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microbial genetics
microbial genetics

... verifiable bases. But the firm establishment of such a chromosomal mechanism of inheritance does not necessarily preclude a role for other extra nuclear cell parts. In fact, when certain mutants demonstrated an inheritance very different from normal Mendelian inheritance patterns, geneticists were f ...
module 12: mendelian genetics 2 - Peer
module 12: mendelian genetics 2 - Peer

... Patterns of inheritance are often much more complex than those encountered in the first genetics module, Module 11. Mammals, birds, plants like garden peas and insects have thousands of different genes in their genomes. Frequently scientists wish to study inheritance patterns for two or more genes s ...
Leukaemia Section t(1;11)(p32;q23)  Atlas of Genetics and Cytogenetics
Leukaemia Section t(1;11)(p32;q23) Atlas of Genetics and Cytogenetics

... About half cases were ALLs and half cases AMLs. There were 17 ALLs, (mainly CD19+, CD10-) 2 biphenotypic leukaemias, 15 AMLs (of which were three M4-AMLs and nine M5-AMLs), and two MDS. There were at least nine cases of secondary leukaemia (and also 3 cases of "relapse", but each time with a differe ...
RNA gene prediction
RNA gene prediction

... Developed at University of Copenhagen Statistical significance is the measure for gene prediction. Ґ High quality data set based on similarity in SwissPRot is extracted from genome. Ґ Data set used to estimate the HMM where based on ORF score and length statistical significance is calculated. Proble ...
Lenny Moss (2001) "DECONSTRUCTING THE GENE"
Lenny Moss (2001) "DECONSTRUCTING THE GENE"

Genetic and biochemical approaches towards unravelling the
Genetic and biochemical approaches towards unravelling the

... genes encoding the gallate decarboxylase enzyme as well as a putative second tannase enzyme. In this work, S. gallolyticus tannase and gallate decarboxylase encoding genes involved in tannin degradation have been identified and their expression comparatively studied. In addition a novel tannase has ...
Oncology and Genetics Doctoral School
Oncology and Genetics Doctoral School

... the efficacy of new molecules, but definitive results are not available yet. Rb2 monitors cell cycle progression mostly by interaction with HCC g with E2F family members of transcription factors and with D cyclins. Its expression levels correlate inversely prognosis and VEGF production. Since angiog ...
Genes
Genes

... small effect ...
Can 2 Brown-Eyed Parents have a Blue
Can 2 Brown-Eyed Parents have a Blue

... In genetics, there are 2 ways to describe individuals… ...
Genes and Cleft Lip and Palate
Genes and Cleft Lip and Palate

... dominant forms of clefting, only one gene in the pair needs to be altered for the carrier to have a cleft. The gene is present on one of the autosomes, i.e. chromosomes number 1-22. Even though the other gene in the pair has the usual DNA sequence it cannot compensate for the altered gene. When a pe ...
Paralogous gene conversion, allelic divergence of attacin genes
Paralogous gene conversion, allelic divergence of attacin genes

... study the differential expression of attacin gene in BmNPV resistance. In addition to that the organization of paralogous attacin genes, their tissue specific expression and variation in the promoter and coding regions were analyzed. The attacin cDNA sequence (accession no. S78369) was blast (BLAST) ...
asexual seed formation for agricultural crop improvement
asexual seed formation for agricultural crop improvement

... a deeper knowledge of reproductive development in plants. We have isolated one gene, which was termed APOSTART because of its START domain and its putative involvement in apomixis (Albertini et al. 2005, Plant Phys 138:2185-2199). Our previous results demonstrate that some APOSTART members are expre ...
Practice exam (2012) key
Practice exam (2012) key

... PCB5065 Fall 2012 - Exam 4 - Chase page 1 of 4 ...
the PDF - Breastcancer.org
the PDF - Breastcancer.org

... (none have receptors) and 100% (all have receptors). 2. An Allred score between 0 and 8. This scoring system is named for the doctor who developed it. The system looks at what percentage of cells test positive for hormone receptors, along with how well the receptors show up after staining (this is ...
a new set of hereditary cancer tests
a new set of hereditary cancer tests

... that predispose a person to breast, ovarian, and uterine (endometrial) cancer and, in some cases, other cancers or noncancerous conditions. Identifying a causative genetic variant provides valuable information for the patient’s diagnosis, treatment and risk reduction options, surveillance (early scr ...
Gene Section WWC1 (WW and C2 domain containing 1)
Gene Section WWC1 (WW and C2 domain containing 1)

... kinase aurora and is required for precise mitotic spindle assembly and chromosome alignment (Xiao et al., 2011b; Zhang et al., 2012). Additionally, KIBRA is also regulated by cyclin-dependent kinase 1 (CDK1) and cell division cycle 14A/B phosphatases (CDC14A, CDC14B) and thus regulates cell-cycle pr ...
function Complex genomic rearrangements lead to novel primate gene
function Complex genomic rearrangements lead to novel primate gene

... RBD) related to the one present in RanBP1, a variable number of zinc-finger motifs, and a C terminus with homology to cyclophilin A (Fig. 1A). In addition to the human RanBP2 ortholog, we detected eight partial copies located in regions that have arisen from intrachromosomal segmental duplications ( ...
Genes, Chromosomes, and Numbers
Genes, Chromosomes, and Numbers

D melanogaster - GEP Community Server
D melanogaster - GEP Community Server

... 2. Other repetitious DNA, derived from transposable elements, also causes difficulties; because one finds nearly identical sequences located in different regions of the genome, mistakes can be made in assembling sequence data. High quality discrepancies can identify these. 3. Much of the repetitous ...
Origins of Eukaryotic Sexual Reproduction
Origins of Eukaryotic Sexual Reproduction

... diploids when the mating-type locus is homozygous (a/a and a/a) and the cells switch to a specialized mating cell type called opaque (Miller and Johnson 2002). Cell – cell fusion then generates tetraploid cells, and adverse media conditions stimulate random chromosome loss to return to a diploid, or ...
Biochemical and genetic characterization of the
Biochemical and genetic characterization of the

... previously designated as S.cerevisiae DNA ligase II In a previous study we described the partial purification and characterization of a 90 kDa DNA ligase that we designated DNA ligase II, since it had different biochemical properties than Cdc9 DNA ligase and was not recognized by a Cdc9 antiserum (2 ...
Chapter 11
Chapter 11

...  Imagine that each gene has two alleles, one light and one dark, that demonstrate incomplete dominance.  An AABBCC individual is dark and aabbcc is light ...
Roots Redefined: Anatomical and Cenetic Analysis of Root
Roots Redefined: Anatomical and Cenetic Analysis of Root

... root and they subsequently acquired root cap characteristics. Upon ablation of cortical initials, pericycle initial cells expanded, divided into the resulting cavity, and subsequently formed cortical parenchyma and endodermis. These and related experiments show that positional information is importa ...
BLOOD CLOTTING CONDITIONS (HEREDITARY THROMBOPHILIAS)
BLOOD CLOTTING CONDITIONS (HEREDITARY THROMBOPHILIAS)

... all have a 1 chance in 2 (50%) of also having a mutation. Screening may be performed through specialised blood tests through your family doctor, or genetic testing may be offered if the gene mutations have been identified in your family. If you are identified as having a gene mutation but do not hav ...
Section 18-1
Section 18-1

... Derived characters – characteristics that appear in recent parts of a lineage but not in its older members ...
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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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