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1. Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines

2. Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species

3. Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species (vol 15, 63, 2017)

4. Initial sequencing and analysis of the human genome

5. The genomes of two key bumblebee species with primitive eusocial organization.

7. The genome of the model beetle and pest tribolium castaneum

8. Butterfly genome reveals promiscuous exchange of mimicry adaptations among species

10. Somatic mutations affect key pathways in lung adenocarcinoma

11. Experiences in providing a community educational resource for the All of Us Researcher Workbench.

12. Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample.

13. Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences.

14. Genomic analysis of two phlebotomine sand fly vectors of Leishmania from the New and Old World.

15. Variants in genes coding for collagen type IV α-chains are frequent causes of persistent, isolated hematuria during childhood.

16. Accuracy and applications of sequencing and genotyping approaches for CYP2A6 and homologous genes.

17. Implementation of preemptive DNA sequence-based pharmacogenomics testing across a large academic medical center: The Mayo-Baylor RIGHT 10K Study.

18. CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project.

19. Targeted Genotyping in Clinical Pharmacogenomics: What Is Missing?

20. Novel Anaplastic Thyroid Cancer PDXs and Cell Lines: Expanding Preclinical Models of Genetic Diversity.

21. A High-throughput Approach to Identify Effective Systemic Agents for the Treatment of Anaplastic Thyroid Carcinoma.

22. Pharmacogenomics of Nicotine Metabolism: Novel CYP2A6 and CYP2B6 Genetic Variation Patterns in Alaska Native and American Indian Populations.

23. Cohort Profile: The Right Drug, Right Dose, Right Time: Using Genomic Data to Individualize Treatment Protocol (RIGHT Protocol).

24. Pharmacogenomic Next-Generation DNA Sequencing: Lessons from the Identification and Functional Characterization of Variants of Unknown Significance in CYP2C9 and CYP2C19 .

25. Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies syndrome due to disruption of BPTF in a 35-year-old man initially diagnosed with Silver-Russell syndrome.

26. Whole-Organ Genomic Characterization of Mucosal Field Effects Initiating Bladder Carcinogenesis.

27. Blood pressure signature genes and blood pressure response to thiazide diuretics: results from the PEAR and PEAR-2 studies.

28. Genetic Variants Influencing Plasma Renin Activity in Hypertensive Patients From the PEAR Study (Pharmacogenomic Evaluation of Antihypertensive Responses).

29. Novel CYP2A6 diplotypes identified through next-generation sequencing are associated with in-vitro and in-vivo nicotine metabolism.

30. Whole Transcriptome Sequencing Analyses Reveal Molecular Markers of Blood Pressure Response to Thiazide Diuretics.

31. Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes.

32. Erratum to: Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species.

33. Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species.

34. Genome-Wide Prioritization and Transcriptomics Reveal Novel Signatures Associated With Thiazide Diuretics Blood Pressure Response.

35. Multifaceted biological insights from a draft genome sequence of the tobacco hornworm moth, Manduca sexta.

36. The ethics of conducting molecular autopsies in cases of sudden death in the young.

37. Postmortem genetic screening for the identification, verification, and reporting of genetic variants contributing to the sudden death of the young.

38. Differentially expressed gene transcripts using RNA sequencing from the blood of immunosuppressed kidney allograft recipients.

39. The genomes of two key bumblebee species with primitive eusocial organization.

40. A massive expansion of effector genes underlies gall-formation in the wheat pest Mayetiola destructor.

41. The first myriapod genome sequence reveals conservative arthropod gene content and genome organisation in the centipede Strigamia maritima.

42. Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems.

43. Comparative validation of the D. melanogaster modENCODE transcriptome annotation.

44. Genetic alterations associated with progression from pancreatic intraepithelial neoplasia to invasive pancreatic tumor.

45. Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis.

46. Whole-exome sequencing combined with functional genomics reveals novel candidate driver cancer genes in endometrial cancer.

47. Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis.

48. Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes.

49. High frequency of PIK3R1 and PIK3R2 mutations in endometrial cancer elucidates a novel mechanism for regulation of PTEN protein stability.

50. A genetic map of Xenopus tropicalis.

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