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  1. AU=Douglas M G
  2. AU="Monyo, E S"
  3. AU="Nguyen Thanh Nguyen"
  4. AU="Zhang, Yueqian"
  5. AU=Lima Emerson Q
  6. AU="Neil K. Taunk, MD"
  7. AU="Letourneau-Guillon, Laurent"
  8. AU="Dziuba, Marina V"
  9. AU="Aleksander Zińczuk"
  10. AU="Rowe, Logan M."
  11. AU="Sharma N." AU="Sharma N."
  12. AU=Yuan Shu
  13. AU="Ye Liu"
  14. AU="Bezerra, Antônio Diego M"
  15. AU="HE Xiufeng"
  16. AU=Freeman Hugh J AU=Freeman Hugh J
  17. AU="Choi, John Kim"
  18. AU="Streng, Bianca M M"
  19. AU="Franklin, Renty B"
  20. AU="Tetri, Laura H"
  21. AU="Badve, Sunil V"
  22. AU=Zhang Yinan
  23. AU="Piquero, Nicole Leeper"
  24. AU="Russo, Giorgio Ivan" AU="Russo, Giorgio Ivan"
  25. AU=Pourdowlat Guitti
  26. AU="Frisenda, Riccardo"
  27. AU=Palmucci Stefano

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  1. Artikel ; Online: Concentration and heritability of immunoglobulin G and natural antibody immunoglobulin M in dairy and beef colostrum along with serum total protein in their calves.

    Altvater-Hughes, Tess E / Hodgins, Douglas C / Wagter-Lesperance, Lauraine / Beard, Shannon C / Cartwright, Shannon L / Mallard, Bonnie A

    Journal of animal science

    2022  Band 100, Heft 2

    Abstract: Immunoglobulin (Ig) G and natural antibody (NAb) IgM are passively transferred to the neonatal calf ... serum total protein [STP] <5.2 g/dL) is still a common concern. The objectives of this study were to: (1 ... cows had significantly greater colostral IgG (146.5 ± 9.5 standard error of the mean [SEM] g/L ...

    Abstract Immunoglobulin (Ig) G and natural antibody (NAb) IgM are passively transferred to the neonatal calf through bovine colostrum. Maternal IgG provides pathogen- or vaccine-specific protection and comprises about 85% of colostral Ig. NAb-IgM is less abundant but provides broad and nonspecific reactivity, potentially contributing to protection against the dissemination of pathogens in the blood (septicemia) in a calf's first days of life. In the dairy and beef industries, failure of passive transfer (FPT) of colostral Ig (serum total protein [STP] <5.2 g/dL) is still a common concern. The objectives of this study were to: (1) compare colostral IgG concentrations and NAb-IgM titers between dairy and beef cows; (2) assess the effect of beef breed on colostral IgG; (3) compare passive transfer of colostral Ig in dairy and beef calves; and (4) estimate the heritability of colostral IgG and NAb-IgM. Colostrum was collected from Holstein dairy (n = 282) and crossbred beef (n = 168) cows at the University of Guelph dairy and beef research centers. Colostral IgG was quantified by radial immunodiffusion and NAb-IgM was quantified by an enzyme-linked immunosorbent assay. In dairy (n = 308) and beef (n = 169) calves, STP was estimated by digital refractometry. Beef cows had significantly greater colostral IgG (146.5 ± 9.5 standard error of the mean [SEM] g/L) than dairy cows (92.4 ± 5.2 g/L, P <0.01). Beef cows with a higher proportion of Angus ancestry had significantly lower colostral IgG (125.5 ± 5.8 g/L) than cows grouped as "Other" (142.5 ± 4.9 g/L, P = 0.02). Using the FPT cutoff, 13% of dairy and 16% of beef calves had FPT; still, beef calves had a significantly larger proportion with excellent passive transfer (STP ≥6.2 g/dL, P <0.01). The heritability of colostral IgG was 0.04 (±0.14) in dairy and 0.14 (±0.32) in beef. Colostral NAb-IgM titers in dairy (12.12 ± 0.22, log2 [reciprocal of titer]) and beef cows (12.03 ± 0.19) did not differ significantly (P = 0.71). The range of NAb-IgM titers was 9.18-14.60, equivalent to a 42-fold range in antibody concentration. The heritability of colostral NAb was 0.24 (±0.16) in dairy and 0.11 (±0.19) in beef cows. This study is the first to compare colostral NAb-IgM between dairy and beef cows. Based on the range in NAb-IgM titers and the heritability, selective breeding may improve colostrum quality and protection for neonatal calves in the early days of life.
    Mesh-Begriff(e) Animals ; Animals, Newborn ; Cattle ; Colostrum/metabolism ; Female ; Immunodiffusion/veterinary ; Immunoglobulin G ; Immunoglobulin M ; Pregnancy
    Chemische Substanzen Immunoglobulin G ; Immunoglobulin M
    Sprache Englisch
    Erscheinungsdatum 2022-01-13
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 390959-1
    ISSN 1525-3163 ; 0021-8812
    ISSN (online) 1525-3163
    ISSN 0021-8812
    DOI 10.1093/jas/skac006
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Mitochondrial Migraine: Disentangling the angiopathy paradigm in m.3243A>G patients.

    Smeitink, Jan / Koene, Saskia / Beyrath, Julien / Saris, Christiaan / Turnbull, Douglas / Janssen, Mirian

    JIMD reports

    2019  Band 46, Heft 1, Seite(n) 52–62

    Abstract: ... with migraine is the spectrum of disorders caused by the m.3243A>G mutation in the mitochondrial transfer RNA ... but compared to the general population, m.3243A>G patients have a higher migraine prevalence. This burdensome ... symptom might sometimes even be the only clinical feature in maternal relatives carrying the m.3243A>G ...

    Abstract Migraine, characterized by recurrent attacks of predominantly unilateral throbbing headache, affects approximately 15% of the adult population and is an important cause of disability worldwide. Knowledge required for the development of new classes of antimigraine drugs might come from studying rare metabolic diseases associated with migraine. An illustrative example of a monogenetic disorder associated with migraine is the spectrum of disorders caused by the m.3243A>G mutation in the mitochondrial transfer RNA Leucine. Reported migraine prevalence figures in patients with this particular mutation vary considerably, but compared to the general population, m.3243A>G patients have a higher migraine prevalence. This burdensome symptom might sometimes even be the only clinical feature in maternal relatives carrying the m.3243A>G mutation. Although the exact sequence of events and the relative importance of factors underlying migraine in m.3243A>G MELAS spectrum disorders are still enigmatic, substantial evidence in man exist that dysfunctional mitochondria in both the vascular, the smooth muscle cells and the neuronal system and the interaction between these are at the starting point of the migraine developing pathophysiological cascade. Exclusively based on results of studies performed in patients harboring the m.3243A>G mutation, either in vivo or ex vivo, we here summarize our current understanding of mitochondrial angiopathy associated migraine in m.3243A>G patients which knowledge might lead to potential new avenues for migraine drug development.
    Sprache Englisch
    Erscheinungsdatum 2019-03-14
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2672872-2
    ISSN 2192-8312 ; 2192-8304
    ISSN (online) 2192-8312
    ISSN 2192-8304
    DOI 10.1002/jmd2.12017
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Artikel ; Online: Raised levels of immunoglobulin G, A and M are associated with an increased risk of total and cause-specific mortality: the Vietnam Experience Study.

    Phillips, Anna C / Carroll, Douglas / Drayson, Mark T / Batty, G David

    Journal of epidemiology and community health

    2014  Band 69, Heft 2, Seite(n) 129–135

    Abstract: ... this body of work by examining whether higher levels of serum Ig G, A and M are associated with increased mortality ...

    Abstract Background: Immunoglobulins (Ig) are essential for combating infectious disease. However, high levels are associated with a range of diseases and/or poor health behaviours, such as autoimmune diseases, chronic infection, HIV and excessive alcohol consumption. In the present analyses, we extend this body of work by examining whether higher levels of serum Ig G, A and M are associated with increased mortality risk.
    Methods: Participants were 4255 Vietnam-era, former US army personnel (the Vietnam Experience Study). From military service files, telephone interviews in 1983 and a medical examination in 1986, sociodemographic, and health data were collected. Contemporary morning fasted blood samples were taken from which IgG, IgA and IgM concentrations were determined. Mortality surveillance over 15 years gave rise to deaths ascribed to all-causes, cardiovascular disease mortality, all cancers combined mortality, external cause and 'other' causes (predominantly comprising deaths due to infectious disease). Cox proportional hazard models were utilised to compute HRs per SD increase in Ig which were first adjusted for age and then additionally adjusting for a range of candidate confounders.
    Results: In multiply adjusted analyses, in general, the higher the immunoglobulin concentration, the greater the risk of death. Thus, IgA (HR=2.0 95% CI 1.47 to 2.73), IgM (HR=1.5 95% CI 1.11 to 1.91) and IgG (HR=5.8 95% CI 3.38 to 9.95) were positively related to all-cause mortality. Corresponding results for 'other' causes of mortality were 4.7 (2.64 to 8.19), 3.5 (2.29 to 5.45) and 33.4 (15.13 to 73.64).
    Conclusions: In the present study, high levels of Ig are associated with an elevated risk of death from total and 'other' causes, mainly infectious disease. High levels of Ig, particularly IgG, may signal subclinical disease.
    Mesh-Begriff(e) Adult ; Biomarkers/blood ; Cardiovascular Diseases/blood ; Cardiovascular Diseases/mortality ; Cause of Death ; Communicable Diseases/blood ; Communicable Diseases/mortality ; Humans ; Immunoglobulin A/blood ; Immunoglobulin G/blood ; Immunoglobulin M/blood ; Immunoglobulins/blood ; Male ; Middle Aged ; Neoplasms/blood ; Neoplasms/mortality ; Proportional Hazards Models ; Retrospective Studies ; Risk Assessment ; United States/epidemiology ; Veterans/statistics & numerical data ; Vietnam Conflict
    Chemische Substanzen Biomarkers ; Immunoglobulin A ; Immunoglobulin G ; Immunoglobulin M ; Immunoglobulins
    Sprache Englisch
    Erscheinungsdatum 2014-09-29
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 391868-3
    ISSN 1470-2738 ; 0142-467X ; 0141-7681 ; 0143-005X
    ISSN (online) 1470-2738
    ISSN 0142-467X ; 0141-7681 ; 0143-005X
    DOI 10.1136/jech-2014-204345
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel ; Online: Italian nursing students and professional socialisation: Response to the commentary. Bagnasco, A., Aleo, G., Timmins, F., DeVries, J. Bressan, V., Bianchi, M., and Sasso, L. The 800 pound Gorilla and the Smoking Gun-a response to Sabatino et al 2015 regarding Italian nurse education and practice.

    Stievano, Alessandro / Affonso, Dyanne / Rocco, Gennaro / Sabatino, Laura / Olsen, Douglas

    Nurse education in practice

    2017  Band 26, Seite(n) 89–90

    Sprache Englisch
    Erscheinungsdatum 2017-07-29
    Erscheinungsland Scotland
    Dokumenttyp Journal Article
    ZDB-ID 2058575-5
    ISSN 1873-5223 ; 1471-5953
    ISSN (online) 1873-5223
    ISSN 1471-5953
    DOI 10.1016/j.nepr.2017.07.009
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  5. Artikel ; Online: Plasma membrane microdomains containing vesicular stomatitis virus M protein are separate from microdomains containing G protein and nucleocapsids.

    Swinteck, B Dancho / Lyles, Douglas S

    Journal of virology

    2008  Band 82, Heft 11, Seite(n) 5536–5547

    Abstract: ... Glycoprotein (G protein) and M protein microdomains were not colocalized in the plasma membrane outside ... whether G protein or M protein was colocalized with VSV nucleocapsid protein (N protein) outside the budding ... of approximately 600 nm. In contrast to the case for G protein, M protein was not colocalized with these areas ...

    Abstract Immunogold electron microscopy and analysis were used to determine the organization of the major structural proteins of vesicular stomatitis virus (VSV) during virus assembly. We determined that matrix protein (M protein) partitions into plasma membrane microdomains in VSV-infected cells as well as in transfected cells expressing M protein. The sizes of the M-protein-containing microdomains outside the virus budding sites (50 to 100 nm) were smaller than those at sites of virus budding (approximately 560 nm). Glycoprotein (G protein) and M protein microdomains were not colocalized in the plasma membrane outside the virus budding sites, nor was M protein colocalized with microdomains containing the host protein CD4, which efficiently forms pseudotypes with VSV envelopes. These results suggest that separate membrane microdomains containing either viral or host proteins cluster or merge to form virus budding sites. We also determined whether G protein or M protein was colocalized with VSV nucleocapsid protein (N protein) outside the budding sites. Viral nucleocapsids were observed to cluster in regions of the cytoplasm close to the plasma membrane. Membrane-associated N protein was colocalized with G protein in regions of plasma membrane of approximately 600 nm. In contrast to the case for G protein, M protein was not colocalized with these areas of nucleocapsid accumulation. These results suggest a new model of virus assembly in which an interaction of VSV nucleocapsids with G-protein-containing microdomains is a precursor to the formation of viral budding sites.
    Mesh-Begriff(e) Animals ; Cell Line ; Cricetinae ; Cytoplasm/metabolism ; Membrane Glycoproteins/metabolism ; Membrane Microdomains/metabolism ; Membrane Microdomains/ultrastructure ; Microscopy, Immunoelectron ; Nucleocapsid/metabolism ; Vesicular stomatitis Indiana virus/metabolism ; Vesicular stomatitis Indiana virus/ultrastructure ; Viral Envelope Proteins/metabolism ; Viral Matrix Proteins/metabolism ; Viral Matrix Proteins/ultrastructure
    Chemische Substanzen G protein, vesicular stomatitis virus ; M protein, Vesicular stomatitis virus ; Membrane Glycoproteins ; Viral Envelope Proteins ; Viral Matrix Proteins
    Sprache Englisch
    Erscheinungsdatum 2008-03-26
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/JVI.02407-07
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  6. Artikel ; Online: Re: Adjuvant radiotherapy for pathological T3N0M0 prostate cancer significantly reduces risk of metastases and improves survival: long-term followup of a randomized clinical trial I. M. Thompson, C. M. Tangen, J. Paradelo, M. S. Lucia, G. Miller, D. Troyer, E. Messing, J. Forman, J. Chin, G. Swanson, E. Canby-Hagino and E. D. Crawford J Urol 2009; 181: 956-962.

    Cheng, Tina / Heng, Daniel Y / Stewart, Douglas

    The Journal of urology

    2009  Band 182, Heft 5, Seite(n) 2531–2; discussion 2532–4

    Mesh-Begriff(e) Follow-Up Studies ; Humans ; Male ; Neoplasm Metastasis ; Neoplasm Staging ; Prostatic Neoplasms/mortality ; Prostatic Neoplasms/pathology ; Prostatic Neoplasms/radiotherapy ; Radiotherapy, Adjuvant ; Randomized Controlled Trials as Topic ; Risk Factors ; Survival Rate ; Time Factors
    Sprache Englisch
    Erscheinungsdatum 2009-11
    Erscheinungsland United States
    Dokumenttyp Comment ; Letter
    ZDB-ID 3176-8
    ISSN 1527-3792 ; 0022-5347
    ISSN (online) 1527-3792
    ISSN 0022-5347
    DOI 10.1016/j.juro.2009.07.053
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Artikel ; Online: Sodhi, N.S., G. Acciaioli, M. Erb and A. Khee-Jin Tan (eds.) 2008. Biodiversity and Human Livelihoods in Protected Areas

    Douglas Clark

    International Journal of the Commons, Vol 3, Iss 1, Pp 153-

    Case studies from the Malay Archipelago. Cambridge: Cambridge University Press.

    2009  Band 155

    Schlagwörter Political science ; J ; Political institutions and public administration (General) ; JF20-2112
    Erscheinungsdatum 2009-05-01T00:00:00Z
    Verlag Utrecht University Library Open Access Journals
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  8. Artikel ; Online: Sodhi, N.S., G. Acciaioli, M. Erb and A. Khee-Jin Tan (eds.) 2008. Biodiversity and Human Livelihoods in Protected Areas

    Douglas Clark

    International Journal of the Commons, Vol 3, Iss 1, Pp 153-

    Case studies from the Malay Archipelago. Cambridge: Cambridge University Press.

    2009  Band 155

    Schlagwörter Political science ; J ; Political institutions and public administration (General) ; JF20-2112
    Erscheinungsdatum 2009-05-01T00:00:00Z
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  9. Artikel ; Online: Commentary on "common genetic polymorphisms modify the effect of smoking on absolute risk of bladder cancer." Garcia-Closas M, Rothman N, Figueroa JD, Prokunina-Olsson L, Han SS, Baris D, Jacobs EJ, Malats N, De Vivo I, Albanes D, Purdue MP, Sharma S, Fu YP, Kogevinas M, Wang Z, Tang W, Tardón A, Serra C, Carrato A, García-Closas R, Lloreta J, Johnson A, Schwenn M, Karagas MR, Schned A, Andriole G Jr., Grubb R 3rd, Black A, Gapstur SM, Thun M, Diver WR, Weinstein SJ, Virtamo J, Hunter DJ, Caporaso N, Landi MT, Hutchinson A, Burdett L, Jacobs KB, Yeager M, Fraumeni JF Jr., Chanock SJ, Silverman DT, Chatterjee N, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.: Cancer Res 2013;73(7):2211-20 [Epub 2013 Mar 27].

    Scherr, Douglas S

    Urologic oncology

    2014  Band 32, Heft 2, Seite(n) 213–214

    Abstract: Bladder cancer results from the combined effects of environmental and genetic factors, smoking being the strongest risk factor. Evaluating absolute risks resulting from the joint effects of smoking and genetic factors is critical to assess the public ... ...

    Abstract Bladder cancer results from the combined effects of environmental and genetic factors, smoking being the strongest risk factor. Evaluating absolute risks resulting from the joint effects of smoking and genetic factors is critical to assess the public health relevance of genetic information. Analyses included up to 3,942 cases and 5,680 controls of European background in seven studies. We tested for multiplicative and additive interactions between smoking and 12 susceptibility loci, individually and combined as a polygenic risk score (PRS). Thirty-year absolute risks and risk differences by levels of the PRS were estimated for U.S. males aged 50 years. Six of 12 variants showed significant additive gene-environment interactions, most notably NAT2 (P = 7×10(-4)) and UGT1A6 (P = 8×10(-4)). The 30-year absolute risk of bladder cancer in U.S. males was 6.2% for all current smokers. This risk ranged from 2.9% for current smokers in the lowest quartile of the PRS to 9.9% for current smokers in the upper quartile. Risk difference estimates indicated that 8,200 cases would be prevented if elimination of smoking occurred in 100,000 men in the upper PRS quartile compared with 2,000 cases prevented by a similar effort in the lowest PRS quartile (P(additive) = 1×10(-4)). Thus, the potential impact of eliminating smoking on the number of bladder cancer cases prevented is larger for individuals at higher than lower genetic risk. Our findings could have implications for targeted prevention strategies. However, other smoking-related diseases, as well as practical and ethical considerations, need to be considered before any recommendations could be made.
    Mesh-Begriff(e) Carcinoma in Situ/etiology ; Female ; Humans ; Male ; Polymorphism, Genetic ; Smoking/adverse effects ; Urinary Bladder Neoplasms/etiology
    Sprache Englisch
    Erscheinungsdatum 2014-02
    Erscheinungsland United States
    Dokumenttyp Comment ; Journal Article
    ZDB-ID 1336505-8
    ISSN 1873-2496 ; 1078-1439
    ISSN (online) 1873-2496
    ISSN 1078-1439
    DOI 10.1016/j.urolonc.2013.08.015
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel: Identification of Aurora-A as a Direct Target of E2F3 during G₂/M Cell Cycle Progression

    He, Lili / Yang, Hua / Ma, Yihong / Pledger, W. Jack / Cress, W. Douglas / Cheng, Jin Q

    Journal of biological chemistry. 2008 Nov. 7, v. 283, no. 45

    2008  

    Abstract: Aurora-A is a centrosome kinase and plays a pivotal role in G₂/M cell cycle progression. Expression ... G₂/M, and decrease rapidly after mitosis. Previous studies have shown regulation of the Aurora ... knockdown of E2F3 decreases mRNA and protein levels of Aurora-A and delays G₂/M entry. Further, E2F3 ...

    Abstract Aurora-A is a centrosome kinase and plays a pivotal role in G₂/M cell cycle progression. Expression of Aurora-A is cell cycle-dependent. Levels of Aurora-A mRNA and protein are low in G₁/S, accumulate during G₂/M, and decrease rapidly after mitosis. Previous studies have shown regulation of the Aurora-A protein level during the cell cycle through the ubiquitin-proteasome pathway. However, the mechanism of transcriptional regulation of Aurora-A remains largely unknown. Here, we demonstrated that E2F3 modulates Aurora-A mRNA expression during the cell cycle. Ectopic expression of E2F3 induces Aurora-A expression. Stable knockdown of E2F3 decreases mRNA and protein levels of Aurora-A and delays G₂/M entry. Further, E2F3 directly binds to Aurora-A promoter and stimulates the promoter activity. Deletion and mutation analyses of the Aurora-A promoter revealed that a region located 96-bp upstream of the transcription initiation site is critical for the activation of the promoter by E2F3. In addition, expression of E2F3 positively correlates with the protein level of Aurora-A in human ovarian cancer examined. These results indicate for the first time that Aurora-A is transcriptionally regulated by E2F3 during the cell cycle and that E2F3 is a causal factor for up-regulation of Aurora-A in a subset of human ovarian cancer. Thus, the E2F3-Aurora-A axis could be an important target for cancer intervention.
    Sprache Englisch
    Erscheinungsverlauf 2008-1107
    Umfang p. 31012-31020.
    Erscheinungsort American Society for Biochemistry and Molecular Biology
    Dokumenttyp Artikel
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    Datenquelle NAL Katalog (AGRICOLA)

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