• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 89
  • 13
  • 13
  • 9
  • 4
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • Tagged with
  • 177
  • 177
  • 177
  • 32
  • 32
  • 32
  • 31
  • 31
  • 24
  • 23
  • 23
  • 23
  • 23
  • 22
  • 22
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
91

Vztah atraktivity a MHC: Role menstruačního cyklu a partnerského statusu. / Vztah atraktivity a MHC: Role menstruačního cyklu a partnerského statusu.

Vávrová, Kateřina January 2011 (has links)
Extremely polymorphic genes of major histocompatibility complex (MHC) play a significant role in the function of immune system by recognizing heterogeneous particles, mainly pathogenic origin. Previous research on various vertebrate species indicates that MHC influences individual body odour and mate choice preferences. Many individuals tend to prefer MHC dissimilar partner so that warrants them an offspring resistant against wider spectrum of infections. Research on MHC-related mate preferences in humans, however, is inconclusive to date. Several studies indicate that women not taking hormonal contraceptives prefer the smell of MHC dissimilar partners while other studies have not come to this conclusion. This can be caused by the absence of potentially influencing factors like the menstrual cycle phase. The aim of this study was to test MHC-similarity mate choice preferences in odour, facial and vocal modalities. In particular, we focused on a potential effect of hormonal contraception. Furtermore, we tested preferential shifts across the menstrual cycle by comparing women's preferences in the follicular and the luteal phase in pill and non-pill users. A group of 52 women in different phases of their menstrual cycle rated odour samples, photos and vocal recordings taken from 51 men. All...
92

Genetic Diversities among Founder Populations of the Endangered Avian Species, the Japanese Crested Ibis and the Oriental Stork in Japan / 希少鳥類トキおよびコウノトリの国内始祖集団における遺伝的多様性に関する研究

Taniguchi, Yukio 25 January 2016 (has links)
京都大学 / 0048 / 新制・論文博士 / 博士(農学) / 乙第12986号 / 論農博第2826号 / 新制||農||1038(附属図書館) / 学位論文||H28||N4961(農学部図書室) / 32456 / 名古屋大学大学院農学研究科生化学制御専攻 / (主査)教授 祝前 博明, 教授 今井 裕, 教授 廣岡 博之 / 学位規則第4条第2項該当 / Doctor of Agricultural Science / Kyoto University / DFAM
93

The Effects of a Set of Novel Compounds on Interferon-gamma Induced Major Histocompatibility Complex (MHC) Class II Molecules in Cultured Thyroid Cells

Allen, Abigail E. 25 September 2018 (has links)
No description available.
94

Rheumatoid factor recognizes specific domains of the IgG heavy chain complexed with HLA class II molecules / リウマトイド因子はHLA class IIと複合体を構成するIgG重鎖の特定のドメインを認識する

Zhang, Shanshan 23 January 2024 (has links)
京都大学 / 新制・課程博士 / 博士(医学) / 甲第24991号 / 医博第5025号 / 新制||医||1069(附属図書館) / 京都大学大学院医学研究科医学専攻 / (主査)教授 生田 宏一, 教授 椛島 健治, 教授 上野 英樹 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM
95

Characterization of major histocompatibility complex class I loci of the lark sparrow (Chondestes grammacus) and insights into avian MHC evolution

Lyons, Amanda C. 26 November 2013 (has links)
No description available.
96

β2m antibody is a suitable antibody to detect major histocompatibility complex class Ι as well as α chain antibody in healthy tissues and tissues infected with mouse parvovirus 1

Alhawsawi, Sana Mahmoud 27 May 2015 (has links)
No description available.
97

The Role of Demographic History in Shaping Genetic Diversity in the Galapagos Penguin (Spheniscus mendiculus) and the Magellanic Penguin (Spheniscus magellanicus)

Arauco-Shapiro, Gabriella 26 July 2017 (has links)
No description available.
98

Identification of major histocompatibility complex haplotypes in goldfish, Carassius auratus

Maxey, Gail D. 04 August 2009 (has links)
Development of techniques for observing variability at the major histocompatibility complex (MHC) of fishes could prove an important first step in understanding the genetic bases of disease resistance. In this study, using goldfish (Carassius auratus) as a model system, three approaches to generating antisera to putative MHC molecules and two methods for detecting antibody reactivities were evaluated. Seven full-sib families were produced, and red blood cells (RBCs) of goldfish family members were screened for reactivity with a panel of absorbed antisera. The antisera panel consisted of fish anti-fish, chicken anti-chicken, and chicken anti-fish antisera. The fish anti-fish antisera was produced by injecting RBCs from each parent into its mate, and the chicken anti-fish antisera was produced by injecting parental goldfish RBCs into chickens. The chicken anti-chicken antisera were obtained from a genetics laboratory where MHC-specific antisera had been prepared previously. The pattern of presence or absence of agglutination upon mixing with the respective reagents in this panel of antisera was regarded as the phenotype of the individual tested. Agglutinations observed macroscopically or microscopically were easily scored as positive or negative. Particular phenotypes were observed among individuals both within and between families. The large numbers of phenotypes observed may indicate: (1) the need for additional absorptions in the preparation of antisera, or (2) segregation of additional sets of phenotypic MHC haplotypes in the tetraploid goldfish. The utility of chicken anti-chicken reagents in serotyping of fish was demonstrated. Use of the traditional approach to conducting hemagglutination assays limited the number of assays executed because of the amount of blood required. In order to minimize the sample volumes required, antibody reactivities were evaluated by flow cytometry employing appropriate fluorescein labeled antibodies. Using this approach, scoring of positive and negative results was equivocal, and results did not always agree with those scored by hemagglutination assays. Results of this study strongly suggest that the development of immune allo- and xeno-antisera and use of hemagglutination assays can be used to characterize genetic variability of the MHC of fishes. Understanding of immunogenetic variability in fishes could be used to develop strains resistant to economically important fish pathogens. / Master of Science
99

Determination of the Expression Patterns of Bovine Non-Classical Major Histocompatibility Complex (MHC) Class I Proteins

Parasar, Parveen 01 December 2013 (has links)
My dissertation hypothesis is that bovine trophoblast cells express cell-surface and secreted non-classical major histocompatibility complex class I (MHC-Ib) proteins which inhibit NK cells and other leukocytes by binding to inhibitory receptors (e.g., LILRB1, LILRB2, KIR2DL4, and/or CD94/NKG2A). Extremely polymorphic and ubiquitously expressed classical MHC class I (MHC-Ia) proteins, which present foreign antigenic peptides to CD8+ T lymphocytes, are involved in acceptance or rejection of tissue grafts. Non-classical MHC class I (MHC-Ib) glycoproteins, such as Human Leukocyte Antigen-G (HLA-G) and murine Qa-2, are important modulators of the maternal immune system during pregnancy. MHC-Ib proteins are: (a) oligomorphic or monomorphic, (b) expressed in specific tissues under specific condtions, and (c) produced as surface and/or soluble isoforms due to alternative splicing. Third trimester-bovine trophoblast cells express both MHC-Ia and MHC-Ib proteins. The MHC-Ib proteins expressed by trophoblast cells during the third trimester of pregnancy are encoded by four bovine leukocyte antigen (BoLA) loci: BoLA-NC1, BoLA-NC2, BoLA-NC3, and BoLA-NC4. Two MHC-Ia (N*01701 and N*01802) and three MHC-Ib (NC1*00501, NC3*00101 and NC4*00201) proteins showed cell-surface expression in transfection studies performed in murine P815 and human K562 cells. Two additional isoforms, NC1*00401 and NC2*00102, were not detected on the surface of these cells. Nevertheless, both class Ia proteins, N*01701 and N*01802, and five class Ib proteins, NC1*00401, NC1*00501, NC2*00102, NC3*00101, and NC4*00201, were detected in crude cell lysates on Western blots. Precipitation of proteins from culture supernatants showed that cell-surface MHC-Ia (N*01701 and N*01802) and MHC-Ib proteins (NC1*00501, NC3*00101, and NC4*00201) are shed from the surface of these cells into the media. The mechanism of shedding of these proteins is, however, not known. Monoclonal antibodies W6/32, IL-A88, H1A, H6A, H11A, H58A, and PT-85A recognized surface MHC-I isoforms with varying affinity. We were able to develop a sandwich enzyme-linked immunosorbent assay (ELISA) using either H1A or IL-A88 antibody as the capture antibody and the W6/32 antibody for detection. We produced monoclonal antibodies against cattle NC1*00501 and NC3*00101 proteins. One monoclonal antibody generated against BoLA-NC3*00101 was highly specific. Unfortunately, due to failure to clone the NC3*00101- hybridoma, we no longer have an infinite source of this monoclonal antibody for NC3*00101. We eluted peptides from NC3*00101-transfected MHC-null K562 cells and identified peptides using liquid chromatography-mass spectrum (LC-MS) analysis. Analysis of peptide binding data using the SAS Proc mixed statistical program, suggested that the peptide EVTNQLVVL is a potential peptide ligand, which can be used to make tetramers for enumeration of antigen-specific leukocytes.
100

Early Epigenetic Regulation of the Adaptive Immune Response Gene CIITA

Mehta, Ninad T 01 December 2010 (has links)
The precise regulation of Major Histocompatibility class II (MHC-II) genes plays an important role in the control of the adaptive immune response. MHC-II genes are expressed constitutively in only a few cell types, but their expression can be induced by the inflammatory response cytokine interferon gamma (INF-γ). The regulation of MHC-II is controlled by a Master Regulator, the class II transactivator (CIITA). Multiple studies have shown that CIITA regulated expression of MHC-II is controlled and induced by INF-γ. It has been also shown that a functional CIITA gene is necessary for the expression of MHC-II genes. CIITA is thus a general regulator of both constitutive and inducible MHC-II expression. Although much is known about the transcription factors necessary for CIITA expression, there is little information as to the epigenetic modifications and the requisite enzymes needed to provide these transcription factors access to DNA. Previous studies in the Greer lab have shown that increased levels of acetylation of histones H3 upon INF-γ stimulation, as does tri-methylation of H3K4 upon prolonged cytokine stimulation. Similar observations were made at early time points post IFN-γ stimulation, where there is an instantaneous increase in the levels of H3K18ac and H3K4me3. In contrast to this, the levels of silencing modifications begin to drop with in the first 20 minutes of IFN-γ stimulation. The binding of STAT1 reaches its peak at about 60 minutes and the first transcripts for the protein start to appear as early as 40 minutes post the cytokines stimulation. Our study is the first to link the rapidly occurring epigenetic changes at the CIITA promoter pIV to EZH2

Page generated in 0.0908 seconds