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The Parasexual Cycle in Candida albicans Provides an
The Parasexual Cycle in Candida albicans Provides an

... In addition, several isolates had undergone extensive genetic recombination between homologous chromosomes, including multiple gene conversion events. Progeny strains exhibited altered colony morphologies on laboratory media, demonstrating that the parasexual cycle generates phenotypic variants of C ...
1 FRQ-interacting RNA Helicase (FRH) Mediates Negative and
1 FRQ-interacting RNA Helicase (FRH) Mediates Negative and

... allele, frhR806H, clock function is completely disturbed, while roles of FRH essential for viability are left intact. FRHR806H still interacts with FRQ, but interaction between the FRQ-FRHR806H complex (FFC) and WCC is severely affected. Phosphorylation of WC-1 is reduced in the mutant leading to co ...
Forche et al. 2008 PLoS Biology
Forche et al. 2008 PLoS Biology

... In addition, several isolates had undergone extensive genetic recombination between homologous chromosomes, including multiple gene conversion events. Progeny strains exhibited altered colony morphologies on laboratory media, demonstrating that the parasexual cycle generates phenotypic variants of C ...
Cell Death and Unbalanced Growth` in Neurospora
Cell Death and Unbalanced Growth` in Neurospora

... between the two classes of mutants. A very similar phenomenon was described by Fries (1948)in Ophiostoma and by Macdonald & Pontecorvo (1953)in Aspergillus nidulans. Macdonald & Pontecorvo showed that spores of a biotin-requiring mutant died off rapidly in a biotin-deficient medium. The very interes ...
Human pigmentation variation: Evolution, genetic basis, and
Human pigmentation variation: Evolution, genetic basis, and

... Pigmentation, which is primarily determined by the amount, the type, and the distribution of melanin, shows a remarkable diversity in human populations, and in this sense, it is an atypical trait. Numerous genetic studies have indicated that the average proportion of genetic variation due to differe ...
Human pigmentation variation: Evolution, genetic basis, and
Human pigmentation variation: Evolution, genetic basis, and

... Pigmentation, which is primarily determined by the amount, the type, and the distribution of melanin, shows a remarkable diversity in human populations, and in this sense, it is an atypical trait. Numerous genetic studies have indicated that the average proportion of genetic variation due to differe ...
org.Mm.eg.db
org.Mm.eg.db

... assigned in the literature, users are cautioned that this map may produce multiple matching results for a single gene symbol. Users should map back from the entrez gene IDs produced to determine which result is the one they want when this happens. Because of this problem with redundant assigment of ...
the hemophilia gene, click here
the hemophilia gene, click here

... chromosome is arranged in thousands of units called genes. There are between 30,000 and 40,000 genes in each cell of the body. Each one of the genes is in charge of telling the body to produce certain proteins. Some genes decide, for example, the colour of the eyes. Chromosomes come in pairs and eve ...
as Adobe PDF - Edinburgh Research Explorer
as Adobe PDF - Edinburgh Research Explorer

... arrows). The observed expression is broader than that of the endogenous dac gene, which is limited to the hind- ...
ADRC2010_GetTheMostOutofFlyBase
ADRC2010_GetTheMostOutofFlyBase

... – Controlled Vocabularies, Term Reports and TermLink – QueryBuilder and Templates ...
In this work, the quantitative assessment of cell lysis was performed
In this work, the quantitative assessment of cell lysis was performed

... induction (data not shown). Lysis occurred in exponential and early stationary phases, but never in late stationary phase. Lysis behavior in high copy plasmid had a high variability between different experiments carried out in separate days, in fact lysis entity in exponential phase and early statio ...
Fulltext - Jultika
Fulltext - Jultika

... kilodalton membrane-associated collagen with interrupted triple helices multiple epiphyseal dysplasia magnetic resonance imaging messenger RNA collagen with multiple triple helix domains and interruptions amino non-collagenous domain osteoarthritis or osteoarthrosis Online Mendelian Inheritance in M ...
The virulence plasmids of Salmonella
The virulence plasmids of Salmonella

... binding to a proximal region, which is essential to activate spvA transcription. Expression of spvR is self-regulated, and the structure of its promoter is similar to that of spvA. A weak interaction with SpvR seems to favor spvR expression, whereas a stronger interaction is required to activate the ...
LINKAGE AND MAPPING IN EUKARYOTES
LINKAGE AND MAPPING IN EUKARYOTES

... fter Sutton suggested the chromosomal theory of inheritance in 1903, evidence accumulated that genes were located on chromosomes. For example, Morgan showed by an analysis of inheritance patterns that the white-eye locus in Drosophila is located on the X chromosome. Given that any organism has many ...
MATRILINEAL, a sperm-specific phospholipase, triggers maize
MATRILINEAL, a sperm-specific phospholipase, triggers maize

... and signalling (Table 2 and Extended Data Table 6). Given the intensive communication between the two gametophytes and the dynamic membrane reshuffling involved in fertilization28, we speculate that some of these differentially expressed genes may mediate one or more of the pleiotropic phenotypes tr ...
BLASTOCYST TRANSFER
BLASTOCYST TRANSFER

... reach the blastocyst stage (X and 21) ...
The full-length HIV-1 molecular clone pLAI 61 was used to produce
The full-length HIV-1 molecular clone pLAI 61 was used to produce

... numbers refer to the position on the genomic HIV-1 RNA transcript, with +1 being the capped G residue. Supplementary Table 1 lists all oligonucleotides used in this study. The tat exon 1 was amplified by PCR on pLAI with primers NotI-WdV005 and WdV002; tat exon 2 with primers WdV007 and NotI-WdV004; ...
Isolation and characterization of an RNA that binds with high affinity
Isolation and characterization of an RNA that binds with high affinity

... motif is indicated by box and the core element that is required for binding to Tat protein is indicated by red. ...
Telomere maintenance without telomerase
Telomere maintenance without telomerase

... a genome-wide hyper-recombination phenotype. However, this analysis did not exclude the possibility that in a cell that lacked telomerase, unreplicated telomeres could themselves become hyper-recombinogenic, a point that will be re-addressed later in this review. Although all survivors recovered fro ...
Syllabus PDF
Syllabus PDF

... a) All recommendations involving clinical medicine must be based on evidence that is accepted within the profession of medicine as adequate justification for their indications and contraindications in the care of patients. b) All scientific research referred to, reported or used in CME in support or ...
History of Discoveries in Molecular Biology
History of Discoveries in Molecular Biology

... The idea was not the product of a painstaking laboratory discipline, but was conceived while cruising in a Honda Civic on Highway 128 from San Francisco to Mendocino. "I do my best thinking while driving," the scientist with the tanned face and bleached hair once explained. For this brilliant idea b ...
The amelogenin gene
The amelogenin gene

... of the developing enamel matrix. This protein is now well characterized from the data of amino acid sequences which have been shown to be at a high degree of homology between all species investigated to date. The gene structure of this protein has been demonstrated and it is confirmed that there are ...
Meiosis: Chapter 10 - University at Buffalo
Meiosis: Chapter 10 - University at Buffalo

... Learning Objectives 1. Recognize how the number and type of chromosomes differ in a gamete compared to a somatic (body) cell. 2. Describe how chromosomes are separated in meiosis and how this differs from mitosis. 3. Apply the knowledge of how chromosomes separate during meiosis and the rules of pr ...
Visceral endoderm-restricted translation of Otx1
Visceral endoderm-restricted translation of Otx1

... In particular Otx1 null mice are viable and show spontaneous epileptic seizures and abnormalities affecting the dorsal telencephalic cortex. Otx2 null mice die early in development and fail in specification of the rostral neuroectoderm and proper gastrulation. In order to determine whether Otx1−/− a ...
Processing the RefSeq and CCDS Annotation Datasets Using the SAS System: Creation of Gene Reference
Processing the RefSeq and CCDS Annotation Datasets Using the SAS System: Creation of Gene Reference

... (Line 45). Finally, we designate this region as the “Promoter”, but it could also be called “5’ genomic”. After we have acquired the promoter, the data step will now be within the region designated as the gene, that is beyond TXSTART (or TXEND, for minus-strand genes). The first and last exons are h ...
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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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