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Radiation Hybrid Mapping: A Somatic Cell Genetic Method for
Radiation Hybrid Mapping: A Somatic Cell Genetic Method for

... Despite these technical advances, present-day maps of human chromosomes are ,very crude in molecular terms. On average, 1 percent meiotic recombination between two markers on a human chromosome corresponds to 1 megabase pairs (Mb) of DNA. In situ hybridization can localize markers to within 2 percen ...
Word - NIEHS SNPs Program - University of Washington
Word - NIEHS SNPs Program - University of Washington

... 7. Close the VG2 image and Select Display Type windows and return to the Genome Variation Server Page. Now, change the allele frequency cutoff to 5. How many SNPs have a minor allele frequency of 5% or greater? 8. Now deselect HapMap-CEU-Panel and select EGP-CEPH-Panel, enter 0 in the allele frequen ...
Extra-chromosomal telomeric DNA in cells from
Extra-chromosomal telomeric DNA in cells from

... less telomere shortening relative to Atm+/+ cells than observed at chromosome ends by Q-FISH (Fig. 1). Alternatively, a high proportion of Atm–/– interphase cells could have been in S-phase or telomeres in Atm –/– cells could be replicated earlier than those in wild-type cells. To study these possib ...
Molecular Mechanisms of Plant and Microbe Coexistence
Molecular Mechanisms of Plant and Microbe Coexistence

... stress response in plant roots of rice and barley (Marschner and Crowley 1998). Ice nucleation activity expressed by rhizosphere populations of Pseudomonas fluorescens Pf5 decreased from 1 to 2 days after the bacterium was inoculated onto root surfaces, suggesting that iron became more available to ...
gene (Pun1? - UC Davis Plant Sciences
gene (Pun1? - UC Davis Plant Sciences

... • AT3 activity remains to be elucidated – Mutants may identify accumulation of intermediates ...
Relationships Between RNA Polymerase II Activity and Spt
Relationships Between RNA Polymerase II Activity and Spt

... yeast genome and many of these exhibit modulation by many factors (Martens et al. 2004, 2005; Hainer et al. 2011; Bird et al. 2006). Furthermore, widespread antisense transcription is being revealed as a mechanism for shaping gene regulation in a number of ways, including transcription over promoter ...
Full-Text PDF
Full-Text PDF

... δ-carotene (ε,ψ-carotene) to produce α-carotene. No ε-cyclization activity was identified for BfLCYB. Sequence comparison showed that BfLCYB shares conserved domains with other functionally characterized lycopene cyclases from different organisms and belongs to a group of ancient lycopene cyclases. ...
Information Encoding in Biological Molecules: DNA and
Information Encoding in Biological Molecules: DNA and

... • The microRNA bantam regulates the Drosophila (fruitfly) gene hid by binding the 3’ UTR. Hid is involved in apoptosis, and it is possible that binding sites for bantam could be found in the 3’ UTR of other apoptosis genes as well. Obtain the 3’ UTR sequence of all Drosophila genes known to be invol ...
Replication timing as an epigenetic mark
Replication timing as an epigenetic mark

... Developmental regulation is a key hallmark of an epigenetic mark.7 While the aforementioned observations make a strong case for the mitotic inheritance of replication timing profiles in a given cell type, evidence for developmental regulation has been primarily anecdotal.12 As described, the first a ...
Prentice Hall Biology
Prentice Hall Biology

... each with half the number of stage of mitosis. opposite ends of the cell. chromosomes as the original. ...
SNP presentation
SNP presentation

... about of lactase produced generally decreases- making it harder to digest milk There is a SNP in the region that turns off the lactase gene: G allele: lactase shut off adulthood (GG is lactose intolerant) A allele : lactase produced into adulthood (AA & AG are lactose tolerant) ...
A missense mutation in growth differentiation factor 9 (GDF9) is
A missense mutation in growth differentiation factor 9 (GDF9) is

... Results: A QTL-region was identified on sheep chromosome 5, close to the growth differentiation factor 9 (GDF9), which is known to be a strong candidate gene for increased ovulation rate/litter size. Sequencing of the GDF9 coding region in the most extreme sires (high and low BLUP values) revealed a ...
GENE-CBR - Indiana University School of Informatics
GENE-CBR - Indiana University School of Informatics

... Machine Learning and Data Mining techniques but … Its capacity for generating enormous amounts of data is, however, also an handicap: great amount of data belonging to each individual (thousands of genes) • efficiency and memory problems ...
A novel locus of Yersinia enterocolitica serotype O:3 involved in
A novel locus of Yersinia enterocolitica serotype O:3 involved in

... pRV16, the roughing was a little more prominent than with YeO3-RfbR12/pRV16. The inability to trans-complement the phage receptor with any of the constructs was intriguing; either the genes were not properly expressed from the plasmids, some important gene(s) were missing or the presence of the plas ...
Lecture 7 POWERPOINT here
Lecture 7 POWERPOINT here

... Different AA’s are linked together via PEPTIDE bonds The individual amino acids within a protein are known as RESIDUES The smallest known P’ is just nine residues long - oxytocin The largest is over 25,000 residues - the structural protein titin ...
カイコの油蚕変異体に関する
カイコの油蚕変異体に関する

... International Silkworm Genome Consortium 2008) and a highdensity linkage map (Yamamoto et al., 2006, 2008), molecular genetic studies on the oily mutants have become more active, and the responsible genes for oily mutants have been further identified. The ow (waxy translucent) mutant has a 25-bp in ...
Issue #11 August 2011 In This Issue Taking A Swing DBAF Funds
Issue #11 August 2011 In This Issue Taking A Swing DBAF Funds

... genes controlling many aspects of human growth and development ..... including erythropoiesis. The human glucocorticoid receptor gene is complex, expressing a number of different forms of the protein with likely influence how different tissues respond to glucocorticoids. There are two major forms of ...
Chromosome Analysis Suite 3.1 (ChAS 3.1)
Chromosome Analysis Suite 3.1 (ChAS 3.1)

... ChAS 3.1 includes a table with the following calls made for each mutation: “high confidence,”, “lower confidence,” and “undetected.” The thresholds for the “high-confidence” calls were established based on separations between the normal reference and mutant calls that resulted in 95% sensitivity and ...
Fanconi anemia and RAD50 deficiency: genetic and functional
Fanconi anemia and RAD50 deficiency: genetic and functional

... oxygen species and other DNA damaging agents. FA is caused by biallelic mutations in at least 11 different genes which appear to function in the maintenance of genomic stability. Eight of the FA genes form a nuclear core complex with a catalytic function involving ubiquitination of the central FANCD ...
Multiple Barriers to Nonhomologous DNA End Joining
Multiple Barriers to Nonhomologous DNA End Joining

... ABSTRACT Repair of meiotic double-strand breaks (DSBs) uses the homolog and recombination to yield crossovers while alternative pathways such as nonhomologous end joining (NHEJ) are suppressed. Our results indicate that NHEJ is blocked at two steps of DSB repair during meiotic prophase: first by the ...
Animal models for Klinefelter`s syndrome and their relevance for the
Animal models for Klinefelter`s syndrome and their relevance for the

... significantly lower in cognitive exercises (DeLisi et al., 2005) while young boys have impaired executive skills of social processing supposed to be linked to X chromosome-dependent effects in areas of cognitive strength (Temple and Sanfilippo, 2003; van Rijn et al., 2006). To date, it is not clear wh ...
Developing a Gene Therapy for Motor Neuron Disease
Developing a Gene Therapy for Motor Neuron Disease

... founder of the modern hospice movement. What is MND? Motor neuron disease (MND) has first been described by the French neurologist Jean-Martin Charcot in 1869. MND is a term used for a group of diseases which are caused by the death of motor neurons in the brain and spinal cord leading to progressiv ...
From DNA to Disorder - Liberty Union High School District
From DNA to Disorder - Liberty Union High School District

... 80% of achondroplasia cases; however, it can still be inherited. Over 80% of individuals with achondroplasia have parents with normal stature and have achondroplasia as the result of a de novo gene mutation. Such parents have a low probability of having another child with achondroplasia. An individu ...
The Drosophila small conductance calcium
The Drosophila small conductance calcium

... I would also like to thank the members of my thesis committee: James Maylie, Richard Walker, and Peter Gillespie. They, along with John, have picked me up when I have stumbled through this process. Scientifically I could not have imagined a better group of mentors. I would like to thank all of the m ...
Parental Methamphetamine Exposure Affects Offspring`s Behavior and
Parental Methamphetamine Exposure Affects Offspring`s Behavior and

...  Light/dark box:Maternally influenced phenotye (dependent on dam treatment (“METH induced”) and sexually dimorphic ...
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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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