Literature DB >> 434110

Myelin deficiency (md): a neurologic mutant in the Wistar rat.

C K Csiza, A de Lahunta.   

Abstract

Myelin deficiency (md), a newly discovered neurologic mutation in the Wistar rat, is transmitted by an X-linked, recessive lethal gene. Male rats are affected, and the first symptom is a head tremor recognizable at 12 to 15 days of age. The tremors become generalized within a few days and disappear when the animal is at rest. In the later stages, from 17 to 21 days of age, the slightest disturbance will precipitate a generalized seizure. Pups die within 30 days after birth. The only gross postmortem change is a gray color of the spinal cord instead of its normally white appearance. Microscopic findings reveal total lack of myelin formation at all levels of the central nervous system.

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Year:  1979        PMID: 434110      PMCID: PMC2042295     

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  8 in total

1.  SCHILDER'S DISEASE (SUDANOPHILIC LEUCODYSTROPHY) IN FIVE MALE MEMBERS OF ONE FAMILY.

Authors:  L CROME; M ZAPELLA
Journal:  J Neurol Neurosurg Psychiatry       Date:  1963-10       Impact factor: 10.154

2.  SEQUENCE OF MYELINIZATION IN THE BRAIN OF THE ALBINO RAT. A. CEREBRAL CORTEX, THALAMUS AND RELATED STRUCTURES.

Authors:  S JACOBSON
Journal:  J Comp Neurol       Date:  1963-08       Impact factor: 3.215

Review 3.  Neurochemistry as a diagnostic aid in the congenital tremor syndrome of piglets.

Authors:  D S Patterson; J T Done
Journal:  Br Vet J       Date:  1977 Mar-Apr

4.  A neurological mutation (msd) of the mouse causing a deficiency of myelin synthesis.

Authors:  H Meier; A D MacPike
Journal:  Exp Brain Res       Date:  1970-06-25       Impact factor: 1.972

5.  Histochemical, ultrastructural and biochemical studies of a case with leukodystrophy due to congenital deficiency of myelin.

Authors:  M Adachi; L Schneck; J Torii; B W Volk
Journal:  J Neuropathol Exp Neurol       Date:  1970-10       Impact factor: 3.685

6.  Absence of cerebral myelin sheaths in a case of presumed Pelizaeus-Merzbacher disease. Electron microscopic and biochemical studies.

Authors:  I Watanabe; R McCaman; P Dyken; W Zeman
Journal:  J Neuropathol Exp Neurol       Date:  1969-04       Impact factor: 3.685

7.  Microchemical studies of postnatal development in rat cerebrum. 2. Formation of myelin.

Authors:  N H Bass; M G Netsky; E Young
Journal:  Neurology       Date:  1969-04       Impact factor: 9.910

8.  MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM.

Authors:  R L SIDMAN; M M DICKIE; S H APPEL
Journal:  Science       Date:  1964-04-17       Impact factor: 47.728

  8 in total
  17 in total

Review 1.  Cellular and molecular aspects of myelin protein gene expression.

Authors:  A T Campagnoni; W B Macklin
Journal:  Mol Neurobiol       Date:  1988       Impact factor: 5.590

2.  Endpoints in myelin-deficient (MD) rats.

Authors:  Jacek M Kwiecien; Kathleen H Delaney
Journal:  Comp Med       Date:  2010-10       Impact factor: 0.982

Review 3.  The myelin mutants as models to study myelin repair in the leukodystrophies.

Authors:  Ian D Duncan; Yoichi Kondo; Su-Chun Zhang
Journal:  Neurotherapeutics       Date:  2011-10       Impact factor: 7.620

4.  Myelination and axonal electrical activity modulate the distribution and motility of mitochondria at CNS nodes of Ranvier.

Authors:  Nobuhiko Ohno; Grahame J Kidd; Don Mahad; Sumiko Kiryu-Seo; Amir Avishai; Hitoshi Komuro; Bruce D Trapp
Journal:  J Neurosci       Date:  2011-05-18       Impact factor: 6.167

5.  Tremors in Samoyed pups with oligodendrocyte deficiencies and hypomyelination.

Authors:  J F Cummings; B A Summers; A de Lahunta; C Lawson
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

6.  Transferrin is an essential factor for myelination.

Authors:  A Espinosa de los Monteros; S Kumar; P Zhao; C J Huang; R Nazarian; T Pan; S Scully; R Chang; J de Vellis
Journal:  Neurochem Res       Date:  1999-02       Impact factor: 3.996

7.  Abnormal compact myelin in the myelin-deficient rat: absence of proteolipid protein correlates with a defect in the intraperiod line.

Authors:  I D Duncan; J P Hammang; B D Trapp
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

8.  Shaking rat Kawasaki (SRK): a new neurological mutant rat in the Wistar strain.

Authors:  H Aikawa; I Nonaka; M Woo; T Tsugane; K Esaki
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

9.  Distribution of central nervous system lesions in beta-mannosidosis.

Authors:  K L Lovell; M Z Jones
Journal:  Acta Neuropathol       Date:  1983       Impact factor: 17.088

10.  Mutation in the myelin proteolipid protein gene alters BK and SK channel function in the caudal medulla.

Authors:  Catherine A Mayer; Wendy B Macklin; Nanthawan Avishai; Kannan Balan; Christopher G Wilson; Martha J Miller
Journal:  Respir Physiol Neurobiol       Date:  2009-10-04       Impact factor: 1.931

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