1 to 10 of 15 literature results

• Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array.

  Glioblastomas (GBs) are malignant CNS tumors often associated with devastating symptoms. Patients with GB have a very poor prognosis, and despite trea…

  Authors: Helena Nord, Christian Hartmann, Robin Andersson, Uwe Menzel, Susan Pfeifer, Arkadiusz Piotrowski, Adam Bogdan, Wojciech Kloc, Johanna Sandgren, Tommie Olofsson,…

  Source: Neuro-oncology. 2009 Dec

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• Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array.

  To further explore the extent of structural large-scale variation in the human genome, we assessed copy number variations (CNVs) in a series of 71 hea…

  Authors: Teresita Díaz de Ståhl, Johanna Sandgren, Arkadiusz Piotrowski, Helena Nord, Robin Andersson, Uwe Menzel, Adam Bogdan, Ann-Charlotte Thuresson, Andrzej Poplawski, Desiree von Tell,…

  Source: Human mutation. 2008 Mar

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• Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

  A previously detected copy number polymorphism (Ep CNP) in patients affected with neuroectodermal tumors led us to investigate its frequency and lengt…

  Authors: Cecilia de Bustos, Teresita Díaz de Ståhl, Arkadiusz Piotrowski, Kiran K Mantripragada, Patrick G Buckley, Eva Darai, Caisa M Hansson, Gintautas Grigelionis, Uwe Menzel, Jan P Dumanski

  Source: Genomics. 2006 Aug

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

  Schwannomatosis is characterized by multiple peripheral and cranial nerve schwannomas that occur in the absence of bilateral 8th cranial nerve schwann…

  Authors: Patrick G Buckley, Kiran K Mantripragada, Teresita Díaz de Ståhl, Arkadiusz Piotrowski, Caisa M Hansson, Hajnalka Kiss, David Vetrie, Ingemar T Ernberg, Magnus Nordenskjöld, Lars Bolund,…

  Source: Human mutation. 2005 Dec

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• Expression of FcgammaRIII is required for development of collagen-induced arthritis.

  Circulating immune complexes are implicated in the pathogenesis of rheumatic immune disorders and the interaction of these immune complexes with IgG F…

  Authors: Teresita Díaz de Ståhl, Maria Andrén, Pernilla Martinsson, J Sjef Verbeek, Sandra Kleinau

  Source: European journal of immunology. 2002 Oct

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• Chromosome 22 array-CGH profiling of breast cancer delimited minimal common regions of genomic imbalances and revealed frequent intra-tumoral genetic heterogeneity.

  Breast cancer is a common malignancy and the second most frequent cause of death among women. Our aim was to perform DNA copy number profiling of 22q …

  Authors: Magdalena Benetkiewicz, Arkadiusz Piotrowski, Teresita Díaz De Ståhl, Michal Jankowski, Dariusz Bala, Jacek Hoffman, Ewa Srutek, Ryszard Laskowski, Wojciech Zegarski, Jan P Dumanski

  Source: International journal of oncology. 2006 Oct

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

  Schwannomas may develop sporadically or in association with NF2 and schwannomatosis. The fundamental aberration in schwannomas is the bi-allelic inact…

  Authors: Teresita Díaz de Ståhl, Caisa M Hansson, Cecilia de Bustos, Kiran K Mantripragada, Arkadiusz Piotrowski, Magdalena Benetkiewicz, Caroline Jarbo, Leif Wiklund, Tiit Mathiesen, Gunnar Nyberg,…

  Source: Human genetics. 2005 Oct

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• Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma.

  Urinary bladder cancer is a heterogeneous disease with tumors ranging from papillary noninvasive (stage Ta) to solid muscle infiltrating tumors (stage…

  Authors: Helena Nord, Ulrika Segersten, Johanna Sandgren, Kenneth Wester, Christer Busch, Uwe Menzel, Jan Komorowski, Jan P Dumanski, Per-Uno Malmström, Teresita Díaz de Ståhl

  Source: International journal of cancer. Journal international du cancer. 2010 Mar 15

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• A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.

  Five patients were previously described with the Opitz (GBBB) syndrome (OMIM 145410) phenotype and 22q11.2 deletion determined by FISH but the precise…

  Authors: Robert P Erickson, Teresita Díaz de Ståhl, Carl E G Bruder, Jan P Dumanski

  Source: American journal of medical genetics. Part A. 2007 Dec 15

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• Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array.

  Neurofibromatosis Type I (NF1) is an autosomal dominant disorder characterized by the development of both benign and malignant tumors. The lifetime ri…

  Authors: Kiran K Mantripragada, Teresita Díaz de Ståhl, Chris Patridge, Uwe Menzel, Robin Andersson, Nadia Chuzhanova, Lan Kluwe, Abhijit Guha, Victor Mautner, Jan P Dumanski,…

  Source: Genes, chromosomes & cancer. 2009 Oct

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