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Chapter 01 An Introduction to Biology
Chapter 01 An Introduction to Biology

... 2. Which of the following is likely NOT a common feature shared among all living organisms? A. All living organisms use energy. B. All living organisms maintain organization. C. All living organisms have evolved over the course of many generations. D. All living organisms maintain some level of home ...
APDC Unit XI Meiosis
APDC Unit XI Meiosis

... • Fragmentation (& regeneration) – body breaks into parts & all of them can grow into adults • Advantages *best in stable environments* • Don’t need partner (good for isolated or nonmotile) • Multitudes of offspring in short time (colonize quickly) ...
Identification of a Novel Point Mutation of Mouse Proto
Identification of a Novel Point Mutation of Mouse Proto

... hemoglobin concentration (MCHC, the ratio of MCH to MCV); platelet counts (PLT); and mean platelet volume (MPV, the average volume of individual platelets). The P-values were evaluated using an unpaired two-tailed t-test using Prism software (GraphPad Software, San Diego) between the blood parameter ...
NIH Public Access - University of Chicago
NIH Public Access - University of Chicago

... The transcription factors EBF and Pax5 play major roles in B cell fate specification and commitment by activating B lineage genes and concomitantly repressing genes of alternate lineages8,19,20. EBF initiates restriction of alternate lineage options and B cell fate commitment independently of Pax5 ( ...
題目: Regulatory mechanism of floral coloration in Oncidium cultivars
題目: Regulatory mechanism of floral coloration in Oncidium cultivars

... isomerase (OgCHI), dihydroflavonol 4-reductase (OgDFR) and anthocyanidin synthase (OgANS) were isolated and their expression patterns were characterized. Northern blot analysis confirmed that although they are active during floral development, OgCHI and OgDFR genes are specifically down-regulated in ...
Fulltext PDF - Indian Academy of Sciences
Fulltext PDF - Indian Academy of Sciences

... protein factor identified on the cell surface only in males. This is the H-Y antigen and for many years it was thought to be involved in male determination. The identification of a female mouse carrying an active H-Y antigen gene translocated from the Y-chromosome to the X chromosome disproved this ...
the art and design of genetic screens
the art and design of genetic screens

... than 20 times this rate. A disadvantage of EMS in the past has been that it was very difficult and laborious to map point mutations to specific genes. This problem has been solved largely by the development of single nucleotide polymorphism (SNP) maps that allow the rapid meiotic mapping of mutation ...
Body Axis Determination in Birds and Mammals
Body Axis Determination in Birds and Mammals

... Segment identity controlled by segment identity (aka homeotic, aka selector) genes. Discovered through homeotic mutations. This is a mutation that causes the transformation of one structure to another homologous structure. (Homologs have evolutionarily related ancestry—both derived from a common anc ...
HLRCC Science
HLRCC Science

... strand of mRNA is separated from the DNA template, and the two DNA strands reunite. The new strand of mRNA is complementary to the DNA strand that made it. For example, a DNA sequence of ATCGTTACC would result in an mRNA sequence of UAGCAAUGG. mRNA is the direct code for proteins. It dictates the s ...
Biology is immature Biosemiotics. Epilogue
Biology is immature Biosemiotics. Epilogue

... multicellular organisms are integrative structures interacting with their surroundings via the activity of individual cells (Hoffmeyer 2008, 116). The lineage is the subject that may eventually learn to cope with changes in the ecological niche conditions or, otherwise, go extinct. According to pres ...
Datasheet for Onchocerca volvulus chitinase (OvCHT1)
Datasheet for Onchocerca volvulus chitinase (OvCHT1)

... (pH 7.5), 1 mM EDTA) mixed and left on ice for 15 minutes. After centrifugation to settle the resin, the supernatant was collected containing the unbound protein sample. The resin was then washed twice with 1 ml of binding buffer, centrifuged, and the wash samples collected. The chitinase activity o ...
Why the
Why the

... (Lahn) and David C. Page of the Whitehead Institute for Biomedical Research in Cambridge, Mass., showed that the Y lost the ability to swap DNA with the X in an unexpected, stepwise fashion— first involving a swath of DNA surrounding the SRY gene and then spreading, in several discrete blocks, down ...
mendel`s legacy
mendel`s legacy

... 1. An allele is each of two alternative forms of a gene. 2. In meiosis, the two alleles of each gene are segregated when the two chromosomes in each pair of homologues are separated into different gametes. Alleles of genes located on different chromosomes or far apart on the same chromosome assort i ...
NOTE: The provided figures may be useful and beneficial
NOTE: The provided figures may be useful and beneficial

Ethylene and Sub1
Ethylene and Sub1

... • EIN3 is usually recruited for degradation by the SCFEBF complex. • Ethylene signalling prevents EIN3 degradation thereby allowing it to activate transcription. • The protein EBF1 that marks out EIN3 for ubiquitin dependent destruction is also controlled by ubiquitin dependent destruction. ...
A haploid-specific transcriptional response to
A haploid-specific transcriptional response to

... mating-type status in the regulation of microtubule properties (2), the maintenance of cell wall integrity (3) and DNA repair by non-homologous end-joining (NHEJ) (4). Galitski et al. (5) investigated the contributions of mating-type and ploidy to 45 gene expression in three isogenic sets of yeast s ...
Slides
Slides

... that you and your part go for genetic counselling. Your partner will also be screened for thalassaemia If you and your partner are both carrier there is a 1in 4 chance that your child will have thalassaemia major ...
Wanganui High School
Wanganui High School

... coordination, shaking, loss of memory and mental deterioration. It is caused by a dominant allele and so only needs one parent to pass it on. There are no symptoms usually until people are in their 40’s – which is usually after they have had children of their own. They have a 50% chance of passing o ...
Chapter 17.
Chapter 17.

... Inheritance of metabolic diseases suggested that genes coded for enzymes  each disease (phenotype) is caused by non-functional gene product ...
Chapter 17. - Cloudfront.net
Chapter 17. - Cloudfront.net

... Inheritance of metabolic diseases suggested that genes coded for enzymes  each disease (phenotype) is caused by non-functional gene product ...
Abstract/Session Information for Program Number 1264
Abstract/Session Information for Program Number 1264

... ossification. Until now, transcriptional repressors of Runx2 in vivo have yet to be identified. By combining SNP analysis of control and CCD subjects and cross species sequence analysis, we have identified conserved GATA domain binding sites in the RUNX2 promoter. Because TRPS1 is the only GATA doma ...
Year 1 Medical Genetics Final Examination March 1, 1996
Year 1 Medical Genetics Final Examination March 1, 1996

... A. usually require loss of both alleles before cell transformation occurs B. a single mutation can activate these genes to suppress vital cellular pathways resulting in aberrant cell growth and proliferation C. loss of heterozygosity for these genes is a hallmark feature found in cancers due to tumo ...
Genetics and genomics
Genetics and genomics

Microbial Genetics Lab
Microbial Genetics Lab

... covered by high-density probes. These allow the identification of transcription start sites and operons and thus regions important in gene regulation. In this experiment we would isolate RNAs from a control cyanobacterium and a mutant cyanobacterium, e.g. one with a defect in photosynthetic electron ...
Characterization of a heat-active archaeal β
Characterization of a heat-active archaeal β

... The gene bgl1 was amplified (for: GGATCCGTAAAGTTCCCTAAAGG, BamHI recognition site is underlined, rev: GTCGACCTAAGTAAGAACGTTTGG, SalI recognition site is underlined) and ligated into subcloning vector pJET (Thermo Scientific, Schwerte, Germany) prior to transformation of E. coli NovaBlue. The plasmids ...
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NEDD9

Neural precursor cell expressed developmentally down-regulated protein 9 (NEDD-9) is a protein that in humans is encoded by the NEDD9 gene. NEDD-9 is also known as enhancer of filamentation 1 (EF1), CRK-associated substrate-related protein (CAS-L), and Cas scaffolding protein family member 2 (CASS2). An important paralog of this gene is BCAR1.
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