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Genetic susceptibility to Grave`s disease
Genetic susceptibility to Grave`s disease

... CD40, which is expressed primarily on B-cells and other APCs (15), has a fundamental role in B-cell activation and antibody secretion (16,17). The wholegenome linkage study done by Tomer identified a locus on chromosome 20q that was linked with GD. Fine mapping identified the CD40 gene as the GD sus ...
Simulating and cleaning gene expression data using
Simulating and cleaning gene expression data using

... p × n matrix of regression coefficients associated with X, m × k matrix of unobserved covariates introducing systematic noise, k × n matrix of regression coefficients associated with W m × n matrix of random noise. ...
Name
Name

... 45. Now that you have the mRNA codons, you can translate them into the corresponding amino acid using The Universal Genetic Code chart provided by your teacher. This is also very fun! The first three letters of each amino acid should be used as an abbreviation on the next page. As you can see, amino ...
Leukaemia Section t(3;8)(q26;q24) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Leukaemia Section t(3;8)(q26;q24) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... Note: Aberrant EVI1 expression usually occurs in AML, MDS or CML-BC as a result of translocation involving 3q26. The most common ones are inv(3)(q21q26), t(3;3) and t(3;21)(q26;q22). The partner genes of EVI1 are identified as Ribophorin I in inv(3)(q21q26) and t(3;3), AML/ MDS1 /EAP in t(3;21), and ...
2006 bradley de novo
2006 bradley de novo

... design an amphipathic segment of α-helical secondary structure, a binary pattern of P-N-P-P-N-N-P is used. Our initial α-helical design focused on the four-helix bundle motif (Fig. 3). In this structure, the hydrophobic face of each helix is oriented toward the central core of the bundle, whereas th ...
A novel C. elegans zinc finger transcription factor, lsy
A novel C. elegans zinc finger transcription factor, lsy

... for lateral symmetry (lsy) defects under a stereomicroscope equipped with a fluorescent light source. Screening through 12,200 haploid genomes, we identified a total of 10 mutant alleles that display a ‘two ASER’ phenotype in which the ASEL neuronal fate has switched to an ASER neuronal fate (see Fi ...
Conservation ofParaHoxgenes` function in patterning of the
Conservation ofParaHoxgenes` function in patterning of the

... date one of these three genes, Xlox has not been reported from any ecdysozoan taxa and both Xlox and Gsx are absent in nematodes. There is evidence that the ParaHox genes were ancestrally a single chromosomal cluster. Colinear expression of the ParaHox genes in anterior, middle, and posterior tissue ...
Oncogenic potential of the DNA replication licensing protein
Oncogenic potential of the DNA replication licensing protein

... often led to the identi®cation of proto-oncogenes or tumor suppressor genes (Jonkers and Berns, 1996; Nusse and Varmus, 1982; Ben-David et al., 1991; Morishita et al., 1988). In this study, we investigated whether CDT1 can function as an oncogene. We demonstrate that CDT1 is highly expressed in huma ...
Antibiotics II
Antibiotics II

... conditions, where a patient might have a stop codon in an important gene, which may predispose the patient toward a particular syndrome or disease, like cystic fibrosis, for example. This means that the aminoglycosides would have to have an effect of the patient’s ribosome (not the bacterial ribosom ...
The Drosophila Tissue Polarity Gene inturned Functions Prior to
The Drosophila Tissue Polarity Gene inturned Functions Prior to

... et al. 1993; WONGand ADLER 1993) that are assembled at the distal-most vertex of each of the polygonally shaped pupal wing cells (WONGand ADLER 1993). The prehair being formed at the distal vertex appears to be essential for the development of distal polarity as mutations in six tissue polarity gene ...
Biological Ontologies in Rice Databases. An Introduction to the
Biological Ontologies in Rice Databases. An Introduction to the

... contrast, Oryzabase, as described below, has defined fine developmental stages of rice in embryogenesis and vegetative and reproductive phases and therefore this has been introduced into the GRO [see Appendix 1 (14)]. We expect to provide detailed information on the developmental stages of other pla ...
overview of inheritance - American Heart Association
overview of inheritance - American Heart Association

... evaluated by geneticists in order to determine the cause of the cardiomyopathy so therapy can be optimized for them. Genetic evaluation is also useful in determining if any other members of the family are at risk for cardiomyopathy so they can also receive the best medical care. Part of this evaluat ...
Developmental timing in Dictyostelium is regulated by the Set1 histone methyltransferase
Developmental timing in Dictyostelium is regulated by the Set1 histone methyltransferase

... methyltransferase. In the absence of Set1, cells display unusually rapid development, characterized by precocious aggregation of amoebae into multicellular aggregates. Early differentiation markers are abundantly expressed in growing set1 cells, indicating the differentiation program is ectopically ...
Nucleus and Mitochondria: structure and disease
Nucleus and Mitochondria: structure and disease

... Two types of proteins make up the nuclear lamina. Lamin A and C are encoded by the same gene by are slightly different due to alternative splicing of their mRNA. Lamin B is essential. ...
Gene Section FANCC (Fanconi anaemia complementation group C) Atlas of Genetics and Cytogenetics
Gene Section FANCC (Fanconi anaemia complementation group C) Atlas of Genetics and Cytogenetics

... repair, FANCD2 return to the non-ubiquinated form. FANCC may have mutlifunctional roles, in addition to its involvement in the FA pathway. FANCC binds to cdc2 (mitotic cyclin-dependent kinase), STAT1, GRP94 (a chaperon protein), NADPH, and a number of other proteins; involved in DNA repair and in su ...
Accepted version  - Queen Mary University of London
Accepted version - Queen Mary University of London

... evidence of a central role in activating both benznidazole and nifurtimox, is a NADHdependent mitochondrial type I NTR (5). In the case of nifurtimox, the active metabolite is an unsaturated open chain nitrile (19). ...
2015 Pearson Education, Inc.
2015 Pearson Education, Inc.

Question 1 _____/ 30 points Question 2 _____/ 20 points Question 3
Question 1 _____/ 30 points Question 2 _____/ 20 points Question 3

... 100 cells) of spontaneous reversion to the Leu+ phenotype. Of the three classes of elements you are considering, which type of element is most likely to be responsible for this “unstable” allele. Explain your choice. This mutation is most likely caused by (3), the DNA virus that inserts by CSSR. The ...
Meiosis and mitosis
Meiosis and mitosis

... end of each chapter covered • As stated on the website you need to present a doctor’s note to the instructor within 48h of missing a quiz or a test • If you have a legitimate reason for missing a ...
McGrath, Patrick: Uses of the Singular Value Decompositions in Biology
McGrath, Patrick: Uses of the Singular Value Decompositions in Biology

... basis that this matrix can be decomposed into. Some common basis would be the sine and cosine waves of a Fourier transform, or the exponential functions of a Laplace transform. However the SVD is the only decomposition that causes the columns of the weight matrix to be orthonormal. The singular valu ...
Genetic Toggle Switch without Cooperative Binding
Genetic Toggle Switch without Cooperative Binding

... concluded that for Hill-coefficient h=1 there is a single steady state solution and no bistability. • Conclusion - cooperative binding (Hill-coefficient h>1) is required for a switch Gardiner, Cantor and Collins, Nature, 403, 339 (2000) Cherry and Adler, J. Theor. Biol. 203, 117 (2000) ...
aps4-artifact
aps4-artifact

... disease. Both of their parents died in a car crash in their thirties. Sue, another sister, refuses to be tested. a. Draw a pedigree for this family b. What is the risk that Sam’s daughter has inherited HD? Sam’s wife does not have the disease. c. What is the risk that Sam’s son has inherited HD? d. ...
Studying Variation in Gene Expression of
Studying Variation in Gene Expression of

... VII. Reflection and Application Questions: 14. Review the lab introduction. What do they mean by gene expression? 15. Why might it be beneficial to the plant to not express the chlorophyll gene when there is no light? 16. How do you know that the plants grown in the dark had the gene, but were not e ...
nsfrui2004 - Mount Holyoke College
nsfrui2004 - Mount Holyoke College

... {Fortier, 2003 #545} (see below). Tina and Priya have done confocal microscopy to examine changes in cell shape during early leg development in control and ßFTZ-F1 mutant prepupae. Tina has also made "movies" of leg morphogenesis in wild-type animals and ßFTZ-F1 mutant animals expressing GFP in thei ...
The Modular Structure and Function of the Wheat HI Promoter with S
The Modular Structure and Function of the Wheat HI Promoter with S

... Fig. 1 Nucleotide and deduced amino acid sequences of wheat HI genes, TH315 (A) and TH325 (B). The deduced amino acid sequences are shown in single capital letters below the nucleotide sequences. The asterisks denote the stop codons. The transcriptional initiation site (+1), the deletion points desc ...
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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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