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1. An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activity

2. Deficiency of ribosomal protein S26, which is mutated in a subset of patients with Diamond Blackfan anemia, impairs erythroid differentiation

3. Distinct ribosome maturation defects in yeast models of Diamond-Blackfan anemia and Shwachman-Diamond syndrome

4. An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activity

5. Early Onset Colorectal Cancer: An Emerging Cancer Risk in Patients with Diamond Blackfan Anemia

6. Rare ribosomopathies: insights into mechanisms of cancer

7. p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia-proteins: RPS19 versus RPL5.

8. Variations of the UNC13D gene in patients with autoimmune lymphoproliferative syndrome.

9. A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia

10. Whole Genome Sequencing of Diamond Blackfan Anemia Syndrome Patients Detects Mutations That Alter mRNA Splicing

11. Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with <scp>TP</scp> 53 mutations

12. Pathogenic germline IKZF1 variant alters hematopoietic gene expression profiles

13. Proapoptotic Requirement of Ribosomal Protein L11 in Ribosomal Stress-Challenged Cortical Neurons

14. Author Correction: Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

15. Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis

16. Ribosomopathies Through a Diamond Lens

17. Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with

18. Molecular convergence in ex vivo models of Diamond-Blackfan anemia

19. Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy

20. Exploiting pre-rRNA processing in Diamond Blackfan anemia gene discovery and diagnosis

21. A new system for naming ribosomal proteins

22. Whole Genome Sequencing Identifies Small Deletions in Ribosomal Genes Causing Diamond Blackfan Anemia

23. Disease Modeling and Phenotype Rescue Using Inducible Pluripotent Stem Cells from Patients with Diamond-Blackfan Anemia

24. IB4-binding sensory neurons in the adult rat express a novel 3′ UTR-extended isoform ofCaMK4that is associated with its localization to axons

25. Diminutive somatic deletions in the 5q region lead to a phenotype atypical of classical 5q− syndrome

26. Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation

27. Impaired growth, hematopoietic colony formation, and ribosome maturation in human cells depleted of Shwachman-Diamond syndrome protein SBDS

28. Ribosomal protein gene deletions in Diamond-Blackfan anemia

29. Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia

30. Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype

31. Diamond-Blackfan Anemia: Diagnosis, Treatment, and Molecular Pathogenesis

32. Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia

33. Bmi1 promotes erythroid development through regulating ribosome biogenesis

34. Immunophenotypic Profiling of Erythroid Progenitor-Derived Extracellular Vesicles in Diamond-Blackfan Anaemia: A New Diagnostic Strategy

35. Human RPS19, the gene mutated in Diamond-Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits

36. Ribosomes and marrow failure: coincidental association or molecular paradigm?

37. Ribosomal proteins Rps0 and Rps21 of Saccharomyces cerevisiae have overlapping functions in the maturation of the 3' end of 18S rRNA

38. Fetal Erythropoiesis Is Defective in Rpl11 Heterozygous Mice and Increases in Severity in Young Animals

39. Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia

40. Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia families

41. Bidirectional Regulation of Mitochondrial Gene Expression during Developmental Neuroplasticity of Visual Cortex

42. Rpm2, the Protein Subunit of Mitochondrial RNase P in Saccharomyces cerevisiae, Also Has a Role in the Translation of Mitochondrially Encoded Subunits of Cytochrome c Oxidase

43. Genes Encoding Ribosomal Proteins Rps0A/B of Saccharomyces cerevisiae Interact With TOM1 Mutants Defective in Ribosome Synthesis

44. Finding a diamond in the (mouse is) rough

45. Proteasome Mutants, pre4-2 and ump1-2, Suppress the Essential Function but Not the Mitochondrial RNase P Function of the Saccharomyces cerevisiae Gene RPM2

46. Variations of the UNC13D Gene in Patients with Autoimmune Lymphoproliferative Syndrome

47. Mitochondrial function is impaired in yeast and human cellular models of Shwachman Diamond syndrome

48. Genetics of the Ribosomopathies

49. Toward the Humanities Digital Library: Building the Local Organization

50. Yeast Proteins Related to the p40/Laminin Receptor Precursor Are Essential Components of the 40 S Ribosomal Subunit

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