Cited by 336Multiple Sclerosis Research StudiesHereditary Neurological DisordersNeurogenesis and neuroplasticity mechanisms

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.

Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice

ROACH, A, TAKAHASHI, N, PRAVTCHEVA, D, RUDDLE, F, HOOD, L·1985·Cell

DOI 10.1016/s0092-8674(85)80110-0

Open this paper in CoChat — free account

Abstract

The gene for mouse myelin basic protein (MBP) was mapped to chromosome 18 by hybridization of cloned MBP probes to DNA from hamster-mouse hybrid cell lines, showing it to be linked to the shiverer mutation which causes abnormal CNS myelination. Genomic blotting experiments show that in the mutants five of six exons which constitute the wild-type gene have been deleted. In shiverer brains the steady state level of transcripts that initiate correctly at the 5' end of the remaining exon 1 is reduced 16-fold. These RNAs are not spliced correctly and are not efficiently polyadenylated. It is proposed that the partial deletion of the MBP gene is an important part of the shiverer lesion.

Integrity signals

Registry

Crossref · 10.1016/s0092-8674(85)80110-0

Cites

32 of 32 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Detection of specific sequences among DNA fragments separated by gel electrophoresis
Southern, E. M. (1975) · Journal of Molecular Biology · doi:10.1016/s0022-2836(75)80083-0 · Cited by 32,245
Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease
Chirgwin, J. M., Przybyla, A., MacDonald, R. J., & Rutter, W. J. (1979) · Biochemistry · doi:10.1021/bi00591a005 · Cited by 21,460
[57] Sequencing end-labeled DNA with base-specific chemical cleavages
Maxam, A. M., & Gilbert, W. (1980) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(80)65059-9 · Cited by 13,943
Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I
Rigby, P. W. J., Dieckmann, M., Rhodes, C., & Berg, P. R. (1977) · Journal of Molecular Biology · doi:10.1016/0022-2836(77)90052-3 · Cited by 11,400
A general method for isolation of high molecular weight DNA from eukaryotes
Blin, N., & Stafford, D. W. (1976) · Nucleic Acids Research · doi:10.1093/nar/3.9.2303 · Cited by 2,743
[68] Transcription maps of polyoma virus-specific RNA: Analysis by two-dimensional nuclease S1 gel mapping
Favaloro, J. M., Treisman, R., & Kamen, R. (1980) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(80)65070-8 · Cited by 1,292
Methylmercury as a reversible denaturing agent for agarose gel electrophoresis
Bailey, J. M., & Davidson, N. (1976) · Analytical Biochemistry · doi:10.1016/s0003-2697(76)80049-8 · Cited by 1,286
Transcriptional Control Signals of a Eukaryotic Protein-Coding Gene
McKnight, S. L., & Kingsbury, R. (1982) · Science · doi:10.1126/science.6283634 · Cited by 1,259
Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes
Treisman, R., Orkin, S. H., & Maniatis, T. (1983) · Nature · doi:10.1038/302591a0 · Cited by 590
Three regions upstream from the cap site are required for efficient and accurate transcription of the rabbit β-globin gene in mouse 3T6 cells
Dierks, P. M., van Ooyen, A., Cochran, M. D., Dobkin, C., Reiser, J., & Weissmann, C. (1983) · Cell · doi:10.1016/0092-8674(83)90055-7 · Cited by 538

Show all 32 references

Sorted by citations

Items 201–300 of 335

The Evolution of Myelin: Theories and Application to Human Disease
Knowles, L. W. (2017) · Journal of Evolutionary Medicine · doi:10.4303/jem/235996 · Cited by 16
Intrinsic neuronal physiology and the functions, dysfunctions and development of neocortex
Connors, B. W. (1994) · Progress in brain research · doi:10.1016/s0079-6123(08)60540-3 · Cited by 17
Po mRNA expression in cultures of Schwann cells and neurons that lack basal lamina and myelin
Brunden, K. R., & Brown, D. T. (1990) · Journal of Neuroscience Research · doi:10.1002/jnr.490270206 · Cited by 17
Molecular biology of myelination
Monuki, E. S., & Lemke, G. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195082937.003.0007 · Cited by 17
Multiple Sclerosis: Multiple Etiologies, Multiple Genes?
Tienari, P. J. (1994) · Annals of Medicine · doi:10.3109/07853899409147901 · Cited by 15
Myelin Basic Protein Is an Endogenous Inhibitor of the High‐Affinity Cannabinoid Binding Site in Brain
Nye, J. S., Voglmaier, S. M., Martenson, R. E., & Snyder, S. H. (1988) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1988.tb10589.x · Cited by 15
DNase I sensitivity of immunoglobulin light chain genes in Abelson murine leukemia virus transformed pre-B cell lines
Persiani, D. M., & Selsing, E. (1989) · Nucleic Acids Research · doi:10.1093/nar/17.13.5339 · Cited by 15
The 3’UTRs of Myelin Basic Protein mRNAs Regulate Transport, Local Translation and Sensitivity to Neuronal Activity in Zebrafish
Torvund‐Jensen, J., Steengaard, J., Askebjerg, L. B., Kjær-Sørensen, K., & Laursen, L. S. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00185 · Cited by 16
Palmitoylethanolamide and White Matter Lesions: Evidence for Therapeutic Implications
Valenza, M., Facchinetti, R., Steardo, L., & Scuderi, C. (2022) · Biomolecules · doi:10.3390/biom12091191 · Cited by 15
Nerve conduction velocity measurements reveal the functional deficit in ceramide galactosyl transferase-deficient (cgt−/−) mice
Haupt, W. F., & Stoffel, W. (2003) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2003.09.004 · Cited by 14
The Myelin‐Deficient Rat Has a Single Base Substitution in the Third Exon of the Myelin Proteolipid Protein Gene
Simons, R., & Riordan, J. R. (1990) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1990.tb02360.x · Cited by 14
Expression of only one myelin basic protein allele in mouse is compatible with normal myelination
Roch, J., Cooper, B. J., Ramirez, R., & Matthieu, J. (1987) · Molecular Brain Research · doi:10.1016/0169-328x(87)90045-3 · Cited by 14
Microstructural analysis of the effects of incorporation of myelin basic protein in phospholipid layers
Cristofolini, L., Fontana, M. P., Serra, F., Fasano, A., Riccio, P., & Konovalov, O. (2005) · European Biophysics Journal · doi:10.1007/s00249-005-0489-5 · Cited by 14
Temporal and spatial transcriptomic dynamics across brain development in Xenopus laevis tadpoles
Ta, A. C., Huang, L.-C., McKeown, C. R., Bestman, J. E., Keuren‐Jensen, K. R. V., & Cline, H. T. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab387 · Cited by 13
Regional analysis of myelin basic protein across postnatal brain development of C57BL/6J mice
Ozarkar, S., Patel, R. K. R., Vulli, T., Friar, C. A., Burette, A. C., & Philpot, B. D. (2025) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2025.1535745 · Cited by 15
Localization and partial characterization of a 60 kDa citrulline‐containing transport form of myelin basic protein from MO3‐13 cells and human white matter
Ursell, M. R., McLaurin, J., Wood, D. D., Ackerley, C., Moscarello, M. A., & Russell, J. T. (1995) · Journal of Neuroscience Research · doi:10.1002/jnr.490420106 · Cited by 13
Genetic alterations in the mouse myelin basic proteins result in a range of dysmyelinating disorders
Jacobs, E. C. (2004) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2004.10.008 · Cited by 13
Isolation and identification of proteolipid proteins injimpy mouse brain
Fannon, A. M., Mastronardi, F. G., & Moscarello, M. A. (1994) · Neurochemical Research · doi:10.1007/bf00968710 · Cited by 13
Comparison of the distribution of Na+, K+-ATPase and myelin-associated glycoprotein (MAG) in the optic nerve, spinal cord and trigeminal ganglion of shiverer (shi/shi) and control (+/+) mice
Sheedlo, H. J., & Siegel, G. J. (1987) · Brain Research · doi:10.1016/0006-8993(87)90273-3 · Cited by 13
Phase separation of myelin sheath in Triton X-114 solution: predominant localization of the 21.5-kDa isoform of myelin basic protein in the lipid raft-associated domain
Uruse, M., Yamamoto, M., Sugawa, M., Matsuura, K., Sato, Y., Seiwa, C., Watanabe, K., Aiso, S., & Asou, H. (2014) · The Journal of Biochemistry · doi:10.1093/jb/mvu005 · Cited by 12
The impact of erdosteine on cisplatin-induced ototoxicity: a proteomics approach
Sofia Waissbluth, A., Garnier, D., Akinpelu, O. V., Salehi, P., & Daniel, S. J. (2016) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-016-4399-1 · Cited by 14
K + channel distribution and clustering in developing and hypomyelinated axons of the optic nerve
Ames, J., Lior, E., & Eter, P. (2000) · Cited by 12
Immunological Aspects of Axon Injury in Multiple Sclerosis
Howe, C. L. (2007) · Current topics in microbiology and immunology · doi:10.1007/978-3-540-73677-6_5 · Cited by 11
Reduced Levels of a Specific Myelin-Associated Oligodendrocytic Basic Protein Isoform in shiverer Myelin
Montague, P., Kirkham, D., McCallion, A. S., Davies, R. W., Kennedy, P. G. E., Klugmann, M., Nave, K., & Griffiths, I. R. (1999) · Developmental Neuroscience · doi:10.1159/000017364 · Cited by 12
Chromosome assignments of the genes for glucocorticoid receptor, myelin basic protein, leukocyte common antigen, and TRPM2 in the rat
Goldner-Sauvé, A. J., Szpirer, C., Szpirer, J., Levan, G., & Gasser, D. L. (1991) · Biochemical Genetics · doi:10.1007/bf00590108 · Cited by 12
An autosomal dominant mutation of facial development in a transgenic mouse
Wakasugi, S., Iwanaga, T., Inomoto, T., Tengan, T., Maeda, S., Uehira, M., Araki, K., Miyazaki, J., Eto, K., 島田, 和., et al. (1988) · Developmental Genetics · doi:10.1002/dvg.1020090306 · Cited by 12
Acute but not inherited demyelination in mouse models leads to brain tissue stiffness changesPreprint
Eberle, D., Fodelianaki, G., Kurth, T., Jagielska, A., Möllmert, S., Ulbricht, E., Wagner, K., Taubenberger, A. V., Träber, N., Escolano, J.-C., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/449603 · Cited by 12
Myelin repair by transplantation of myelin‐forming cells in globoid cell leukodystrophy
Kondo, Y., & Duncan, I. D. (2016) · Journal of Neuroscience Research · doi:10.1002/jnr.23909 · Cited by 11
Transcriptional Fingerprint of Hypomyelination in Zfp191 null and Shiverer ( Mbp shi ) Mice
Aaker, J., Elbaz, B., Wu, Y., Looney, T. J., Zhang, L., Lahn, B. T., & Popko, B. (2016) · ASN NEURO · doi:10.1177/1759091416670749 · Cited by 11
Cellular and Molecular Aspects of Myelin Protein Gene Expression
Campagnoni, A. T., & Macklin, W. B. (1989) · Humana Press eBooks · doi:10.1007/978-1-4612-4520-9_2 · Cited by 12
Recent Advances in Studies on Genes for Myelin Proteins
Ikenaka, K., Okano, H., Tamura, T., & Mikoshiba, K. (1991) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.1991.00181.x · Cited by 11
Mitochondrial Dynamics in Physiology and Pathology of Myelinated Axons
Sui, Y., Nguyen, H. B., Thai, T. Q., Ikenaka, K., & Ohno, N. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-32-9636-7_10 · Cited by 10
B-cell function in CNS inflammatory demyelinating disease: a complexity of roles and a wealth of possibilities
Fillatreau, S., & Anderton, S. M. (2007) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.3.4.565 · Cited by 11
Embryonic stem cell rescue of tremor and ataxia in myelin-deficient shiverer mice
Low, H. P., Greco, B. M., Tanahashi, Y., Gallant, J., Jones, S. N., Billings‐Gagliardi, S., Recht, L. D., & Schwartz, W. J. (2008) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2008.09.037 · Cited by 10
Phylogenetically Conserved Amino Acids of MBP and P0 from Amphibian Myelin
Karthigasan, J., Bauer, T. K., Teplow, D. B., Saavedra, R. A., & Kirschner, D. A. (1992) · Journal of Molecular Neuroscience · doi:10.1007/bf03380137 · Cited by 9
Neuronal Expression of Reporter Genes in the Intact Nervous System of Aplysia
Kaang, B. (1996) · Molecules and Cells · doi:10.1016/s1016-8478(23)07311-9 · Cited by 9
The genes coding for alpha and beta catenin (Catna1 and Catnb) and Plakoglobin (Jup) map to mouse Chromosomes 18, 9, and 11, respectively
Gu�net, J. L., Simon‐Chazottes, D., Ringwald, M., & Kemler, R. (1995) · Mammalian Genome · doi:10.1007/bf00364802 · Cited by 9
Shiverer∗jimpy double mutant mice. III. Comparison of shimld∗jpmsd and shi∗jp phenotypes demonstrates dissimilar interactions of allelic mutations
Billings‐Gagliardi, S., Kerner, A., Kirschner, D. A., & Wolf, M. K. (1987) · Molecular Brain Research · doi:10.1016/0169-328x(87)90027-1 · Cited by 9
Differential recognition of MBP epitopes in BALB/c mice determines the site of inflammatory disease induction
Yoshizawa, I., Bronson, R. T., Ben-Nun, A., Richert, J. R., Dorf, M. E., & Abromson‐Leeman, S. R. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)00101-5 · Cited by 9
Spontaneous Remyelination and Intracerebral Grafting of Myelinating Cells in Mammals
Gumpel, M., Gout, O., & Gansmüller, A. (1989) · Springer eBooks · doi:10.1007/978-3-642-48369-1_5 · Cited by 9
Insertional mutagenesis inducing hypomyelination in transgenic mice
Orian, J. M., Mitchell, A. W. S., Marshman, W. E., Webb, G. C., Ayers, M. M., Grail, D., Ford, J. H., Kaye, A. H., & Gonzales, M. F. (1994) · Journal of Neuroscience Research · doi:10.1002/jnr.490390512 · Cited by 8
Animal Models and the Science of Movement Disorders
LeDoux, M. S. (2005) · Elsevier eBooks · doi:10.1016/b978-012088382-0/50003-7 · Cited by 8
Rumpshaker Behaves like Juvenile-Lethal Plp Mutations When Combined with Shiverer in Double Mutant Mice
Billings‐Gagliardi, S., Nunnari, J. J., & Wolf, M. K. (2001) · Developmental Neuroscience · doi:10.1159/000048691 · Cited by 8
Two‐Photon Fluorescent Imaging of Myelination in the Spinal Cord
Condie, A. G., Gerson, S. L., Miller, R. H., & Wang, Y. (2012) · ChemMedChem · doi:10.1002/cmdc.201200343 · Cited by 8
Agathisflavone Modifies Microglial Activation State and Myelination in Organotypic Cerebellar Slices Culture
de Almeida, M. M. A., Pieropan, F., Footz, T. K., David, J. M., David, J. P., da Silva, V. D. A., Souza, C. D. S., Voronova, A., Butt, A. M., & Costa, S. L. (2021) · Journal of Neuroimmune Pharmacology · doi:10.1007/s11481-021-09991-6 · Cited by 10
Reversal of Immunodominance Aong Autoantigenic T-cell Epitopes
Fairchild, P. J. (1999) · Autoimmunity · doi:10.3109/08916939908993802 · Cited by 8
Molecular biology of myelin basic protein: Gene rearrangement and expression of anti-sense RNA in myelin-deficient mutants
Mikoshiba, K., Aruga, J., & Okano, H. (1991) · Comparative Biochemistry and Physiology Part C Comparative Pharmacology · doi:10.1016/0742-8413(91)90181-r · Cited by 8
Remyelination of a Chemically Induced Demyelinated Lesion in the Spinal Cord of the Adult Shiverer Mouse by Transplanted Oligodendrocytes
Gout, O., Gansmüller, A., & Gumpel, M. (1990) · Springer eBooks · doi:10.1007/978-3-642-83968-9_13 · Cited by 8
Glial Transplants: An in vivo Analysis of Extrinsic and Intrinsic Determinants of Dysmyelination in Genetic Variants
Lachapelle, F. (1995) · Brain Pathology · doi:10.1111/j.1750-3639.1995.tb00606.x · Cited by 8
A multipoint genetic linkage map of mouse chromosome 18
Johnson, K. R., & Davisson, M. T. (1992) · Genomics · doi:10.1016/0888-7543(92)90029-r · Cited by 8
Shiverer and Other Marker Models Used in Intracerebral Transplantations of Glial Cells
Gumpel, M. (1991) · Methods in neurosciences · doi:10.1016/b978-0-12-185263-4.50030-3 · Cited by 8
Impaired myelin ultrastructure is reversed by citalopram treatment in a mouse model for major depressive disorder
Israel‐Elgali, I., Pan, H., Oved, K., Pillar, N., Levy, G., Barak, B., Carneiro, A. M. D., Gurwitz, D., & Shomron, N. (2023) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2023.09.012 · Cited by 8
Myelin dysfunction/degradation in the central nervous system: why are myelin sheaths susceptible to damage?
Bradl, M. (1999) · Springer eBooks · doi:10.1007/978-3-7091-6369-6_2 · Cited by 7
Quaking*Shiverer Double-Mutant Mice Survive for at Least 100 Days with No CNS Myelin
Wolf, M. K., Nunnari, J. N., & Billings‐Gagliardi, S. (1999) · Developmental Neuroscience · doi:10.1159/000017415 · Cited by 7
Evidence that CNS Hypomyelination Does Not Cause Death of Jimpy-msd Mutant Mice
Billings‐Gagliardi, S., Nunnari, J. N., Nadon, N. L., & Wolf, M. K. (1999) · Developmental Neuroscience · doi:10.1159/000017414 · Cited by 7
Molecular Genetic Insights Into Neurologic Diseases
Breakefield, X. O., & Cambi, F. (1987) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.10.030187.002535 · Cited by 7
Morphometric and freeze‐fracture studies on peripheral nerve in shiverer mice
Panagopoulos, G., King, R. H. M., Gabriel, G., Stolinski, C., Sofer, D., Lachapelle, F., & Thomas, P. K. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902860304 · Cited by 6
Genes coding for proteins in central nervous system myelin
THOMPSON, R. J. (1992) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1992.tb00813.x · Cited by 6
Developmental axon diameter growth of central nervous system axons does not depend on ensheathment or myelination by oligodendrocytesPreprint
Bin, J. M., Emberley, K., Buscham, T. J., Eichel‐Vogel, M. A., Doan, R. A., Steyer, A. M., Nolan, M. F., Möbius, W., Monk, K. R., Werner, H. B., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.10.632348 · Cited by 5
Cerebellar soluble lectin and its glycoprotein ligands in the developing brain of control and dysmyelinating mutant mice
Li, W.-X., Kuchler‐Bopp, S., Zaepfel, M., Badache, A., Thomas, D., Vincendon, G., Baumann, N., & Zanetta, J. (1993) · Neurochemistry International · doi:10.1016/0197-0186(93)90005-p · Cited by 5
Gene Therapy For Inherited Diseases Of The Central Nervous System
Pierson, T. M., & Wolfe, J. H. N. (2005) · Neurological disease and therapy · doi:10.1201/9780849358364.ch4 · Cited by 5
Die Myelinmembran des Zentralnervensystems — essentielle makromolekulare Strukturen und Funktion
Stoffel, W. (1990) · Angewandte Chemie · doi:10.1002/ange.19901020905 · Cited by 5
Progenitor Cells of the Adult Human Subcortical White Matter
Roy, N. S., Windrem, M. S., & Goldman, S. A. (2004) · Elsevier eBooks · doi:10.1016/b978-012439510-7/50063-2 · Cited by 4
Quaking*shiverer double mutant mice: morphological phenotypes support possible dual actions of the shiverer locus
Wolf, M. K., & Billings‐Gagliardi, S. (1988) · Brain Research · doi:10.1016/0006-8993(88)90256-9 · Cited by 4
Cytoplasmic domains of the myelin-associated glycoprotein
Kursula, P. (2000) · Cited by 4
STRUCTURAL, FUNCTIONAL, AND CLINICAL ASPECTS OF MYELIN PROTEINS
Epand, R. M. (1988) · Elsevier eBooks · doi:10.1016/b978-0-12-470348-3.50014-8 · Cited by 4
Transcriptional upregulation of myelin components in spontaneous myelin basic protein-deficient mice
Staats, K. A., Pombal, D., Schönefeldt, S., Helleputte, L. V., Maurin, H., Dresselaers, T., Govaerts, K., Himmelreich, U., LEUVEN, F. V., Bosch, L. V. D., et al. (2015) · Brain Research · doi:10.1016/j.brainres.2015.02.021 · Cited by 3
Chapter 3 Molecular genetic analyses of myelin deficiency and cerebellar ataxia
Mikoshiba, K., Okano, H., Miyawaki, A., Furuichi, T., & Ikenaka, K. (1995) · Progress in brain research · doi:10.1016/s0079-6123(08)63281-1 · Cited by 4
Abnormal Regulation of the Myelin Basic Protein Gene during Development of the Myelin‐Deficient Mousea
Matthieu, J., Toŝić, M., & Gardinier, M. V. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb42396.x · Cited by 3
(Na++K+)-adenosinetriphosphatase in the brain of Shiverer (Shi/Shi) mice
Sheedlo, H. J., Siegel, G. J., Desmond, T. J., & Ernst, S. A. (1987) · Neurochemical Research · doi:10.1007/bf00971708 · Cited by 3
Manipulating the Mouse Genome: New Approaches for the Dissection of Mouse Development
Yamamura, K., & Wakasugi, S. (1991) · Development Growth & Differentiation · doi:10.1111/j.1440-169x.1991.00093.x · Cited by 3
Chimeric and Molecular Genetic Analysis of Myelin‐Deficient (Shiverer and Mld) Mutant Mice
Mikoshiba, K., Okano, H., Aruga, J., Tamura, T.-A., Miura, M., Ikenaka, K., & Nakagawa, T. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb42391.x · Cited by 3
Remyelination in Multiple Sclerosis
Stangel, M., Pul, R., Skripuletz, T., Trebst, C., Voß, E. V., & Gudi, V. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-384913-7.00009-5 · Cited by 3
MULTIPLE SCLEROSIS: REMYELINATION
Kocsis, J. D., Sasaki, M., Lankford, K. L., & Radtke, C. (2008) · Elsevier eBooks · doi:10.1016/b978-012373994-0.50020-8 · Cited by 3
Crosstalks Between Myelinating Cells and the Axonal Cytoskeleton
Perrot, R., & Eyer, J. (2010) · Advances in neurobiology · doi:10.1007/978-1-4419-6787-9_25 · Cited by 2
Central nervous system regeneration approach in the toxic cuprizone model of de- and remyelination
Tejedor, L. S. (2015) · Cited by 2
Molecular Biology of the Genes Encoding the Major Myelin Proteins
Lemke, G. (1987) · Springer eBooks · doi:10.1007/978-1-4615-7488-0_2 · Cited by 2
Glial Abnormalities in Genetically Determined Disorders of Myelin
Vela, J. M., Dalmau, I., González, B., & Castellano, B. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5737-1_18 · Cited by 1
Cell Therapy for Pediatric Disorders of Glia
Osório, M. J., & Goldman, S. A. (2016) · Springer eBooks · doi:10.1007/978-1-4899-7654-3_15 · Cited by 1
Modeling Disorders of Movement
LeDoux, M. S. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405195-9.00002-0 · Cited by 1
Leukodystrophies
Garbern, J. Y. (2005) · Neurological disease and therapy · doi:10.1201/9780849358364.ch20 · Cited by 1
Live imaging of autoimmune responses in distinct milieus of the central nervous system
Schlosser, C. S. (2013) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-4014 · Cited by 1
Myelin Basic Protein Gene Expression, Oligodendrocyte Metabolism and Myelin Stability in the MLD Mutant Mouse
Matthieu, J., Omlin, F. X., Roch, J., & Cooper, B. J. (1987) · Springer eBooks · doi:10.1007/978-1-4757-0354-2_2 · Cited by 1
Curing the shiverer mutant
Milner, R. J. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90002-6 · Cited by 1
From Myelin Basic Protein to Myelin Deficient Mice
Tosic, M., & Matthieu, J. (1990) · Springer eBooks · doi:10.1007/978-3-642-83968-9_34 · Cited by 1
Selective Alteration of the Ventilatory Response to Hypoxia Results from Mutation in the Myelin Proteolipid Protein Gene
Miller, M. J., Haxhiu, M. A., Kangas, C. D., Georgiadis, P., Gudz, T. I., & Macklin, W. B. (2004) · Advances in experimental medicine and biology · doi:10.1007/0-387-27023-x_14 · Cited by 1
The role of oligodendrocytes in higher-order circuit functions
Corona, S. Y. M. (2018) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7137
Expression of Nervous System cDNAs in Glial and Non-Glial Cell Lines
Allinquant, B., Staugaitis, S. M., D’Urso, D., Almazán, G., Chin, S., Brophy, P., & Colman, D. (1990) · Springer eBooks · doi:10.1007/978-3-642-83968-9_23 · Cited by 1
Role of microglia in myelin turnover
Safaiyan, S. (2016) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-5727
Unravelling the Role Cortical Myelination Plays in Higher Brain Functions
Subramanian, S. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8448 · Cited by 1
Dialogues: Communication Between Axons and Myelinating Glia
Gould, R. M., & Brady, S. T. (2005) · Elsevier eBooks · doi:10.1016/b978-012738761-1/50003-1 · Cited by 1
Absence of MBP 3’ UTR in Mice Disrupts mRNA Transport, Myelination, and Motor LearningPreprint
Nowacki, J. C., Bulen, H. L., Meservey, L. M., Richardson, H. S., Valenzuela, A., Nguyen, H., Cheng, Z., Zeng, H., & Fu, M. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.23.696264 · Cited by 1
Zentrale Myelinisierungsstörungen: Biologische Grundlagen, transgene Modelle und molekulare Pathologie
Nave, K. (1999) · Springer eBooks · doi:10.1007/978-3-662-07096-3_12 · Cited by 1
Genetically Defined Myelin Disorders
Johnson, R. S., & Riordan, J. R. (1992) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4899-6732-9_3 · Cited by 1
Role of miRNAs in Oligodendrocyte Development
Budde, H. (2010) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-381
The Function of Oligodendrocytes in the Maturation of the Brain
Stoffel, W. (1993) · Springer eBooks · doi:10.1007/978-3-642-84949-7_3
Essential Macromolecular Structures for the Function of the Myelin Membrane of Central Nervous System
Stoffel, W. (1990) · Springer eBooks · doi:10.1007/978-3-642-84224-5_10
Regulation of Oligodendrocyte Differentiation: Relevance for Remyelination
Maier, O. (2012) · InTech eBooks · doi:10.5772/37892
Molecular-Biology Approaches to Genetic Defects of the Mammalian Nervous System
Sutcliffe, J. G., & Travis, G. H. (1991) · Progress in nucleic acid research and molecular biology · doi:10.1016/s0079-6603(08)60011-2
ReducedS-adenosylmethionine: Protein-lysineN-methyltransferase activity (protein methylase III) in shiverer mutant mouse brain
Chanderkar, L. P., Shanker, G., Knobler, R. L., LUBLIN, F. D., Paik, W. K., & Kim, S. (1987) · Neurochemical Research · doi:10.1007/bf00972296

Authors: ROACH, A., TAKAHASHI, N., PRAVTCHEVA, D., RUDDLE, F., & HOOD, L.
Affiliations: California Institute of Technology (US)
Yale University (US)
ORCID: HOOD, L
Venue: Cell
Publisher: Elsevier BV
Published: 1985-08
Volume: 42
Issue: 1
Pages: 149-155
ISSN: 0092-8674 (ISSN-L)
DOI: 10.1016/s0092-8674(85)80110-0
OpenAlex: W2151814085
Cited by: 336
References: 32
Citations by year: 2025: 5 · 2024: 2 · 2023: 3 · 2022: 5 · 2021: 6 · 2020: 3 · 2019: 3 · 2018: 6 · 2017: 4 · 2016: 13 · 2015: 6 · 2014: 5 · 2013: 6 · 2012: 3
FWCI: 21.88
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Cell (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health
Topics: Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: myelin basic protein, chromosome 18, gene mapping, partial gene deletion, CNS myelination, alternative splicing, transcription initiation, polyadenylation, exon deletion
MeSH terms: Animals, Base Sequence, Brain, Chromosome Deletion, Chromosome Mapping, Myelin Basic Protein, Genes, Genetic Linkage, Mice, Neurologic Mutants, Mutation, Poly A, RNA Splicing, RNA, Messenger, Transcription, Genetic, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Chromosomal mapping of mouse myelin basic protein gene and structure and transcription of the partially deleted gene in shiverer mutant mice

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks