Pages that link to "Q48755346"
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The following pages link to Online Mendelian Inheritance in Man (OMIM). (Q48755346):
Displaying 50 items.
- Analyzing effects of naturally occurring missense mutations (Q21284966) (← links)
- Modeling effects of human single nucleotide polymorphisms on protein-protein interactions (Q24643464) (← links)
- UCbase & miRfunc: a database of ultraconserved sequences and microRNA function (Q24656355) (← links)
- ALAD porphyria is a conformational disease (Q24680334) (← links)
- Sequence variation in G-protein-coupled receptors: analysis of single nucleotide polymorphisms (Q24804913) (← links)
- Differential gene expression in anatomical compartments of the human eye. (Q24814005) (← links)
- Bias of selection on human copy-number variants (Q25257186) (← links)
- Future vision of the GDB human genome database (Q28141392) (← links)
- Rapid screening for improved solubility of small human proteins produced as fusion proteins in Escherichia coli (Q28345106) (← links)
- Identification and characterization of lncRNA mediated transcriptional dysregulation dictates lncRNA roles in glioblastoma (Q28397795) (← links)
- Human cancer protein-protein interaction network: a structural perspective (Q28472174) (← links)
- Chapter 3: Small molecules and disease (Q28484584) (← links)
- Resources for functional genomics studies in Drosophila melanogaster (Q28657863) (← links)
- Collection of variation causing disease--the Human Variome Project (Q28710284) (← links)
- A corpus for plant-chemical relationships in the biomedical domain (Q28829710) (← links)
- RefSeq and LocusLink: NCBI gene-centered resources (Q29547259) (← links)
- Structural and functional impact of cancer-related missense somatic mutations (Q30404960) (← links)
- Chapter 2: Data-driven view of disease biology (Q30585186) (← links)
- AnsNGS: An Annotation System to Sequence Variations of Next Generation Sequencing Data for Disease-Related Phenotypes (Q30620435) (← links)
- Exploring histones and their relatives with the Histone Sequence Database (Q30661958) (← links)
- The Eukaryotic Promoter Database, EPD: new entry types and links to gene expression data (Q30667284) (← links)
- Introduction to resources in molecular genetics (Q30677311) (← links)
- Association of genes to genetically inherited diseases using data mining (Q30692445) (← links)
- WormQTLHD--a web database for linking human disease to natural variation data in C. elegans (Q30692701) (← links)
- NCBI Reference Sequence project: update and current status (Q30722205) (← links)
- Use of molecular variation in the NCBI dbSNP database (Q30829552) (← links)
- Improved locus-specific database for OPA1 mutations allows inclusion of advanced clinical data. (Q30854410) (← links)
- Identification of brain proteins that interact with 2-methylnorharman. An analog of the parkinsonian-inducing toxin, MPP . (Q30868164) (← links)
- Identifying core gene modules in glioblastoma based on multilayer factor-mediated dysfunctional regulatory networks through integrating multi-dimensional genomic data (Q30887798) (← links)
- A comprehensive curated resource for follicle stimulating hormone signaling. (Q31034780) (← links)
- Online genetic databases informing human genome epidemiology (Q33289920) (← links)
- SNP and mutation data on the web - hidden treasures for uncovering (Q33351962) (← links)
- Clique-based data mining for related genes in a biomedical database (Q33476564) (← links)
- Analysis of AML genes in dysregulated molecular networks (Q33504376) (← links)
- Recent advances in predicting gene-disease associations (Q33631987) (← links)
- Similarly strong purifying selection acts on human disease genes of all evolutionary ages (Q33633483) (← links)
- An integrated approach to inferring gene-disease associations in humans (Q33669063) (← links)
- When the human viral infectome and diseasome networks collide: towards a systems biology platform for the aetiology of human diseases. (Q33799911) (← links)
- Central mutation databases--a review (Q33804818) (← links)
- Online medical genetics resources: a US perspective (Q33805206) (← links)
- MyGeneFriends: A Social Network Linking Genes, Genetic Diseases, and Researchers (Q33861503) (← links)
- Saturation of the Human Phenome (Q33885880) (← links)
- IthaGenes: an interactive database for haemoglobin variations and epidemiology (Q33945880) (← links)
- Genestrace: phenomic knowledge discovery via structured terminology. (Q33950144) (← links)
- Are splicing mutations the most frequent cause of hereditary disease? (Q33985993) (← links)
- An integrative approach to ortholog prediction for disease-focused and other functional studies (Q34006468) (← links)
- Systems pharmacology of arrhythmias (Q34111154) (← links)
- miRWalk – Database: Prediction of possible miRNA binding sites by “walking” the genes of three genomes (Q34186822) (← links)
- "Guilt by association" is the exception rather than the rule in gene networks (Q34220929) (← links)
- Large-scale functional organization of long-range chromatin interaction networks (Q34275017) (← links)