Search

Your search keyword '"Dna mutational analysis"' showing total 116,536 results

Search Constraints

Start Over You searched for: Descriptor "Dna mutational analysis" Remove constraint Descriptor: "Dna mutational analysis"
116,536 results on '"Dna mutational analysis"'

Search Results

1. Mutational signatures in 175 Chinese gastric cancer patients.

2. Conserved regulatory motifs in the juxtamembrane domain and kinase N-lobe revealed through deep mutational scanning of the MET receptor tyrosine kinase domain.

3. popDMS infers mutation effects from deep mutational scanning data.

4. Computationally restoring the potency of a clinical antibody against Omicron.

5. Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients.

6. Integrated mutational landscape analysis of poorly differentiated high-grade neuroendocrine carcinoma of the uterine cervix.

7. Timing and Ideal Patient for an Appropriate Search for Somatic RET Mutation in Medullary Thyroid Cancer.

8. Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment.

9. Precision oncology platforms: practical strategies for genomic database utilization in cancer treatment

10. Rosace: a robust deep mutational scanning analysis framework employing position and mean-variance shrinkage

11. A case of double‐negative prostate cancer with BRCA2 mutation and high tumor mutation burden treated sequentially with olaparib and pembrolizumab

12. Shifting the Cancer Screening Paradigm: Developing a Multi-Biomarker Class Approach to Multi-Cancer Early Detection Testing.

13. Clinical and molecular spectrum of a large Egyptian cohort with ALS2‐related disorders of infantile‐onset of clinical continuum IAHSP/JPLS

14. Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis.

15. Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies

16. Differential Expression of MED12-Associated Coding RNA Transcripts in Uterine Leiomyomas

17. Iris and Ciliary Body Melanocytomas Are Defined by Solitary GNAQ Mutation Without Additional Oncogenic Alterations

19. Inspiring basic and applied research in genome integrity mechanisms: Dedication to Samuel H. Wilson.

20. Deciphering tumor immune microenvironment differences between high-grade serous and endometrioid ovarian cancer to investigate their potential in indicating immunotherapy response

21. Inhibition of ceramide accumulation in AdipoR1-/- mice increases photoreceptor survival and improves vision

22. Co‐occurrence of BAP1 and SF3B1 mutations in uveal melanoma induces cellular senescence

23. Differential immunohistochemical and molecular profiling of conventional and aggressive components of chromophobe renal cell carcinoma: pitfalls for diagnosis

24. Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia

25. MASSIVE ADVANCING NONEXUDATIVE TYPE 1 CHOROIDAL NEOVASCULARIZATION IN CTRP5 LATE-ONSET RETINAL DEGENERATION: Longitudinal Findings on Multimodal Imaging and Implications for Age-Related Macular Degeneration.

26. Improving the value of molecular testing: current status and opportunities in colorectal cancer precision medicine.

27. Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

28. An interesting case of isolated false‐negative hepatitis B surface antigen in a blood donor.

29. Deciphering tumor immune microenvironment differences between high-grade serous and endometrioid ovarian cancer to investigate their potential in indicating immunotherapy response.

30. Predictive Value of Ultrasound Imaging Characteristics and a BRAF V600E Nomogram for Central Lymph Node Metastasis Risk in Papillary Thyroid Microcarcinoma.

32. Constitutively Activating GNAS Somatic Mutation in Right Ventricular Outflow Tract Tachycardia.

33. Cutaneous Lymphadenoma Is a Distinct Trichoblastoma-like Lymphoepithelial Tumor With Diffuse Androgen Receptor Immunoreactivity, Notch1 Ligand in Reed-Sternberg–like Cells, and Common EGFR Somatic Mutations

34. The N-terminal domain of SARS-CoV-2 nsp1 plays key roles in suppression of cellular gene expression and preservation of viral gene expression

35. NR4A family members regulate T cell tolerance to preserve immune homeostasis and suppress autoimmunity.

36. Population sequencing data reveal a compendium of mutational processes in the human germ line.

38. Resolving pathogenicity classification for the CDH1 c.[715G>A] (p.Gly239Arg) Variant

39. EXO5-DNA structure and BLM interactions direct DNA resection critical for ATR-dependent replication restart

40. Cancer of Unknown Primary in the Molecular Era

41. LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS—SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED

42. NUBPL mitochondrial disease: new patients and review of the genetic and clinical spectrum.

43. TERT promoter mutations and other prognostic factors in patients with advanced urothelial carcinoma treated with an immune checkpoint inhibitor

44. Mitochondrial DNA mutations in Medulloblastoma

45. De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

46. Molecular diagnosis of diffuse glioma using a chip-based digital PCR system to analyze IDH, TERT, and H3 mutations in the cerebrospinal fluid.

47. Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1

48. Shifting the Cancer Screening Paradigm: Developing a Multi-Biomarker Class Approach to Multi-Cancer Early Detection Testing

49. Sensitive detection of tumor mutations from blood and its application to immunotherapy prognosis

50. Kickboxing a cardiomyopathy: mitochondrial sequencing provides answer for young athlete and her family

Catalog

Books, media, physical & digital resources