| P2093 | author name string | Zhang Y | |
| | Post JC | |
| | Ehrlich GD | |
| | Gorry MC | |
| P2860 | cites work | The human fibroblast growth factor receptor genes: a common structural arrangement underlies the mechanisms for generating receptor forms that differ in their third immunoglobulin domain | Q24306718 |
| | Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome | Q24310222 |
| | Fibroblast growth factor receptor 3 is a negative regulator of bone growth | Q24322706 |
| | Cloning and characterization of multiple human genes and cDNAs encoding highly related type II keratin 6 isoforms | Q28118270 |
| | Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability | Q28270811 |
| | Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes | Q28300015 |
| | Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras | Q28609649 |
| | Ligand-independent activation of fibroblast growth factor receptors by point mutations in the extracellular, transmembrane, and kinase domains | Q28609650 |
| | Multiple interdependent sequence elements control splicing of a fibroblast growth factor receptor 2 alternative exon | Q28609655 |
| | Genomic structure and complete sequence of the human FGFR4 gene | Q32128060 |
| | Single base mutation in the pro alpha 2(I) collagen gene that causes efficient splicing of RNA from exon 27 to exon 29 and synthesis of a shortened but in-frame pro alpha 2(I) chain | Q33633029 |
| | Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development. | Q34427515 |
| | PCR amplification of up to 35-kb DNA with high fidelity and high yield from lambda bacteriophage templates | Q35100239 |
| | Alternative mRNA splicing | Q35237442 |
| | Exon/intron structure of aldehyde dehydrogenase genes supports the "introns-late" theory. | Q36240600 |
| | K-sam gene encodes secreted as well as transmembrane receptor tyrosine kinase | Q36930426 |
| | Differential expression of the fibroblast growth factor receptor (FGFR) multigene family in normal human adult tissues | Q38474392 |
| | Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome | Q39425084 |
| | Fibroblast growth factors in mammalian development | Q40425812 |
| | Fibroblast-growth-factor receptor mutations in human skeletal disorders | Q40960541 |
| | Sequence requirements for regulated RNA splicing of the human fibroblast growth factor receptor-1 alpha exon | Q41134892 |
| | Fibroblast growth factors, their receptors and receptor disorders | Q41491086 |
| | The heparan sulfate-fibroblast growth factor family: diversity of structure and function. | Q41680432 |
| | Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson—Weiss syndrome | Q42677643 |
| | Unique expression pattern of the FGF receptor 3 gene during mouse organogenesis | Q46371402 |
| | The evolution of an intron: analysis of a long, deletion-prone intron in the human dystrophin gene | Q47333248 |
| | FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome | Q48030449 |
| | Conserved use of a non-canonical 5' splice site (/GA) in alternative splicing by fibroblast growth factor receptors 1, 2 and 3. | Q48038229 |
| | Genomic organization of the human fibroblast growth factor receptor 3 (FGFR3) gene and comparative sequence analysis with the mouse Fgfr3 gene | Q48051872 |
| | Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3. | Q49042849 |
| | Structural and Functional Diversity in the FGf Receptor Multigene Family | Q55919452 |
| | Genomic structure of the downstream part of the human FLT3 gene: exon/intron structure conservation among genes encoding receptor tyrosine kinases (RTK) of subclass III | Q72120035 |
| | Neuronal adhesion molecules signal through FGF receptor | Q72580622 |
| | Two gene duplication events in the human and primate dopamine D5 receptor gene family | Q72630169 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | human fibroblast | Q101404861 |
| P304 | page(s) | 69-79 | |
| P577 | publication date | 1999-04-01 | |
| P1433 | published in | Gene | Q5531065 |
| P1476 | title | Genomic organization of the human fibroblast growth factor receptor 2 (FGFR2) gene and comparative analysis of the human FGFR gene family | |
| P478 | volume | 230 | |