These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

176 related articles for article (PubMed ID: 7649548)

  • 1. Mutations of the fibroblast growth factor receptor-3 gene in one familial and six sporadic cases of achondroplasia in Japanese patients.
    Ikegawa S; Fukushima Y; Isomura M; Takada F; Nakamura Y
    Hum Genet; 1995 Sep; 96(3):309-11. PubMed ID: 7649548
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia.
    Rousseau F; Bonaventure J; Legeai-Mallet L; Pelet A; Rozet JM; Maroteaux P; Le Merrer M; Munnich A
    Nature; 1994 Sep; 371(6494):252-4. PubMed ID: 8078586
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Common mutations in the fibroblast growth factor receptor 3 (FGFR 3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism.
    Bonaventure J; Rousseau F; Legeai-Mallet L; Le Merrer M; Munnich A; Maroteaux P
    Am J Med Genet; 1996 May; 63(1):148-54. PubMed ID: 8723101
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A glycine 375-to-cysteine substitution in the transmembrane domain of the fibroblast growth factor receptor-3 in a newborn with achondroplasia.
    Superti-Furga A; Eich G; Bucher HU; Wisser J; Giedion A; Gitzelmann R; Steinmann B
    Eur J Pediatr; 1995 Mar; 154(3):215-9. PubMed ID: 7758520
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Achondroplasia is defined by recurrent G380R mutations of FGFR3.
    Bellus GA; Hefferon TW; Ortiz de Luna RI; Hecht JT; Horton WA; Machado M; Kaitila I; McIntosh I; Francomano CA
    Am J Hum Genet; 1995 Feb; 56(2):368-73. PubMed ID: 7847369
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations of the fibroblast growth factor receptor-3 gene in achondroplasia.
    Rousseau F; Bonaventure J; Legeai-Mallet L; Pelet A; Rozet JM; Maroteaux P; Le Merrer M; Munnich A
    Horm Res; 1996; 45(1-2):108-10. PubMed ID: 8742128
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chinese achondroplasia is also defined by recurrent G380R mutations of the fibroblast growth factor receptor-3 gene.
    Niu DM; Hsiao KJ; Wang NH; Chin LS; Chen CH
    Hum Genet; 1996 Jul; 98(1):65-7. PubMed ID: 8682509
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mutations of the fibroblast growth factor receptor 3 gene in achondroplasia].
    Zhao P; Ma H; Wang Y; Mi Z; Wu Y; Jiang M; Gao H; Li Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Feb; 16(1):16-8. PubMed ID: 9949234
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and molecular characteristics of Thai patients with achondroplasia.
    Shotelersuk V; Ittiwut C; Srivuthana S; Wacharasindhu S; Aroonparkmongkol S; Mutirangura A; Poovorawan Y
    Southeast Asian J Trop Med Public Health; 2001 Jun; 32(2):429-33. PubMed ID: 11556601
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in fibroblast growth-factor receptor 3 in sporadic cases of achondroplasia occur exclusively on the paternally derived chromosome.
    Wilkin DJ; Szabo JK; Cameron R; Henderson S; Bellus GA; Mack ML; Kaitila I; Loughlin J; Munnich A; Sykes B; Bonaventure J; Francomano CA
    Am J Hum Genet; 1998 Sep; 63(3):711-6. PubMed ID: 9718331
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia.
    Shiang R; Thompson LM; Zhu YZ; Church DM; Fielder TJ; Bocian M; Winokur ST; Wasmuth JJ
    Cell; 1994 Jul; 78(2):335-42. PubMed ID: 7913883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasia.
    Tonoki H; Nakae J; Tajima T; Shinohara N; Monji J; Satoh S; Fujieda K
    Jpn J Hum Genet; 1995 Dec; 40(4):347-9. PubMed ID: 8851771
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation in the gene encoding the fibroblast growth factor receptor-3 in Korean children with achondroplasia.
    Yang SW; Kitoh H; Yamada Y; Goto H; Ogasawara N
    Acta Paediatr Jpn; 1998 Aug; 40(4):324-7. PubMed ID: 9745773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fibroblast growth factor receptor-3 as a therapeutic target for Achondroplasia--genetic short limbed dwarfism.
    Aviezer D; Golembo M; Yayon A
    Curr Drug Targets; 2003 Jul; 4(5):353-65. PubMed ID: 12816345
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia.
    Bellus GA; McIntosh I; Smith EA; Aylsworth AS; Kaitila I; Horton WA; Greenhaw GA; Hecht JT; Francomano CA
    Nat Genet; 1995 Jul; 10(3):357-9. PubMed ID: 7670477
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data.
    Tsai FJ; Tsai CH; Chang JG; Wu JY
    Am J Med Genet; 1999 Sep; 86(3):300-1. PubMed ID: 10482885
    [No Abstract]   [Full Text] [Related]  

  • 17. Analysis of the FGFR3 gene in Japanese patients with achondroplasia and hypochondroplasia.
    Katsumata N; Mikami S; Nagashima-Miyokawa A; Nimura A; Sato N; Horikawa R; Tanae A; Tanaka T
    Endocr J; 2000 Mar; 47 Suppl():S121-4. PubMed ID: 10890199
    [TBL] [Abstract][Full Text] [Related]  

  • 18. An uncommon G375C substitution in a newborn with achondroplasia.
    Addor MC; Gudinchet F; Truttmann A; Schorderet DF
    Genet Couns; 2000; 11(2):169-74. PubMed ID: 10893668
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.
    Vajo Z; Francomano CA; Wilkin DJ
    Endocr Rev; 2000 Feb; 21(1):23-39. PubMed ID: 10696568
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasia.
    Bonaventure J; Rousseau F; Legeai-Mallet L; Le Merrer M; Munnich A; Maroteaux P
    Acta Paediatr Suppl; 1996 Oct; 417():33-8. PubMed ID: 9055906
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.