Immunoglobulins in milk from cows immunized with oral strains of Actinomyces, Prevotella, Porphyromonas, and Fusobacterium

Autor: Nobuhiro Takahashi, G. Eisenhuth, Ignatius K Lee, S. Binion, Charles F. Schachtele, N. Laible

Publikováno v: Journal of dental research. 71(8)

Immunization of pregnant cows with bacteria leads to the presence of high concentrations of specific antibodies in colostrum and milk. A total of 14 cows was immunized with single strains of heat-killed oral bacteria or pools of strains of Actinomyce

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dd5d4a28303acb7bf8037b8f0d52e96
https://pubmed.ncbi.nlm.nih.gov/1354674

Aberrant neurodevelopment in human iPS cell-derived models of Alexander disease.

Autor: Matusova Z; Laboratory of Gene Expression, Institute of Biotechnology of the Czech Academy of Sciences, Vestec, Czechia.; Faculty of Science, Charles University, Prague, Czechia., Dykstra W; Department of Translational Neuroscience, University Medical Centre Utrecht Brain Centre, Utrecht University, Utrecht, The Netherlands., de Pablo Y; Laboratory of Astrocyte Biology and CNS Regeneration, Center for Brain Repair, Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden., Zetterdahl OG; Stem Cells, Aging and Neurodegeneration Lab, Department of Experimental Medical Science, Faculty of Medicine, Lund Stem Cell Center, Lund University, Lund, Sweden.; Glial and Neuronal Biology Lab, Department of Experimental Medical Science, Faculty of Medicine, Lund Stem Cell Center, Lund University, Lund, Sweden., Canals I; Glial and Neuronal Biology Lab, Department of Experimental Medical Science, Faculty of Medicine, Lund Stem Cell Center, Lund University, Lund, Sweden.; Division of Metabolism, University Children's Hospital Zurich, University of Zurich, Zurich, Switzerland.; ITINERARE-Innovative therapies in rare diseases, University Research Priority Program, University of Zurich, Zurich, Switzerland., van Gelder CAGH; Oncode Institute and Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands., Vos HR; Oncode Institute and Molecular Cancer Research, Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands., Pérez-Sala D; Centro de Investigaciones Biológicas Margarita Salas, Madrid, Spain., Kubista M; Laboratory of Gene Expression, Institute of Biotechnology of the Czech Academy of Sciences, Vestec, Czechia.; Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden., Abaffy P; Laboratory of Gene Expression, Institute of Biotechnology of the Czech Academy of Sciences, Vestec, Czechia., Ahlenius H; Stem Cells, Aging and Neurodegeneration Lab, Department of Experimental Medical Science, Faculty of Medicine, Lund Stem Cell Center, Lund University, Lund, Sweden., Valihrach L; Laboratory of Gene Expression, Institute of Biotechnology of the Czech Academy of Sciences, Vestec, Czechia.; Department of Cellular Neurophysiology, Institute of Experimental Medicine of the Czech Academy of Sciences, Prague, Czechia., Hol EM; Department of Translational Neuroscience, University Medical Centre Utrecht Brain Centre, Utrecht University, Utrecht, The Netherlands., Pekny M; Laboratory of Astrocyte Biology and CNS Regeneration, Center for Brain Repair, Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.; University of Newcastle, Newcastle, New South Wales, Australia.

Publikováno v: Glia [Glia] 2025 Jan; Vol. 73 (1), pp. 57-79. Date of Electronic Publication: 2024 Sep 23.

A 235 Kb deletion at 17q21.33 encompassing the COL1A1, and two additional secondary copy number variants in an infant with type I osteogenesis imperfecta: A rare case report.

Autor: Numbere, Numbereye¹ (AUTHOR), Weber, David R.² (AUTHOR), Porter, George³ (AUTHOR), Iqbal, Mohammed A.¹ (AUTHOR) anwar_iqbal@urmc.rochester.edu

Publikováno v: Molecular Genetics & Genomic Medicine. Jun2020, Vol. 8 Issue 6, p1-5. 5p.

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Delayed cortical development in mice with a neural specific deletion of β1 integrin.

Autor: Rashid, Mamunur, Olson, Eric C.

Publikováno v: Frontiers in Neuroscience; 2023, p1-15, 15p