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Genomic Survey and Gene Expression Analysis
Genomic Survey and Gene Expression Analysis

... maturation and germination, floral induction and development, and photomorphogenesis, and are also involved in stress and hormone signaling. We have identified 89 bZIP transcription factor-encoding genes in the rice (Oryza sativa) genome. Their chromosomal distribution and sequence analyses suggest ...
Not now, but soon: Justification for continued research on CRISPR
Not now, but soon: Justification for continued research on CRISPR

... for a halt on research and clinical application of CRISPR-Cas93. The members of the group consisted of Edward Lanphier (one of the scientists responsible for developing a technological predecessor to CRISPR-Cas9) and four of his colleagues. They expressed concern over the safety and ethics of CRISPR ...
16p13 deletions FTNW - Unique The Rare Chromosome Disorder
16p13 deletions FTNW - Unique The Rare Chromosome Disorder

Analysis of DNA transcription termination sequences of gene coding
Analysis of DNA transcription termination sequences of gene coding

... dissociation of TEC into RNA, DNA and an RNA polymerase, what means the ending of transcription. In this study, the sequences located between phaC1 and phaZ genes in Pseudomonas species were analysed to identify the bacteria for Rho-independent transcription terminator. Five of studied sequences (tw ...
PDF
PDF

c. MUTANTS  OF PARAMECIUM  DEFECTIVE  IN  CHEMOKINESIS
c. MUTANTS OF PARAMECIUM DEFECTIVE IN CHEMOKINESIS

... to connect the test and control arms. Cells are allowed to distribute themselves between the two arms for 30 min at which time the stopcock is turned to seal the arms, the arms are emptied and the number of cells in each arm counted. The index of attraction and repulsion is Iche (number of cells in ...
Chromatin Signature Identifies Monoallelic Gene Expression Across
Chromatin Signature Identifies Monoallelic Gene Expression Across

... genes predicted as MAE in GM12878 showed only minor changes compared to our previous study, consistent with the use of slightly different ChIP-Seq datasets. To note, in this context, the use of quantile rank is equivalent to quantile normalization, but without requiring a reference dataset. Conseque ...
DNA Denaturing through UV-C Photon Dissipation: A
DNA Denaturing through UV-C Photon Dissipation: A

... 1988; 2009, Yarus and Christian, 1989) but also a UV-C dissipative era for the beginnings of life. When in such complexes and in water, RNA and DNA act as quenching molecules, providing the pigment molecule with an extremely rapid, sub picosecond, dexcitation channel (Pecourt et al. 2000) for passin ...
array CGH - Unique The Rare Chromosome Disorder Support Group
array CGH - Unique The Rare Chromosome Disorder Support Group

Fetal Hemoglobin Levels in Sickle Cell Disease and
Fetal Hemoglobin Levels in Sickle Cell Disease and

... the peripheral circulation of F cells compared with RBCs containing no detectable Hb F.9 In SS individuals, the variation in F-cell production as measured by the percent F reticulocytes is the major variable contributing to differences in Hb F levels. The broad distribution of Hb F levels in normal ...
Full Text  - The International Journal of Developmental Biology
Full Text - The International Journal of Developmental Biology

... In the mouse. the initial distribution of the Pax2gene transcripts is in postmitotic cells on both sides of the sulcus limitans of the neural tube, and later in the intermediate zone of the spinal cord, myelencephalon and metencephalon (Names at af., 1990; Asano and Gruss. 1992). Pax2 is also expres ...
Dragon Genetics -- Independent Assortment and Genetic Linkage
Dragon Genetics -- Independent Assortment and Genetic Linkage

... each other during the formation of eggs or sperm. Therefore, the traits determined by these two genes are inherited independently. For example, the wing gene and the horn gene are located on different chromosomes so they are inherited independently. Genes on different chromosomes are inherited indep ...
Coding Regions of MSX1 do not Contribute to Non
Coding Regions of MSX1 do not Contribute to Non

... examined regions of MSX1, two exons including intronicexonic boundaries in Turkish NS-CL/P patients. There are some reports that researchers found no MSX1 mutations in patients with clefts [8, 9]. According to the previous studies, mutations in MSX1 can contribute to NSCL/P as many as 2% of the tota ...
Non-Type 1 Cystinuria Marker DNA Test for Mastiff
Non-Type 1 Cystinuria Marker DNA Test for Mastiff

... turn  negative  after  castration,  and  are  therefore  not  as  informative  for  puppies  and  neutered   males.  Urine  testing  for  males  can  be  done  at  any  time,  but  is  not  generally  useful  before  2  years.   3. ...
Transgenic Tobacco Plants with Bacillus thuringiensis 8
Transgenic Tobacco Plants with Bacillus thuringiensis 8

... weights of tobacco budworm larvae and protection levels of transgenic plants from insect attack were measured. Protection levels were decided by comparing leaf areas consumed by larvae. In T2 transgenic plants, two leaves from each plant were individually wrapped with two layers of gauze and ten thi ...
Antibiotic resistance genes and identification of staphylococci
Antibiotic resistance genes and identification of staphylococci

... These results confirm the large spread of multidrugresistant bacteria, including staphylococci, which can be isolated from different environments, such as clinical, animal and food samples (Santos Sanches et al., 2000; Khan et al., 2005). The fact that 72.7% of our isolates carried two tetracycline r ...
Homoeotic and atavic mutations in insects Two main types of
Homoeotic and atavic mutations in insects Two main types of

... (telotype) are developmentally identical. From this it is concluded that the function of the wildtype allele is to repress the developmental characteristic of the telotype in the affected organ or region (autotype). Since homoeotic mutations are specific to compartments and double mutants show an ad ...
Review Set for 2.4 *Heredity
Review Set for 2.4 *Heredity

... counselor tells them that they are both carriers of a certain genetic disease. What does this mean? • A. They are both immune to the disease, and it is very likely that their children will also be immune to it. • B. There is a very high probability that one or both of them will develop the disease a ...
Neurogenetics User Manual
Neurogenetics User Manual

SEARCH_16S: A new algorithm for identifying 16S
SEARCH_16S: A new algorithm for identifying 16S

... Of the 6,487 finished assemblies, 6,401 had feature tables provided by NCBI. SEARCH_16S and NCBI reported the same number of 16S genes (i.e., number of paralogs) in 5,724 (88%). A total of 26,816 genes were reported with 24,402 (91%) reported by both. A gene was considered to be reported by both met ...
Albinism - OG
Albinism - OG

jxb.oxfordjournals.org - Oxford Academic
jxb.oxfordjournals.org - Oxford Academic

... endosperm. Moreover, amylose content is one of the key factors used for evaluating rice grain quality (Fitzgerald et  al., 2009; Jeon et  al., 2010). However, how these genes are regulated during rice seed development remains poorly understood. The rice Wx gene encodes the OsGBSSI, a key enzyme for ...
Introduction to Genetics
Introduction to Genetics

... from each parent Each parent contributes one of its two alleles (at random) to its offspring For example, a parent with genotype Aa (a heterozygote for alleles A and a) has a 50% probability of passing an A allele onto its offspring and a 50% probability of passing along an a allele. ...
Slides
Slides

... 2. Extension causes displacement of strand on other side of nick 3. D-loop is cleaved, invading strand is ligated to newly created 3′-end of the homologous strand 4. 3′-end of newly synthesized strand & the 5′-end of a homologous strand are ligated forming a ...
chapter 15 the nervous system
chapter 15 the nervous system

... Describe the part of the brain mainly involved in each of the following situations: 21. You studying for an upcoming biology exam. 22. You are rushing to class because you are late and almost fall on an icy patch of pavement, but manage to keep your balance. 23. You feel angry and embarrassed when y ...
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Nutriepigenomics

Nutriepigenomics is the study of food nutrients and their effects on human health through epigenetic modifications. There is now considerable evidence that nutritional imbalances during gestation and lactation are linked to non-communicable diseases, such as obesity, cardiovascular disease, diabetes, hypertension, and cancer. If metabolic disturbances occur during critical time windows of development, the resulting epigenetic alterations can lead to permanent changes in tissue and organ structure or function and predispose individuals to disease.
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