27 results on '"Baker, Carl A"'
Search Results
2. NONHUMAN GENOMICS: Long-read sequence assembly of the gorilla genome
3. Association of Baseline Visual Acuity and Retinal Thickness With 1-Year Efficacy of Aflibercept, Bevacizumab, and Ranibizumab for Diabetic Macular Edema
4. Panretinal Photocoagulation vs Intravitreous Ranibizumab for Proliferative Diabetic Retinopathy: A Randomized Clinical Trial
5. HUMAN GENOMICS: Global diversity, population stratification, and selection of human copy-number variation
6. Assessing the Effect of Personalized Diabetes Risk Assessments During Ophthalmologic Visits on Glycemic Control: A Randomized Clinical Trial
7. Gibbon genome and the fast karyotype evolution of small apes
8. Pilot Study of Individuals With Diabetic Macular Edema Undergoing Cataract Surgery
9. Great ape genetic diversity and population history
10. Global increases in both common and rare copy number load associated with autism
11. Macular Edema After Cataract Surgery in Eyes Without Preoperative Central-Involved Diabetic Macular Edema
12. Support for the N -Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families
13. A framework for human microbiome research
14. Structure, function and diversity of the healthy human microbiome
15. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
16. Evaluation of Masking Study Participants to Intravitreal Injections in a Randomized Clinical Trial
17. XPC Branch-Point Sequence Mutations Disrupt U2 snRNP Binding, Resulting in Abnormal pre-mRNA Splicing in Xeroderma Pigmentosum Patients
18. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
19. A burst of segmental duplications in the genome of the African great ape ancestor
20. Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes
21. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
22. Increased expression of VEGF121/VEGF165–189 ratio results in a significant enhancement of human prostate tumor angiogenesis
23. Phenotypic Heterogeneity in the XPB DNA Helicase Gene (ERCC3): Xeroderma Pigmentosum Without and With Cockayne Syndrome
24. Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients
25. Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer risk
26. The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function
27. A Hemolytic-Uremic Syndrome with the Acquired Immunodeficiency Syndrome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.