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10. Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO. Lo Iacono N; Blair HC; Poliani PL; Marrella V; Ficara F; Cassani B; Facchetti F; Fontana E; Guerrini MM; Traggiai E; Schena F; Paulis M; Mantero S; Inforzato A; Valaperta S; Pangrazio A; Crisafulli L; Maina V; Kostenuik P; Vezzoni P; Villa A; Sobacchi C J Bone Miner Res; 2012 Dec; 27(12):2501-10. PubMed ID: 22836362 [TBL] [Abstract][Full Text] [Related]
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13. New knowledge on critical osteoclast formation and activation pathways from study of rare genetic diseases of osteoclasts: focus on the RANK/RANKL axis. Crockett JC; Mellis DJ; Scott DI; Helfrich MH Osteoporos Int; 2011 Jan; 22(1):1-20. PubMed ID: 20458572 [TBL] [Abstract][Full Text] [Related]
14. RANK-dependent autosomal recessive osteopetrosis: characterization of five new cases with novel mutations. Pangrazio A; Cassani B; Guerrini MM; Crockett JC; Marrella V; Zammataro L; Strina D; Schulz A; Schlack C; Kornak U; Mellis DJ; Duthie A; Helfrich MH; Durandy A; Moshous D; Vellodi A; Chiesa R; Veys P; Lo Iacono N; Vezzoni P; Fischer A; Villa A; Sobacchi C J Bone Miner Res; 2012 Feb; 27(2):342-51. PubMed ID: 22271396 [TBL] [Abstract][Full Text] [Related]
15. PDK1 is important lipid kinase for RANKL-induced osteoclast formation and function via the regulation of the Akt-GSK3β-NFATc1 signaling cascade. Xiao D; Zhou Q; Gao Y; Cao B; Zhang Q; Zeng G; Zong S J Cell Biochem; 2020 Nov; 121(11):4542-4557. PubMed ID: 32048762 [TBL] [Abstract][Full Text] [Related]
16. Osteoclasts from patients with autosomal dominant osteopetrosis type I caused by a T253I mutation in low-density lipoprotein receptor-related protein 5 are normal in vitro, but have decreased resorption capacity in vivo. Henriksen K; Gram J; Høegh-Andersen P; Jemtland R; Ueland T; Dziegiel MH; Schaller S; Bollerslev J; Karsdal MA Am J Pathol; 2005 Nov; 167(5):1341-8. PubMed ID: 16251418 [TBL] [Abstract][Full Text] [Related]
17. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. Frattini A; Orchard PJ; Sobacchi C; Giliani S; Abinun M; Mattsson JP; Keeling DJ; Andersson AK; Wallbrandt P; Zecca L; Notarangelo LD; Vezzoni P; Villa A Nat Genet; 2000 Jul; 25(3):343-6. PubMed ID: 10888887 [TBL] [Abstract][Full Text] [Related]
18. SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. Pangrazio A; Fasth A; Sbardellati A; Orchard PJ; Kasow KA; Raza J; Albayrak C; Albayrak D; Vanakker OM; De Moerloose B; Vellodi A; Notarangelo LD; Schlack C; Strauss G; Kühl JS; Caldana E; Lo Iacono N; Susani L; Kornak U; Schulz A; Vezzoni P; Villa A; Sobacchi C J Bone Miner Res; 2013 May; 28(5):1041-9. PubMed ID: 23280965 [TBL] [Abstract][Full Text] [Related]
19. RANKL coordinates cell cycle withdrawal and differentiation in osteoclasts through the cyclin-dependent kinase inhibitors p27KIP1 and p21CIP1. Sankar U; Patel K; Rosol TJ; Ostrowski MC J Bone Miner Res; 2004 Aug; 19(8):1339-48. PubMed ID: 15231022 [TBL] [Abstract][Full Text] [Related]
20. Disease status in autosomal dominant osteopetrosis type 2 is determined by osteoclastic properties. Chu K; Snyder R; Econs MJ J Bone Miner Res; 2006 Jul; 21(7):1089-97. PubMed ID: 16813529 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]