interacts with the origin of replication component, CDC6, and has been linked to regulation of autophagy. ^[2]

Small Gene Within

In this study we demonstrate that Sir2 and the condensin complex are recruited to the RE exclusively in MATa cells, specifically to the promoter of a small gene within the right half of the RE known as RDT1. ^[1] In this study we demonstrate that Sir2 and the condensin complex are recruited to the RE exclusively in MATa cells, specifically to the promoter of a small gene within the right half of the RE known as RDT1. ^[2]

Essential Gene Within

This results in a preference for Tn5-Puror insertions transcribed toward a downstream essential or quasi-essential gene within the same operon. ^[1] We combine computational and synthetic biology approaches to rationally design an overlapping reading frame expressing an essential gene within an existing gene to protect. ^[2]

Ancestral Gene Within

As provided by several orthology databases, hierarchical orthologous groups (HOGs) are sets of genes that are inferred to have descended from a common ancestral gene within a species clade. ^[1] In silico analysis of the Psav DAPP‐PG 722 genome revealed the presence of a single gene coding for a Na+/Ca2+ exchanger (cneA), which is a widely conserved and ancestral gene within the P. ^[2]

gene within one

The paper provides a clinical description and analysis of two melanoma cases with mutations in the BRAF and NRAS gene within one tumor. ^[1] The paper provides a clinical description and analysis of two melanoma cases with mutations in the BRAF and NRAS gene within one tumor. ^[2]