| scholarly article | Q13442814 |
| P50 | author | Nicholas J. Schork | Q63005429 |
| P2093 | author name string | Ali Torkamani | |
| P2860 | cites work | Initial sequencing and analysis of the human genome | Q21045365 |
| GeneWise and Genomewise | Q21061201 | ||
| Predicting deleterious amino acid substitutions | Q22065761 | ||
| The Sequence of the Human Genome | Q22065842 | ||
| Are rare variants responsible for susceptibility to complex diseases? | Q22337172 | ||
| The protein kinase complement of the human genome | Q24324497 | ||
| The Pfam protein families database | Q24599089 | ||
| The Croonian Lecture 1997. The phosphorylation of proteins on tyrosine: its role in cell growth and disease | Q24677033 | ||
| The amino-acid mutational spectrum of human genetic disease | Q24793270 | ||
| The PROSITE database. | Q25257913 | ||
| Crystallographic and solution studies of an activation loop mutant of the insulin receptor tyrosine kinase: insights into kinase mechanism | Q27629016 | ||
| Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies | Q27824769 | ||
| Characterization of single-nucleotide polymorphisms in coding regions of human genes | Q28138557 | ||
| Somatic mutation of the Peutz-Jeghers syndrome gene, LKB1/STK11, in malignant melanoma | Q28141888 | ||
| A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms | Q28203288 | ||
| InterProScan--an integration platform for the signature-recognition methods in InterPro | Q29547336 | ||
| The druggable genome | Q29547361 | ||
| PANTHER: a library of protein families and subfamilies indexed by function | Q29547480 | ||
| Prediction of deleterious human alleles | Q29614367 | ||
| On the allelic spectrum of human disease | Q29616298 | ||
| The pleckstrin homology domain of Bruton tyrosine kinase interacts with protein kinase C | Q30047790 | ||
| Analysis and prediction of functionally important sites in proteins | Q33267765 | ||
| A single amino acid substitution in the activation loop defines the decoy characteristic of VEGFR-1/FLT-1 | Q34333820 | ||
| Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2. | Q34381015 | ||
| PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level. | Q35557599 | ||
| Kinomics: methods for deciphering the kinome | Q36079218 | ||
| Growth factors and cancer | Q36441643 | ||
| Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects. | Q37585393 | ||
| Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas | Q45345804 | ||
| KinMutBase: a registry of disease-causing mutations in protein kinase domains | Q46439138 | ||
| Human Gene Mutation Database (HGMD): 2003 update | Q47903166 | ||
| Selective Pressures at a Codon-level Predict Deleterious Mutations in Human Disease Genes | Q57837778 | ||
| Selective constraints, amino acid composition, and the rate of protein evolution | Q73606206 | ||
| The common variants/multiple disease hypothesis of common complex genetic disorders | Q76318556 | ||
| Sequence-based prediction of pathological mutations | Q80610312 | ||
| The eukaryotic protein kinase superfamily: kinase (catalytic) domain structure and classification 1 | Q107343694 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 49-58 | |
| P577 | publication date | 2007-05-11 | |
| P1433 | published in | Genomics | Q5533503 |
| P1476 | title | Distribution analysis of nonsynonymous polymorphisms within the human kinase gene family. | |
| P478 | volume | 90 |
| Q41125698 | Analysis of somatic mutations across the kinome reveals loss-of-function mutations in multiple cancer types |
| Q37478203 | Analytical methods for inferring functional effects of single base pair substitutions in human cancers |
| Q31033195 | Characterization of pathogenic germline mutations in human protein kinases |
| Q36752464 | Congenital disease SNPs target lineage specific structural elements in protein kinases |
| Q34324927 | Disease-related mutations predicted to impact protein function |
| Q28394818 | Getting personalized cancer genome analysis into the clinic: the challenges in bioinformatics |
| Q42352597 | HUMAN KINASES DISPLAY MUTATIONAL HOTSPOTS AT COGNATE POSITIONS WITHIN CANCER. |
| Q42409589 | Investigating the linkage between disease-causing amino acid variants and their effect on protein stability and binding |
| Q34088851 | Kinase mutations in human disease: interpreting genotype-phenotype relationships |
| Q36324695 | Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease |
| Q64923711 | Orange is the new black: Kinases are the new master regulators of tumor suppression. |
| Q37448909 | Predicting potentially functional SNPs in drug-response genes. |
| Q38987589 | Structure-functional prediction and analysis of cancer mutation effects in protein kinases. |
| Q89521806 | Variation benchmark datasets: update, criteria, quality and applications |
Search more.