429 results on '"Sood, Raman"'
Search Results
2. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
3. Dysregulated myosin in Hermansky-Pudlak syndrome lung fibroblasts is associated with increased cell motility
4. A robust pipeline for efficient knock-in of point mutations and epitope tags in zebrafish using fluorescent PCR based screening
5. Guided genetic screen to identify genes essential in the regeneration of hair cells and other tissues
6. Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development
7. Large-scale generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes
8. Correction: ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
9. ATP6V1H Deficiency Impairs Bone Development through Activation of MMP9 and MMP13.
10. Organ specific microenvironmental MR1 expression in cutaneous melanoma
11. Macrophage mediated mesoscale brain mechanical homeostasis mechanically imaged via optical tweezers and Brillouin microscopyin vivo
12. Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy
13. Regulation of a novel isoform of Receptor Expression Enhancing Protein REEP6 in rod photoreceptors by bZIP transcription factor NRL
14. Role of RUNX1 in hematological malignancies
15. Human macrophages survive and adopt activated genotypes in living zebrafish
16. A novel de novo TP63 mutation in whole‐exome sequencing of a Syrian family with Oral cleft and ectrodactyly.
17. Genomic Landscape of Patients with GermlineRUNX1Variants and Familial Platelet Disorder with Myeloid Malignancy
18. Fluorescent PCR–based Screening Methods for Precise Knock-in of Small DNA Fragments and Point Mutations in Zebrafish
19. Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41
20. Additional file 1 of A robust pipeline for efficient knock-in of point mutations and epitope tags in zebrafish using fluorescent PCR based screening
21. Additional file 2 of A robust pipeline for efficient knock-in of point mutations and epitope tags in zebrafish using fluorescent PCR based screening
22. A high-throughput functional genomics workflow based on CRISPR/Cas9-mediated targeted mutagenesis in zebrafish
23. Zrsr2 Is Essential for the Embryonic Development and Splicing of Minor Introns in RNA and Protein Processing Genes in Zebrafish
24. Cover Image, Volume 173A, Number 11, November 2017
25. A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non‐coding element
26. A Comprehensive Review of Indel Detection Methods for Identification of Zebrafish Knockout Mutants Generated by Genome-Editing Nucleases
27. Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
28. Identification of benzodiazepine Ro5-3335 as an inhibitor of CBF leukemia through quantitative high throughput screen against RUNX1-CBFβ interaction
29. Additional file 5 of Dysregulated myosin in Hermansky-Pudlak syndrome lung fibroblasts is associated with increased cell motility
30. brca2 in zebrafish ovarian development, spermatogenesis, and tumorigenesis
31. Understanding and Editing the Zebrafish Genome
32. Differential requirement for Gata1 DNA binding and transactivation between primitive and definitive stages of hematopoiesis in zebrafish
33. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis
34. Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
35. Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2and DDX41
36. Compound heterozygous KCTD7 variants in progressive myoclonus epilepsy
37. Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development
38. Clinical and genomic analysis of a large Chinese family with familial cortical myoclonic tremor with epilepsy and SAMD12 intronic repeat expansion
39. A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region
40. Human SHPRH suppresses genomic instability through proliferating cell nuclear antigen polyubiquitination
41. Rare hypomorphic human variation in the heptahelical domain ofSMOcontributes to holoprosencephaly phenotypes
42. Cover, Volume 41, Issue 12
43. Zrsr2 Deficient Zebrafish Display Hematopoietic Defects and U12-Type Intron Retention in mRNA Processing Genes
44. A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45
45. Localization of a novel melanoma susceptibility locus to 1p22
46. Isolation and characterization of the human homeobox gene HOX D1
47. A steroid-independent regimen of bortezomib, liposomal doxorubicin and thalidomide demonstrate high response rates in newly diagnosed multiple myeloma patients
48. High-throughput generation and phenotypic characterization of zebrafish CRISPR mutants of DNA repair genes
49. Functional analysis ofSonic Hedgehogvariants associated with holoprosencephaly in humans using a CRISPR/Cas9 zebrafish model
50. BE4max and AncBE4max Are Efficient in Germline Conversion of C:G to T:A Base Pairs in Zebrafish
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