Literature DB >> 33864620

MYRF: A Mysterious Membrane-Bound Transcription Factor Involved in Myelin Development and Human Diseases.

Hao Huang1, Fang Zhou1, Shiyou Zhou2, Mengsheng Qiu3.   

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Year:  2021        PMID： 33864620      PMCID： PMC8192642          DOI： 10.1007/s12264-021-00678-9

Source DB:  PubMed          Journal:  Neurosci Bull        ISSN： 1995-8218            Impact factor:   5.271


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  3 in total

Review 1.  Review of the phenotypic spectrum associated with haploinsufficiency of MYRF.

Authors:  Linda Z Rossetti; Kevin Glinton; Bo Yuan; Pengfei Liu; Nishitha Pillai; Elizabeth Mizerik; Pilar Magoulas; Jill A Rosenfeld; Lefkothea Karaviti; Vernon R Sutton; Seema R Lalani; Daryl A Scott
Journal:  Am J Med Genet A       Date:  2019-05-08       Impact factor: 2.802

2.  Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos.

Authors:  David Khorram; Michael Choi; Ben R Roos; Edwin M Stone; Teresa Kopel; Richard Allen; Wallace L M Alward; Todd E Scheetz; John H Fingert
Journal:  Mol Vis       Date:  2015-09-01       Impact factor: 2.367

3.  Autosomal dominant nanophthalmos and high hyperopia associated with a C-terminal frameshift variant in MYRF.

Authors:  Owen M Siggs; Emmanuelle Souzeau; James Breen; Ayub Qassim; Tiger Zhou; Andrew Dubowsky; Jonathan B Ruddle; Jamie E Craig
Journal:  Mol Vis       Date:  2019-09-21       Impact factor: 2.367
  3 in total
  1 in total

Review 1.  A Glance at the Molecules That Regulate Oligodendrocyte Myelination.

Authors:  Shunqi Wang; Yingxing Wang; Suqi Zou
Journal:  Curr Issues Mol Biol       Date:  2022-05-15       Impact factor: 2.976
  1 in total

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