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PubMed 17345627 Over-expression of BMP4 and BMP5 in a child with axial skeletal malformations and heterotopic ossification: a new syndrome. Bone morphogenetic proteins (BMPs) are a highly conserved class of signaling 1.4 KB 2017-09-11 49 36 2021-12-05
PubMed 18165598 The differential effects of bupivacaine and lidocaine on prostaglandin E2 release, cyclooxygenase gene expression and pain in a clinical pain model. BACKGROUND: In addition to blocking nociceptive inp 1.75 KB 2015-11-23 26 37 2021-12-05
PubMed 18179903 Mutation analysis of CHRNA1, CHRNB1, CHRND, and RAPSN genes in multiple pterygium syndrome/fetal akinesia patients. Multiple pterygium syndromes (MPS) comprise a group of multiple congenital anomaly d 1.41 KB 2015-11-23 26 38 2021-12-05
PubMed 18366737 The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. BACKGROUND: Fumarate hydratase (HGNC approv 2.43 KB 2015-11-24 26 40 2021-12-05
PubMed 18507837 Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort. INTRODUCTION: Somatic alterations have been shown to correla 1.99 KB 2015-11-24 26 42 2021-12-05
PubMed 18593936 Curcumin decreases specificity protein expression in bladder cancer cells. Curcumin is the active component of tumeric, and this polyphenolic compound has been extensively investigated as an anticance 1.6 KB 2015-11-24 26 50 2021-12-05
PubMed 19160446 P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? The chromosomal region 12q24 has been previously implicated by linkage studies of both bipolar disorder and unipolar mood disorder 1.27 KB 2025-10-02 29 21 2021-12-05
PubMed 19508969 Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). BACKGROUND: Nephronophthisis (NPHP), a rare recessive cystic kidney disease, is the most frequent g 1.96 KB 2015-11-25 27 53 2021-12-05
PubMed 19549709 Efficacy of everolimus (RAD001) in patients with advanced NSCLC previously treated with chemotherapy alone or with chemotherapy and EGFR inhibitors. BACKGROUND: Treatment options are scarce in pretrea 1.57 KB 2015-11-25 25 33 2021-12-05
PubMed 19779499 Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family. Hypokalaemic periodic paralysis (HypoPP) is an autosomal dominant disorder, which is charact 1.24 KB 2015-11-25 25 23 2021-12-05