spitz


REFERENCES

Ahmad, I., Dooley, C. M. and Afiat, S. (1998). Involvement of Mash1 in EGF-mediated regulation of differentiation in the vertebrate retina. Dev. Biol. 194(1): 86-98. PubMed Citation: 9473334

Andrew, D. J., et al. (1997). The Drosophila dCREB-A gene is required for dorsal/ventral patterning of the larval cuticle. Development 124: 181-193. PubMed Citation: 9006079

Austin, C. L., Manivannan, S. N. and Simcox, A. (2014). TGF-alpha ligands can substitute for the neuregulin Vein in Drosophila development. Development 141: 4110-4114. PubMed ID: 25336739

Bang, A. G. and Kintner, C. (2000). Rhomboid and Star facilitate presentation and processing of the Drosophila TGF-alpha homolog Spitz. Genes Dev. 14: 177-186. PubMed Citation: 10652272

Bergmann, A., Tugentman, M., Shilo, B.-Z. and Steller, H. (2002). Regulation of cell number by MAPK-dependent control of apoptosis: A mechanism for trophic survival signaling. Dev. Cell 2: 159-170. 11832242

Brachmann, R., et al. (1989). Transmembrane TGF-alpha precursors activate EGF/TGF-alpha receptors. Cell 56(4): 691-700. 89136015

Brodu, V., Elstob, P. R. and Gould, A. P. (2004). EGF receptor signaling regulates pulses of cell delamination from the Drosophila ectoderm. Dev. Cell 7: 885-895. 15572130

Brown, K. E. and Freeman, M. (2003). Egfr signalling defines a protective function for ommatidial orientation in the Drosophila eye. Development 130: 5401-5412. 14507785

Buff, E., et al. (1998). Signalling by the Drosophila epidermal growth factor receptor is required for the specification and diversification of embryonic muscle progenitors. Development 125: 2075-2086. PubMed Citation: 9570772

Buse, P., et al. (1995). Transforming growth factor-alpha abrogates glucocorticoid-stimulated tight junction formation and growth suppression in rat mammary epithelial tumor cells. J. Biol. Chem. 270: 6505-6514. PubMed Citation: 7896785

Caussanel, V., et al. (1996). Cellular distribution of EGF, TGFalpha and their receptor during postnatal development and spermatogenesis of the boar testis. Mol. Cell. Endocrinol. 123(1): 61-69. PubMed Citation: 8912812

Chafino, S., Martin, D. and Franch-Marro, X. (2021). Activation of EGFR signaling by Tc-Vein and Tc-Spitz regulates the metamorphic transition in the red flour beetle Tribolium castaneum. Sci Rep 11(1): 18807. PubMed ID: 34552169

Chang, C., Newman, A. P. and Sternberg, P. W. (1999). Reciprocal EGF signaling back to the uterus from the induced C. elegans vulva coordinates morphogenesis of epithelia. Curr. Biol. 9(5): 237-46. PubMed Citation: 10074449

Chang, J., et al. (2001). The CNS midline cells control the spitz class and Egfr signaling genes to establish the proper cell fate of the Drosophila ventral neuroectoderm. Int. J. Dev. Biol. 45(5-6): 715-24. 11669373

Chen, M. H., Li, Y. J., Kawakami, T., Xu, S. M. and Chuang, P. T. (2004). Palmitoylation is required for the production of a soluble multimeric Hedgehog protein complex and long-range signaling in vertebrates. Genes Dev. 18: 641-659. 15075292

Cheung, P., et al. (2000). Synergistic coupling of histone H3 phosphorylation and acetylation in response to epidermal growth factor stimulation. Molec. Cell 5: 905-915. PubMed Citation: 10911985

Cordero, J. B., Stefanatos, R. K., Myant, K., Vidal, M. and Sansom, O. J. (2012). Non-autonomous crosstalk between the Jak/Stat and Egfr pathways mediates Apc1-driven intestinal stem cell hyperplasia in the Drosophila adult midgut. Development 139: 4524-4535. PubMed ID: 23172913

Cruz, J., Martin, D. and Franch-Marro, X. (2020). Egfr signaling is a major regulator of ecdysone biosynthesis in the Drosophila prothoracic gland. Curr Biol 30(8): 1547-1554. PubMed ID: 32220314

Daniel, A., Dumstrei, K., Lengyel, J. A. and Hartenstein, V. (1999). The control of cell fate in the embryonic visual system by atonal, tailless and EGFR signaling. Development 126: 2945-2954. PubMed Citation: 10357938

Dardik, A., Smith, R. M. and Schultz, R. M. (1992). Colocalization of transforming growth factor-alpha and a functional epidermal growth factor receptor (EGFR) to the inner cell mass and preferential localization of the EGFR on the basolateral surface of the trophectoderm in the mouse blastocyst. Dev. Biol. 154(2): 396-409. PubMed Citation: 1426645

del Álamo, A., Terriente, J. and Díaz-Benjumea, F. J. (2002). Spitz/EGFr signalling via the Ras/MAPK pathway mediates the induction of bract cells in Drosophila legs. Development 129: 1975-1982. 11934863

DeWitt, A., et al. (2002). Affinity regulates spatial range of EGF receptor autocrine ligand binding. Dev. Bio. 250: 305-316. 12376105

Ding J., et al. (1998). Cripto is required for correct orientation of the anterior-posterior axis in the mouse embryo. Nature 395(6703): 702-7. PubMed Citation: 9790191

Doetsch, F., et al. (1999). Subventricular zone astrocytes are neural stem cells in the adult mammalian brain. Cell 97: 703-716. PubMed Citation: 10380923

Doetsch, F., et al. (2002). EGF converts transit-amplifying neurogenic precursors in the adult brain into multipotent stem cells. Neuron 36: 1021-1034. 12495619

Dumstrei, K., et al. (1998). EGFR signaling is required for the differentiation and maintenance of neural progenitors along the dorsal midline of the Drosophila embryonic head. Development 125(17): 3417-3426

Ebner, R. and Derynck, R. (1991). Epidermal growth factor and transforming growth factor-alpha: differential intracellular routing and processing of ligand-receptor complexes. Cell Regul. 2(8): 599-612

Elstob, P. R., Brodu, V. and Gould, A. P. (2001). spalt-dependent switching between two cell fates that are induced by the Drosophila EGF receptor. Development 128: 723-732. 11171397

Fang, Y. and Sheffield, L. G. (1998). Regulation of epidermal growth factor expression in mammary epithelial cells by a Yin-Yang-1-like element. J. Mol. Endocrinol. 20(3): 337-344

Ferguson, K. M., et al. (2003). EGF activates its receptor by removing interactions that autoinhibit ectodomain dimerization. Mol. Cell 11: 507-517. 12620237

Foronda, D., Martín, P., Sánnchez-Herrero, E. (2012). Drosophila Hox and sex-determination genes control segment elimination through EGFR and extramacrochetae activity. PLoS Genet. 8(8): e1002874. PubMed Citation: 22912593

Frankfort, B. J., et al. (2001). senseless repression of rough is required for r8 photoreceptor differentiation in the developing Drosophila eye. Neuron 32: 403-414. 11709152

Freeman, M. (1994). The spitz gene is required for photoreceptor determination in the Drosophila eye where it interacts with the EGF receptor. Mech Dev 48: 25-33

Freeman, M. (1996). Reiterative use of the EGF Receptor triggers differentiation of all cell types in the Drosophila eye. Cell 87: 651-660

Gallio, M. and Kylsten, P. (2000). Providencia may help find a function for a novel, widespread protein family. Curr. Biol. 10: R693-R694. 11050401

Gandrillon, O., et al. (1999). TGF-beta cooperates with TGF-alpha to induce the self-renewal of normal erythrocytic progenitors: evidence for an autocrine mechanism. EMBO J. 18(10): 2764-2781

Garrett, T. P. J., et al. (2002). Crystal structure of a truncated epidermal growth factor receptor extracellular domain bound to transforming growth factor alpha. Cell 110: 763-773. 12297049

Gilboa, L. and Lehmann, R. (2006). Soma-germline interactions coordinate homeostasis and growth in the Drosophila gonad. Nature 443: 97-100. Medline abstract: 16936717

Golembo, M., Raz, E. and Shilo, B.-Z. (1996). The Drosophila embryonic midline is the site of Spitz processing, and induces activation of the EGF receptor in the ventral ectoderm. Development 122, 3363-3370

Golembo, M., et al. (1999). Vein expression is induced by the EGF receptor pathway to provide a positive feedback loop in patterning the Drosophila embryonic ventral ectoderm. Genes Dev. 13(2): 158-162

González-Gaitán, M. and Jäckle, H. (2000). Tip cell-derived RTK signaling initiates cell movements in the Drosophila stomatogastric nervous system anlage. EMBO Reports 1: 366-371. 11269504

Goto, S., Taniguchi, M., Muraoka, M., Toyoda, H., Sado, Y., Kawakita, M. and Hayashi, S. (2001). UDP-sugar transporter implicated in glycosylation and processing of Notch. Nat. Cell Biol. 3: 816-822. 11533661

Gritti, A., et al. (1999). Epidermal and fibroblast growth factors behave as mitogenic regulators for a single multipotent stem cell-like population from the subventricular region of the adult mouse forebrain. J. Neurosci. 19(9): 3287-97

Gutzwiller, L. M., et al. (2010). Proneural and abdominal Hox inputs synergize to promote sensory organ formation in the Drosophila abdomen. Dev. Biol. 348(2): 231-43. PubMed Citation: 20875816

Hammerle, B. and Tejedor, F. J. (2007). A novel function of DELTA-NOTCH signalling mediates the transition from proliferation to neurogenesis in neural progenitor cells. PLoS One 2: e1169. PubMed ID: 18000541

Hatini, V. and DiNardo, S. (2001). Distinct signals generate repeating Striped pattern in the embryonic parasegment. Mol. Cell 7: 151-160. 11172720

Held, L. I., Jr. (2002). Bristles induce bracts via the EGFR pathway on Drosophila legs. Mech. Dev. 117: 225-234. 12204262

Hornstein, I., Mortin, M. A. and Katzav, S. (2003). DroVav, the Drosophila melanogaster homologue of the mammalian Vav proteins, serves as a signal transducer protein in the Rac and DER pathways. Oncogene 22: 6774-6784. PubMed citation: 14555990

Howes, R., Wasserman, J. D. and Freeman, M. (1998). In vivo analysis of argos structure-function. Sequence requirements for inhibition of the Drosophila epidermal growth factor receptor. J. Biol. Chem. 273(7): 4275-4281

Hsiung, F., et al. (2001). Function of the Drosophila TGF-alpha homolog Spitz is controlled by Star and interacts directly with Star. Mech. Dev. 107: 13-23. 11520660

Huang, Z., Shilo, B. Z. and Kunes, S. (1998). A retinal axon fascicle uses spitz, an EGF receptor ligand, to construct a synaptic cartridge in the brain of Drosophila. Cell 95: 693-703. PubMed ID: 9845371

Jiang, H. and Edgar, B. A. (2009). EGFR signaling regulates the proliferation of Drosophila adult midgut progenitors. Development 136(3): 483-93. PubMed Citation: 19141677

Kashimata, M. and Gresik, E. W. (1997). Epidermal growth factor system is a physiological regulator of development of the mouse fetal submandibular gland and regulates expression of the alpha6-integrin subunit. Dev. Dyn. 208(2): 149-161

Kashiwagi, M., Kuroki, T. and Huh, N. (1997). Specific inhibition of hair follicle formation by epidermal growth factor in an organ culture of developing mouse skin. Dev. Biol. 189(1): 22-32

Kerber, B., Fellert, S. and Hoch, M., (1998). Seven-up, the Drosophila homolog of the COUP-TF orphan receptors, controls cell proliferation in the insect kidney. Genes Dev. 12(12): 1781-1786

Klein, D. E., Stayrook, S. E., Shi, F., Narayan, K. and Lemmon, M. A. (2008). Structural basis for EGFR ligand sequestration by Argos. Nature 453(7199): 1271-5. PubMed citation: 18500331

Kuo, Y. M., et al. (1996). Salivary duct determination in Drosophila: roles of the EGF receptor signaling pathway and the transcription factors Fork head and Trachealess. Development 122: 1909-17

Lee, J. R., Urban, S. Garvey, C. F. and Freeman, M. (2001). Regulated intracellular ligand transport and proteolysis control EGF signal activation in Drosophila. Cell 107: 161-171. 11672524

Lesokhin, A. M., et al. (1999). Several levels of EGF receptor signaling during photoreceptor specification in wild-type, Ellipse, and null mutant Drosophila. Dev. Biol. 205(1): 129-44

Li-Kroeger, D. et al. (2008). Hox and senseless antagonism functions as a molecular switch to regulate EGF secretion in the Drosophila PNS. Dev. Cell 15: 298-308. PubMed Citation: 18694568

Lillien, L. (1995). Changes in retinal fate induced by overexpression of EGF receptor. Nature 377: 158-162

Luer, K., et al. (1997). Induction of identified mesodermal cells by CNS midline progenitors in Drosophila. Development 124(14): 2681-2690

Luetteke, N. C., et al. (1993). TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice. Cell 73: 263-78

Luetteke, N. C., et al. (1999). Targeted inactivation of the EGF and amphiregulin genes reveals distinct roles for EGF receptor ligands in mouse mammary gland development. Development 126(12): 2739-2750

Mark, M. D. and Storm, D. R. (1997). Coupling of epidermal growth factor (EGF) with the antiproliferative activity of cAMP induces neuronal differentiation. J. Biol. Chem. 272(27): 17238-17244

Mayer, U. and Nusslein-Volhard, C. (1988). A group of genes required for pattern formation in the ventral ectoderm of the Drosophila embryo. Genes Dev 2: 1496-511

McDonald, J. A., Pinheiro, E. M., Kadlec, L., Schupbach, T. and Montell, D. J. (2006). Multiple EGFR ligands participate in guiding migrating border cells. Dev. Biol. 296(1): 94-103. 16712835

Mendonsa, E. S. and Riley, B. B. (1999). Genetic analysis of tissue interactions required for otic placode induction in the zebrafish. Dev. Biol. 206(1): 100-12

Miura, G. I., et al. (2006). Palmitoylation of the EGFR ligand Spitz by Rasp increases Spitz activity by restricting its diffusion. Dev. Cell 10: 167-176. 16459296

Morante, J., Vallejo, D. M., Desplan, C. and Dominguez, M. (2013). Conserved miR-8/miR-200 defines a glial niche that controls neuroepithelial expansion and neuroblast transition. Dev Cell. PubMed ID: 24139822

Moriai, T., et al. (1994). A variant epidermal growth factor receptor exhibits altered type alpha transforming growth factor binding and transmembrane signaling. Proc. Natl. Acad. Sci. 91: 10217-10221

Moriki, T., Maruyama, H. and Maruyama, I. N. (2001). Activation of preformed EGF receptor dimers by ligand-induced rotation of the transmembrane domain. J. Mol. Biol. 311: 1011-1026. 11531336

Mortensen, E. R., et al. (1997). Epidermal growth factor and okadaic acid stimulate Sp1 proteolysis. J. Biol. Chem. 272(26): 16540-16547

Nagaraj, R., et al. (1999). Role of the EGF receptor pathway in growth and patterning of the Drosophila wing through the regulation of vestigial. Development 126: 975-985

Ogiso, H., et al. (2002). Crystal structure of the complex of human epidermal growth factor and receptor extracellular domains. Cell 110: 775-787. 12297050

Pasnuri, N., Jaiswal, M., Ray, K. and Mazumder, A. (2023). Buffered EGFR signaling regulated by spitz-to-argos expression ratio is a critical factor for patterning the Drosophila eye. PLoS Genet 19(2): e1010622. PubMed ID: 36730442

Patel, P. H., Dutta, D. and Edgar, B. A. (2015). Niche appropriation by Drosophila intestinal stem cell tumours. Nat Cell Biol 17: 1182-1192. PubMed ID: 26237646

Philippar, U., et al. (2008). A Mena invasion isoform potentiates EGF-induced carcinoma cell invasion and metastasis. Dev. Cell 15(6): 813-28. PubMed Citation: 19081071

Pittelkow, M. R., et al. (1993). Autonomous growth of human keratinocytes requires epidermal growth factor receptor occupancy. Cell Growth Differ. 4(6): 513-521

Rather, P. N., et al. (1999). Providencia stuartii genes activated by cell-to-cell signaling and identification of a gene required for production or activity of an extracellular factor. J. Bacteriol. 181: 7185-7191. 10572119

Reddy, C. C., Wells, A. and Lauffenburger, D. A. (1996). Receptor-mediated effects on ligand availability influence relative mitogenic potencies of epidermal growth factor and transforming growth factor alpha. J. Cell Physiol. 166(3): 512-522

Reich, A. and Shilo, B.-Z. (2002). Keren, a new ligand of the Drosophila epidermal growth factor receptor, undergoes two modes of cleavage. EMBO J. 21: 4287-4296. 12169631

Reneker, L. W., et al. (1995). TGF alpha can act as a chemoattractant to perioptic mesenchymal cells in developing mouse eyes. Development 121: 1669-1680.

Rhee, S. G. (2001). Regulation of phosphoinositide-specific phospholipase C. Annu. Rev. Biochem. 70: 281-312. 11395409

Roy, S., Hsiung, F. and Kornberg, T. B. (2011). Specificity of Drosophila cytonemes for distinct signaling pathways. Science 332(6027): 354-8. PubMed Citation: 21493861

Rusten, T. E., et al. (2001). Spalt modifies EGFR-mediated induction of chordotonal precursors in the embryonic PNS of Drosophila promoting the development of oenocytes. Development 128: 711-722. 11171396

Rutledge, B. J., et al. (1992). The Drosophila spitz gene encodes a putative EGF-like growth factor involved in dorsal-ventral axis formation and neurogenesis. Genes Dev 6: 1503-17

Sarkar, A., et al. (2007). Antagonistic roles of Rac and Rho in organizing the germ cell microenvironment. Curr. Biol. 17(14): 1253-8. PubMed citation: 17629483

Saxena, A., Denholm, B., Bunt, S., Bischoff, M., VijayRaghavan, K. and Skaer, H. (2014). Epidermal growth factor signalling controls Myosin II planar polarity to orchestrate convergent extension movements during Drosophila tubulogenesis. PLoS Biol 12: e1002013. PubMed ID: 25460353

Schlesinger, A., Kiger, A., Perrimon, N. and Shilo, B.-Z. (2004). Small Wing PLCγ is required for ER retention of cleaved Spitz during eye development in Drosophila. Dev. Cell 7: 535-545. 15469842

Schnepp, B., et al. (1996). Vein is a novel component in the Drosophila epidermal growth factor receptor pathway with similarity to the neuregulins. Genes Dev. 10: 2302-13

Schnepp, B. (1998). EGF domain swap converts a Drosophila EGF receptor activator into an inhibitor. Genes Dev. 12: 908-913

Schweitzer, R., et al. (1995). Secreted Spitz triggers the DER signaling pathway and is a limiting component in embryonic ventral ectoderm determination. Genes Dev 9: 1518-1529

Selva, E. M., Hong, K., Baeg, G. H., Beverley, S. M., Turco, S. J., Perrimon, N. and Hacker, U. (2001). Dual role of the fringe connection gene in both heparan sulphate and fringe-dependent signalling events. Nat. Cell Biol. 3: 809-815. 11533660

Shen, M. M., Wang, H. and Leder, P. (1997). A differential display strategy identifies Cryptic, a novel EGF-related gene expressed in the axial and lateral mesoderm during mouse gastrulation. Development 124: 429-442

Shvartsman, S. Y., Muratov, C. B. and Lauffenburger, D. A. (2002). Modeling and computational analysis of EGF receptor-mediated cell communication in Drosophila oogenesis. Development 129: 2577-2589. 12015287

Siegenthaler, J. A., Ashique, A. M., Zarbalis, K., Patterson, K. P., Hecht, J. H., Kane, M. A., Folias, A. E., Choe, Y., May, S. R., Kume, T., Napoli, J. L., Peterson, A. S. and Pleasure, S. J. (2009). Retinoic acid from the meninges regulates cortical neuron generation. Cell 139: 597-609. PubMed ID: 19879845

Simcox, A. (1997). Differential requirement for EGF-like ligands in Drosophila wing development. Mech Dev 62 (1): 41-50. PubMed Citation: 9106165

Sinenko, S. A., Shim, J. and Banerjee, U. (2011). Oxidative stress in the haematopoietic niche regulates the cellular immune response in Drosophila. EMBO Rep. 13(1): 83-9. PubMed Citation: 22134547

Smith, J. E., Cummings, C. A. and Cronmiller, C. (2002). daughterless coordinates somatic cell proliferation, differentiation and germline cyst survival during follicle formation in Drosophila. Development 129: 3255-3267. 12070099

Sonnenfeld, M. J., Barazesh, N., Sedaghat, Y. and Fan, C. (2004). The jing and ras1 pathways are functionally related during CNS midline and tracheal development. Mech. Dev. 121: 1531-1547. 15511644

Stemerdink, C. and Jacobs, J. R. (1997). Argos and Spitz group genes function to regulate midline glial cell number in Drosophila embryos. Development 124(19): 3787-3796. PubMed ID: 9367434

Strand, M. and Micchelli, C. A. (2013). Regional control of Drosophila gut stem cell proliferation: EGF establishes GSSC proliferative set point & controls emergence from quiescence. PLoS One 8: e80608. PubMed ID: 24236188

Sturtevant, M. A., Roark, M. and Bier, E. (1993). The Drosophila rhomboid gene mediates the localized formation of wing veins and interacts genetically with components of the EGF-R signaling pathway. Genes Dev. 7: 961-73

Su, M.-T., et al. (1999). The Drosophila homeobox genes zfh-1 and even-skipped are required for cardiac-specific differentiation of a numb-dependent lineage decision. Development 126: 3241-3251. PubMed ID: 10375513

Sutcliffe, B., Forero, M. G., Zhu, B., Robinson, I. M. and Hidalgo, A. (2013). Neuron-type specific functions of DNT1, DNT2 and Spz at the Drosophila neuromuscular junction. PLoS One 8: e75902. PubMed ID: 24124519

Szuts, D., Freeman, M. and Bienz, M. (1997). Antagonism between EGFR and Wingless signalling in the larval cuticle of Drosophila. Development 124(16): 3209-3219

Tio, M., Ma, C. and Moses, K. (1994). spitz, a Drosophila homolog of transforming growth factor-alpha, is required in the founding photoreceptor cells of the compound eye facets. Mech Dev 48: 13-23

Tio, M. and Moses, K. (1997). The Drosophila TGFalpha homolog Spitz acts in photoreceptor recruitment in the developing retina. Development 124: 343-351

Tropepe, V., et al. (1999). Distinct neural stem cells proliferate in response to EGF and FGF in the developing mouse telencephalon. Dev. Biol. 208(1): 166-88

Tsruya, R., et al. (2002). Intracellular trafficking by Star regulates cleavage of the Drosophila EGF receptor ligand Spitz. Genes Dev. 16: 222-234. 11799065

Turing, A. M. (1952). The chemical basis of morphogenesis. Philos. Trans. R. Soc. London B237: 37-72

Urban, S., Lee, J. R. and Freeman, M. (2001). Drosophila Rhomboid-1 defines a family of putative intramembrane serine proteases. Cell 107: 173-182. 11672525

Urban, S., Lee, J. R. and Freeman, M. (2002). A family of Rhomboid intramembrane proteases activates all Drosophila membrane-tethered EGF ligands. EMBO J. 21: 4277-4286. 12169630

van de Poll, M. L., et al. (1998). Identification of the minimal requirements for binding to the human epidermal growth factor (EGF) receptor using chimeras of human EGF and an EGF repeat of Drosophila Notch. J. Biol. Chem. 273(26): 16075-16081

Wasserman, J. D. and Freeman, M. (1998). An autoregulatory cascade of EGF receptor signaling patterns the Drosophila egg. Cell 95(3): 355-64

Wessells, R. J., et al. (1999). Tissue-specific regulation of vein/EGF receptor signaling in Drosophila. Dev. Biol. 216(1): 243-59.

Witt, L. M. et al. (2010). Atonal, senseless, and abdominal-A regulate rhomboid enhancer activity in abdominal sensory organ precursors. Dev. Biol. 344: 1060-1070. PubMed Citation: 20478292

Xu, C., et al. (1998). Specific arrest of cardiogenesis in cultured embryonic stem cells lacking Cripto-1. Dev. Biol. 196(2): 237-247. PubMed Citation: 9576836

Xu, C., et al. (1999). Abrogation of the Cripto gene in mouse leads to failure of postgastrulation morphogenesis and lack of differentiation of cardiomyocytes. Development 126(3): 483-494. PubMed Citation: 9876177

Xu, N., et al. (2011). EGFR, Wingless and JAK/STAT signaling cooperatively maintain Drosophila intestinal stem cells. Dev. Biol 354(1): 31-43. PubMed Citation: 21440535

Yamaguchi, M., et al. (1995). Opposite effects of transforming growth factor alpha and epidermal growth factor on mouse placental lactogen I secretion. Proc. Natl. Acad. Sci. 92: 2830-4. PubMed Citation: 7535931

Yang, L. and Baker, N. E. (2003). Cell cycle withdrawal, progression, and cell survival regulation by EGFR and its effectors in the differentiating Drosophila eye. Developmental Cell 4: 359-369. 12636917

Yano, H., et al. (2005). Distinct functional units of the Golgi complex in Drosophila cells. Proc. Natl. Acad. Sci 102: 13467-13472. 16174741

Yarnitzky, T., Min, L. and Volk, T. (1998). An interplay between two EGF-receptor ligands, Vein and Spitz, is required for the formation of a subset of muscle precursors in Drosophila. Mech. Dev. 79(1-2): 73-82. PubMed Citation: 10349622

Yasugi, T., Umetsu, D., Murakami, S., Sato, M. and Tabata, T. (2008). Drosophila optic lobe neuroblasts triggered by a wave of proneural gene expression that is negatively regulated by JAK/STAT. Development 135: 1471-1480. PubMed ID: 18339672

Yasugi, T., Sugie, A., Umetsu, D. and Tabata, T. (2010). Coordinated sequential action of EGFR and Notch signaling pathways regulates proneural wave progression in the Drosophila optic lobe. Development 137: 3193-3203. PubMed ID: 20724446

Zhang, J., Talbot, W. S. and Schier, A. F. (1998). Positional cloning identifies zebrafish one-eyed pinhead as a permissive EGF-related ligand required during gastrulation. Cell 92(2): 241-251. PubMed Citation: 9458048

Yu, L., Lee, T., Lin, N. and Wolf, M. J. (2010). Affecting Rhomboid-3 function causes a dilated heart in adult Drosophila. PLoS Genet. 6(5): e1000969. PubMed Citation: 20523889


spitz: Biological Overview | Evolutionary Homologs | Regulation | Developmental Biology | Effects of Mutation

date revised: 17 November 2021
 

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