Daniel Sinnett
Sinnett, Daniel, 1963-
Sinnett, Daniel
VIAF ID: 105554326 (Personal)
Permalink: http://viaf.org/viaf/105554326
Preferred Forms
- 100 0 _ ‡a Daniel Sinnett
- 100 1 _ ‡a Sinnett, Daniel
- 100 1 _ ‡a Sinnett, Daniel
- 100 1 _ ‡a Sinnett, Daniel ‡d 1963-
-
4xx's: Alternate Name Forms (2)
Works
Title | Sources |
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Étude de la rétroposition des séquences Alu chez l'humain. | |
Isolation of cosmid and BAC DNA from E. coli | |
Isolation of stable bacterial artificial chromosome DNA using a modified alkaline lysis method | |
Joint genotype inference with germline and somatic mutations | |
KMT2E-ASNS: a novel relapse-specific fusion gene in early T-cell precursor acute lymphoblastic leukemia. | |
Lesch-Nyhan syndrome: molecular investigation of three French Canadian families using a hypoxanthine-guanine phosphoribosyltransferase cDNA probe | |
Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11 | |
LncRNAs downregulated in childhood acute lymphoblastic leukemia modulate apoptosis, cell migration, and DNA damage response | |
Localization and role of NPC1L1 in cholesterol absorption in human intestine | |
Localization, function and regulation of the two intestinal fatty acid-binding protein types. | |
Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancer | |
Mapping cis-acting regulatory variation in recombinant congenic strains | |
Methylation analysis of the glypican 3 gene in embryonal tumours | |
miR-431-5p Knockdown Protects Against Angiotensin II-Induced Hypertension and Vascular Injury | |
Modification in oxidative stress, inflammation, and lipoprotein assembly in response to hepatocyte nuclear factor 4alpha knockdown in intestinal epithelial cells | |
Molecular genetics of cancer | |
Molecular Profiling of Hard-to-Treat Childhood and Adolescent Cancers | |
Mutational and expression analysis of the chromosome 12p candidate tumor suppressor genes in pre-B acute lymphoblastic leukemia. | |
Mutational dynamics of early and late relapsed childhood ALL: rapid clonal expansion and long-term dormancy | |
Novel associations between activating killer-cell immunoglobulin-like receptor genes and childhood leukemia | |
Nutriepigenomics and malnutrition | |
Nutrition education and cooking workshops for families of children with cancer: a feasibility study | |
An optimized workflow to improve reliability of detection of KIAA1549:BRAF fusions from RNA sequencing data | |
Overall informativity, OI, in DNA polymorphisms revealed by inter-Alu PCR: detection of genomic rearrangements | |
Paraoxonase 1, 2 and 3 DNA variants and susceptibility to childhood inflammatory bowel disease. | |
Parental smoking, CYP1A1 genetic polymorphisms and childhood leukemia (Québec, Canada) | |
Patterns of variation in DNA segments upstream of transcription start sites | |
The peptidomimetic CXCR4 antagonist TC14012 recruits beta-arrestin to CXCR7: roles of receptor domains | |
Physical mapping of the G-protein coupled receptor 19 (GPR19) in the chromosome 12p12.3 region frequently rearranged in cancer cells | |
A pilot study to evaluate paclitaxel (Taxol) as primary medical treatment for patients with inoperable stage III and IV breast carcinoma | |
Polymorphisms of the vincristine pathway and response to treatment in children with childhood acute lymphoblastic leukemia | |
Population genomics in a disease targeted primary cell model | |
Preconceptional paternal exposure to pesticides and increased risk of childhood leukaemia | |
Prenatal diagnosis using DNA probes in twins at risk for Duchenne muscular dystrophy | |
Prevention of Long-term Adverse Health Outcomes With Cardiorespiratory Fitness and Physical Activity in Childhood Acute Lymphoblastic Leukemia Survivors | |
Promoter SNPs in G1/S checkpoint regulators and their impact on the susceptibility to childhood leukemia. | |
A protective role of IL-37 in cancer: a new hope for cancer patients | |
Psychosocial Intervention Programs for Parents of Children with Cancer: A Systematic Review and Critical Comparison of Programs' Models and Development | |
Rapid Detection of CYP1A1, CYP2D6, and NAT Variants by Multiplex Polymerase Chain Reaction and Allele-Specific Oligonucleotide Assay | |
Rare allelic forms of PRDM9 associated with childhood leukemogenesis. | |
Rationale for an international consortium to study inherited genetic susceptibility to childhood acute lymphoblastic leukemia | |
Recurrent somatic BRAF insertion (p.V504_R506dup): a tumor marker and a potential therapeutic target in pilocytic astrocytoma. | |
Replication analysis confirms the association of ARID5B with childhood B-cell acute lymphoblastic leukemia | |
Reply to Comments by Kraft and Wilson and by Weinberg and Mitchell on “Parental Genotypes in the Risk of a Complex Disease”. | |
Research- and Practice-Based Nutrition Education and Cooking Workshops in Pediatric Oncology: Protocol for Implementation and Development of Curriculum. | |
Role of NOS3 DNA variants in externalizing behavioral problems observed in childhood leukemia survivors | |
Role of rs10406069 in miR-5196 in hyperdiploid childhood acute lymphoblastic leukemia | |
Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity | |
Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus | |
SNooPer: a machine learning-based method for somatic variant identification from low-pass next-generation sequencing | |
Spontaneous brain oscillations as neural fingerprints of working memory capacities: A resting-state MEG study. | |
Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process | |
Subcellular proteomics of cell differentiation: Quantitative analysis of the plasma membrane proteome of Caco-2 cells | |
A survey of genetic and epigenetic variation affecting human gene expression | |
Syndrome de Lesch-Nyhan détection des porteuses et caractérisation des mutations responsables de ce désordre génétique | |
Tissue distribution and regulation of the small Sar1b GTPase in mice. | |
To disclose, or not to disclose? Context matters | |
The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers | |
TR-16PERSONALIZED TARGETED THERAPY IN REFRACTORY OR RELAPSED CANCER IN CHILDHOOD (TRICEPS STUDY). | |
Tracking Silent Hypersensitivity Reactions to Asparaginase during Leukemia Therapy Using Single-Chip Indirect Plasmonic and Fluorescence Immunosensing. | |
Trametinib for progressive pediatric low-grade gliomas | |
TRPV4 and KRAS and FGFR1 gain-of-function mutations drive giant cell lesions of the jaw | |
Variable continental distribution of polymorphisms in the coding regions of DNA-repair genes. | |
Very long intergenic non-coding RNA transcripts and expression profiles are associated to specific childhood acute lymphoblastic leukemia subtypes | |
The VIE study: feasibility of a physical activity intervention in a multidisciplinary program in children with cancer | |
Visual short term memory related brain activity predicts mathematical abilities | |
Vitamin D nutritional status and bone turnover markers in childhood acute lymphoblastic leukemia survivors: A PETALE study | |
Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood ALL patients | |
Whole-exome sequencing of a rare case of familial childhood acute lymphoblastic leukemia reveals putative predisposing mutations in Fanconi anemia genes | |
Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans |