Search Results
52. Loss of PRDM1/BLIMP-1 function contributes to poor prognosis of activated B-cell-like diffuse large B-cell lymphoma
53. Machine learning and data mining in complex genomic data a review on the lessons learned in Genetic Analysis Workshop Nineteen
54. Pathogenic Mutations in Cancer-Predisposing Genes: A Survey of 300 Patients with Whole-Genome Sequencing and Lifetime Electronic Health Records
55. Supplemental Data: PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism
56. The intolerance to functional genetic variation of protein domains predicts the localization of pathogenic mutations within genes
57. Association of Researcher Characteristics with Views on Return of Incidental Findings from Genomic Research
58. Characterization of a novel fusion gene EML4-NTRK3 in a case of recurrent congenital fibrosarcoma
59. Researchers’ views on informed consent for return of secondary results in genomic research
60. The Need for Vigilance in the Marketing of Genomic Tests in Psychiatry
61. Broadening horizons: holistic viewpoints from the Biology of Genomes
62. Characterizing The Genetic Basis Of Transcriptome Diversity Through Rna-sequencing Of 922 Individuals
63. Correction: A dual clustering framework for association screening with whole genome sequencing data and longitudinal traits
64. CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites
65. Genetics of follicular lymphoma transformation
66. Genome characterization of Long Island tick rhabdovirus, a new virus identified in Amblyomma americanum ticks
67. Informed consent for return of incidental findings in genomic research
68. Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function
69. Models of Consent to Return of Incidental Findings in Genomic Research
70. One in Four Individuals of African-American Ancestry Harbors a 5.5kb Deletion at chromosome 11q13.1
71. Placental Genome and Maternal-Placental Genetic Interactions: A Genome-Wide and Candidate Gene Association Study of Placental Abruption
72. Processes and factors involved in decisions regarding return of incidental genomic findings in research
73. Should Life Insurers Have Access to Genetic Test Results?
74. Viral diversity and clonal evolution from unphased genomic data
75. Creation and characterization of BAC-transgenic mice with physiological over-expression of epitope-tagged RCAN1 (DSCR1)
76. De novo likelihood-based measures for comparing genome assemblies
77. Genetic Polymorphisms of XRCC1 and Leukemia Risk: A Meta-Analysis of 19 Case-Control Studies
78. Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes
79. Genome-Wide and Differential Proteomic Analysis of Hepatitis B Virus and Aflatoxin B1 Related Hepatocellular Carcinoma in Guangxi, China
80. Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci
81. Genotyping Serotonin Transporter Polymorphisms 5-httlpr And Rs25531 In European- And African-american Subjects From The National Institute Of Mental Health’s Collaborative Center For Genomic Studies
82. Researchers’ views on return of incidental genomic research results: qualitative and quantitative findings
83. Return of Secondary Genomic Findings vs Patient Autonomy: Implications for Medical Care
84. Synonymous site conservation in the HIV-1 genome
85. Transcriptome sequencing and microarray design for functional genomics in the extremophile Arabidopsis relative Thellungiella salsuginea (Eutrema salsugineum)
86. Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals
87. Integrative genomic approaches in cervical cancer: implications for molecular pathogenesis
88. Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation
89. Identification of Copy Number Gain and Overexpressed Genes on Chromosome Arm 20q by an Integrative Genomic Approach in Cervical Cancer: Potential Role in Progression
90. Prediction of enzyme function based on 3D templates of evolutionarily important amino acids
91. Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair
92. Characterizing the expression of the human olfactory receptor gene family using a novel DNA microarray
93. Gene Dosage Alterations Revealed by cDNA Microarray Analysis in Cervical Cancer: Identification of Candidate Amplified and Overexpressed Genes
94. Loss of spermatogonia and wide-spread DNA methylation defects in newborn male mice deficient in DNMT3L
95. Molecular Cytogenetic Applications in Analysis of the Cancer Genome
96. Detecting transcriptionally active regions using genomic tiling arrays
97. Loss of LIN-35, the Caenorhabditis elegans ortholog of the tumor suppressor p105Rb, results in enhanced RNA interference
98. Genomic Profiling Maps Loss of Heterozygosity and Defines the Timing and Stage Dependence of Epigenetic and Genetic Events in Wilms’ Tumors
99. Lack of PTEN sequesters CHK1 and initiates genetic instability
100. CisOrtho: A program pipeline for genome-wide identification of transcription factor target genes using phylogenetic footprinting
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