Literature DB >> 4123573

Genetic kyphoscoliosis in mice.

A G Dickinson, V M Meikle.   

Abstract

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Year:  1973        PMID： 4123573     DOI： 10.1016/s0140-6736(73)91186-0

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  5 in total

1.  A new early-onset neuromuscular disorder associated with kyphoscoliosis peptidase (KY) deficiency.

Authors:  Carola Hedberg-Oldfors; Niklas Darin; Mia Olsson Engman; Zacharias Orfanos; Christer Thomsen; Peter F M van der Ven; Anders Oldfors
Journal:  Eur J Hum Genet       Date:  2016-08-03       Impact factor: 4.246

2.  Progressive hereditary spastic paraplegia caused by a homozygous KY mutation.

Authors:  Yuval Yogev; Yonatan Perez; Iris Noyman; Anwar Abu Madegem; Hagit Flusser; Zamir Shorer; Eugene Cohen; Leonid Kachko; Analia Michaelovsky; Ruth Birk; Arie Koifman; Max Drabkin; Ohad Wormser; Daniel Halperin; Rotem Kadir; Ohad S Birk
Journal:  Eur J Hum Genet       Date:  2017-05-10       Impact factor: 4.246

3.  Changes in mouse intervertebral-disc proteoglycan synthesis with age. Hereditary kyphoscoliosis is associated with elevated synthesis.

Authors:  G Venn; R M Mason
Journal:  Biochem J       Date:  1986-03-01       Impact factor: 3.857

4.  Transcriptional upregulation of Bag3, a chaperone-assisted selective autophagy factor, in animal models of KY-deficient hereditary myopathy.

Authors:  Elliot J Jokl; Gideon L Hughes; Tobias Cracknell; Mary E Pownall; Gonzalo Blanco
Journal:  Dis Model Mech       Date:  2018-07-06       Impact factor: 5.758

5.  A cell autonomous torsinA requirement for cholinergic neuron survival and motor control.

Authors:  Samuel S Pappas; Jay Li; Tessa M LeWitt; Jeong-Ki Kim; Umrao R Monani; William T Dauer
Journal:  Elife       Date:  2018-08-17       Impact factor: 8.140
  5 in total

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