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  1. AU="Moretti, Alessandra"
  2. AU=Chintagumpala Murali
  3. AU="Cameron, Sharon Tracey"
  4. AU="Innao, Vanessa"
  5. AU="Lopez-Paz, Cristina"
  6. AU="Rattenbacher, Bernd"
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  14. AU="Nitta, Takashi"
  15. AU="Catanesi, M. G."
  16. AU="Kim, E. J."
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  20. AU="Gallagher, Julia E"
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  29. AU=Wang Heping
  30. AU="Miyazaki, Masashi"
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  34. AU="Li, Baohua"
  35. AU="Zhang, Nasen Jonathan"
  36. AU="Scotlandi, Katia"
  37. AU="Thomson, M A"
  38. AU=New Sophie E P
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  40. AU="Staehelin, Cornelia"
  41. AU="Akhtar, Suraiya"
  42. AU="Georgel, Philippe"
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  44. AU="Charron, Morgane"
  45. AU="Leona S. Alizadeh" AU="Leona S. Alizadeh"
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  66. AU="Chowdhury, Muhtamim"
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  69. AU="Simpson, Tina Y"
  70. AU="Li, Peirang"
  71. AU="Zhang, Zhao-Liang"
  72. AU="Perner, Sven"
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  1. Artikel ; Online: Ex vivo Culture and Contractile Force Measurements of Non-human Primate Heart Slices.

    Poch, Christine M / Dendorfer, Andreas / Laugwitz, Karl-Ludwig / Moretti, Alessandra

    Bio-protocol

    2023  Band 13, Heft 13, Seite(n) e4750

    Abstract: Cardiovascular diseases are the leading cause of death and morbidity worldwide. Patient mortality has been successfully reduced by nearly half in the last four decades, mainly due to advances in minimally invasive surgery techniques and interventional ... ...

    Abstract Cardiovascular diseases are the leading cause of death and morbidity worldwide. Patient mortality has been successfully reduced by nearly half in the last four decades, mainly due to advances in minimally invasive surgery techniques and interventional cardiology methods. However, a major hurdle is still the translational gap between preclinical findings and the conversion into effective therapies, which is partly due to the use of model systems that fail to recapitulate key aspects of human physiology and disease. Large animal models such as pigs and non-human primates are highly valuable because they closely resemble humans but are costly and time intensive. Here, we provide a method for long-term ex vivo culture of non-human primate (NHP) myocardial tissue that offers a powerful alternative for a wide range of applications including electrophysiology studies, drug screening, and gene function analyses.
    Sprache Englisch
    Erscheinungsdatum 2023-07-05
    Erscheinungsland United States
    Dokumenttyp Journal Article
    ZDB-ID 2833269-6
    ISSN 2331-8325 ; 2331-8325
    ISSN (online) 2331-8325
    ISSN 2331-8325
    DOI 10.21769/BioProtoc.4750
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel ; Online: Designer pigs for xenogeneic heart transplantation and beyond.

    Wolf, Eckhard / Reichart, Bruno / Moretti, Alessandra / Laugwitz, Karl-Ludwig

    Disease models & mechanisms

    2023  Band 16, Heft 5

    Abstract: The 2-month-survival of a terminally ill patient who received a genetically modified pig heart has demonstrated that cardiac xenotransplantation could provide a therapeutic option for patients who cannot receive a human organ. Genetic engineering to ... ...

    Abstract The 2-month-survival of a terminally ill patient who received a genetically modified pig heart has demonstrated that cardiac xenotransplantation could provide a therapeutic option for patients who cannot receive a human organ. Genetic engineering to overcome transplant rejection mechanisms, coagulation dysregulation and overgrowth of xeno-hearts has been the key to this success. The concept of exogenesis - the replacement of specific cellular populations and tissue structures of a pig heart with human cells - is a promising extension of xenotransplantation because it could further reduce immunological and physiological obstacles. Additionally, in the aim of preventing the need for heart transplant, tailored pig models mimicking monogenic cardiac disorders have been developed to test new cellular and molecular therapies. Thus, genetically engineered pigs provide a powerful platform for xenogeneic, exogenic and endogenic restoration of cardiac function.
    Mesh-Begriff(e) Animals ; Humans ; Swine ; Transplantation, Heterologous ; Heart Transplantation ; Heart ; Genetic Engineering ; Graft Rejection/genetics ; Animals, Genetically Modified
    Sprache Englisch
    Erscheinungsdatum 2023-05-30
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2451104-3
    ISSN 1754-8411 ; 1754-8403
    ISSN (online) 1754-8411
    ISSN 1754-8403
    DOI 10.1242/dmm.050177
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  3. Buch ; Online ; Dissertation / Habilitation: Cardiac progenitors repopulate left ventricular myocardium in an ex vivo 3D tissue model

    Reiter, Franziska Cäcilia [Verfasser] / Moretti, Alessandra [Akademischer Betreuer] / Moretti, Alessandra [Gutachter] / Sinnecker, Daniel [Gutachter]

    2023  

    Verfasserangabe Franziska Cäcilia Reiter ; Gutachter: Alessandra Moretti, Daniel Sinnecker ; Betreuer: Alessandra Moretti
    Schlagwörter Medizin, Gesundheit ; Medicine, Health
    Thema/Rubrik (Code) sg610
    Sprache Englisch
    Verlag Universitätsbibliothek der TU München
    Erscheinungsort München
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  4. Buch ; Online ; Dissertation / Habilitation: 3D Cardiac Tissue Engineering for Studying Hypoplastic Left Heart Syndrome and other Disease Phenotypes

    Poch, Christine Maria [Verfasser] / Moretti, Alessandra [Akademischer Betreuer] / Moretti, Alessandra [Gutachter] / Kossatz, Susanne [Gutachter] / Mägdefessel, Lars [Gutachter]

    2022  

    Verfasserangabe Christine Maria Poch ; Gutachter: Alessandra Moretti, Susanne Kossatz, Lars Mägdefessel ; Betreuer: Alessandra Moretti
    Schlagwörter Medizin, Gesundheit ; Medicine, Health
    Thema/Rubrik (Code) sg610
    Sprache Englisch
    Verlag Universitätsbibliothek der TU München
    Erscheinungsort München
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  5. Buch ; Online ; Dissertation / Habilitation: Defining early steps of human cardiac progenitor lineage segregation, fate decision and gene regulatory elements

    Zawada, Dorota Marta [Verfasser] / Moretti, Alessandra [Akademischer Betreuer] / Moretti, Alessandra [Gutachter] / Wahl-Schott, Christian [Gutachter] / Gagneur, Julien [Gutachter]

    2023  

    Verfasserangabe Dorota Marta Zawada ; Gutachter: Alessandra Moretti, Christian Wahl-Schott, Julien Gagneur ; Betreuer: Alessandra Moretti
    Schlagwörter Medizin, Gesundheit ; Medicine, Health
    Thema/Rubrik (Code) sg610
    Sprache Englisch
    Verlag Universitätsbibliothek der TU München
    Erscheinungsort München
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  6. Artikel ; Online: Generation of heterozygous (MRli003-A-3) and homozygous (MRli003-A-4) TRPM4 knockout human iPSC lines.

    Zhang, Fangfang / Meier, Anna B / Lipp, Peter / Laugwitz, Karl-Ludwig / Dorn, Tatjana / Moretti, Alessandra

    Stem cell research

    2022  Band 60, Seite(n) 102731

    Abstract: TRPM4 is a ... ...

    Abstract TRPM4 is a Ca
    Mesh-Begriff(e) CRISPR-Cas Systems/genetics ; Gene Editing ; Heterozygote ; Homozygote ; Humans ; Induced Pluripotent Stem Cells/metabolism ; Mutation/genetics ; TRPM Cation Channels/genetics ; TRPM Cation Channels/metabolism
    Chemische Substanzen TRPM Cation Channels ; TRPM4 protein, human
    Sprache Englisch
    Erscheinungsdatum 2022-02-26
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2393143-7
    ISSN 1876-7753 ; 1873-5061
    ISSN (online) 1876-7753
    ISSN 1873-5061
    DOI 10.1016/j.scr.2022.102731
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  7. Buch ; Online ; Dissertation / Habilitation: Advanced hiPSC-based platforms for in vitro modeling of cardiac development, disease, and therapy

    Meier, Anna Béatrice [Verfasser] / Moretti, Alessandra [Akademischer Betreuer] / Moretti, Alessandra [Gutachter] / Saur, Dieter [Gutachter] / Biel, Martin [Gutachter] / Laugwitz, Karl-Ludwig [Gutachter]

    2022  

    Verfasserangabe Anna Béatrice Meier ; Gutachter: Alessandra Moretti, Dieter Saur, Martin Biel, Karl-Ludwig Laugwitz ; Betreuer: Alessandra Moretti
    Schlagwörter Naturwissenschaften ; Science
    Thema/Rubrik (Code) sg500
    Sprache Englisch
    Verlag Universitätsbibliothek der TU München
    Erscheinungsort München
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  8. Buch ; Online ; Dissertation / Habilitation: Klinischer Verlauf von Erwachsenen mit Fallot'scher Tetralogie oder Pulmonalatresie mit Ventrikelseptumdefekt über einem Alter von 40 Jahren

    Schwall, Laurent Louis Aloyse Verfasser] / [Ewert, Peter [Akademischer Betreuer] / Ewert, Peter [Gutachter] / Moretti, Alessandra [Gutachter]

    2023  

    Verfasserangabe Laurent Louis Aloyse Schwall ; Gutachter: Peter Ewert, Alessandra Moretti ; Betreuer: Peter Ewert
    Schlagwörter Medizin, Gesundheit ; Medicine, Health
    Thema/Rubrik (Code) sg610
    Sprache Deutsch
    Verlag Universitätsbibliothek der TU München
    Erscheinungsort München
    Dokumenttyp Buch ; Online ; Dissertation / Habilitation
    Datenquelle Digitale Dissertationen im Internet

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  9. Artikel ; Online: Generation of heterozygous (MRli003-A-1) and homozygous (MRli003-A-2) MYH10 knockout human iPSC lines.

    Zhang, Fangfang / Meier, Anna B / Laugwitz, Karl-Ludwig / Dorn, Tatjana / Moretti, Alessandra

    Stem cell research

    2021  Band 57, Seite(n) 102612

    Abstract: Myosin-10, also known as non-muscle myosin IIB, is a cytoskeletal protein implicated in cardiac development and disease. In humans, it is encoded by the MYH10 gene. Using CRISPR/Cas9 gene editing technology, we generated two MYH10 knockout human iPSC ... ...

    Abstract Myosin-10, also known as non-muscle myosin IIB, is a cytoskeletal protein implicated in cardiac development and disease. In humans, it is encoded by the MYH10 gene. Using CRISPR/Cas9 gene editing technology, we generated two MYH10 knockout human iPSC lines - one heterozygous (MRli003-A-1) and one homozygous (MRli003-A-2) - by introducing a frameshift deletion in exon 2. We then verified that both lines had maintained pluripotency, parental cell morphology, trilineage differentiation potential and a normal karyotype.
    Sprache Englisch
    Erscheinungsdatum 2021-11-29
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 2393143-7
    ISSN 1876-7753 ; 1873-5061
    ISSN (online) 1876-7753
    ISSN 1873-5061
    DOI 10.1016/j.scr.2021.102612
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  10. Artikel ; Online: Genome editing for Duchenne muscular dystrophy: a glimpse of the future?

    Kupatt, Christian / Windisch, Alina / Moretti, Alessandra / Wolf, Eckhard / Wurst, Wolfgang / Walter, Maggie C

    Gene therapy

    2021  Band 28, Heft 9, Seite(n) 542–548

    Abstract: Mutations in Dystrophin, one of the largest proteins in the mammalian body, are causative for a severe form of muscle disease, Duchenne Muscular Dystrophy (DMD), affecting not only skeletal muscle, but also the heart. In particular, exons 45-52 ... ...

    Abstract Mutations in Dystrophin, one of the largest proteins in the mammalian body, are causative for a severe form of muscle disease, Duchenne Muscular Dystrophy (DMD), affecting not only skeletal muscle, but also the heart. In particular, exons 45-52 constitute a hotspot for DMD mutations. A variety of molecular therapies have been developed, comprising vectors encoding micro- and minidystrophins as well as utrophin, a protein with partially overlapping functions. With the advent of the CRISPR-Cas9-nuclease, genome editing offers a novel option of correction of the disease-cuasing mutations. Full restoration of the healthy gene by homology directed repair is a rare event. However, non-homologous end-joining (NHEJ) may restore the reading frame by causing exon excision. This approach has first been demonstrated in mice and then translated to large animals (dogs, pigs). This review discusses the potential opportunities and limitations of genome editing in DMD, including the generation of appropriate animal models as well as new developments in genome editing tools.
    Mesh-Begriff(e) Animals ; CRISPR-Cas Systems ; Disease Models, Animal ; Dogs ; Gene Editing ; Genetic Therapy ; Mice ; Muscular Dystrophy, Duchenne/genetics ; Muscular Dystrophy, Duchenne/therapy ; Swine
    Sprache Englisch
    Erscheinungsdatum 2021-02-02
    Erscheinungsland England
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1191036-7
    ISSN 1476-5462 ; 0969-7128
    ISSN (online) 1476-5462
    ISSN 0969-7128
    DOI 10.1038/s41434-021-00222-4
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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