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1. Generation of Pearl/Calcium Phosphate Composite Particles and Their Integration into Porous Chitosan Scaffolds for Bone Regeneration

2. Agreement between two large pan-cancer CRISPR-Cas9 gene dependency data sets

3. Transcriptomic Remodelling of Fetal Endothelial Cells During Establishment of Inflammatory Memory

4. Sexual Dimorphism in Innate Immunity: The Role of Sex Hormones and Epigenetics

5. Triiodothyronine (T3) Induces Limited Transcriptional and DNA Methylation Reprogramming in Human Monocytes

6. A Potential Role for Epigenetically Mediated Trained Immunity in Food Allergy

7. Unsupervised correction of gene-independent cell responses to CRISPR-Cas9 targeting

8. Mutational signatures of ionizing radiation in second malignancies

9. Supplementary Information from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

10. Supplementary Glioma Genes from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

11. Supplementary Glioma Gene Mutations from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

12. Data from A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

13. Project Score database: a resource for investigating cancer cell dependencies and prioritizing therapeutic targets

14. Gender-affirming hormone therapy induces specific DNA methylation changes in blood

15. Pan-cancer proteomic map of 949 human cell lines

16. Gender Affirming Hormone Therapy induces specific DNA methylation changes in blood

17. Development of the Fearless, Tearless Transition model of care for adolescents with an intellectual disability and/or autism spectrum disorder with mental health comorbidities

18. A Potential Role for Epigenetically Mediated Trained Immunity in Food Allergy

19. The mutational signature profile of known and suspected human carcinogens in mice

20. Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples

21. Agreement between two large pan-cancer CRISPR-Cas9 gene dependency data sets

22. Agreement between two large pan-cancer CRISPR-Cas9 gene dependency datasets

23. Author Correction: Landscape of somatic mutations in 560 breast cancer whole-genome sequences

24. Immunological imprinting of humoral immunity to SARS-CoV-2 in children

25. The perspectives of obese women receiving antenatal care: A qualitative study of women's experiences

26. Mutational signatures of ionizing radiation in second malignancies

27. Landscape of somatic mutations in 560 breast cancer whole-genome sequences

28. The Collaborative Recordist

29. COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

30. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

31. Mutations in the BRWD3 Gene Cause X-Linked Mental Retardation Associated with Macrocephaly

32. The BioMart community portal: an innovative alternative to large, centralized data repositories

33. A comprehensive multicenter comparison of whole genome sequencing pipelines using a uniform tumor-normal sample pair

34. Somatic mutations of the histone H3K27 demethylase gene UTX in human cancer

35. AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes

36. The Relationship Between Tourism Education and The Tourism Industry: Implications for Tourism Education

37. Innovations in Tourism Education and Training

38. Dimensions of the Education—Industry Interface for Tourism

39. BioMart Central Portal: An open database network for the biological community

40. Data mining using the Catalogue of Somatic Mutations in Cancer BioMart

41. Annotating Whole Genome Sequencing in COSMIC (The Catalogue of Somatic Mutations in Cancer)

42. Systematic sequencing of renal carcinoma reveals inactivation of histone modifying genes

43. X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment

44. Patterns of somatic mutation in human cancer genomes

45. Mutations in CUL4B, Which Encodes a Ubiquitin E3 Ligase Subunit, Cause an X-linked Mental Retardation Syndrome Associated with Aggressive Outbursts, Seizures, Relative Macrocephaly, Central Obesity, Hypogonadism, Pes Cavus, and Tremor

46. Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation

47. Mutation analysis of 24 known cancer genes in the NCI-60 cell line set

48. A Hypermutation Phenotype and Somatic MSH6 Mutations in Recurrent Human Malignant Gliomas after Alkylator Chemotherapy

49. Sequence analysis of the protein kinase gene family in human testicular germ-cell tumors of adolescents and adults

50. Prodromal Urticaria with Seronegative Rheumatoid Arthritis

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