Mark Noble

ORCID: 0000-0002-9618-120X
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About
Contact & Profiles
Research Areas
  • Neurogenesis and neuroplasticity mechanisms
  • Pluripotent Stem Cells Research
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Glioma Diagnosis and Treatment
  • RNA Research and Splicing
  • Virus-based gene therapy research
  • CRISPR and Genetic Engineering
  • Liver physiology and pathology
  • Neuroscience and Neuropharmacology Research
  • Gene Regulatory Network Analysis
  • Advanced Fluorescence Microscopy Techniques
  • Cardiac Ischemia and Reperfusion
  • Birth, Development, and Health
  • MicroRNA in disease regulation
  • Epigenetics and DNA Methylation
  • Single-cell and spatial transcriptomics
  • Cell Image Analysis Techniques
  • Axon Guidance and Neuronal Signaling
  • Genomics and Chromatin Dynamics
  • Nerve injury and regeneration
  • RNA Interference and Gene Delivery
  • Metabolomics and Mass Spectrometry Studies
  • Congenital heart defects research
  • Microfluidic and Bio-sensing Technologies
  • Immune cells in cancer

Yale University
2023-2025

University of South Florida
2016

Madison Group (United States)
2011

Ludwig Cancer Research
1989-2007

Mirus Bio (United States)
2004-2007

University of Rochester
2005-2006

University of Rochester Medical Center
2001-2006

Huntsman Cancer Institute
1996-2003

University of Utah
1996-2003

Western University
2000

Proton nuclear magnetic resonance (1H NMR) spectroscopy is a noninvasive technique that can provide information on wide range of metabolites. Marked abnormalities 1H NMR brain spectra have been reported in patients with neurological disorders, but their neurochemical implications may be difficult to appreciate because data are obtained from heterogeneous tissue regions composed several cell populations. The purpose this study was examine the profile major neural types. This helpful...

10.1523/jneurosci.13-03-00981.1993 article EN cc-by-nc-sa Journal of Neuroscience 1993-03-01

We have found that glial progenitor cells isolated from the optic nerves of adult rats are fundamentally different their counterparts in perinatal animals. In our studies on bipotential oligodendrocyte-type-2 astrocyte (O-2A) cells, we seen O-2Aadult can be distinguished O-2Aperinatal progenitors by morphology and antigenic phenotype, much longer cell cycle time (65 h versus 18 h), slower rate migration (4 microns h-1 21 h-1), course differentiation into oligodendrocytes or type-2 astrocytes...

10.1242/dev.105.2.387 article EN Development 1989-02-01
James R. Xue Ava Mackay-Smith Kousuke Mouri Meilín Fernández García Michael X. Dong and 95 more Jared F. Akers Mark Noble Xue Li Kerstin Lindblad‐Toh Elinor K. Karlsson James P. Noonan Terence D. Capellini Kristen Brennand Ryan Tewhey Pardis C. Sabeti Steven K. Reilly Gregory Andrews Joel Armstrong Matteo Bianchi Bruce W. Birren Kevin R. Bredemeyer Ana M. Breit Matthew J. Christmas Hiram Clawson Joana Damas Federica Di Palma Mark Diekhans Michael X. Dong Eduardo Eizirik Kaili Fan Cornelia Fanter Nicole M. Foley Karin Forsberg‐Nilsson Carlos J. Garcia John Gatesy Steven Gazal Diane P. Genereux Linda Goodman Jenna Grimshaw Michaela K. Halsey Andrew J. Harris Glenn Hickey Michael Hiller Allyson G. Hindle Robert Hubley Graham M. Hughes Jeremy Johnson David Juan Irene M. Kaplow Elinor K. Karlsson Kathleen C. Keough Bogdan Kirilenko Klaus‐Peter Koepfli Jennifer M. Korstian Amanda Kowalczyk Sergey V. Kozyrev Alyssa J. Lawler Colleen Lawless Thomas Lehmann Danielle L. Levesque Harris A. Lewin Xue Li Abigail Lind Kerstin Lindblad‐Toh Ava Mackay-Smith Voichita D. Marinescu Tomás Marquès‐Bonet Victor C. Mason Jennifer R. S. Meadows Wynn K. Meyer Jill E. Moore Lucas R. Moreira Diana D. Moreno-Santillán Kathleen M. Morrill Gerard Muntané William J. Murphy Arcadi Navarro Martin Nweeia Sylvia Ortmann Austin Osmanski Benedict Paten Nicole S. Paulat Andreas Pfenning BaDoi N. Phan Katherine S. Pollard Henry Pratt David A. Ray Steven K. Reilly Jeb Rosen Irina Ruf Louise Ryan Oliver A. Ryder Pardis C. Sabeti Daniel E. Schäffer Aitor Serres Beth Shapiro Arian F. A. Smit Mark S. Springer Chaitanya Srinivasan Cynthia Steiner

Conserved genomic sequences disrupted in humans may underlie uniquely human phenotypic traits. We identified and characterized 10,032 human-specific conserved deletions (hCONDELs). These short (average 2.56 base pairs) are enriched for brain functions across genetic, epigenomic, transcriptomic datasets. Using massively parallel reporter assays six cell types, we discovered 800 hCONDELs conferring significant differences regulatory activity, half of which enhance rather than disrupt function....

10.1126/science.abn2253 article EN Science 2023-04-27

We have isolated a tripotential glial precursor cell population from spinal cords of E13.5 rats. In vitro, these A2B5 + E-NCAM − glial-restricted (GRP) cells can undergo extensive self-renewal, and differentiate into oligodendrocytes two distinct astrocyte populations, but do not neurons. The differentiation potential GRP is retained through at least three cycles expansion recloning. Unlike oligodendrocyte-type 2 progenitor cells, freshly respond to platelet-derived growth factor as mitogen...

10.1073/pnas.95.7.3996 article EN Proceedings of the National Academy of Sciences 1998-03-31

ABSTRACT We have found that CNTF and LIF are pleiotropic modulators of development in the O-2A lineage. Both molecules enhanced generation oligodendrocytes cultures dividing progenitors. also promoted oligodendrocyte maturation, as determined by expression myelin basic protein, could promote survival to an extent comparable with insulin-like growth factor-1 or insulin. In addition, both differentiation progenitors into type-2 astrocytes but only when applied presence extra-cellular matrix...

10.1242/dev.120.1.143 article EN Development 1994-01-01

We have shown previously that oligodendrocyte-type-2 astrocyte (O-2A) progenitor cells isolated from adult rat optic nerves can be distinguished in vitro their perinatal counterparts on the basis of much slower rates division, differentiation, and migration when grown presence cortical astrocytes or PDGF. This behavior is consistent with vivo observations there only a modest production oligodendrocytes CNS. As such inconsistent likely need for rapid generation following demyelinating damage...

10.1083/jcb.118.4.889 article EN The Journal of Cell Biology 1992-08-15

Delivery is increasingly being recognized as the critical hurdle holding back tremendous promise of nucleic acid-based therapies that include gene therapy and more recently siRNA-based therapeutics. While numerous candidate genes (and siRNA sequences) with therapeutic potential have been identified, their utility has not yet realized because inefficient and/or unsafe delivery technologies. We now describe an intravascular, nonviral methodology enables efficient repeatable acids to muscle...

10.1016/j.ymthe.2004.05.004 article EN cc-by-nc-nd Molecular Therapy 2004-06-22

Changes in gene regulation have been linked to the expansion of human cerebral cortex and neurodevelopmental disorders, potentially by altering neural progenitor proliferation. However, effects genetic variation within regulatory elements on progenitors remain obscure. We use sgRNA-Cas9 screens stem cells (hNSCs) disrupt 10,674 genes 26,385 conserved regions 2,227 enhancers active developing determine Genes with proliferation phenotypes are associated disorders show biased expression...

10.1016/j.celrep.2024.113693 article EN cc-by-nc-nd Cell Reports 2024-01-23

We have been studying the differing characteristics of oligodendrocyte-type-2 astrocyte (O-2A) progenitors isolated from optic nerves perinatal and adult rats. These two cell types display striking differences in their vitro phenotypes. In addition, O-2Aperinatal progenitor population appears to a limited life-span vivo, while O-2Aadult appear be maintained throughout life. seem largely disappeared nerve by 1 mo after birth, are not detectable cultures derived contrast, can first 7-d-old...

10.1083/jcb.116.1.167 article EN The Journal of Cell Biology 1992-01-01

The central nervous system of individuals with multiple sclerosis contains lesions specifically characterized by breakdown myelin sheaths associated a general failure repair demyelinating damage. cause is unknown. Although immune mechanisms have been implicated in this breakdown, no convincing demonstrations specific reaction against yet provided patients. Similarly, the cellular biological which underlie are We found that (i) oligodendrocytes, cells produce system, and (ii)...

10.1073/pnas.86.22.9025 article EN Proceedings of the National Academy of Sciences 1989-11-01

Abstract Cell culture techniques, high‐resolution in vitro 1 H NMR spectroscopy, and chromatographic analyses were used to compare the properties of three types human brain nervous system tumours. lines immunocytochemically characterized at all stages with specific antibodies. Intracellular metabolites present cell extracts analysed by spectroscopy high performance liquid chromatography (HPLC). The spectra from meningiomas, neuroblastomas, glioblastomas displayed, addition similarities —...

10.1002/nbm.1940080605 article EN NMR in Biomedicine 1995-09-01

Anemia frequently accompanies chronic diseases such as progressive renal failure, acquired immunodeficiency syndrome, and cancer. Patients are currently treated with erythropoietin (EPO) replacement therapy, using various recombinant human EPO protein formulations. Although this treatment is effective, gene therapy could be more economical convenient for the long-term management of disease. The objective study was to develop a naked DNA-based protocol that fill need. Hydrodynamic limb vein...

10.1089/hum.2006.186 article EN Human Gene Therapy 2007-03-01

Abstract Human Accelerated Regions (HARs) are highly conserved across species but exhibit a significant excess of human-specific sequence changes, suggesting they may have gained novel functions in human evolution. HARs include transcriptional enhancers with activity and been implicated the evolution brain. However, our understanding how contributed to uniquely features brain is hindered by lack insight into genes pathways that regulate. It unclear whether acted altering expression gene...

10.1101/2024.06.25.600691 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-06-26
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