Found: 65
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Increased expression of VEGF.
- Published in:
- International Journal of Cancer, 2007, v. 120, n. 10, p. 2096, doi. 10.1002/ijc.22461
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- Publication type:
- Article
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
- Published in:
- Molecular Autism, 2018, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13229-018-0247-z
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- Publication type:
- Article
Indexical contextualism and the challenges from disagreement.
- Published in:
- Philosophical Studies, 2012, v. 157, n. 1, p. 107, doi. 10.1007/s11098-010-9621-1
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- Publication type:
- Article
Alpha Satellite Insertion Close to an Ancestral Centromeric Region.
- Published in:
- Molecular Biology & Evolution, 2021, v. 38, n. 12, p. 5576, doi. 10.1093/molbev/msab244
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- Publication type:
- Article
An Absolutist Theory of Faultless Disagreement in Aesthetics.
- Published in:
- Pacific Philosophical Quarterly, 2017, v. 98, n. 3, p. 429, doi. 10.1111/papq.12102
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- Publication type:
- Article
Support for the N -methyl-d-aspartate receptor hypofunction hypothesis of schizophrenia from exome sequencing in multiplex families.
- Published in:
- 2013
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- Publication type:
- Journal Article
Support for the N-Methyl-D-Aspartate Receptor Hypofunction Hypothesis of Schizophrenia From Exome Sequencing in Multiplex Families.
- Published in:
- JAMA Psychiatry, 2013, v. 70, n. 6, p. 582, doi. 10.1001/jamapsychiatry.2013.1195
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- Publication type:
- Article
Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 1, p. 84
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- Publication type:
- Article
Global increases in both common and rare copy number load associated with autism.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2870, doi. 10.1093/hmg/ddt136
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- Publication type:
- Article
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.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 3, p. 343
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- Publication type:
- Article
An evolutionary driver of interspersed segmental duplications in primates.
- Published in:
- Genome Biology, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s13059-020-02074-4
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- Publication type:
- Article
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
- Published in:
- Nature, 2012, v. 485, n. 7397, p. 246, doi. 10.1038/nature10989
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- Publication type:
- Article
A burst of segmental duplications in the genome of the African great ape ancestor.
- Published in:
- 2009
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- Publication type:
- Correction notice
A burst of segmental duplications in the genome of the African great ape ancestor.
- Published in:
- Nature, 2009, v. 457, n. 7231, p. 877, doi. 10.1038/nature07744
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- Publication type:
- Article
Effect of Initial Management With Aflibercept vs Laser Photocoagulation vs Observation on Vision Loss Among Patients With Diabetic Macular Edema Involving the Center of the Macula and Good Visual Acuity: A Randomized Clinical Trial.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Panretinal Photocoagulation vs Intravitreous Ranibizumab for Proliferative Diabetic Retinopathy: A Randomized Clinical Trial.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 4, p. 407, doi. 10.1038/ejhg.2009.190
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- Publication type:
- Article
Excess of rare, inherited truncating mutations in autism.
- Published in:
- Nature Genetics, 2015, v. 47, n. 6, p. 582, doi. 10.1038/ng.3303
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- Publication type:
- Article
Refining analyses of copy number variation identifies specific genes associated with developmental delay.
- Published in:
- Nature Genetics, 2014, v. 46, n. 10, p. 1063, doi. 10.1038/ng.3092
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- Publication type:
- Article
Corrigendum: A copy number variation morbidity map of developmental delay.
- Published in:
- Nature Genetics, 2014, v. 46, n. 9, p. 1040, doi. 10.1038/ng0914-1040a
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- Publication type:
- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- 2012
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- Publication type:
- Correction notice
A copy number variation morbidity map of developmental delay.
- Published in:
- Nature Genetics, 2011, v. 43, n. 9, p. 838, doi. 10.1038/ng.909
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- Publication type:
- Article
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 585, doi. 10.1038/ng.835
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- Publication type:
- Article
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
- Published in:
- Nature Genetics, 2010, v. 42, n. 3, p. 203, doi. 10.1038/ng.534
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- Publication type:
- Article
Personalized copy number and segmental duplication maps using next-generation sequencing.
- Published in:
- Nature Genetics, 2009, v. 41, n. 10, p. 1061, doi. 10.1038/ng.437
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- Publication type:
- Article
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
- Published in:
- Nature Genetics, 2009, v. 41, n. 2, p. 160, doi. 10.1038/ng.292
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- Publication type:
- Article
A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
- Published in:
- Nature Genetics, 2008, v. 40, n. 3, p. 322, doi. 10.1038/ng.93
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- Publication type:
- Article
Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes.
- Published in:
- PLoS Genetics, 2011, v. 7, n. 11, p. 1, doi. 10.1371/journal.pgen.1002334
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- Publication type:
- Article
Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 5, p. 1, doi. 10.1371/journal.pgen.1000962
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- Publication type:
- Article
Expressivism and Moral Dilemmas: A Response to Marino.
- Published in:
- Ethical Theory & Moral Practice, 2011, v. 14, n. 4, p. 445, doi. 10.1007/s10677-010-9255-6
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- Publication type:
- Article
293. Optimizing the Efficacy of Spliceosome-Mediated RNA Trans-Splicing (SMaRT™) for Suicide Gene Therapy of Cervical Cancer
- Published in:
- 2005
- By:
- Publication type:
- Abstract
Philippine Security in the Age of Terror: National, Regional, and Global Challenges in the Post-9/11 World.
- Published in:
- 2010
- By:
- Publication type:
- Book Review
Improved assembly and variant detection of a haploid human genome using single‐molecule, high‐fidelity long reads.
- Published in:
- Annals of Human Genetics, 2020, v. 84, n. 2, p. 125, doi. 10.1111/ahg.12364
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- Publication type:
- Article
Evidence for opposing selective forces operating on human-specific duplicated TCAF genes in Neanderthals and humans.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25435-4
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- Publication type:
- Article
PHILIPPINE FOLLIES.
- Published in:
- 2017
- By:
- Publication type:
- Excerpt
US-Southeast Asia Relations: Obama Passes.
- Published in:
- Comparative Connections: A Triannual E-Journal on East Asian Bilateral Relations, 2014, v. 15, n. 1, p. 47
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- Publication type:
- Article
Gibbon genome and the fast karyotype evolution of small apes.
- Published in:
- Nature, 2014, v. 513, n. 7517, p. 195, doi. 10.1038/nature13679
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- Publication type:
- Article
A Step Forward in Understanding Treatment Approaches for Diabetic Macular Edema.
- Published in:
- 2023
- By:
- Publication type:
- journal article
Assessment of the DRCR Retina Network Approach to Management With Initial Observation for Eyes With Center-Involved Diabetic Macular Edema and Good Visual Acuity: A Secondary Analysis of a Randomized Clinical Trial.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Visual Field Changes Over 5 Years in Patients Treated With Panretinal Photocoagulation or Ranibizumab for Proliferative Diabetic Retinopathy.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Month 12 Outcomes After Treatment Change at Month 6 Among Poor Responders to Aflibercept or Bevacizumab in Eyes With Macular Edema Secondary to Central or Hemiretinal Vein Occlusion: A Secondary Analysis of the SCORE2 Study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Five-Year Outcomes of Panretinal Photocoagulation vs Intravitreous Ranibizumab for Proliferative Diabetic Retinopathy: A Randomized Clinical Trial.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Association of Baseline Visual Acuity and Retinal Thickness With 1-Year Efficacy of Aflibercept, Bevacizumab, and Ranibizumab for Diabetic Macular Edema.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Assessing the Effect of Personalized Diabetes Risk Assessments During Ophthalmologic Visits on Glycemic Control: A Randomized Clinical Trial.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Assessing the Effect of Personalized Diabetes Risk Assessments During Ophthalmologic Visits on Glycemic Control.
- Published in:
- JAMA Ophthalmology, 2015, v. 133, n. 8, p. 888, doi. 10.1001/jamaophthalmol.2015.1312
- By:
- Publication type:
- Article
Pilot Study of Individuals With Diabetic Macular Edema Undergoing Cataract Surgery.
- Published in:
- JAMA Ophthalmology, 2014, v. 132, n. 2, p. 224, doi. 10.1001/jamaophthalmol.2013.6209
- By:
- Publication type:
- Article
Four-Year Visual Outcomes in the Protocol W Randomized Trial of Intravitreous Aflibercept for Prevention of Vision-Threatening Complications of Diabetic Retinopathy.
- Published in:
- JAMA: Journal of the American Medical Association, 2023, v. 329, n. 5, p. 376, doi. 10.1001/jama.2022.25029
- By:
- Publication type:
- Article
Cancer centers and the National Cancer Institute.
- Published in:
- Cancer (0008543X), 1972, v. 29, n. 4, p. 823, doi. 10.1002/1097-0142(197204)29:4<823::AID-CNCR2820290405>3.0.CO;2-9
- By:
- Publication type:
- Article
Jesse P. Greenstein, Ph.D. (1902-1959).
- Published in:
- Cancer (0008543X), 1959, v. 12, n. 4, p. i, doi. 10.1002/1097-0142(195907/08)12:4<::AID-CNCR2820120402>3.0.CO;2-A
- By:
- Publication type:
- Article
XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients.
- Published in:
- Human Mutation, 2010, v. 31, n. 2, p. 167, doi. 10.1002/humu.21166
- By:
- Publication type:
- Article