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Estimating lethal allele frequencies in complex pedigrees via gene
Estimating lethal allele frequencies in complex pedigrees via gene

... expected lethal allele frequency from known individual genotypes (carriers) among a set of relevant ancestors. Here we used a Fortran program written by LIDAUER and ESSL (1994) based on a concept developed by ALLAIRE et al. (1982). With this program, only six generations of each reference animal are ...
Tumor Suppressor Genes
Tumor Suppressor Genes

... In fact, a simple genetic model could be invoked to explain these observations. It depended on the observation, made frequently in genetics, that the phenotype of a mutant, inactive allele is recessive in the presence of an intact, wildtype allele. The hypothesis went like this. Imagine that normal ...
Evolution exam questions
Evolution exam questions

... 25. The most important EVOLUTIONARY consequence of chromosomal inversions is: a. they prevent selection from acting on the alleles within the inverted region, thereby increasing genetic diversity. b. they prevent specific groups of alleles from being separated by crossing-over, allowing them to be ...
Regionalization in the mammalian telencephalon - Fishell Lab
Regionalization in the mammalian telencephalon - Fishell Lab

... at distinct times, over a much more protracted period of development. The possibility that regional determination occurs at different times in different mammals warrants further investigation. Another issue that arises from these experiments is whether all cells or only a subpopulation of more pluri ...
Two distinct tumor suppressor loci within chromosome 11p15
Two distinct tumor suppressor loci within chromosome 11p15

... chromosome 11p is a more common event in human breast cancer than previously appreciated (3,4). LOH occurred in at least one marker on the short arm of chromosome 11 in 56 of 94 (60%) informative tumors. The overall frequency of LOH for each marker varies from 16 to 60%, with two peaks seen at marke ...
Specialized adaptation of a lactic acid bacterium to the milk
Specialized adaptation of a lactic acid bacterium to the milk

... development [11–16], and several of the clustered regularly interspaced short palindromic repeats (CRISPR) regions not present in both CNRZ1066 and LMG 18311 that are involved in bacteriophage defense [17, 18]. Interestingly, long before even the notion of a genome had even been conceived, S. ther ...
Design a Kid
Design a Kid

... Determine eye color: Dark eyes are dominant over light. Darker eyes are produced in the presence of more active alleles. In this situation, the large letters (A or B) represent alleles which are active in depositing dark pigment. Small letters (a and b) represent alleles which deposit little pigment ...
PDF + SI - Development - The Company of Biologists
PDF + SI - Development - The Company of Biologists

... at the primitive streak, in neural crest cells delaminating from the neural tube, in the presomitic mesoderm and the lateral plate mesoderm among other EMT territories (Nieto et al. 1994, Acloque et al 2011, Blanco et al. 2007, Morales et al. 2007, Dale et al. 2007, Niessen et al. 2008). Snail1 mous ...
Section 11-1
Section 11-1

... Normal human body cells each contain 46 chromosomes. The cell division process that body cells undergo is called mitosis and produces daughter cells that are virtually identical to the parent cell. Working with a partner, discuss and answer the questions that follow. ...
network - bioinf leipzig
network - bioinf leipzig

... Interactions between TFs, miRNAs, other ncRNAs, and histone modifications • TFs bind as monomers, homo-dimers, or hetero-dimers • Multiple TFs (~7-10) cooperate to regulate gene expression • TFs regulate the expression of other TFs • Feedback loops, autoregulation … •  Network • Add epigenetic mod ...
Slide 1
Slide 1

... Abnormal numbers of sex chromosomes do not usually affect survival  The following table lists the most common human sex chromosome abnormalities. In general, – a single Y chromosome is enough to produce “maleness,” even in combination with several X chromosomes, and – the absence of a Y chromosome ...
Functional genomics of plant photosynthesis in
Functional genomics of plant photosynthesis in

... that are unable to perform photosynthesis, and lightsensitive mutants can be maintained in complete darkness (Fig. 2). Plants such as Arabidopsis or maize with mutations that affect photosynthesis are often inviable or at least susceptible to light-induced photo-oxidation, which can complicate bioch ...
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics
Leukaemia Section 12p abnormalities in myeloid malignancies Atlas of Genetics and Cytogenetics

... generally associated with a poor prognosis; however, different clinical courses are defined concerning the magnitude of 12p; a group with small deletions has a better prognosis than patients with 12p abnormalities in general and a lower tendency to additional chromosomal rearrangements; submicroscop ...
Phenotypic data in FlyBase
Phenotypic data in FlyBase

... function beyond predicted functions, and reveals the involvement of gene products in processes without constraint to lists of `candidate genes' about which something is already known. Different alleles, with distinct molecular lesions in or around the transcription unit, may have different mutant ph ...
PhenoLink - a web-tool for linking phenotype Lactobacillus plantarum strains
PhenoLink - a web-tool for linking phenotype Lactobacillus plantarum strains

... very large and noisy with many features (e.g., genes, metabolite abundances). Thus, associating phenotypes to ~omics data requires an approach that is robust to noise and can handle large and diverse data sets. Results: We developed a web-tool PhenoLink (http://bamics2.cmbi.ru.nl/websoftware/phenoli ...
Centromere Locations and Associated Chromosome
Centromere Locations and Associated Chromosome

... pericentromeric region of the ancestral species, although its position still cannot be determined precisely (Figure 2). We examined our results to see whether any gene copy number differences are suggested, because it has been found that the centromeric regions of A. thaliana have significantly fewe ...
Vegetative incompatibility in filamentous fungi: Podospora and
Vegetative incompatibility in filamentous fungi: Podospora and

... Heterokaryon incompatibility is a widespread phenomenon in filamentous fungi, but its biological significance remains obscure. Heterokaryon incompatibility may constitute an allorecognition (nonself-recognition) system that preserves fungal individuality by preventing heterokaryon formation between ...
HS-SCI-APB-Unit 3 -- Chapter 13- Meiosis and Sexual Life Cycles
HS-SCI-APB-Unit 3 -- Chapter 13- Meiosis and Sexual Life Cycles

... copies of each chromosome, as flies and humans do-and the progeny is going to be diploid, then you've got to make sperm and eggs that have only one copy of each chromosome, so that when those sperm and egg come together you restore the right chromosome number. And to produce sperm and eggs with only ...
Genetics of Bacteriophage P22. II. Gene Order and Gene Function.
Genetics of Bacteriophage P22. II. Gene Order and Gene Function.

... Fie. 1. The genetic m&p of phage P22 drawn approximately to scale. The genetic size of each gene is indicated; this was determined by the largest frequency of recombination between mutations in a complementation group. Also shown are frequencies of recombination between particular mutants in the var ...
A xylem-specific cellulose synthase gene from aspen (Populus
A xylem-specific cellulose synthase gene from aspen (Populus

Chromosomal Abnormalities
Chromosomal Abnormalities

... B. The chromosome can be divided into three regions, the p, or short arm, the q, or long arm and the centromere (the primary constriction found in each chromosome). During meiosis or mitosis, the centromere is the point at which sister chromatids are held together. Each arm is further subdivided int ...
Phenotype
Phenotype

Genetics of fibrosing lung diseases REVIEW
Genetics of fibrosing lung diseases REVIEW

... cytosine)), but none of these associations have been replicated by others. Unlike in IPF, immunological inflammation seems to be more prominent in the pathogenesis of scleroderma lung fibrosis, being an autoimmune disease with specific autoantibodies, such as antitopoisomerase antibodies, in patient ...
PDF File - Friends Science Publishers
PDF File - Friends Science Publishers

... populations revealed that the bh genes were hemizygouseffective and dosage-independent. The F1 monosomic analysis showed that the bh genes of Yupi Branching were recessive (Peng et al., 1998b). Disomics. The plants with disomic genetic constitution are also important for the evolutionary perspective ...
Genetics Simplified
Genetics Simplified

... Heredity • Heredity is the passing of traits from parent to offspring. ...
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Genomic imprinting

Genomic imprinting is the epigenetic phenomenon by which certain genes are expressed in a parent-of-origin-specific manner. If the allele inherited from the father is imprinted, it is thereby silenced, and only the allele from the mother is expressed. If the allele from the mother is imprinted, then only the allele from the father is expressed. Forms of genomic imprinting have been demonstrated in fungi, plants and animals. Genomic imprinting is a fairly rare phenomenon in mammals; most genes are not imprinted.In insects, imprinting affects entire chromosomes. In some insects the entire paternal genome is silenced in male offspring, and thus is involved in sex determination. The imprinting produces effects similar to the mechanisms in other insects that eliminate paternally inherited chromosomes in male offspring, including arrhenotoky.Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. It is an epigenetic process that involves DNA methylation and histone methylation without altering the genetic sequence. These epigenetic marks are established (""imprinted"") in the germline (sperm or egg cells) of the parents and are maintained through mitotic cell divisions in the somatic cells of an organism.Appropriate imprinting of certain genes is important for normal development. Human diseases involving genomic imprinting include Angelman syndrome and Prader–Willi syndrome.
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