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48,733 results on '"GENES"'

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1. Human Gingival Fibroblast Growth and Function in Response to Laser-Induced Meso- and Microscale Hybrid Topography on Dental Implant Healing Abutments.

2. The prominent pervasive oncogenic role and tissue specific permissiveness of RAS gene mutations.

3. Decoding biology with massively parallel reporter assays and machine learning.

4. Developmental assembly of multi-component polymer systems through interconnected synthetic gene networks in vitro.

5. Mycobacteria that cause tuberculosis have retained ancestrally acquired genes for the biosynthesis of chemically diverse terpene nucleosides.

6. Impact of essential genes on the success of genome editing experiments generating 3313 new genetically engineered mouse lines

7. A novel reporter for helicase activity in translation uncovers DDX3X interactions

8. Multiplex profiling of developmental cis-regulatory elements with quantitative single-cell expression reporters

9. Seedless fruit in Annona squamosa L. is monogenic and conferred by INO locus deletion in multiple accessions.

10. A Prognostic Model Based on Cisplatin-Resistance Related Genes in Oral Squamous Cell Carcinoma.

11. Functional analysis of the mating type genes in Verticillium dahliae.

12. Transcriptional and metabolic profiling of sulfur starvation response in two monocots.

13. A single-cell atlas enables mapping of homeostatic cellular shifts in the adult human breast.

14. MRI Surveillance and Breast Cancer Mortality in Women With BRCA1 and BRCA2 Sequence Variations

15. Advancing the scale of synthetic biology via cross-species transfer of cellular functions enabled by iModulon engraftment.

16. A view of the pan‐genome of domesticated Cowpea (Vigna unguiculata [L.] Walp.)

17. POPULATION HISTORY AND GENETIC STRUCTURE IN THE WESTERN ATLANTIC SURFCLAM SUBSPECIES (SPISULA SOLIDISSIMA SPP.)

20. Risk-reducing mastectomy and breast cancer mortality in women with a BRCA1 or BRCA2 pathogenic variant: an international analysis

21. Nuclear to cytoplasmic transport is a druggable dependency in MYC-driven hepatocellular carcinoma.

22. Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants

23. Functional annotation of variants of the BRCA2 gene via locally haploid human pluripotent stem cells

24. Analysis of five near-complete genome assemblies of the tomato pathogen Cladosporium fulvum uncovers additional accessory chromosomes and structural variations induced by transposable elements effecting the loss of avirulence genes.

25. Nasopharyngeal lymphatic plexus is a hub for cerebrospinal fluid drainage

26. The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species

27. Barcoded overexpression screens in gut Bacteroidales identify genes with roles in carbon utilization and stress resistance

28. HDAC activity is dispensable for repression of cell-cycle genes by DREAM and E2F:RB complexes

29. One hundred years of comparative genetic and physical mapping in cultivated oat (Avena sativa)

30. Dissection of a rapidly evolving wheat resistance gene cluster by long-read genome sequencing accelerated the cloning of Pm69

31. Characteristic spatial and frequency distribution of mutations in SCN1A.

32. SLC2A1 variants cause late-onset epilepsy and the genetic-dependent stage feature: For the China Epilepsy Gene 1.0 Project.

33. Molecular analysis of inherited disorders of cornification in polish patients show novel variants and functional data and provokes questions on the significance of secondary findings.

34. Identifying low-density, ancestry-informative SNP markers through whole genome resequencing in Indian, Chinese, and wild yak.

35. Transcriptomic analysis of the 12 major human breast cell types reveals mechanisms of cell and tissue function.

36. Orphan genes are not a distinct biological entity.

37. Ionising radiation exposure-induced regulation of selected biomarkers and their impact in cancer and treatment.

38. De novo and inherited monoallelic variants in TUBA4A cause ataxia and spasticity.

39. A mutation in the PRKAR1B gene drives pathological mechanisms of neurodegeneration across species.

40. Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis.

41. GDF5 as a rejuvenating treatment for age-related neuromuscular failure.

42. Clinical validation of the Ion Torrent Oncomine Myeloid Assay GX v2 on the Genexus Integrated Sequencer as a stand-alone assay for single-nucleotide variants, insertions/deletions, and fusion genes: Challenges, performance, and perspectives.

43. Linkage equilibrium between rare mutations.

44. An explanation for the sister repulsion phenomenon in Patterson's f-statistics.

45. Defects in the central metabolism prevent thymineless death in Escherichia coli, while still allowing significant protein synthesis.

46. ERBB2 amplification in gastric cancer: a genomic insight into ethnic disparities.

47. Bioinformatic and experimental data pertaining to the role of the NLRP3 inflammasome in ovarian cancer.

48. Reference Gene Selection for RT-qPCR Normalization in Toxoplasma gondii Exposed to Broxaldine.

49. Comparative Efficacy of Adagrasib and Sotorasib in KRAS G12C-Mutant NSCLC: Insights from Pivotal Trials.

50. Splicing Dysregulation of Non-Canonical GC-5′ Splice Sites of Breast Cancer Susceptibility Genes ATM and PALB2.

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