Zobrazeno 1 - 10
of 110
pro vyhledávání: '"K, Mantripragada"'
Autor:
Meena Upadhyaya, Victor Mautner, Abhijit Guha, Jan P. Dumanski, Ian M. Frayling, Rosalie E. Ferner, Nadia Chuzhanova, Lan Kluwe, Gillian Spurlock, Kiran K. Mantripragada
Supplementary Table S2 from High-Resolution DNA Copy Number Profiling of Malignant Peripheral Nerve Sheath Tumors Using Targeted Microarray-Based Comparative Genomic Hybridization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71fe6c17f408412f1784f7cd11e2834f
https://doi.org/10.1158/1078-0432.22439398
https://doi.org/10.1158/1078-0432.22439398
Autor:
Meena Upadhyaya, Victor Mautner, Abhijit Guha, Jan P. Dumanski, Ian M. Frayling, Rosalie E. Ferner, Nadia Chuzhanova, Lan Kluwe, Gillian Spurlock, Kiran K. Mantripragada
Purpose: Neurofibromatosis type 1 (NF1) is an autosomal dominant condition that predisposes to benign and malignant tumors. The lifetime risk of a malignant peripheral nerve sheath tumor (MPNST) in NF1 is ∼10%. These tumors have a poor survival rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::092b2dcf26307acb9228bdcb19ab9096
https://doi.org/10.1158/1078-0432.c.6516865
https://doi.org/10.1158/1078-0432.c.6516865
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Genes, brain, and behavior. 14(6)
Previous studies suggest that a single nucleotide polymorphism in the catechol-O-methyltransferase (COMT) gene (val158met) may modulate reward-guided decision making in healthy individuals. The polymorphism affects dopamine catabolism and thus modula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b87f1cc4bbb0b9cba51172b7254b0e93
https://pubmed.ncbi.nlm.nih.gov/26096878
https://pubmed.ncbi.nlm.nih.gov/26096878
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Translational Psychiatry
The variant at rs1006737 in the L-type voltage-gated calcium channel (alpha 1c subunit) CACNA1C gene is reliably associated with both bipolar disorder and schizophrenia. We investigated whether this risk variant affects reward responsiveness because
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8981290a5284ea2ed5f3fffb2292abb2
https://pubmed.ncbi.nlm.nih.gov/25290268
https://pubmed.ncbi.nlm.nih.gov/25290268
Publikováno v:
Current topics in behavioral neurosciences. 4
Schizophrenia is a severe, debilitating and common psychiatric disorder, which directly affects approximately 1% of the population worldwide. Although previous studies have unequivocally shown that schizophrenia has a strong genetic component, our un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d80366f079cddb61a581ff519825b842
https://pubmed.ncbi.nlm.nih.gov/21312414
https://pubmed.ncbi.nlm.nih.gov/21312414
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Magdalena, Benetkiewicz, Yun, Wang, Marci, Schaner, Pei, Wang, Kiran K, Mantripragada, Patrick G, Buckley, Gunnar, Kristensen, Anne-Lise, Børresen-Dale, Jan P, Dumanski
Publikováno v:
Genes, chromosomescancer. 42(3)
Previous low-resolution studies of chromosome 22 in ovarian carcinoma have suggested its involvement in the development of the disease. We report a high-resolution analysis of DNA copy number and gene expression of 22q in 18 ovarian carcinomas using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a7d4c925f3c8220a966efd26d2226a89
https://pubmed.ncbi.nlm.nih.gov/15578687
https://pubmed.ncbi.nlm.nih.gov/15578687
Autor:
Kiran K, Mantripragada, Patrick G, Buckley, Magdalena, Benetkiewicz, Cecilia, De Bustos, Carina, Hirvelä, Caroline, Jarbo, Carl E G, Bruder, Helena, Wensman, Tiit, Mathiesen, Gunnar, Nyberg, Laura, Papi, V Peter, Collins, Koichi, Ichimura, Gareth, Evans, Jan P, Dumanski
Publikováno v:
International journal of oncology. 22(3)
Previous low-resolution schwannoma studies have reported diverse frequencies (30-80%) of 22q deletions, involving the neurofibromatosis-2 tumor suppressor (NF2) gene. We constructed an array spanning 11 million base pairs of 22q encompassing the NF2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::da2e10ed7f0e3cce13531c47921461ad
https://pubmed.ncbi.nlm.nih.gov/12579316
https://pubmed.ncbi.nlm.nih.gov/12579316