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1. A Neutralizing Antibody Recognizing Primarily N-Linked Glycan Targets the Silent Face of the HIV Envelope

2. Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma

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3. Maturation and Diversity of the VRC01-Antibody Lineage over 15 Years of Chronic HIV-1 Infection

4. Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease

5. Biogeography and individuality shape function in the human skin metagenome

6. Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

7. Topographic diversity of fungal and bacterial communities in human skin

8. Co-evolution of a broadly neutralizing HIV-1 antibody and founder virus

9. Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates

10. Developmental pathway for potent V1V2-directed HIV-neutralizing antibodies

11. A Neutralizing Antibody Recognizing Primarily N-Linked Glycan Targets the Silent Face of the HIV Envelope

12. The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

13. An intermediate grade of finished genomic sequence suitable for comparative analyses

14. Co-evolution of a broadly neutralizing HIV-1 antibody and founder virus

15. Longitudinal shift in diabetic wound microbiota correlates with prolonged skin defense response

16. Maturation and Diversity of the VRC01-Antibody Lineage over 15 Years of Chronic HIV-1 Infection

17. Effort required to finish shotgun-generated genome sequences differs significantly among vertebrates

18. Somatic Mutational Landscape of AML with Inv(16) and t(8;21) Identifies Two Distinct Patterns in Relapse Tumors

19. Gene-Based Sequencing Identifies Lipid-Influencing Variants with Ethnicity-Specific Effects in African Americans

20. Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome

21. Erratum: Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum

22. Analyses of deep mammalian sequence alignments and constraint predictions for 1% of the human genome

23. TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

24. Somatic mutational landscape of AML with inv(16) or t(8;21) identifies patterns of clonal evolution in relapse leukemia

25. Whole-genome sequencing identifies a recurrent functional synonymous mutation in melanoma

26. Targeted Deep Re-Sequencing Implicates Rare and Low Frequency Coding Variants in IL23R, MEFV, TLR4, and NOD2 in Behcet's Disease

27. Corrigendum: TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum.

28. Familial Kyphoscoliosis: Association with the IRX Homeobox Gene Family.