Reciprocal relationship in gene expression between FGFR1 and FGFR3: implication for tumorigenesisJANG, Jun-Hyeog.Oncogene (Basingstoke). 2005, Vol 24, Num 5, pp 945-948, issn 0950-9232, 4 p.Article

Targeting FGFR3 in multiple myeloma: inhibition of t(4;14)-positive cells by SU5402 and PD173074GRAND, E. K; CHASE, A. J; HEATH, C et al.Leukemia. 2004, Vol 18, Num 5, pp 962-966, issn 0887-6924, 5 p.Article

Thanatophoric Dysplasia Caused by Double Missense FGFR3 MutationsPANNIER, Stéphanie; MARTINOVIC, Jelena; HEUERTZ, Solange et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 6, pp 1296-1301, issn 1552-4825, 6 p.Article

FGFR3 and PIK3CA mutations in stucco keratosis and dermatosis papulosa nigraHAFNER, C; LANDTHALER, M; MENTZEL, T et al.British journal of dermatology (1951). 2010, Vol 162, Num 3, pp 508-512, issn 0007-0963, 5 p.Article

Identification of ID-1 as a potential target gene of MMSET in multiple myelomaHUDLEBUSCH, Heidi Rye; THEILGAARD-MÖNCH, Kim; LODAHL, Marianne et al.British journal of haematology. 2005, Vol 130, Num 5, pp 700-708, issn 0007-1048, 9 p.Article

An activating Fgfr3 mutation affects trabecular bone formation via a paracrine mechanism during growthMUGNIERY, Emilie; DACQUIN, Romain; MARTY, Caroline et al.Human molecular genetics (Print). 2012, Vol 21, Num 11, pp 2503-2513, issn 0964-6906, 11 p.Article

Directionally specific paracrine communication mediated by epithelial FGF9 to stromal FGFR3 in two-compartment premalignant prostate tumorsCHENGLIU JIN; FEN WANG; XIAOCHONG WU et al.Cancer research (Baltimore). 2004, Vol 64, Num 13, pp 4555-4562, issn 0008-5472, 8 p.Article

Growth references for height, weight, and head circumference for Argentine children with achondroplasiaDEL PINO, Mariana; FANO, Virginia; LEJARRAGA, Horacio et al.European journal of pediatrics. 2011, Vol 170, Num 4, pp 453-459, issn 0340-6199, 7 p.Article

Tumour formation by single fibroblast growth factor receptor 3-positive rhabdomyosarcoma-initiating cellsHIROTSU, M; SETOGUCHI, T; MATSUNOSHITA, Y et al.British journal of cancer. 2009, Vol 101, Num 12, pp 2030-2037, issn 0007-0920, 8 p.Article

Disruption of a Sox9―β-catenin circuit by mutant Fgfr3 in thanatophoric dysplasia type IISHUNG, Chia-Yi; OTA, Sara; ZHOU, Zi-Qiang et al.Human molecular genetics (Print). 2012, Vol 21, Num 21, pp 4628-4644, issn 0964-6906, 17 p.Article

Étude préliminaire des mutations des gènes p53 et FGFR3 sur le culot urinaire des tumeurs de la vessie = Preliminary study of p53 and FGFR3 gene mutations in the urine for bladder tumorsNOËL, N; COUTEAU, J; MAILLET, G et al.Progrès en urologie (Paris). 2013, Vol 23, Num 1, pp 29-35, issn 1166-7087, 7 p.Article

Mutational activation of FGFR3: no involvement in the development of renal cell carcinomaSTOEHR, C. G; STOEHR, R; HARTMANN, A et al.Journal of cancer research and clinical oncology. 2012, Vol 138, Num 2, pp 359-361, issn 0171-5216, 3 p.Article

Mise au point sur la mutation FGFR3 et le phénotype épigénétique MRES dans la carcinogenèse vésicale = Update on FGFR3 mutation and MRES phenotype in urothelial carcinogenesisMASSON-LECOMTE, A; VORDOS, D; DE LA TAILLE, A et al.Progrès en urologie (Paris). 2013, Vol 23, Num 2, pp 96-98, issn 1166-7087, 3 p.Article

No Evidence of FGFR3 Mutations in Prostate CancerZUIVERLOON, Tahlita C. M; BOORMANS, Joost L; TRAPMAN, Jan et al.The Prostate. 2011, Vol 71, Num 6, pp 637-641, issn 0270-4137, 5 p.Article

Non-invasive prenatal detection of achondroplasia in size-fractionated cell-free DNA by MALDI-TOF MS assayYING LI; PAGE-CHRISTIAENS, Godelieve C. M. L; GILLE, Johan J. P et al.Prenatal diagnosis. 2007, Vol 27, Num 1, pp 11-17, issn 0197-3851, 7 p.Article

Acanthosis nigricans nævoïde ou « RAVEN » (rounded and velvety epidermal nevus): trois cas = Nevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal nevus): Three casesPETIT, A; LEMARCHAND-VENENCIE, F; PINQUIER, L et al.Annales de dermatologie et de vénéréologie. 2012, Vol 139, Num 3, pp 183-188, issn 0151-9638, 6 p.Article

Achondroplasia With Synostosis of Multiple SuturesGEORGOULIS, George; ALEXIOU, George; PRODROMOU, Neofytos et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 8, pp 1969-1971, issn 1552-4825, 3 p.Article

The novel JAK inhibitor AZD1480 blocks STAT3 and FGFR3 signaling, resulting in suppression of human myeloma cell growth and survivalSCUTO, A; KREJCI, P; KRETZNER, L et al.Leukemia. 2011, Vol 25, Num 3, pp 538-550, issn 0887-6924, 13 p.Article

Mild Isolated Craniosynostosis Due To a Novel FGFR3 Mutation, p.Ala334ThrBARROSO, Eva; PEREZ-CARRIZOSA, Virginia; GARCIA-RECUERO, Ignacio et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 3050-3053, issn 1552-4825, 4 p.Article

Clinical and Molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 (FGFR3) in PortugalALMEIDA, M. R; CAMPOS-XAVIER, A. B; SOUSA, S et al.Clinical genetics. 2009, Vol 75, Num 2, pp 150-156, issn 0009-9163, 7 p.Article

Clinical significance of cyclin D1, fibroblast growth factor receptor 3, and p53 immunohistochemistry in plasma cell myeloma treated with a thalidomide-based regimenKELLEY, Todd W; BAZ, Rachid; HUSSEIN, Mohamad et al.Human pathology. 2009, Vol 40, Num 3, pp 405-412, issn 0046-8177, 8 p.Article

FGFR3 and PIK3CA mutations are involved in the molecular pathogenesis of solar lentigoHAFNER, C; STOEHR, R; VAN OERS, J. M. M et al.British journal of dermatology (1951). 2009, Vol 160, Num 3, pp 546-551, issn 0007-0963, 6 p.Article

Mutant fibroblast growth factor receptor 3 induces intracellular signaling and cellular transformation in a cell type- and mutation-specific mannerDI MARTINO, E; L'HOTE, C. G; KENNEDY, W et al.Oncogene (Basingstoke). 2009, Vol 28, Num 48, pp 4306-4316, issn 0950-9232, 11 p.Article

Chromosome 9 deletions are more frequent than FGFR3 mutations in flat urothelial hyperplasias of the bladderVAN OERS, Johanna M. M; ADAM, Christoph; KNUECHEL, Ruth et al.International journal of cancer. 2006, Vol 119, Num 5, pp 1212-1215, issn 0020-7136, 4 p.Article

Medial temporal lobe dysgenesis in hypochondroplasiaKANNU, Peter; HAYES, Ian M; MANDELSTAM, Simone et al.American journal of medical genetics. 2005, Vol 138A, Num 4, pp 389-391, issn 0148-7299, 3 p.Article