نتایج جستجو برای: frameshift mutations

تعداد نتایج: 174767  

Journal: :Human molecular genetics 1997
J Meyer P Südbeck M Held T Wagner M L Schmitz F D Bricarelli E Eggermont U Friedrich O A Haas A Kobelt J G Leroy L Van Maldergem E Michel B Mitulla R A Pfeiffer A Schinzel H Schmidt G Scherer

It has previously been shown that, in the heterozygous state, mutations in the SOX9 gene cause campomelic dysplasia (CD) and the often associated autosomal XY sex reversal. In 12 CD patients, 10 novel mutations and one recurrent mutation were characterized in one SOX9 allele each, and in one case, no mutation was found. Four missense mutations are all located within the high mobility group (HMG...

Journal: :Blood 2017
Idoia García-Ramírez Saber Tadros Inés González-Herrero Alberto Martín-Lorenzo Guillermo Rodríguez-Hernández Dalia Moore Lucía Ruiz-Roca Oscar Blanco Diego Alonso-López Javier De Las Rivas Keenan Hartert Romain Duval David Klinkebiel Martin Bast Julie Vose Matthew Lunning Kai Fu Timothy Greiner Fernando Rodrigues-Lima Rafael Jiménez Francisco Javier García Criado María Begoña García Cenador Paul Brindle Carolina Vicente-Dueñas Ash Alizadeh Isidro Sánchez-García Michael R Green

CREBBP is targeted by inactivating mutations in follicular lymphoma (FL) and diffuse large B-cell lymphoma (DLBCL). Here, we provide evidence from transgenic mouse models that Crebbp deletion results in deficits in B-cell development and can cooperate with Bcl2 overexpression to promote B-cell lymphoma. Through transcriptional and epigenetic profiling of these B cells, we found that Crebbp inac...

2014
Brenton G Mar Lars B Bullinger Kathleen M McLean Peter V Grauman Marian H Harris Kristen Stevenson Donna S Neuberg Amit U Sinha Stephen E Sallan Lewis B Silverman Andrew L Kung Luca Lo Nigro Benjamin L Ebert Scott A Armstrong

Relapsed paediatric acute lymphoblastic leukaemia (ALL) has high rates of treatment failure. Epigenetic regulators have been proposed as modulators of chemoresistance, here, we sequence genes encoding epigenetic regulators in matched diagnosis-remission-relapse ALL samples. We find significant enrichment of mutations in epigenetic regulators at relapse with recurrent somatic mutations in SETD2,...

Journal: :Carcinogenesis 2000
S E Andrew X S Xu A Baross-Francis L Narayanan K Milhausen R M Liskay F R Jirik P M Glazer

DNA mismatch repair (MMR) deficiency leads to an increased mutation frequency and a predisposition to neoplasia. 'Knockout' mice deficient in the MMR proteins Msh2 and Pms2 crossed with mutation detection reporter (supF, lacI and cII) transgenic mice have been used to facilitate a comparison of the changes in mutation frequency and spectra. We find that the mutation frequency was consistently h...

2015
Manuel C Lemos Rajesh V Thakker

Pseudohypoparathyroidism type 1a (PHP1a) is characterized by hypocalcaemia and hyperphosphatemia due to parathyroid hormone resistance, in association with the features of Albright's hereditary osteodystrophy (AHO). PHP1a is caused by maternally inherited inactivating mutations of Gs-alpha, which is encoded by a complex imprinted locus termed GNAS. Paternally inherited mutations can lead either...

Journal: :The Journal of clinical investigation 2015
Keith A Choate Yin Lu Jing Zhou Peter M Elias Samir Zaidi Amy S Paller Anita Farhi Carol Nelson-Williams Debra Crumrine Leonard M Milstone Richard P Lifton

Widespread reversion of genetic disease is rare; however, such events are particularly evident in some skin disorders in which normal clones develop on a background of affected skin. We previously demonstrated that mutations in keratin 10 (KRT10) cause ichthyosis with confetti (IWC), a severe dominant disorder that is characterized by progressive development of hundreds of normal skin spots via...

Journal: :Journal of bacteriology 2006
Megan N Hersh Liza D Morales Kimberly J Ross Susan M Rosenberg

Escherichia coli strains carrying null alleles of genes encoding single-strand-specific exonucleases ExoI and ExoVII display elevated frameshift mutation rates but not base substitution mutation rates. We characterized increased spontaneous frameshift mutation in ExoI- ExoVII- cells and report that some of this effect requires RecA, an inducible SOS DNA damage response, and the low-fidelity, SO...

2002
Alexis Hernández

We study compact non-supersymmetric Z N orbifolds in various dimensions. We compute the spectrum of several tachyonic type II and heterotic examples and partially classify tachyon-free heterotic models. We also discuss the relation to compactification on K3 and Calabi-Yau manifolds.

Journal: :Biochimica et biophysica acta 2010
Masaki Takahashi Mineyuki Mizuguchi Hiroyuki Shinoda Tomoyasu Aizawa Makoto Demura Hitoshi Okazawa Keiichi Kawano

Polyglutamine tract-binding protein-1 (PQBP-1) is a nuclear protein that interacts with various proteins, including RNA polymerase II and the spliceosomal protein U5-15kD. PQBP-1 is known to be associated with X-linked mental retardation in which a frameshift mutation in the PQBP-1 gene occurs. In the present study, we demonstrate that PQBP-1 binds to U5-15kD via a continuous 23-residue segment...

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