190 results on '"Nadaf, Javad"'
Search Results
2. Molecular characterization of DICER1-mutated pituitary blastoma
3. Invasive growth of brain metastases is linked to CHI3L1 release from pSTAT3-positive astrocytes.
4. Identity and Nature of Neural Stem Cells in the Adult Human Subventricular Zone
5. A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
6. DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis
7. Exomic and epigenomic analysis of pulmonary blastoma
8. Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant
9. Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy
10. Author Correction: Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy
11. Ovarian small cell carcinoma in one of a pair of monozygous twins
12. NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
13. Supplementary Data from Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer
14. Data from Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
15. Supplementary Table 3 from Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
16. Supplementary Tables and Figures from Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
17. Supplementary Table 2 from Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
18. Histone H3K36 mutations promote sarcomagenesis through altered histone methylation landscape
19. PRAME protein expression in DICER1 ‐related tumours
20. Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer
21. Germline and somatic FGFR1 abnormalities in dysembryoplastic neuroepithelial tumors
22. Abstract 1569: pSTAT3+ stromal cells drive the invasive growth of brain metastases
23. Glioblastoma scRNA-seq shows treatment-induced, immune-dependent increase in mesenchymal cancer cells and structural variants in distal neural stem cells
24. Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer
25. Abstract 2056: The genomic landscape of carriers of rare variants in FANCI, a new candidate ovarian cancer predisposing gene
26. Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome
27. ExomeAI: detection of recurrent allelic imbalance in tumors using whole-exome sequencing data
28. Additional file 3 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
29. Additional file 2 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
30. Additional file 4 of A functionally impaired missense variant identified in French Canadian families implicates FANCI as a candidate ovarian cancer-predisposing gene
31. Invasive growth associated with cold-inducible RNA-binding protein expression drives recurrence of surgically resected brain metastases
32. A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients
33. RARE-22. GERMLINE PATHOGENIC VARIANT c.1552G>A;p.E518K IN DGCR8 CONFERS SUSCEPTIBILITY FOR SCHWANNOMATOSIS AND THYROID TUMORS
34. BIOM-03. INVASIVE HISTOPATHOLOGY DRIVES POOR OUTCOMES IN SURGICALLY RESECTED BRAIN METASTASES
35. The genetic analysis of a founder Northern American population of European descent identifiesFANCIas a candidate familial ovarian cancer risk gene
36. Duplication 2p16 is associated with perisylvian polymicrogyria
37. Exome sequencing study of partial agenesis of the corpus callosum in men with developmental delay, epilepsy, and microcephaly
38. Abstract 756: Whole exome sequencing identifies frequent mutations of PTPRB and KDR in secondary angiosarcoma
39. Ovarian small cell carcinoma in one of a pair of monozygous twins
40. Identification of QTL controlling meat quality traits in an F2 cross between two chicken lines selected for either low or high growth rate
41. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients
42. Functional analysis of germline ETV6 variants associated with familial thrombocytopenia and acute lymphoblastic leukemia
43. Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma
44. Abstract 2479: A functionally nullRAD51Dmissense mutation is strongly associated with ovarian carcinoma
45. The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families
46. Transcriptome profiling of granulosa and theca cells during dominant follicle development in the horse
47. Germ-line and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type
48. Abstract LB-019: FGFR1 abnormalities in seizure-associated familial and sporadic dysembryoplastic neuroepithelial tumors
49. LG-26GERMLINE AND SOMATIC FGFR1 ABNORMALITIES IN DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMORS
50. Erratum: Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibility
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