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  1. Article ; Online: The Switch/Sucrose Nonfermentable Subunit ARID1A Mediates Neutrophil-Associated Skin Inflammatory Responses.

    Batzorig, Uyanga / Chen, Yifang / Liu, Ye / Fernández-Méndez, Celia / Mahapatra, Samiksha / Lim, Sung Ha / Hong, Seung-Phil / Sen, George L

    The Journal of investigative dermatology

    2024  

    Language English
    Publishing date 2024-03-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80136-7
    ISSN 1523-1747 ; 0022-202X
    ISSN (online) 1523-1747
    ISSN 0022-202X
    DOI 10.1016/j.jid.2024.03.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: RACK1 Prevents the Premature Differentiation of Epidermal Progenitor Cells by Inhibiting IRF6 Expression.

    Ling, Ji / Tiwari, Manisha / Chen, Yifang / Sen, George L

    The Journal of investigative dermatology

    2021  Volume 142, Issue 5, Page(s) 1499–1502.e4

    MeSH term(s) Cell Differentiation ; Epidermal Cells/metabolism ; Interferon Regulatory Factors/metabolism ; Receptors for Activated C Kinase/genetics ; Receptors for Activated C Kinase/metabolism ; Stem Cells
    Chemical Substances Interferon Regulatory Factors ; Receptors for Activated C Kinase
    Language English
    Publishing date 2021-11-04
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 80136-7
    ISSN 1523-1747 ; 0022-202X
    ISSN (online) 1523-1747
    ISSN 0022-202X
    DOI 10.1016/j.jid.2021.10.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Improved naming in patients with Broca's aphasia with tDCS.

    Bonilha, Leonardo / Rorden, Chris / Roth, Rebecca / Sen, Souvik / George, Mark S / Fridriksson, Julius

    Journal of neurology, neurosurgery, and psychiatry

    2024  Volume 95, Issue 3, Page(s) 273–276

    Abstract: Background: Language impairment (aphasia) is a common neurological deficit after strokes. For individuals with chronic aphasia (beyond 6 months after the stroke), language improvements with speech therapy (ST) are often limited. Transcranial direct ... ...

    Abstract Background: Language impairment (aphasia) is a common neurological deficit after strokes. For individuals with chronic aphasia (beyond 6 months after the stroke), language improvements with speech therapy (ST) are often limited. Transcranial direct current stimulation (tDCS) is a promising approach to complement language recovery but interindividual variability in treatment response is common after tDCS, suggesting a possible relationship between tDCS and type of linguistic impairment (aphasia type).
    Methods: This current study is a subgroup analysis of a randomised controlled phase II futility design clinical trial on tDCS in chronic post-stroke aphasia. All participants received ST coupled with tDCS (n=31) vs sham tDCS (n=39). Confrontation naming was tested at baseline, and 1, 4, and 24 weeks post-treatment.
    Results: Broca's aphasia was associated with maximal adjunctive benefit of tDCS, with an average improvement of 10 additional named items with tDCS+ST compared with ST alone at 4 weeks post-treatment. In comparison, tDCS was not associated with significant benefits for other aphasia types
    Conclusions: These results indicate that adjuvant tDCS can enhance ST to treat naming in Broca's aphasia, and this may guide intervention approaches in future studies.
    MeSH term(s) Humans ; Transcranial Direct Current Stimulation/methods ; Aphasia/etiology ; Aphasia/therapy ; Stroke/complications ; Stroke/therapy ; Language ; Speech Therapy
    Language English
    Publishing date 2024-02-14
    Publishing country England
    Document type Randomized Controlled Trial ; Clinical Trial, Phase II ; Journal Article
    ZDB-ID 3087-9
    ISSN 1468-330X ; 0022-3050
    ISSN (online) 1468-330X
    ISSN 0022-3050
    DOI 10.1136/jnnp-2023-331541
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Novel presentations associated with a PDHA1 variant - Alternating hemiplegia in Hemizygote proband and Guillain Barre Syndrome in Heterozygote mother.

    Sen, Kuntal / Grahame, George / Bedoyan, Jirair K / Gropman, Andrea L

    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

    2021  Volume 31, Page(s) 27–30

    Abstract: We report a 5-year-old male with a PDHA1 variant who presented with alternating hemiplegia of childhood and later developed developmental regression, basal ganglia injury and episodic lactic acidosis. Enzyme assay in lymphocytes confirmed a diagnosis of ... ...

    Abstract We report a 5-year-old male with a PDHA1 variant who presented with alternating hemiplegia of childhood and later developed developmental regression, basal ganglia injury and episodic lactic acidosis. Enzyme assay in lymphocytes confirmed a diagnosis of Pyruvate Dehydrogenase Complex (PDC) deficiency. His mother who was heterozygous for the same variant suffered from ophthalmoplegia, chronic migraine and developed flaccid paralysis at 36 years of age. PDHA1 is the most common genetic cause of PDC deficiency and presents with a myriad of neurological phenotypes including neonatal form with lactic acidosis, non-progressive infantile encephalopathy, Leigh syndrome subtype and intermittent ataxia. The presentations in our 2 patients contribute to the clinical heterogeneity of this neurogenetic condition.
    MeSH term(s) Adult ; Child, Preschool ; Female ; Guillain-Barre Syndrome/genetics ; Hemiplegia/genetics ; Hemizygote ; Heterozygote ; Humans ; Male ; Mothers ; Paraplegia/genetics ; Pedigree ; Phenotype ; Pyruvate Dehydrogenase (Lipoamide)/genetics ; Pyruvate Dehydrogenase Complex Deficiency Disease/diagnosis ; Pyruvate Dehydrogenase Complex Deficiency Disease/genetics
    Chemical Substances Pyruvate Dehydrogenase (Lipoamide) (EC 1.2.4.1)
    Language English
    Publishing date 2021-01-22
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 1397146-3
    ISSN 1532-2130 ; 1090-3798
    ISSN (online) 1532-2130
    ISSN 1090-3798
    DOI 10.1016/j.ejpn.2021.01.006
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: CDK12 Is Necessary to Promote Epidermal Differentiation Through Transcription Elongation.

    Li, Jingting / Tiwari, Manisha / Chen, Yifang / Luanpitpong, Sudjit / Sen, George L

    Stem cells (Dayton, Ohio)

    2022  Volume 40, Issue 4, Page(s) 435–445

    Abstract: Proper differentiation of the epidermis is essential to prevent water loss and to protect the body from the outside environment. Perturbations in this process can lead to a variety of skin diseases that impacts 1 in 5 people. While transcription factors ... ...

    Abstract Proper differentiation of the epidermis is essential to prevent water loss and to protect the body from the outside environment. Perturbations in this process can lead to a variety of skin diseases that impacts 1 in 5 people. While transcription factors that control epidermal differentiation have been well characterized, other aspects of transcription control such as elongation are poorly understood. Here we show that of the two cyclin-dependent kinases (CDK12 and CDK13), that are known to regulate transcription elongation, only CDK12 is necessary for epidermal differentiation. Depletion of CDK12 led to loss of differentiation gene expression and absence of skin barrier formation in regenerated human epidermis. CDK12 binds to genes that code for differentiation promoting transcription factors (GRHL3, KLF4, and OVOL1) and is necessary for their elongation. CDK12 is necessary for elongation by promoting Ser2 phosphorylation on the C-terminal domain of RNA polymerase II and the stabilization of binding of the elongation factor SPT6 to target genes. Our results suggest that control of transcription elongation by CDK12 plays a prominent role in adult cell fate decisions.
    MeSH term(s) Cell Differentiation/genetics ; Cyclin-Dependent Kinases/genetics ; Cyclin-Dependent Kinases/metabolism ; Humans ; Phosphorylation ; RNA Polymerase II/chemistry ; RNA Polymerase II/genetics ; RNA Polymerase II/metabolism ; Transcription Factors/genetics ; Transcription Factors/metabolism
    Chemical Substances Transcription Factors ; CDK12 protein, human (EC 2.7.11.22) ; Cyclin-Dependent Kinases (EC 2.7.11.22) ; RNA Polymerase II (EC 2.7.7.-)
    Language English
    Publishing date 2022-03-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 1143556-2
    ISSN 1549-4918 ; 1066-5099
    ISSN (online) 1549-4918
    ISSN 1066-5099
    DOI 10.1093/stmcls/sxac002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Enhanc(er)ing Skin Stem Cells.

    Wang, Ying / Sen, George L

    Cell stem cell

    2016  Volume 19, Issue 4, Page(s) 415–417

    Abstract: In this issue of Cell Stem Cell, Rinaldi et al. (2016) find an unexpected role for the de novo DNA methyltransferases Dnmt3a and Dnmt3b in the regulation of enhancers. Their findings provide new insight into how regulation of enhancer activity through ... ...

    Abstract In this issue of Cell Stem Cell, Rinaldi et al. (2016) find an unexpected role for the de novo DNA methyltransferases Dnmt3a and Dnmt3b in the regulation of enhancers. Their findings provide new insight into how regulation of enhancer activity through DNA methylation can have dramatic consequences on epidermal stem cell fate decisions.
    MeSH term(s) DNA (Cytosine-5-)-Methyltransferases/genetics ; DNA Methylation ; Stem Cells
    Chemical Substances DNA (Cytosine-5-)-Methyltransferases (EC 2.1.1.37)
    Language English
    Publishing date 2016--06
    Publishing country United States
    Document type Journal Article ; Comment
    ZDB-ID 2375354-7
    ISSN 1875-9777 ; 1934-5909
    ISSN (online) 1875-9777
    ISSN 1934-5909
    DOI 10.1016/j.stem.2016.09.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Regulation of integrin and extracellular matrix genes by HNRNPL is necessary for epidermal renewal.

    Li, Jingting / Chen, Yifang / Tiwari, Manisha / Bansal, Varun / Sen, George L

    PLoS biology

    2021  Volume 19, Issue 9, Page(s) e3001378

    Abstract: ... heterogeneous nuclear ribonucleoprotein L (HNRNPL) binds to these genes on chromatin to promote their expression. HNRNPL recruits RNA ...

    Abstract Stratified epithelia such as the epidermis require coordinated regulation of stem and progenitor cell proliferation, survival, and differentiation to maintain homeostasis. Integrin-mediated anchorage of the basal layer stem cells of the epidermis to the underlying dermis through extracellular matrix (ECM) proteins is crucial for this process. It is currently unknown how the expression of these integrins and ECM genes are regulated. Here, we show that the RNA-binding protein (RBP) heterogeneous nuclear ribonucleoprotein L (HNRNPL) binds to these genes on chromatin to promote their expression. HNRNPL recruits RNA polymerase II (Pol II) to integrin/ECM genes and is required for stabilizing Pol II transcription through those genes. In the absence of HNRNPL, the basal layer of the epidermis where the stem cells reside prematurely differentiates and detaches from the underlying dermis due to diminished integrin/ECM expression. Our results demonstrate a critical role for RBPs on chromatin to maintain stem and progenitor cell fate by dictating the expression of specific classes of genes.
    MeSH term(s) Cell Differentiation ; Cells, Cultured ; Chromatin ; Epidermal Cells/metabolism ; Epidermis/growth & development ; Extracellular Matrix/genetics ; Extracellular Matrix/metabolism ; Heterogeneous-Nuclear Ribonucleoprotein L/metabolism ; Humans ; Integrins/genetics ; Integrins/metabolism ; Stem Cells
    Chemical Substances Chromatin ; Heterogeneous-Nuclear Ribonucleoprotein L ; Integrins
    Language English
    Publishing date 2021-09-20
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2126776-5
    ISSN 1545-7885 ; 1544-9173
    ISSN (online) 1545-7885
    ISSN 1544-9173
    DOI 10.1371/journal.pbio.3001378
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Post-Transcriptional Mechanisms Regulating Epidermal Stem and Progenitor Cell Self-Renewal and Differentiation.

    Li, Jingting / Sen, George L

    The Journal of investigative dermatology

    2016  Volume 136, Issue 4, Page(s) 746–752

    Abstract: Epidermal stem and progenitor cells exist within the basal layer of the epidermis and serve to replenish the loss of differentiated cells because of normal turnover or injury. Current efforts have focused on elucidating the transcriptional regulation of ... ...

    Abstract Epidermal stem and progenitor cells exist within the basal layer of the epidermis and serve to replenish the loss of differentiated cells because of normal turnover or injury. Current efforts have focused on elucidating the transcriptional regulation of epidermal stem cell self-renewal and differentiation. However, recent studies have pointed to an emerging and prominent role for post-transcriptional regulation of epidermal cell fate decisions. In this review, we will focus on post-transcriptional mechanisms including noncoding RNAs, RNA binding proteins, and mRNA decay-mediated control of epidermal stem and progenitor cell function in the skin.
    MeSH term(s) 3' Untranslated Regions ; Animals ; Cell Differentiation ; Cell Proliferation ; Cell Self Renewal ; DEAD-box RNA Helicases/metabolism ; Epidermis/cytology ; Exosomes/metabolism ; Gene Expression Regulation ; Humans ; Mice ; MicroRNAs/genetics ; Mutation ; Proto-Oncogene Proteins/metabolism ; RNA Processing, Post-Transcriptional ; RNA, Long Noncoding/genetics ; Stem Cells/cytology
    Chemical Substances 3' Untranslated Regions ; MicroRNAs ; Proto-Oncogene Proteins ; RNA, Long Noncoding ; DDX6 protein, human (EC 3.6.1.-) ; DEAD-box RNA Helicases (EC 3.6.4.13)
    Language English
    Publishing date 2016-02-11
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 80136-7
    ISSN 1523-1747 ; 0022-202X
    ISSN (online) 1523-1747
    ISSN 0022-202X
    DOI 10.1016/j.jid.2015.12.030
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Remembering one's identity: the epigenetic basis of stem cell fate decisions.

    Sen, George L

    FASEB journal : official publication of the Federation of American Societies for Experimental Biology

    2011  Volume 25, Issue 7, Page(s) 2123–2128

    Abstract: Stem cells serve a vital role in multicellular organisms by constantly replenishing tissue with their differentiated progeny during normal homeostasis or damage. How these cells maintain their identities throughout the life of an organism is an area of ... ...

    Abstract Stem cells serve a vital role in multicellular organisms by constantly replenishing tissue with their differentiated progeny during normal homeostasis or damage. How these cells maintain their identities throughout the life of an organism is an area of intense research. In this review, we explore recent emerging evidence that stem cell fate decisions are based on their epigenome and specific epigenetic factors.
    MeSH term(s) Cell Differentiation ; Cell Proliferation ; DNA Methylation ; DNA-Cytosine Methylases/metabolism ; Histone Demethylases/metabolism ; Histone-Lysine N-Methyltransferase/metabolism ; Histones/metabolism ; Humans ; Methylation ; Stem Cells/cytology ; Stem Cells/metabolism
    Chemical Substances Histones ; Histone Demethylases (EC 1.14.11.-) ; DNA-Cytosine Methylases (EC 2.1.1.-) ; histone methyltransferase (EC 2.1.1.-) ; Histone-Lysine N-Methyltransferase (EC 2.1.1.43)
    Language English
    Publishing date 2011-07
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 639186-2
    ISSN 1530-6860 ; 0892-6638
    ISSN (online) 1530-6860
    ISSN 0892-6638
    DOI 10.1096/fj.11-182774
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: ELL Facilitates RNA Polymerase II-Mediated Transcription of Human Epidermal Proliferation Genes.

    Li, Jingting / Bansal, Varun / Tiwari, Manisha / Chen, Yifang / Sen, George L

    The Journal of investigative dermatology

    2020  Volume 141, Issue 5, Page(s) 1352–1356.e3

    MeSH term(s) Cell Proliferation ; Epidermis/growth & development ; Humans ; RNA Polymerase II/physiology ; Transcription, Genetic ; Transcriptional Elongation Factors/physiology
    Chemical Substances ELL protein, human ; Transcriptional Elongation Factors ; RNA Polymerase II (EC 2.7.7.-)
    Language English
    Publishing date 2020-11-04
    Publishing country United States
    Document type Letter ; Research Support, N.I.H., Extramural
    ZDB-ID 80136-7
    ISSN 1523-1747 ; 0022-202X
    ISSN (online) 1523-1747
    ISSN 0022-202X
    DOI 10.1016/j.jid.2020.09.024
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