SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Niimura Michihito)
 

Search: WFRF:(Niimura Michihito) > Identification of g...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2

Buckley, Patrick G. (author)
Uppsala universitet,Institutionen för genetik och patologi,Dumanski
Mantripragada, Kiran K. (author)
Uppsala universitet,Institutionen för genetik och patologi
Di­az de Ståhl, Teresita (author)
Uppsala universitet,Institutionen för genetik och patologi
show more...
Piotrowski, Arkadiusz (author)
Uppsala universitet,Institutionen för genetik och patologi
Hansson, Caisa M. (author)
Uppsala universitet,Institutionen för genetik och patologi
Kiss, Hajnalka (author)
Vetrie, David (author)
Ernberg, Ingemar T. (author)
Karolinska Institutet
Nordenskjöld, Magnus (author)
Karolinska Institutet
Bolund, Lars (author)
Sainio, Markku (author)
Rouleau, Guy A. (author)
Niimura, Michihito (author)
Wallace, Andrew J. (author)
Evans, D. Gareth R. (author)
Grigelionis, Gintautas (author)
Uppsala universitet,Institutionen för genetik och patologi
Menzel, Uwe (author)
Uppsala universitet,Institutionen för genetik och patologi
Dumanski, Jan P. (author)
Uppsala universitet,Institutionen för genetik och patologi
Dumanski, JE (author)
show less...
 (creator_code:org_t)
Hindawi Limited, 2005
2005
English.
In: Human Mutation. - : Hindawi Limited. - 1059-7794 .- 1098-1004. ; 26:6, s. 540-9
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Schwannomatosis is characterized by multiple peripheral and cranial nerve schwannomas that occur in the absence of bilateral 8th cranial nerve schwannomas. The latter is the main diagnostic criterion of neurofibromatosis type 2 (NF2), which is a related but distinct disorder. The genetic factors underlying the differences between schwannomatosis and NF2 are poorly understood, although available evidence implicates chromosome 22 as the primary location of the gene(s) of interest. To investigate this, we comprehensively profiled the DNA copy number in samples from sporadic and familial schwannomatosis, NF2, and a large cohort of normal controls. Using a tiling-path chromosome 22 genomic array, we identified two candidate regions of copy number variation, which were further characterized by a PCR-based array with higher resolution. The latter approach allows the detection of minute alterations in total genomic DNA, with as little as 1.5 kb per measurement point of nonredundant sequence on the array. In DNA derived from peripheral blood from a schwannomatosis patient and a sporadic schwannoma sample, we detected rearrangements of the immunoglobulin lambda (IGL) locus, which is unlikely to be due to a B-cell specific somatic recombination of IGL. Analysis of normal controls indicated that these IGL rearrangements were restricted to schwannomatosis/schwannoma samples. In the second candidate region spanning GSTT1 and CABIN1 genes, we observed a frequent copy number polymorphism at the GSTT1 locus. We further describe missense mutations in the CABIN1 gene that are specific to samples from schwannomatosis and NF2 and make this gene a plausible candidate for contributing to the pathogenesis of these disorders.

Keyword

IGLV
IGLC
immunoglobulin
genomic array
array-CGH' CABIN1
GSTT1
GSTT2
RAG1
RAG2
B-lymphocyte
schwannoma
MEDICINE
MEDICIN

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view