Literature DB >> 8884266

Mapping of unconventional myosins in mouse and human.

T Hasson1, J F Skowron, D J Gilbert, K B Avraham, W L Perry, W M Bement, B L Anderson, E H Sherr, Z Y Chen, L A Greene, D C Ward, D P Corey, M S Mooseker, N G Copeland, N A Jenkins.   

Abstract

Myosins are molecular motors that move along filamentous actin. Seven classes of myosin are expressed in vertebrates: conventional myosin, or myosin-II, as well as the 6 unconventional myosin classes-I, -V, -VI, -VII, -IX, and -X. We have mapped in mouse 22 probes encompassing all known unconventional myosins and, as a result, have identified 16 potential unconventional myosin genes. These genes include 7 myosins-I, 2 myosins-V, 1 myosin-VI, 3 myosins-VII, 2 myosins-IX, and 1 myosin-X. The map location of 5 of these genes was identified in human chromosomes by fluorescence in situ hybridization.

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Year:  1996        PMID： 8884266     DOI： 10.1006/geno.1996.0488

Source DB:  PubMed          Journal:  Genomics        ISSN： 0888-7543            Impact factor:   5.736


  9 in total

1.  Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.

Authors:  M C Lanasa; W A Hogge; C Kubik; J Blancato; E P Hoffman
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

Review 2.  Unconventional myosins, the basis for deafness in mouse and man.

Authors:  T Hasson
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

3.  Molecular genetic dissection of mouse unconventional myosin-VA: tail region mutations.

Authors:  J D Huang; V Mermall; M C Strobel; L B Russell; M S Mooseker; N G Copeland; N A Jenkins
Journal:  Genetics       Date:  1998-04       Impact factor: 4.562

4.  A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.

Authors:  D A Campbell; D P McHale; K A Brown; L M Moynihan; M Houseman; G Karbani; G Parry; A H Janjua; V Newton; L al-Gazali; A F Markham; N J Lench; R F Mueller
Journal:  J Med Genet       Date:  1997-12       Impact factor: 6.318

5.  Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Authors:  Y Liang; A Wang; F J Probst; I N Arhya; T D Barber; K S Chen; D Deshmukh; D F Dolan; J T Hinnant; L E Carter; P K Jain; A K Lalwani; X C Li; J R Lupski; S Moeljopawiro; R Morell; C Negrini; E R Wilcox; S Winata; S A Camper; T B Friedman
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

6.  Pharmacodynamic genome-wide association study identifies new responsive loci for glucocorticoid intervention in asthma.

Authors:  Y Wang; C Tong; Z Wang; Z Wang; D Mauger; K G Tantisira; E Israel; S J Szefler; V M Chinchilli; H A Boushey; S C Lazarus; R F Lemanske; R Wu
Journal:  Pharmacogenomics J       Date:  2015-01-20       Impact factor: 3.550

7.  Loss of Unconventional Myosin VI Affects cAMP/PKA Signaling in Hindlimb Skeletal Muscle in an Age-Dependent Manner.

Authors:  Lilya Lehka; Dominika Wojton; Małgorzata Topolewska; Vira Chumak; Łukasz Majewski; Maria Jolanta Rędowicz
Journal:  Front Physiol       Date:  2022-06-28       Impact factor: 4.755

8.  Unconventional myosins in inner-ear sensory epithelia.

Authors:  T Hasson; P G Gillespie; J A Garcia; R B MacDonald; Y Zhao; A G Yee; M S Mooseker; D P Corey
Journal:  J Cell Biol       Date:  1997-06-16       Impact factor: 10.539

9.  Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss.

Authors:  Farah Talebi; Farideh Ghanbari Mardasi; Javad Mohammadi Asl; Saeed Tizno; Marziye Najafvand Zadeh
Journal:  Cell J       Date:  2017-12-01       Impact factor: 2.479
  9 in total

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