نتایج جستجو برای: nonrecurrent

تعداد نتایج: 267  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Nicola L P Barnes Sahar Khavari Gary P Boland Angela Cramer W Fiona Knox Nigel J Bundred

The type 1 tyrosine kinase receptor HER2 (c-erbB2/neu) is associated with resistance to hormone therapy and poor survival in invasive breast cancer, whereas HER4 expression is associated with endocrine responsiveness. Patterns of tyrosine kinase receptor coexpression may aid prediction of recurrence risk after surgery for ductal carcinoma in situ (DCIS). Women who had undergone surgery for pure...

2012
Anna Dolnik Julia C. Engelmann Maren Scharfenberger-Schmeer Julian Mauch Sabine Kelkenberg-Schade Berit Haldemann Tamara Fries Jan Krönke Michael W. M. Kühn Peter Paschka Sabine Kayser Stephan Wolf Verena I. Gaidzik Richard F. Schlenk Frank G. Rücker Hartmut Döhner Claudio Lottaz Konstanze Döhner Lars Bullinger

Acute myeloid leukemia (AML) is characterized by molecular heterogeneity. As commonly altered genomic regions point to candidate genes involved in leukemogenesis, we used microarray-based comparative genomic hybridization and single nucleotide polymorphism profiling data of 391 AML cases to further narrow down genomic regions of interest. Targeted resequencing of 1000 genes located in the criti...

Journal: :Genetics 1998
W G Hill

SEWALL WRIGHT suggested that genes of large effect on a quantitative trait could be isolated by recurrent backcrossing with selection on the trait. Loci [quantitative trait loci (QTL)] at which the recurrent and nonrecurrent lines have genes of different large effect on the trait would remain segregating, while other loci would become fixed for the gene carried by the recurrent parent. If the r...

Journal: :Human molecular genetics 2011
Pengfei Liu Ayelet Erez Sandesh C Sreenath Nagamani Weimin Bi Claudia M B Carvalho Alexandra D Simmons Joanna Wiszniewska Ping Fang Patricia A Eng M Lance Cooper V Reid Sutton Elizabeth R Roeder John B Bodensteiner Mauricio R Delgado Siddharth K Prakash John W Belmont Pawel Stankiewicz Jonathan S Berg Marwan Shinawi Ankita Patel Sau Wai Cheung James R Lupski

Genomic instability is a feature of the human Xp22.31 region wherein deletions are associated with X-linked ichthyosis, mental retardation and attention deficit hyperactivity disorder. A putative homologous recombination hotspot motif is enriched in low copy repeats that mediate recurrent deletion at this locus. To date, few efforts have focused on copy number gain at Xp22.31. However, clinical...

Journal: :IEEE transactions on neural networks 2003
Pablo Zegers Malur K. Sundareshan

Generation of desired trajectory behavior using neural networks involves a particularly challenging spatio-temporal learning problem. This paper introduces a novel solution, i.e., designing a dynamic system whose terminal behavior emulates a prespecified spatio-temporal pattern independently of its initial conditions. The proposed solution uses a dynamic neural network (DNN), a hybrid architect...

Journal: :Psychological review 2008
Kevin B MacDonald

This article analyzes the effortful control of automatic processing related to social and emotional behavior, including control over evolved modules designed to solve problems of survival and reproduction that were recurrent over evolutionary time. The inputs to effortful control mechanisms include a wide range of nonrecurrent information--information resulting not from evolutionary regularitie...

Journal: :Blood 2012
Anna Dolnik Julia C Engelmann Maren Scharfenberger-Schmeer Julian Mauch Sabine Kelkenberg-Schade Berit Haldemann Tamara Fries Jan Krönke Michael W M Kühn Peter Paschka Sabine Kayser Stephan Wolf Verena I Gaidzik Richard F Schlenk Frank G Rücker Hartmut Döhner Claudio Lottaz Konstanze Döhner Lars Bullinger

Acute myeloid leukemia (AML) is characterized by molecular heterogeneity. As commonly altered genomic regions point to candidate genes involved in leukemogenesis, we used microarray-based comparative genomic hybridization and single nucleotide polymorphism profiling data of 391 AML cases to further narrow down genomic regions of interest. Targeted resequencing of 1000 genes located in the criti...

Journal: :Genome dynamics 2006
P Stankiewicz J R Lupski

In the past fifteen years, an emerging group of genetic diseases have been described that result from DNA rearrangements rather than from single nucleotide changes. Such conditions have been referred to as genomic disorders. The predominant molecular mechanism underlying the rearrangements that cause this group of diseases and traits is nonallelic homologous recombination (NAHR) (unequal crossi...

Journal: :Genetics 2009
Olivier Cocquempot Véronique Brault Charles Babinet Yann Herault

Polyalanine expansion diseases are proposed to result from unequal crossover of sister chromatids that increases the number of repeats. In this report we suggest an alternative mechanism we put forward while we investigated a new spontaneous mutant that we named "Dyc" for "Digit in Y and Carpe" phenotype. Phenotypic analysis revealed an abnormal limb patterning similar to that of the human inhe...

Journal: :Cancer research 2008
J Guy Lyons Vyomesh Patel Naomi C Roue Sandra Y Fok Lilian L Soon Gary M Halliday J Silvio Gutkind

The transcriptional repressor Snail2 is overexpressed in head and neck squamous cell carcinomas (HNSCC) relative to nonmalignant head and neck mucosal epithelium, and in locally recurrent relative to nonrecurrent HNSCCs. We investigated the mechanisms by which Snails might contribute to the pathogenesis of HNSCCs using cell biological and molecular analyses. Oral keratinocytes that expressed Sn...

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