32 results on '"Hussain, Rafiqul"'
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2. Single-cell DNA sequencing identifies risk-associated clonal complexity and evolutionary trajectories in childhood medulloblastoma development
3. Blood and immune development in human fetal bone marrow and Down syndrome
4. Single-cell insights into immune dysregulation in rheumatoid arthritis flare versus drug-free remission
5. Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2
6. Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
7. Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina.
8. Deciphering the spatio-temporal transcriptional and chromatin accessibility of human retinal organoid development at the single cell level
9. Single cell RNA sequencing reveals transcriptional changes of human choroidal and retinal pigment epithelium cells during fetal development, in healthy adult and intermediate age-related macular degeneration
10. Conjunctival epithelial cells resist productive SARS-CoV-2 infection
11. Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
12. pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation
13. Conjunctival epithelial cells resist productive SARS-CoV-2 infection
14. A single cell atlas of human cornea that defines its development, limbal progenitor cells and their interactions with the immune cells
15. Intrinsic and extrinsic regulation of human fetal bone marrow haematopoiesis and perturbations in Down syndrome
16. Additional file 3 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
17. Additional file 1 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
18. Additional file 4 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
19. Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2
20. RB1 Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development
21. Co-expression of SARS-CoV-2 entry genes in the superficial adult human conjunctival, limbal and corneal epithelium suggests an additional route of entry via the ocular surface
22. MBRS-59. SINGLE-CELL WHOLE-GENOME SEQUENCING DISSECTS INTRA-TUMOURAL GENOMIC HETEROGENEITY AND CLONAL EVOLUTION IN CHILDHOOD MEDULLOBLASTOMA
23. The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease
24. A single cell atlas of human cornea that defines its development, limbal stem and progenitor cells and the interactions with the limbal niche
25. Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2
26. CRX Expression in Pluripotent Stem Cell-Derived Photoreceptors Marks a Transplantable Subpopulation of Early Cones
27. Deconstructing Retinal Organoids: Single Cell RNA-Seq Reveals the Cellular Components of Human Pluripotent Stem Cell-Derived Retina
28. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)
29. Somatic mtDNA variation is an important component of Parkinson's disease
30. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in (A20).
31. Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
32. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).
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