37 results on '"Hussain, Rafiqul"'
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2. Single-cell insights into immune dysregulation in rheumatoid arthritis flare versus drug-free remission
3. Deciphering the spatiotemporal transcriptional and chromatin accessibility of human retinal organoid development at the single-cell level
4. Single-cell DNA sequencing identifies risk-associated clonal complexity and evolutionary trajectories in childhood medulloblastoma development
5. Blood and immune development in human fetal bone marrow and Down syndrome
6. Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2
7. Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
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. Additional file 3 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
16. Additional file 1 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
17. Additional file 4 of Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype
18. Intrinsic and extrinsic regulation of human fetal bone marrow haematopoiesis and perturbations in Down syndrome
19. [In towns and cities]
20. Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2
21. RB1 Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development
22. 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
23. MBRS-59. SINGLE-CELL WHOLE-GENOME SEQUENCING DISSECTS INTRA-TUMOURAL GENOMIC HETEROGENEITY AND CLONAL EVOLUTION IN CHILDHOOD MEDULLOBLASTOMA
24. The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease
25. A single cell atlas of human cornea that defines its development, limbal stem and progenitor cells and the interactions with the limbal niche
26. Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2
27. CRX Expression in Pluripotent Stem Cell-Derived Photoreceptors Marks a Transplantable Subpopulation of Early Cones
28. Deconstructing Retinal Organoids: Single Cell RNA-Seq Reveals the Cellular Components of Human Pluripotent Stem Cell-Derived Retina
29. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)
30. Somatic mtDNA variation is an important component of Parkinson's disease
31. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in (A20).
32. An Induced Pluripotent Stem Cell Model of Hypoplastic Left Heart Syndrome (HLHS) Reveals Multiple Expression and Functional Differences in HLHS-Derived Cardiac Myocytes
33. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency
34. Transferrin gene polymorphism in Alzheimer's disease and dementia with Lewy bodies in humans
35. An Induced Pluripotent Stem Cell Model of Hypoplastic Left Heart Syndrome (HLHS) Reveals Multiple Expression and Functional Differences in HLHS-Derived Cardiac Myocytes.
36. Heteroplasmic mitochondrial DNA variants in cardiovascular diseases
37. Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20).
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