High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas. (Q53663420)

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scientific article published on 28 October 2005

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English	High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas.	scientific article published on 28 October 2005

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scholarly article

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas. (English)

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Arkadiusz Piotrowski

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

Caisa M Hansson

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Caisa M Hansson

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Kiran K Mantripragada

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Kiran K Mantripragada

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

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Caroline Jarbo

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Teresita Díaz de Ståhl

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Teresita Díaz de Ståhl

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

Magdalena Benetkiewicz

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Magdalena Benetkiewicz

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

Cecilia de Bustos

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Cecilia de Bustos

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Europe PubMed Central

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17 May 2018

http://europepmc.org/abstract/MED/16078050

author name string

Leif Wiklund

8

1 reference

Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Gunnar Nyberg

10

1 reference

Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

V Peter Collins

11

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Koichi Ichimura

13

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17 May 2018

http://europepmc.org/abstract/MED/16078050

publication date

28 October 2005

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17 May 2018

http://europepmc.org/abstract/MED/16078050

1 reference

Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

118

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PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

1

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17 May 2018

http://europepmc.org/abstract/MED/16078050

35-44

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Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

Schwannomatosis: a clinical and pathologic study

1 reference

https://api.crossref.org/works/10.1007%2FS00439-005-0002-3

21 January 2018

Familial schwannomatosis: exclusion of the NF2 locus as the germline event

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https://api.crossref.org/works/10.1007%2FS00439-005-0002-3

21 January 2018

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

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Large-scale copy number polymorphism in the human genome

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Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution

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Genomic microarrays in the spotlight

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Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

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Molecular characterization of chromosome 22 deletions in schwannomas

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Molecular recognition by LARGE is essential for expression of functional dystroglycan

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Assembly of microarrays for genome-wide measurement of DNA copy number

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Detection of large-scale variation in the human genome

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Site-specific reciprocal translocation, t(11;22) (q23;q11), in several unrelated families with 3:1 meiotic disjunction

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A group of schwannomas with interstitial deletions on 22q located outside the NF2 locus shows no detectable mutations in the NF2 gene

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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor

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Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility

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Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?

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Genetic aberrations in sporadic and neurofibromatosis 2 (NF2)-associated schwannomas studied by comparative genomic hybridization (CGH).

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Human-specific duplication and mosaic transcripts: the recent paralogous structure of chromosome 22.

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Frequency and distribution of NF2 mutations in schwannomas

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Metabolic gene polymorphism frequencies in control populations

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A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications

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Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity

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Identifiers

10.1007/S00439-005-0002-3

1 reference

Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 May 2018

http://europepmc.org/abstract/MED/16078050

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