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2929 Uppsatser om The Major Histocompatibility Complex (MHC) Genes - Sida 1 av 196
Hund som komparativ modell för autoimmuna sjukdomar :
In this essay dog as a compatible model were put against human. The Major Histocompatibility Complex (MHC) Genes were compared between dogs, human, cat and mouse. To evaluate dog as a model and study similarities and differences was the aim with this review.
Dog as a model contributes to understand mechanisms behind autoimmune diseases and showed clearly histological similarities between human and dogs concerning the skin disease mucous membrane pemphigoid (MMP)/cicatricial pemphgioid (CP). Further genetic evidence motivated the choice of using dog as a comprehensive model when the MHC-complex correlated with hypothyroiditis in Doberman dog as it does in human. Physiological similarities with low levels of thyroid hormones (T3 and T4) together with high level of thyroid releasing hormone (TSH) were found in the same way as in human.
Survey Of Genes Of Escherichia Coli Causing Bovine Mastitis With DNA Microarrays
Background: Mastitis in dairy cattle is a common ailment worldwide. A cause of mastitis can be bacteria such as Escherichia coli. Mastitis is not a deadly ailment and sometimes the dairy cows show no symptoms but if certain virulence genes are present in the bacteria that cause the mastitis, the bacteria can be transmitted to humans and cause severe diseases. The potential presence of enterohemorrhagic Escherichia coli (EHEC) in particular would be a major concern for human health.Aim: The aim for this study was to analyze the presence of virulence genes known to be present in E.coli strains isolated from dairy cows with mastitis in Sweden.Method: A Qiagen BIO ROBOT EZ1 was used to purify DNA from 90 bacterial cultures. A panel of virulence genes were amplified and biotinylated from the purified DNA by PCR and an E.coli based DNA microarray was used to detect presumed virulence genes in E.coli.Result: There were no samples that had all the genes traditionally used to classify E.coli as EHEC or potential EHEC.
Genernas påverkan på köttkvaliteten
Multiple factors are involved in control of beef sensory quality so great variation can be induced. The perception of meat quality can be affected anywhere in the product chain. Both the environment and the set of genes of the animals have an effect on the final output. A problem facing the beef industry today is the significant variations in meat quality between individual animals, which is reflected in the uneven quality of the meat that reaches the consumer. If the quality of meat in stores varies significantly over time, the consumers? trust may decrease.
Syringomyeli hos hund
The canine population has during it?s time with humans gone through at least 2 major genetic bottlenecks, the first when it was separated from the wolf, and the second when it was divided into different breeds. Among other things, this has lead to the accumulation of unwanted genes, such as genes causing disease in dogs. One such inherited disease is syringomyelia, which has proven to be more common than expected, especially in certain smaller breeds such as the Cavalier King Charles Spaniel. Syringomyelia in dogs is often a secondary condition caused by the malformation called occipital hypoplasia.
Utvärtes behandling av sarkoider på häst med Aldara TM eller Xxterra TM : en jämförande pilotstudie
Sarcoid is the most common tumor in horses all over the world. The sarcoid is a benign, locally invasive, usually fibroblastic proliferative skin neoplasm. Even if the etiology is not completley verified, the epidemiology and clinical behavior suggest a infectious intervention, probably BPV type 1 or type 2. However, it is known that the cause is multifactorial. A genetic prepdispositon has been identified associated to genes within the Major Histocompatibility Complex (MHC), but also to breed, age and perhaps gender.
Utvärtes behandling av sarkoider på häst med Aldara eller Xxterra : en jämförande pilotstudie
Sarcoid is the most common tumor in horses all over the world. The sarcoid is a benign, locally invasive, usually fibroblastic proliferative skin neoplasm. Even if the etiology is not completley verified, the epidemiology and clinical behavior suggest a infectious intervention, probably BPV type 1 or type 2. However, it is known that the cause is multifactorial. A genetic prepdispositon has been identified associated to genes within the Major Histocompatibility Complex (MHC), but also to breed, age and perhaps gender.
Lymfocytär tyroidit hos hund (clt) : genetik, patogenes, histologi
Hypotyreoidism är en vanlig endokrin sjukdom hos hundar. Den orsakar nedsatt livskvalitet i form av utbredda symptom från flera olika organsystem och sjukdomen kräver livslång medicinering. En orsak till hypotyreoidism är Canine Lymphocytic Thyroiditis (CLT), en autoimmun sjukdom som står för ett stort antal av sjukdomsfallen hos hund. Mycket talar för att utvecklandet av sjukdomen har en ärftlighetskomponent eftersom den uppträder i mycket hög frekvens inom vissa raser medan det är en tämligen ovanlig åkomma inom andra raser. Studier av hundpopulationer har visat på en genetisk koppling mellan CLT och gener för Dog Leukocyte Antigen II (DLA II) hos vissa raser.
Resistens mot ivermektin : vad vet vi idag?
Hypotyreoidism är en vanlig endokrin sjukdom hos hundar. Den orsakar nedsatt livskvalitet i form av utbredda symptom från flera olika organsystem och sjukdomen kräver livslång medicinering. En orsak till hypotyreoidism är Canine Lymphocytic Thyroiditis (CLT), en autoimmun sjukdom som står för ett stort antal av sjukdomsfallen hos hund. Mycket talar för att utvecklandet av sjukdomen har en ärftlighetskomponent eftersom den uppträder i mycket hög frekvens inom vissa raser medan det är en tämligen ovanlig åkomma inom andra raser. Studier av hundpopulationer har visat på en genetisk koppling mellan CLT och gener för Dog Leukocyte Antigen II (DLA II) hos vissa raser.
Felaktig alternativ splicing: Vissa mutationer i BRCA1, BRCA2, ER? och ER? är starkt förknippade med bröstcancer
Alternative splicing is a process that partly rejects the common definition of a gene ? that one gene codes for one specific protein. By variable combination of coding regions (exons) and exclusion of non-coding regions (introns), formation of several different mRNA-transcripts, and consequently several different proteins, can derive from the same gene. Alternative splicing is an important condition for the development of complex life forms, but it is also a highly sensitive process and inaccurate splicing is the cause of approximately 15 % of mutations that cause genetic diseases. This article presents four genes, BRCA1, BRCA2, ER? and ER?, and inaccurate splicing of these genes increases the risk of developing cancer, particularly breast cancer and ovarian cancer.
Den multifasetterade innovationsprocessen som framgångsfaktor i ett innovativt företag : Ett undersökande case i Serendipityformen
This is a graduation project in Innovation Management, which seeks to enlighten new theories within the major subject ? the multi?faceted innovation process.The reader is hereby invited to an insight in the more complex perspectives of these types of theories than what has previously been explained in simplified ways.We have conducted research on a company within the cleantech market; Cellkraft AB. The company develops and produces fuel cells amongst other products, which have emerged during their research and development in the fuel cell technology. Cellkraft works in a high?tech frontline market where innovation is key.
Fine-Mapping of Equine Multiple Congenital Ocular Anomalies on horse chromosome 6
Multiple Congenital Ocular Anomalities (MCOA) is a genetic disease that affects primarily Silver coloured horses of breeds such as the Rocky and Kentucky mountain horses. In these breeds the Silver dapple colour is very popular leading to an increase of affected horses. The major feature of the disease is ocular cysts of variable size. Large cysts also lead to a variety of secondary syndromes, for example retinal detachment. In previous studies the locus for MCOA has been mapped to an interval of 420 kb on equine chromosome six.
Validering av designverktyg för organisationsprestanda
In today?s constantly changing market place most organizations need to reorganize. Reorganization carries risks that could jeopardize the organization's well-being and profitability. To minimize these risks, companies need a tool to help them analyze how the reorganization will affect the business before they make major changes. Such tool has now been developed by researchers at KTH.
Genetiska defekter hos nötkreatur :
Genetic defects are caused by mutations in major genes where the gene?s protein product has a large impact on the physiology of the animal. The synthesis of the protein can be altered by a change in the nucleotide sequence, which can lead to malformation and in many cases death.One of the main reasons of increase in many genetic defects is the use of few bulls in breeding programmes, causing a reduction of the genetic variation. Genetic defects cause suffering for the animal and influences the production by, for example, increased costs due to misscarriages, lost milk production and expenditure for medical treatment. Bovine Leukocyte Adhesion Deficiency (BLAD) and Complex Vertebral Malformation (CVM) are two genetic defects that were widespread before the causative mutation was discovered.
Evaluation and Comparison of Ecological Models Simulating Nitrogen Processes in Treatment Wetlands,Implemented in Modelica
Two ecological models of nitrogen processes in treatment wetlands have been evaluated and compared. These models have been implemented, simulated, and visualized in the Modelica language. The differences and similarities between the Modelica modeling environment used in this thesis and other environments or tools for ecological modeling have been evaluated. The modeling tools evaluated are PowerSim, Simile, Stella, the MathModelica Model Editor, and WEST. The evaluation and the analysis have been performed using McCall?s factors for software quality (McCall et al, 1977), a correlation analysis and the Constant Comparative Method (Glaser&Strauss, 1999).
Differences of progressive retinal atrophy in dogs
A group of diseases that affect the dog?s sight is progressive retinal atrophy (PRA) a disease that means that the photoreceptors in the retina of the eye either not develop normally or undergo degeneration and thereby causes vision loss and blindness. The disease affects many different breeds and is inherited. What have been shown is that it is different genes that had become mutated in the different breeds, this conclude that despite similar clinical symptoms, the underlying reason could be different. Also the genes that are mutated in dogs and give rise to diseases also exists in humans.