نتایج جستجو برای: sporadic region

تعداد نتایج: 557854  

2013
Shunyao Liao Wenzhong Song Yunqiang Liu Shaoping Deng Yaming Liang Zhenlin Tang Jiyuan Huang Dandan Dong Gang Xu

BACKGROUND Familial papillary thyroid cancer (fPTC) is recognized as a distinct entity only recently and no fPTC predisposing genes have been identified. Several potential regions and susceptibility loci for sporadic PTC have been reported. We aimed to evaluate the role of the reported susceptibility loci and potential risk genomic region in a Chinese familial multinodular goiter (fMNG) with PT...

Journal: :Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2001
S C Costa L S Nascimento F J Ferreira P S Mattos L H Camara-Lopes L S Ward

In addition to the mutations that underlie most cases of the multiple endocrine neoplasia type 1 (MEN1) syndrome, somatic mutations of the MEN1 gene have also been described in sporadic tumors like gastrinomas, insulinomas and bronchial carcinoid neoplasm. We examined exon 2 of this gene, where most of the mutations have been described, in 148 endocrine and nonendocrine sporadic tumors. DNA was...

Journal: :Human molecular genetics 2001
V L Sheen P H Dixon J W Fox S E Hong L Kinton S M Sisodiya J S Duncan F Dubeau I E Scheffer S C Schachter A Wilner R Henchy P Crino K Kamuro F DiMario M Berg R Kuzniecky A J Cole E Bromfield M Biber D Schomer J Wheless K Silver G H Mochida S F Berkovic F Andermann E Andermann W B Dobyns N W Wood C A Walsh

Periventricular heterotopia (PH) is a human neuronal migration disorder in which many neurons destined for the cerebral cortex fail to migrate. Previous analysis showed heterozygous mutations in the X-linked gene filamin 1 (FLN1), but examined only the first six (of 48) coding exons of the gene and hence did not assess the incidence and functional consequences of FLN1 mutations. Here we perform...

Meningioangiomatosis is regarded as a rare benign hamartomatous condition mostly involving the cerebral cortex and overlying leptomeninges. A strong association of MA with neurofibromatosis type 2 has been documented in published articles. Herein we report a case of an otherwise healthy 13-year-old boy with no family history or stigmata of neurofibromatosis who presented with intractable seizur...

Journal: :The Lancet 1873

Journal: :Journal of medical genetics 2006
M Sharma J C Mueller A Zimprich P Lichtner A Hofer P Leitner S Maass D Berg A Dürr V Bonifati G De Michele B Oostra A Brice N W Wood B Muller-Myhsok T Gasser

BACKGROUND Parkinson's disease is a genetically complex disease with mixed mode of inheritance. Recently, a haplotype across the sepiapterin reductase (SPR) gene, which is located in the PARK3 linkage region, was shown to modulate age of onset of Parkinson's disease in sibships from North America. OBJECTIVE To make a thorough assessment of the SPR gene region in sporadic Parkinson's disease. ...

2014
Chao Ling Matthew Pease Lingling Shi Vasu Punj Mark S. Shiroishi Deborah Commins Daniel J. Weisenberger Kai Wang Gabriel Zada

Pituitary adenomas (PAs) are neoplasms that may cause a variety of neurological and endocrine effects. Although known causal contributors include heredity, hormonal influence and somatic mutations, the pathophysiologic mechanisms driving tumorigenesis and invasion of sporadic PAs remain unknown. We hypothesized that alterations in DNA methylation are associated with PA invasion and histopatholo...

2011
Long Phi Le G. Petur Nielsen Andrew Eric Rosenberg Dafydd Thomas Julie M. Batten Vikram Deshpande Joseph Schwab Zhenfeng Duan Ramnik J. Xavier Francis J. Hornicek A. John Iafrate

The molecular events in chordoma pathogenesis have not been fully delineated, particularly with respect to copy number changes. Understanding copy number alterations in chordoma may reveal critical disease mechanisms that could be exploited for tumor classification and therapy. We report the copy number analysis of 21 sporadic chordomas using array comparative genomic hybridization (CGH). Recur...

Journal: :Cancer research 2011
Juhong Jiang Eddy S Yang Guochun Jiang Somaira Nowsheen Hong Wang Tong Wang Yihan Wang Dean Billheimer A Bapsi Chakravarthy Melissa Brown Bruce Haffty Fen Xia

Subcellular localization regulates BRCA1 function, and BRCA1 is exported to the cytoplasm following DNA damage in a p53-dependent manner. Because more than 50% of solid tumors harbor p53 mutations, it is possible that genetically wild-type (wt) BRCA1 is functionally abnormal through compromised nuclear-cytoplasmic shuttling in sporadic breast cancer patients with dysfunctional p53. In this stud...

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