44 results on '"Bandapalli, Obul Reddy"'
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2. Characterization of rare germline variants in familial multiple myeloma
3. Compromised DNA repair is responsible for diabetes‐associated fibrosis
4. Whole Exome-Trio Analysis Reveals Rare Variants Associated with Congenital Pouch Colon
5. Abstract 2058: Identifications of novel variants using system biology-based approaches in NT5C2, its association to relapse acute lymphoblastic leukaemia
6. Editorial: Integrated systems genomic approaches for characterizing uncharacterized proteins
7. Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients
8. Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family
9. Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer
10. Germline Variants of CYBA and TRPM4 Predispose to Familial Colorectal Cancer
11. Whole-Exome Sequencing Identifies a Novel Germline Variant in PTK7 Gene in Familial Colorectal Cancer
12. The Omic Insights on Unfolding Saga of COVID-19
13. Transcription factor TFE3 enhances cell cycle and cancer progression by binding to the hTERT promoter
14. Elevated Expression of the RAGE Variant-V in SCLC Mitigates the Effect of Chemotherapeutic Drugs
15. A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer
16. Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer
17. Characterization of Rare Germline Variants in Familial Multiple Myeloma
18. Hypothetical Proteins as Predecessors of Long Non-coding RNAs
19. Cancer Predisposition Genes in Cancer-Free Families
20. A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer
21. Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing
22. Whole genome sequencing reveals DICER1 as a candidate predisposing gene in familial Hodgkin lymphoma
23. Identification of an Ultra High-Risk and Targetable Molecular Signature in Relapsed Pediatric T-ALL
24. The Combination of MRD and Copy Number Alterations (CNAs) Defines an Ultra-High Risk Group of Children with Primary T-Lymphoblastic Leukemia (T-ALL)
25. Gene Panel Sequencing of Primary and Relapsed Pediatric T-ALL Shows That Relapse-Specific Mutations Are Diverse and Mostly Non-Recurrent
26. Relapsing Pediatric T-Cell Acute Lymphoblastic Leukemia Downregulates T-Cell Properties and Upregulates Cell Adhesion
27. PDX Models Recapitulate Genetics and Epigenetics of Pediatric T-Cell Leukemia
28. PTEN Alterations Are Related to Unfavorable Prognosis in Children with T-Cell Acute Lymphoblastic Leukemia Treated According to ALL IC-BFM Protocols
29. A novel autosomal recessive TERT T1129P mutation in a dyskeratosis congenita family leads to cellular senescence and loss of CD34+ hematopoietic stem cells not reversible by mTOR-inhibition
30. Network Topologies Decoding Cervical Cancer
31. Analysis of global gene expression profiles and invasion related genes of colorectal liver metastasis
32. Analysis of global gene expression profiles and invasion related genes of colorectal liver metastasis
33. Whole-Exome Sequencing Links CARD11 Inactivation with SCID
34. The Favorable Effect of Activating NOTCH1 Receptor Mutations On Long Term Outcome in T-ALL Is Treatment Related and Can Be Separated From NOTCH Pathway Activation by FBXW7 Loss of Function.
35. Cross-species comparison of biological themes and underlying genes on a global gene expression scale in a mouse model of colorectal liver metastasis and in clinical specimens
36. Tissue Inhibitor of Metalloproteinases-1 Promotes Liver Metastasis by Induction of Hepatocyte Growth Factor Signaling
37. Musashi1 Contribution to Glioblastoma Development via Regulation of a Network of DNA Replication, Cell Cycle and Division Genes.
38. Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer.
39. Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways.
40. PTENAlterations Are Related to Unfavorable Prognosis in Children with T-Cell Acute Lymphoblastic Leukemia Treated According to ALL IC-BFM Protocols
41. Whole-Exome Sequencing Links CARD11Inactivation with SCID
42. Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer
43. Familial cancer variant prioritization pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family
44. Increased apoptosis of host cells and tumor cells in the invasion front of colorectal liver metastases.
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