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SPATULA, a bHLH carpel development gene
SPATULA, a bHLH carpel development gene

Characterisation of the katA gene encoding a catalase and evidence
Characterisation of the katA gene encoding a catalase and evidence

... A KatA-de¢cient strain of S. xylosus, designated TX350, was constructed by exchanging the 5P-end of katA for an erythromycin resistance gene, ermB (Fig. 1B). By this replacement, the ¢rst 60 codons of katA including the start codon and ribosome-binding site were removed resulting in a complete block ...
C. neoformans
C. neoformans

... N2 nematodes were fed on lawns of C. neoformans and then at different time-points transferred to lawns of non-pathogenic cryptococci. All nematodes that survived transfer were rescued, regained normal non-distended anatomy and no C. neoformans yeast cells could be cultured followed “grinding” of the ...
Mining Multi-Faceted Overviews of Arbitrary Topics in a Text Collection
Mining Multi-Faceted Overviews of Arbitrary Topics in a Text Collection

... • We evaluated the effectiveness of different facet modeling approaches in Table.4. • Pri and Reg are our prior-based and regularizerbased approacheswith most extensive facet expansion; • Sup represents the result of the system by [11] using the supervised approach • MQR casts this task as a multi-q ...
marker assisted selection in disease resistance breeding
marker assisted selection in disease resistance breeding

... they are generally independent of environmental growth conditions. The only problem with isozymes in MAS is that most cultivars (commercial breeds of plants) are genetically very similar and isozymes do not produce a great amount of polymorphism and polymorphism in the protein primary structure may ...
Meiosis - Myersbiology
Meiosis - Myersbiology

... • Males are an expensive luxury - in most species they contribute little to rearing offspring. ...
pdf
pdf

... not always complete, meaning that nonparental genotypes are seen in a proportion of the progeny. This is explained by crossing over between the gene pairs during meiosis in the parents. Let’s think about the general recombination shown in Fig. 8.1 in this context. The two chromosomes outlined in the ...
Role of two-component systems in the virulence of Streptococcus
Role of two-component systems in the virulence of Streptococcus

... membrane-associated sensor histidine kinase (HK) and a cytoplasmic cognate response regulator (RR). Upon receipt of a specific external stimulus the kinase domain of the HK sensor protein is activated to autophosphorylate a conserved histidine residue. HK proteins tend to be found as homodimers that ...
Interaction of nonsense suppressor tRNAs and codon nonsense
Interaction of nonsense suppressor tRNAs and codon nonsense

... in both a prokaryotic and a eukaryotic host [13]. A temperature-sensitive mutant of E. coli harbors a weak suppressing activity towards a UAG mutation, together with an inability to grow at 43˚C in rich medium. The mutation shows enhanced misreading of UAG/A, but UGA. The mutation gives an increased ...
Chromosomal translocations deregulated BCL6
Chromosomal translocations deregulated BCL6

Complex Heterozygosity Screening with Actin Alanine Scan Alleles
Complex Heterozygosity Screening with Actin Alanine Scan Alleles

... genes has been shown to contribute to tumorigenesis (Santarosa and Ashworth 2004), and complex haploinsufficiency has been shown in mouse models to contribute to early aging (Baker et al. 2006) and tumorigenesis (Ma et al. 2005; Vives et al. 2006). Furthermore, recent genome-wide sequencing of 1092 ...
genotype AND phenotype
genotype AND phenotype

... Brandy has one allele for being tall, and one allele for being short.  Is this genotype or phenotype? Explain how you know. ...
Variation in copper metabolism in Arabidopsis thaliana accessions
Variation in copper metabolism in Arabidopsis thaliana accessions

Gene Section MYB (v-myb myeloblastosis viral oncogene homolog (avian))
Gene Section MYB (v-myb myeloblastosis viral oncogene homolog (avian))

View PDF - BloodMed
View PDF - BloodMed

... in print was short lived; I was hauled up before the Director General of Medical Services for the Far East Land Forces and told that I could be court marshalled for not getting permission from the War House (Office) to publish information about military personnel. `And, in any case', he added, `it i ...
Adrenomedullin Gene Expression Is Developmentally Regulated and
Adrenomedullin Gene Expression Is Developmentally Regulated and

Maneeshi Prasad
Maneeshi Prasad

... Yang, J. et al. (2009) Nat. Neurosci. 12:113. ...
This document has been downloaded from Tampub – The
This document has been downloaded from Tampub – The

... the transcription of genes involved in lipid and cholesterol metabolism. In sterol-depleted cells, SREBF cleavage activating protein (SCAP) forms a complex with SREBF and assists in its transportation to the Golgi apparatus where it can be processed by two specific proteases and then release the ami ...
Glioma heterogeneity and the LAT-1
Glioma heterogeneity and the LAT-1

... Glioma heterogeneity and the L-Amino acid transporter-1 (LAT1): A first step to stratified BPA-based BNCT? ...
Sequence requirements for function of the
Sequence requirements for function of the

... chorion, the follicle cells are destroyed prior to egg-laying, and therefore the mitotic apparatus needs never deal with this unusual DNA onionskin. If amplification is prevented by a trans-acting mutation or a chromosomal rearrangement that moves the origin away from the gene cluster, the resultant ...
17. Prof. K. P. Bhatia: Paroxysmal Movement Disorders
17. Prof. K. P. Bhatia: Paroxysmal Movement Disorders

AP Biology
AP Biology

... is unusual for allele with severe detrimental effects in homozygotes ...
Read the Nobel Lecture
Read the Nobel Lecture

... First we needed an assay – a way to detect if telomere elongation was happening. The first assay we tried explored whether a piece of DNA that included a telomere would incorporate DNA precursors more readily than a piece of DNA containing non-telomeric sequences. The idea was that if there was an ...
abnormalities of chromosome structure
abnormalities of chromosome structure

...  In general, loss of chromosome material has more serious consequences than duplication of chromosome material.  Aneuploidy of the sex chromosomes is less serious than that of the autosomes.  Y chromosome  very little genetic material is located on this chromosome.  X chromosome  inactivation ...
Gene methylation in gastric cancer
Gene methylation in gastric cancer

... Gastric cancer is highly prevalent in Asia, particularly China, and is one of the leading causes of cancer-related death worldwide [1]. There are two main types of gastric adenocarcinoma: intestinal and diffuse. The accepted paradigm for the pathogenesis of the intestinal-type is a multistep progres ...
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Epigenetics of human development

Development before birth, including gametogenesis, embryogenesis, and fetal development, is the process of body development from the gametes are formed to eventually combine into a zygote to when the fully developed organism exits the uterus. Epigenetic processes are vital to fetal development due to the need to differentiate from a single cell to a variety of cell types that are arranged in such a way to produce cohesive tissues, organs, and systems.Epigenetic modifications such as methylation of CpGs (a dinucleotide composed of a 2'-deoxycytosine and a 2' deoxyguanosine) and histone tail modifications allow activation or repression of certain genes within a cell, in order to create cell memory either in favor of using a gene or not using a gene. These modifications can either originate from the parental DNA, or can be added to the gene by various proteins and can contribute to differentiation. Processes that alter the epigenetic profile of a gene include production of activating or repressing protein complexes, usage of non-coding RNAs to guide proteins capable of modification, and the proliferation of a signal by having protein complexes attract either another protein complex or more DNA in order to modify other locations in the gene.
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