Showing 961 - 980 results of 3,155 for search '"phenotype"', query time: 0.10s Refine Results
  1. 961

    Arginase-1-specific T cells target and modulate tumor-associated macrophages by Mads Hald Andersen, Inés Lecoq, Ayako Wakatsuki Pedersen, Evelina Martinenaite, Shamaila Munir Ahmad, Maria Perez-Penco, Lucia Lara de la Torre, Marion Chapellier, Lars Rønn Olsen, Mia Aaboe-Jørgensen, Hannah Jorinde Glöckner, Anne Mette Askehøj Rømer

    Published 2025-01-01
    “…T-cell-mediated changes in the macrophage immune phenotype and cytokine microenvironment were examined using flow cytometry, RT-qPCR and multiplex immunoassay. …”
    Get full text
    Article
  2. 962
  3. 963

    Fhl1, a new spatially specific protein, regulates vein graft neointimal hyperplasia by Chaoqun Wang, Jiantao Chen, Zicong Feng, Bohao Jian, Suiqing Huang, Kangni Feng, Haoliang Liu, Zhuoming Zhou, Ziyin Ye, Jing Lu, Mengya Liang, Zhongkai Wu

    Published 2024-12-01
    “…Spatial transcriptomics profiles and morphological observations demonstrated that a newly generated cell population outside the grafted vein with hybrid phenotype between SMCs and fibroblasts contributes to neointimal formation.…”
    Get full text
    Article
  4. 964

    Modification and analysis of context-specific genome-scale metabolic models: methane-utilizing microbial chassis as a case study by M. A. Kulyashov, R. Hamilton, Y. Afshin, S. K. Kolmykov, T. S. Sokolova, T. M. Khlebodarova, M. G. Kalyuzhnaya, I. R. Akberdin

    Published 2025-01-01
    “…The cellular roles of the tungsten (W)-dependent formate dehydrogenase (fdhAB) and fae homologs (fae1-2 and fae3) were investigated via mutagenesis. The phenotype of the fdhAB mutant followed the model prediction. …”
    Get full text
    Article
  5. 965

    Novel ZAP-70-Related Immunodeficiency Presenting with Epstein–Barr Virus Lymphoproliferative Disorder and Hemophagocytic Lymphohistiocytosis by Moriah Forster, Timothy Moran, Anne Beaven, Timothy Voorhees

    Published 2021-01-01
    “…A deficiency of this kinase leads to a phenotype of severe combined immunodeficiency, while hypomorphic mutations of the kinase lead to more mild immunodeficiency phenotypes. …”
    Get full text
    Article
  6. 966

    Why morphology matters: the negative consequences of hasty descriptions of putative novelties in asexual ascomycetes by Ondřej Koukol, Gregorio Delgado

    Published 2021-09-01
    “…Descriptions of new fungal species have been almost routinely based on phenotypic studies coupled with single or multigene phylogenetic analyses of DNA sequence data. …”
    Get full text
    Article
  7. 967

    A Large PROP1 Gene Deletion in a Turkish Pedigree by Suheyla Gorar, Doga Turkkahraman, Kanay Yararbas

    Published 2018-01-01
    “…This finding is in line with the fact that patients with PROP1 mutations may have different phenotype/genotype correlation.…”
    Get full text
    Article
  8. 968

    Gene Expression during Survival of Escherichia coli O157:H7 in Soil and Water by Ashley D. Duffitt, Robert T. Reber, Andrew Whipple, Christian Chauret

    Published 2011-01-01
    “…These results suggest that E. coli O157:H7 may develop a different phenotype during transport through the environment. …”
    Get full text
    Article
  9. 969

    Spatial stochastic models of cancer: Fitness, migration, invasion by Natalia L. Komarova

    Published 2013-03-01
    “…In this review we concentrateon two phenotypic characteristics of cells: their reproductivepotential and their motility. …”
    Get full text
    Article
  10. 970

    Fatigue and Exercise Intolerance as Initial Manifestations of a Nonsyndromic Mitochondrial Disorder Due to the Variant m.3243A>G by Josef Finsterer, Sinda Zarrouk

    Published 2022-01-01
    “…The variant m.3243A>G may not only manifest as syndromic MID, particularly MELAS but also as nonsyndromic phenotype. MIDs should be considered as differentials of chronic fatigue even if no other phenotypic manifestation of a MID is present.…”
    Get full text
    Article
  11. 971

    The Immune Response Is Involved in Atherosclerotic Plaque Calcification: Could the RANKL/RANK/OPG System Be a Marker of Plaque Instability? by Fabrizio Montecucco, Sabine Steffens, François Mach

    Published 2007-01-01
    “…The accumulation of inflammatory cells and thus high amounts of soluble mediators are responsible for the evolution of some plaques to instable phenotype which may lead to rupture. One condition strongly associated with plaque rupture is calcification, a physiopathological process orchestrated by several soluble factors, including the receptor activator of nuclear factor NFκB ligand (RANKL)/receptor activator of nuclear factor NFκB (RANK)/osteoprotegerin (OPG) system. …”
    Get full text
    Article
  12. 972

    Inflammatory Bowel Disease in Children of Middle Eastern Descent by Christina Mai Ying Naidoo, Steven T. Leach, Andrew S. Day, Daniel A. Lemberg

    Published 2014-01-01
    “…Although there were limitations with this dataset, we estimated a higher prevalence of IBD in Middle Eastern children and they had a different disease phenotype and behavior compared to the control group, with less disease restricted to the colon and likely a more active disease course.…”
    Get full text
    Article
  13. 973

    Hypoxia-Inducible Factor-1 as a Therapeutic Target in Endometrial Cancer Management by Laura M. S. Seeber, Ronald P. Zweemer, René H. M. Verheijen, Paul J. van Diest

    Published 2010-01-01
    “…Tumor hypoxia is important because it renders an aggressive phenotype and leads to radio- and chemo-therapy resistance. …”
    Get full text
    Article
  14. 974

    Development of Multiple Myeloma of the IgA Type in a Patient with Cold Agglutinin Disease: Transformation or Coincidence? by Øystein Sefland, Ulla Randen, Sigbjørn Berentsen

    Published 2019-01-01
    “…For years, she remained asymptomatic apart from the hemolytic anemia until eventually she developed multiple myeloma (MM) of the IgAλ phenotype. Prior to the development of MM, her hemolytic anemia responded to rituximab monotherapy. …”
    Get full text
    Article
  15. 975

    Dysregulation of REST and its target genes impacts the fate of neural progenitor cells in down syndrome by Tan Huang, Sharida Fakurazi, Pike-See Cheah, King-Hwa Ling

    Published 2025-01-01
    “…REST and its target genes may collectively regulate the NPC phenotype.…”
    Get full text
    Article
  16. 976

    A Girl with PRRT2 Mutation Presenting with Benign Familial Infantile Seizures Followed by Autistic Regression by Li Zhang, Zhen-Xia Wan, Jin-Yi Zhu, Hui-Juan Liu, Jin Sun, Xiao-Hui Zou, Ting Zhang, Yan Li

    Published 2024-01-01
    “…In addition to BFIS, PRRT2 mutations are also associated with paroxysmal kinesigenic dyskinesia (PKD) and infantile convulsions and paroxysmal choreoathetosis (ICCA), indicating a complex genotype-phenotype heterogeneity in PRRT2 mutations. This clinical observation highlights the possibility that BFIS patients with PRRT2 mutations may not always have a benign neurodevelopmental prognosis, emphasizing the need for long-term clinical follow-up.…”
    Get full text
    Article
  17. 977

    Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa by A. M. Ali, R. M. Mbwasi, G. Kinabo, E.-J. Kamsteeg, B. C. Hamel, M. C. J. Dekker

    Published 2017-01-01
    “…We highlight the different features present in our patient and describe the etiology of the Freeman–Sheldon phenotype and how its clinical complications can be dealt with. …”
    Get full text
    Article
  18. 978

    Deficiency of ACE2 in Bone-Marrow-Derived Cells Increases Expression of TNF-α in Adipose Stromal Cells and Augments Glucose Intolerance in Obese C57BL/6 Mice by Sean E. Thatcher, Manisha Gupte, Nicholas Hatch, Lisa A. Cassis

    Published 2012-01-01
    “…Deficiency of ACE2 in macrophages has been suggested to promote the development of an inflammatory M1 macrophage phenotype. We evaluated effects of ACE2 deficiency in bone-marrow-derived stem cells on adipose inflammation and glucose tolerance in C57BL/6 mice fed a high fat (HF) diet. …”
    Get full text
    Article
  19. 979

    The Transcriptional Network Structure of a Myeloid Cell: A Computational Approach by Jesús Espinal-Enríquez, Daniel González-Terán, Enrique Hernández-Lemus

    Published 2017-01-01
    “…We present the topological parameters which define the network as well as some global structural features and introduce a relative inuence parameter to quantify the relevance of a transcription factor in the context of induction of a phenotype. Genes like ZHX2, ADNP, or SMAD6 seem to be highly regulated to avoid an avalanche transcription event. …”
    Get full text
    Article
  20. 980

    Expedient Treatment of a Collodion Baby by Michael Chung, Jaime Pittenger, Stuart Tobin, Andrew Chung, Nirmala Desai

    Published 2011-01-01
    “…As the name suggests, the term “collodion baby” refers to a phenotype that can be characterized by a yellow, shiny, tight parchment-like membrane stretched over the skin. …”
    Get full text
    Article