Research Resource: Comprehensive Expression Atlas of the Fibroblast Growth Factor System in Adult Mouse

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works

FGF-21 as a novel metabolic regulator

Kharitonenkov, A., Shiyanova, T. L., Koester, A., Ford, A. M., Micanovic, R., Galbreath, E. J., Sandusky, G. E., Hammond, L. J., Moyers, J. S., Owens, R. A., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23606 · Cited by 2,125 · see citing works

Suppression of Aging in Mice by the Hormone Klotho

Kurosu, H., Yamamoto, M., Clark, J. D., Pastor, J. V., Nandi, A., Gurnani, P., McGuinness, O. P., Chikuda, H., Yamaguchi, M., Kawaguchi, H., et al. (2005) · Science · doi:10.1126/science.1112766 · Cited by 1,935 · see citing works

Klotho converts canonical FGF receptor into a specific receptor for FGF23

Urakawa, I., Yamazaki, Y., Shimada, T., Iijima, K., Hasegawa, H., Okawa, K., Fujita, T., Fukumoto, S., & Yamashita, T. (2006) · Nature · doi:10.1038/nature05315 · Cited by 1,871 · see citing works

Fibroblast growth factor 15 functions as an enterohepatic signal to regulate bile acid homeostasis

Inagaki, T., Choi, M., Moschetta, A., Peng, L., Cummins, C. L., McDonald, J. G., Luo, G., Jones, S. A., Goodwin, B., Richardson, J. A., et al. (2005) · Cell Metabolism · doi:10.1016/j.cmet.2005.09.001 · Cited by 1,865 · see citing works

Endocrine Regulation of the Fasting Response by PPARα-Mediated Induction of Fibroblast Growth Factor 21

Inagaki, T., Dutchak, P., Zhao, G., Ding, X., Gautron, L., Parameswara, V., Li, Y., Goetz, R., Mohammadi, M., Esser, V., et al. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.003 · Cited by 1,504 · see citing works

Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism.

Shimada, T., Kakitani, M., Yamazaki, Y., Hasegawa, H., Takeuchi, Y., Fujita, T., Fukumoto, S., Tomizuka, K., & Yamashita, T. (2004) · Journal of Clinical Investigation · doi:10.1172/jci19081 · Cited by 1,503 · see citing works

Hepatic Fibroblast Growth Factor 21 Is Regulated by PPARα and Is a Key Mediator of Hepatic Lipid Metabolism in Ketotic States

Badman, M. K., Pissios, P., Kennedy, A. R., Koukos, G., Flier, J. S., & Maratos-Flier, E. (2007) · Cell Metabolism · doi:10.1016/j.cmet.2007.05.002 · Cited by 1,495 · see citing works

Cloning and characterization of FGF23 as a causative factor of tumor-induced osteomalacia

Shimada, T., Mizutani, S., Muto, T., Yoneya, T., Hino, R., Takeda, S., Takeuchi, Y., Fujita, T., Fukumoto, S., & Yamashita, T. (2001) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.101545198 · Cited by 1,391 · see citing works

Targeted ablation of Fgf23 demonstrates an essential physiological role of FGF23 in phosphate and vitamin D metabolism

Shimada, T., Kakitani, M., Yamazaki, Y., et al. (2004) · Journal of Clinical Investigation · doi:10.1172/jci200419081 · Cited by 1,368 · see citing works

Regulation of Fibroblast Growth Factor-23 Signaling by Klotho*

Kurosu, H., Ogawa, Y., Miyoshi, M., Yamamoto, M., Nandi, A., Rosenblatt, K., Baum, M., Schiavi, S., Hu, M.-C., Moe, O., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.c500457200 · Cited by 1,356 · see citing works

Fgf10 is essential for limb and lung formation

Sekine, K., Ohuchi, H., Fujiwara, M., Yamasaki, M., Yoshizawa, T., Sato, T., Yagishita, N., Matsui, D., Koga, Y., Itoh, N., et al. (1999) · Nature Genetics · doi:10.1038/5096 · Cited by 1,283 · see citing works

Structural and functional diversity in the FGF receptor multigene family.

Johnson, D. E., & Williams, L. (1993) · Advances in Cancer Research · doi:10.1016/s0065-230x(08)60821-0 · Cited by 1,270 · see citing works

Receptor Specificity of the Fibroblast Growth Factor Family

Zhang, X., Ibrahimi, O. A., Olsen, S. K., Umemori, H., Mohammadi, M., & Ornitz, D. M. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601252200 · Cited by 1,164 · see citing works

Evolution of the Fgf and Fgfr gene families.

Itoh, N., & Ornitz, D. (2004) · Trends in Genetics · doi:10.1016/j.tig.2004.08.007 · Cited by 1,123 · see citing works

Anatomical profiling of nuclear receptor expression reveals a hierarchical transcriptional network

Bookout, A. L., Jeong, Y., Downes, M., Yu, R. T., Evans, R. M., & Mangelsdorf, D. J. (2006) · Cell · doi:10.1016/j.cell.2006.06.049 · Cited by 1,015 · see citing works

The parathyroid is a target organ for FGF23 in rats

Ben‐Dov, I. Z., Galitzer, H., Lavi-Moshayoff, V., Goetz, R. M., Kuro‐o, M., Mohammadi, M., Sirkis, R., Naveh‐Many, T., & Silver, J. (2007) · Journal of Clinical Investigation · doi:10.1172/jci32409 · Cited by 951 · see citing works

Identification of a novel FGF, FGF-21, preferentially expressed in the liver

Nishimura, T., Nakatake, Y., Konishi, M., & Itoh, N. (2000) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(00)00067-1 · Cited by 847 · see citing works

Localisation of a fibroblast growth factor and its effect alone and with hydrocortisone on 3T3 cell growth

Gospodarowicz, D. (1974) · Nature · doi:10.1038/249123a0 · Cited by 788 · see citing works

Determination of ligand-binding specificity by alternative splicing: two distinct growth factor receptors encoded by a single gene.

Miki, T., Bottaro, D., Fleming, T., Smith, C. L., Burgess, W., Chan, A., & Aaronson, S. (1992) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.89.1.246 · Cited by 757 · see citing works

Tissue-specific Expression of βKlotho and Fibroblast Growth Factor (FGF) Receptor Isoforms Determines Metabolic Activity of FGF19 and FGF21

Kurosu, H., Choi, M., Ogawa, Y., Dickson, A. S., Goetz, R., Eliseenkova, A. V., Mohammadi, M., Rosenblatt, K. P., Kliewer, S. A., & Kuro-o, M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m704165200 · Cited by 748 · see citing works

Structural basis for fibroblast growth factor receptor activation

Mohammadi, M., Olsen, S. K., & Ibrahimi, O. A. (2005) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2005.01.008 · Cited by 737 · see citing works

Regulation of Oxidative Stress by the Anti-aging Hormone Klotho*♦

Yamamoto, M., Clark, J. D., Pastor, J. V., Gurnani, P., Nandi, A., Kurosu, H., Miyoshi, M., Ogawa, Y., Castrillón, D. H., Rosenblatt, K. P., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m509039200 · Cited by 727 · see citing works

FGF10 acts as a major ligand for FGF receptor 2 IIIb in mouse multi-organ development.

Ohuchi, H., Hori, Y., Yamasaki, M., Harada, H., Sekine, K., Kato, S., & Itoh, N. (2000) · Biochemical and Biophysical Research Communications - BBRC · doi:10.1006/bbrc.2000.3721 · Cited by 663 · see citing works

βKlotho is required for metabolic activity of fibroblast growth factor 21

Ogawa, Y., Kurosu, H., Yamamoto, M., Nandi, A., Rosenblatt, K. P., Goetz, R., Eliseenkova, A. V., Mohammadi, M., & Kuro-o, M. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701600104 · Cited by 617 · see citing works

Fibroblast Growth Factor 19 Increases Metabolic Rate and Reverses Dietary and Leptin-Deficient Diabetes

Fu, L., John, L. M., Adams, S. H., Yu, X. X., Tomlinson, E., Renz, M. E., Williams, P. M., Soriano, R. H., Corpuz, R. T., Moffat, B., et al. (2004) · Endocrinology · doi:10.1210/en.2003-1671 · Cited by 580 · see citing works

Transgenic Mice Expressing Human Fibroblast Growth Factor-19 Display Increased Metabolic Rate and Decreased Adiposity

Tomlinson, E., Fu, L., John, L., Hultgren, B., Huang, X., Renz, M., Stephan, J. P., Tsai, S. P., Powell-Braxton, L., French, D., et al. (2002) · Endocrinology · doi:10.1210/endo.143.5.8850 · Cited by 576 · see citing works

Identification of a Novel Fibroblast Growth Factor, FGF-23, Preferentially Expressed in the Ventrolateral Thalamic Nucleus of the Brain

Yamashita, T., Yoshioka, M., & Itoh, N. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3696 · Cited by 553 · see citing works

Molecular Insights into the Klotho-Dependent, Endocrine Mode of Action of Fibroblast Growth Factor 19 Subfamily Members

Goetz, R., Beenken, A., Ibrahimi, O., Kalinina, J., Olsen, S., Eliseenkova, A. V., Xu, C.-F., Neubert, T., Zhang, F.-M., Linhardt, R., et al. (2007) · Molecular and Cellular Biology · doi:10.1128/mcb.02249-06 · Cited by 544 · see citing works

FGFR‐4, a novel acidic fibroblast growth factor receptor with a distinct expression pattern.

Partanen, J., Mäkelä, T., Eerola, E., Korhonen, J., Hirvonen, H., Claesson-Welsh, L., & Alitalo, K. (1991) · EMBO Journal · doi:10.1002/j.1460-2075.1991.tb07654.x · Cited by 511 · see citing works

An oncogene isolated by transfection of Kaposi's sarcoma DNA encodes a growth factor that is a member of the FGF family

Bovi, P. D., Curatola, A. M., Kern, F. G., Greco, A., Ittmann, M., & Basilico, C. (1987) · Cell · doi:10.1016/0092-8674(87)90331-x · Cited by 507 · see citing works

Regulation of Fibroblastic Growth Factor 23 Expression but Not Degradation by PHEX

Liu, S., Guo, R., Simpson, L. G., Xiao, Z.-S., Burnham, C. E., & Quarles, L. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304544200 · Cited by 505 · see citing works

Fibroblast Growth Factor-21 Improves Pancreatic β-Cell Function and Survival by Activation of Extracellular Signal–Regulated Kinase 1/2 and Akt Signaling Pathways

Wente, W., Efanov, A. M., Brenner, M. B., Kharitonenkov, A., Koster, A. M., Sandusky, G. E., Sewing, S., Treinies, I., Zitzer, H., & Gromada, J. (2006) · Diabetes · doi:10.2337/db05-1435 · Cited by 497 · see citing works

Klotho, a Gene Related to a Syndrome Resembling Human Premature Aging, Functions in a Negative Regulatory Circuit of Vitamin D Endocrine System

Tsujikawa, H., Kurotaki, Y., Fujimori, T., Fukuda, K., & Nabeshima, Y. (2003) · Molecular Endocrinology · doi:10.1210/me.2003-0048 · Cited by 490 · see citing works

FGFR-3 and FGFR-4 function cooperatively to direct alveogenesis in the murine lung

Weinstein, M. B., Xu, X., Ohyama, K., & Deng, C. (1998) · Development · doi:10.1242/dev.125.18.3615 · Cited by 485 · see citing works

Molecular Cloning of a Novel Cytokine cDNA Encoding the Ninth Member of the Fibroblast Growth Factor Family, which has a Unique Secretion Property

Miyamoto, M., Naruo, K., Seko, C., Matsumoto‐Yoshitomi, S., Kondo, T., & Kurokawa, T. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.7.4251-4259.1993 · Cited by 422 · see citing works

Fibroblast growth factors and their receptors in the central nervous system

Reuß, B., & Halbach, O. V. B. U. (2003) · Cell and Tissue Research · doi:10.1007/s00441-003-0756-7 · Cited by 412 · see citing works

Functional evolutionary history of the mouse Fgf gene family

Itoh, N., & Ornitz, D. M. (2007) · Developmental Dynamics · doi:10.1002/dvdy.21388 · Cited by 409 · see citing works

1α,25-Dihydroxyvitamin D3upregulates FGF23 gene expression in bone: the final link in a renal-gastrointestinal-skeletal axis that controls phosphate transport

Kolek, O. I., Hines, E. R., Jones, M. D., LeSueur, L., Lipko, M. A., Kiela, P. R., Collins, J. F., Haussler, M. R., & Ghishan, F. K. (2005) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00243.2005 · Cited by 408 · see citing works

High‐Throughput Real‐Time Quantitative Reverse Transcription PCR

Bookout, A. L., Cummins, C. L., Mangelsdorf, D. J., Pesola, J. M., & Kramer, M. F. (2006) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb1508s73 · Cited by 401 · see citing works

Cloning and characterization of an androgen-induced growth factor essential for the androgen-dependent growth of mouse mammary carcinoma cells.

Tanaka, A., Miyamoto, K., Minamino, N., Takeda, M., Sato, B., Matsuo, H., & Matsumoto, K. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.19.8928 · Cited by 398 · see citing works

Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice

Falardeau, J., Chung, W. C. J., Beenken, A., Raivio, T., Plummer, L., Sidis, Y., Jacobson-Dickman, E. E., Eliseenkova, A. V., Ma, J., Dwyer, A., et al. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34538 · Cited by 397 · see citing works

α-Klotho as a Regulator of Calcium Homeostasis

Imura, A., Tsuji, Y., Murata, M., Maeda, R., Kubota, K., Iwano, A., Obuse, C., Togashi, K., Tominaga, M., Kita, N., et al. (2007) · Science · doi:10.1126/science.1135901 · Cited by 385 · see citing works

Elevated Cholesterol Metabolism and Bile Acid Synthesis in Mice Lacking Membrane Tyrosine Kinase Receptor FGFR4*

Yu, C., Wang, F., Kan, M., Jin, C., Jones, R. B., Weinstein, M., Deng, C.-X., & Mckeehan, W. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.20.15482 · Cited by 357 · see citing works

Keratinocyte growth factor is a growth factor for type II pneumocytes in vivo.

Ulich, T. R., Yi, E. S., Longmuir, K. J., Yin, S., Biltz, R., Morris, C. F., Housley, R. M., & Pierce, G. F. (1994) · Journal of Clinical Investigation · doi:10.1172/jci117086 · Cited by 351 · see citing works

βKlotho Is Required for Fibroblast Growth Factor (FGF) 21 Signaling through FGF Receptor (FGFR) 1c and FGFR3c

Suzuki, M., Uehara, Y., Motomura-Matsuzaka, K., Oki, J., Koyama, Y., Kimura, M., Asada, M., Komi-Kuramochi, A., Oka, S., & Toru, T. (2008) · Molecular Endocrinology · doi:10.1210/me.2007-0313 · Cited by 345 · see citing works

FGF‐21/FGF‐21 receptor interaction and activation is determined by βKlotho

Kharitonenkov, A., Dunbar, J. D., Bina, H. A., Bright, S. W., Moyers, J. S., Zhang, C., Ding, L., Micanovic, R., Mehrbod, S. F., Knierman, M. D., et al. (2007) · Journal of Cellular Physiology · doi:10.1002/jcp.21357 · Cited by 329 · see citing works

A role for FGF-6 in skeletal muscle regenerationPreprint

Floß, T., Arnold, H.-H., & Braun, T. W. (1997) · Genes & Development · doi:10.1101/gad.11.16.2040 · Cited by 328 · see citing works

Molecular cloning and expression analyses of mouse βklotho, which encodes a novel Klotho family protein

Ito, S., Kinoshita, S., Shiraishi, N., Nakagawa, S., Sekine, S., Fujimori, T., & Nabeshima, Y. (2000) · Mechanisms of Development · doi:10.1016/s0925-4773(00)00439-1 · Cited by 312 · see citing works

Characterization of Recombinant Human Fibroblast Growth Factor (FGF)-10 Reveals Functional Similarities with Keratinocyte Growth Factor (FGF-7)

Igarashi, M., Finch, P. W., & Aaronson, S. A. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.21.13230 · Cited by 307 · see citing works

Identification of a hormonal basis for gallbladder filling

Choi, M., Moschetta, A., Bookout, A., Peng, L., Umetani, M., Holmstrom, S. R., Suino-Powell, K., Xu, H. E., Richardson, J., Gerard, R., et al. (2006) · Nature Medicine · doi:10.1038/nm1501 · Cited by 289 · see citing works

Liver-specific Activities of FGF19 Require Klotho beta

Lin, B. C., Wang, M., Blackmore, C. A., & Desnoyers, L. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m704244200 · Cited by 284 · see citing works

Fibroblast growth factor homologous factors control neuronal excitability through modulation of voltage-gated sodium channels.

Goldfarb, M., Schoorlemmer, J., Williams, A. J., Diwakar, S., Wang, Q., Huang, X., Giza, J. I., Tchetchik, D., Kelley, K., Vega, A. V., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.07.006 · Cited by 266 · see citing works

Targeting FGF19 inhibits tumor growth in colon cancer xenograft and FGF19 transgenic hepatocellular carcinoma models

Desnoyers, L. R., Pai, R., Ferrando, R., Hotzel, K., Le, T., Ross, J., Carano, R., D'Souza, A., Qing, J., Mohtashemi, I., et al. (2008) · Oncogene · doi:10.1038/sj.onc.1210623 · Cited by 266 · see citing works

Impaired negative feedback suppression of bile acid synthesis in mice lacking βKlotho

Ito, S., Fujimori, T., Furuya, A., Satoh, J., Nabeshima, Y., & Nabeshima, Y. (2005) · Journal of Clinical Investigation · doi:10.1172/jci23076 · Cited by 248 · see citing works

Alpha-Klotho as a regulator of calcium homeostasis

Tsuji, Y. (2008) · Kyoto University Research Information Repository (Kyoto University) · Cited by 243 · see citing works

Development of the Thymus Requires Signaling Through the Fibroblast Growth Factor Receptor R2-IIIb

Revest, J., Suniara, R. K., Kerr, K., Owen, J. J. T., & Dickson, C. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.4.1954 · Cited by 242 · see citing works

Fibroblast growth factor homologous factors: evolution, structure, and function.

Goldfarb, M. (2005) · Cytokine & growth factor reviews · doi:10.1016/j.cytogfr.2005.02.002 · Cited by 234 · see citing works

The Fgf Families in Humans, Mice, and Zebrafish: Their Evolutional Processes and Roles in Development, Metabolism, and Disease

Itoh, N. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.1819 · Cited by 224 · see citing works

Keratinocyte growth factor and its receptor are involved in regulating early lung branching

Post, M., Souza, P., Liu, J., Tseu, I., Wang, J., Kuliszewski, M. J., & Tanswell, A. K. (1996) · Development · doi:10.1242/dev.122.10.3107 · Cited by 172 · see citing works

A protein canyon in the FGF–FGF receptor dimer selects from an à la carte menu of heparan sulfate motifs

Mohammadi, M., Olsen, S. K., & Goetz, R. M. (2005) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2005.09.002 · Cited by 158 · see citing works

Regulation of thymic epithelium by keratinocyte growth factor

Erickson, M., Morkowski, S., Lehar, S. M., Gillard, G. O., Beers, C., Dooley, J., Rubin, J. S., Rudensky, A. Y., & Farr, A. G. (2002) · Blood · doi:10.1182/blood-2002-04-1036 · Cited by 154 · see citing works

Patterning of frontal cortex subdivisions by Fgf17

Cholfin, J. A., & Rubenstein, J. L. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0702225104 · Cited by 154 · see citing works

Structure and Expression of the mRNA Encoding a Novel Fibroblast Growth Factor, FGF-18

Ohbayashi, N., Hoshikawa, M., Kimura, S., Yamasaki, M., Fukui, S., & Itoh, N. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.29.18161 · Cited by 152 · see citing works

FGF23 is a hormone-regulating phosphate metabolism—Unique biological characteristics of FGF23

Fukumoto, S., & Yamashita, T. (2007) · Bone · doi:10.1016/j.bone.2006.12.062 · Cited by 148 · see citing works

KGF regulates pulmonary epithelial proliferation and surfactant protein gene expression in adult rat lung

Yano, T., Mason, R. J., Pan, T., Deterding, R. R., Nielsen, L. D., & Shannon, J. M. (2000) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.2000.279.6.l1146 · Cited by 146 · see citing works

Murine FGF-12 and FGF-13: expression in embryonic nervous system, connective tissue and heart

Hartung, H. D., Feldman, B., Lovec, H., Coulier, F., Birnbaum, D., & Goldfarb, M. P. (1997) · Mechanisms of Development · doi:10.1016/s0925-4773(97)00042-7 · Cited by 140 · see citing works

Co-receptor Requirements for Fibroblast Growth Factor-19 Signaling

Wu, X., Ge, H., Gupte, J., Weiszmann, J., Shimamoto, G., Stevens, J., Hawkins, N., Lemon, B., Shen, W., Xu, J., et al. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.c700130200 · Cited by 140 · see citing works

FGF-20, a Novel Neurotrophic Factor, Preferentially Expressed in the Substantia Nigra Pars Compacta of Rat Brain

Ohmachi, S., Watanabe, Y., Mikami, T., Kusu, N., Ibi, T., Akaike, A., & Itoh, N. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3675 · Cited by 139 · see citing works

Fgf-8, activated by proviral insertion, cooperates with the Wnt-1 transgene in murine mammary tumorigenesis

MacArthur, C. A., Shankar, D. B., & Shackleford, G. M. (1995) · Journal of Virology · doi:10.1128/jvi.69.4.2501-2507.1995 · Cited by 139 · see citing works

Characterization and molecular cloning of a putative binding protein for heparin-binding growth factors.

Wu, D., Kan, M., Sato, G. H., Okamoto, T., & Sato, J. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)55368-0 · Cited by 131 · see citing works

Cellular Signaling by Fibroblast Growth Factors (FGFs) and Their Receptors (FGFRs) in Male Reproduction

Cotton, L. M., O’Bryan, M. K., & Hinton, B. T. (2008) · Endocrine Reviews · doi:10.1210/er.2007-0028 · Cited by 129 · see citing works

Isolation of a rearranged human transforming gene following transfection of Kaposi sarcoma DNA.

Bovi, P. D., & Basilico, C. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.16.5660 · Cited by 125 · see citing works

Quantitative analysis of estrogen receptor-? mRNA and its variants in human breast cancers

Iwao, K., Miyoshi, Y., Egawa, C., Ikeda, N., & Noguchi, S. (2000) · International Journal of Cancer · doi:10.1002/1097-0215(20001201)88:5 · Cited by 124 · see citing works

Mouse fibroblast growth factor 10: cDNA cloning, protein characterization, and regulation of mRNA expression

Beer, H., Florence, C., Dammeier, J., McGuire, L., Werner, S., & Duan, D. R. (1997) · Oncogene · doi:10.1038/sj.onc.1201383 · Cited by 122 · see citing works

Expression of fibroblast growth factor-8 and regulation of cognate receptors, fibroblast growth factor receptor-3c and -4, in bovine antral follicles

Junior, J. B., Teixeira, A. B., da Costa, I. B., Glapinski, V. F., Pinto, M. G. L., Giometti, I. C., Barros, C. M., Cao, M., Nicola, E. S., & Price, C. A. (2005) · Reproduction · doi:10.1530/rep.1.00642 · Cited by 122 · see citing works

Inhibition of Fibroblast Growth Factor 19 Reduces Tumor Growth by Modulating β-Catenin Signaling

Pai, R., Dunlap, D. Y., Qing, J., Mohtashemi, I., Hötzel, K., & French, D. M. (2008) · Cancer Research · doi:10.1158/0008-5472.can-07-2325 · Cited by 121 · see citing works

Abnormal social behaviors in mice lacking Fgf17

Scearce-Levie, K. A., Roberson, E. D., Gerstein, H. C., Cholfin, J. A., Mandiyan, V. S., Shah, N. M., Rubenstein, J. L. R., & Mucke, L. (2007) · Genes Brain & Behavior · doi:10.1111/j.1601-183x.2007.00357.x · Cited by 113 · see citing works

Mutations within the FGF5 gene are associated with hair length in cats

Drögemüller, C., Rüfenacht, S., Wichert, B. A., & Leeb, T. (2007) · Animal Genetics · doi:10.1111/j.1365-2052.2007.01590.x · Cited by 108 · see citing works

Identification of a novel mouse membrane-bound family 1 glycosidase-like protein, which carries an atypical active site structure.

Ito, S., Fujimori, T., Hayashizaki, Y., & Nabeshima, Y. (2002) · Biochimica et Biophysica Acta · doi:10.1016/s0167-4781(02)00281-6 · Cited by 108 · see citing works

The fibroblast growth factor-binding protein FGF-BP.

Abuharbeid, S., Czubayko, F., & Aigner, A. (2006) · International Journal of Biochemistry and Cell Biology · doi:10.1016/j.biocel.2005.10.017 · Cited by 105 · see citing works

Structure and Expression of a Novel Fibroblast Growth Factor, FGF-17, Preferentially Expressed in the Embryonic Brain

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Novel secretory heparin-binding factors from human glioma cells (glia-activating factors) involved in glial cell growth. Purification and biological properties.

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