The ephrins and Eph receptors in neural development.
暂无分享,去创建一个
[1] J. Flanagan,et al. Ephrin-B3, a ligand for the receptor EphB3, expressed at the midline of the developing neural tube , 1998, Oncogene.
[2] D. O'Leary,et al. Graded and lamina-specific distributions of ligands of EphB receptor tyrosine kinases in the developing retinotectal system. , 1997, Developmental biology.
[3] David G. Wilkinson,et al. The EphA4 and EphB1 receptor tyrosine kinases and ephrin-B2 ligand regulate targeted migration of branchial neural crest cells , 1997, Current Biology.
[4] S. Fraser,et al. Interactions of Eph-related receptors and ligands confer rostrocaudal pattern to trunk neural crest migration , 1997, Current Biology.
[5] D. Wilkinson,et al. Krox-20 is a key regulator of rhombomere-specific gene expression in the developing hindbrain , 1997, Mechanisms of Development.
[6] M. Barbacid,et al. Aberrant axonal projections in mice lacking EphA8 (Eek) tyrosine protein kinase receptors , 1997, The EMBO journal.
[7] Stephen W. Wilson,et al. Characterisation of five novel zebrafish Eph-related receptor tyrosine kinases suggests roles in patterning the neural plate , 1997, Development Genes and Evolution.
[8] Jürgen Löschinger,et al. Shared and distinct functions of RAGS and ELF‐1 in guiding retinal axons , 1997, The EMBO journal.
[9] E. Pasquale,et al. Tyrosine Phosphorylation of Transmembrane Ligands for Eph Receptors , 1997, Science.
[10] David J. Anderson,et al. Eph Family Transmembrane Ligands Can Mediate Repulsive Guidance of Trunk Neural Crest Migration and Motor Axon Outgrowth , 1997, Neuron.
[11] V. Dixit,et al. Reciprocal expression of the Eph receptor Cek5 and its ligand(s) in the early retina. , 1997, Developmental biology.
[12] Marina P Sánchez,et al. The Eek receptor, a member of the Eph family of tyrosine protein kinases, can be activated by three different Eph family ligands , 1997, Oncogene.
[13] F. Bonhoeffer,et al. Two Eph receptor tyrosine kinase ligands control axon growth and may be involved in the creation of the retinotectal map in the zebrafish. , 1997, Development.
[14] L. Cantley,et al. Recognition of Unique Carboxyl-Terminal Motifs by Distinct PDZ Domains , 1997, Science.
[15] J. Winslow,et al. AL‐1‐induced Growth Cone Collapse of Rat Cortical Neurons is Correlated with REK7 Expression and Rearrangement of the Actin Cytoskeleton , 1997, The European journal of neuroscience.
[16] Jussi Taipale,et al. Growth factors in the extracellular matrix , 1997, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[17] 坂野 誠治. Characterization of a ligand for receptor protein-tyrosine kinase-HTK expressed in immature hematopoietic cells , 1997 .
[18] G. Yancopoulos,et al. Eph family receptors and their ligands distribute in opposing gradients in the developing mouse retina. , 1996, Developmental biology.
[19] W. Harris,et al. Engrailed and retinotectal topography , 1996, Trends in Neurosciences.
[20] M. Nieto. Molecular Biology of Axon Guidance , 1996, Neuron.
[21] C. Ring,et al. Expression pattern of collagen IX and potential role in the segmentation of the peripheral nervous system. , 1996, Developmental biology.
[22] Andrew Lumsden,et al. Patterning the Vertebrate Neuraxis , 1996, Science.
[23] J. Flanagan,et al. Detection of Ligands in Regions Anatomically Connected to Neurons Expressing the Eph Receptor Bsk: Potential Roles in Neuron–Target Interaction , 1996, The Journal of Neuroscience.
[24] T. Pawson,et al. Sek4 and Nuk receptors cooperate in guidance of commissural axons and in palate formation. , 1996, The EMBO journal.
[25] A. Flenniken,et al. Distinct and overlapping expression patterns of ligands for Eph-related receptor tyrosine kinases during mouse embryogenesis. , 1996, Developmental biology.
[26] T. Sargent,et al. Disruption of cell adhesion in Xenopus embryos by Pagliaccio, an Eph-class receptor tyrosine kinase. , 1996, Developmental biology.
[27] F. Bonhoeffer,et al. Chromophore-assisted laser inactivation of a repulsive axonal guidance molecule , 1996, Current Biology.
[28] T. Pawson,et al. Bidirectional signalling through the EPH-family receptor Nuk and its transmembrane ligands , 1996, Nature.
[29] I. Black,et al. Regulation of topographic projection in the brain: Elf-1 in the hippocamposeptal system. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[30] B. Fredette,et al. Inhibition of motor axon growth by T-cadherin substrata. , 1996, Development.
[31] M. Sheng,et al. PDZs and Receptor/Channel Clustering: Rounding Up the Latest Suspects , 1996, Neuron.
[32] Andrew P. McMahon,et al. Engrailed-1 as a target of the Wnt-1 signalling pathway in vertebrate midbrain development , 1996, Nature.
[33] D. Cerretti,et al. Ligand Activation of ELK Receptor Tyrosine Kinase Promotes Its Association with Grb10 and Grb2 in Vascular Endothelial Cells* , 1996, The Journal of Biological Chemistry.
[34] A. Flenniken,et al. Elk-L3, a novel transmembrane ligand for the Eph family of receptor tyrosine kinases, expressed in embryonic floor plate, roof plate and hindbrain segments. , 1996, Oncogene.
[35] John G Flanagan,et al. Topographically Specific Effects of ELF-1 on Retinal Axon Guidance In Vitro and Retinal Axon Mapping In Vivo , 1996, Cell.
[36] D. O'Leary,et al. Retroviral Misexpression of engrailed Genes in the Chick Optic Tectum Perturbs the Topographic Targeting of Retinal Axons , 1996, The Journal of Neuroscience.
[37] A. Iwama,et al. Characterization of a ligand for receptor protein-tyrosine kinase HTK expressed in immature hematopoietic cells. , 1996, Oncogene.
[38] L. Berg,et al. A new member of the Eph family of receptors that lacks protein tyrosine kinase activity. , 1996, Oncogene.
[39] M. Yamagata,et al. Visual projection map specified by topographic expression of transcription factors in the retina , 1996, Nature.
[40] J. Sanes,et al. The Eph Kinase Ligand AL-1 Is Expressed by Rostral Muscles and Inhibits Outgrowth from Caudal Neurons , 1996, Molecular and Cellular Neuroscience.
[41] R. Klein,et al. Similarities and Differences in the Way Transmembrane-Type Ligands Interact with the Elk Subclass of Eph Receptors , 1996, Molecular and Cellular Neuroscience.
[42] P. Chambon,et al. The expression pattern of the mouse receptor tyrosine kinase gene MDK1 is conserved through evolution and requires Hoxa-2 for rhombomere-specific expression in mouse embryos. , 1996, Developmental biology.
[43] Uwe Drescher,et al. Rostral optic tectum acquires caudal characteristics following ectopic Engrailed expression , 1996, Current Biology.
[44] T. Pawson,et al. Nuk Controls Pathfinding of Commissural Axons in the Mammalian Central Nervous System , 1996, Cell.
[45] A. Flenniken,et al. Eph Receptors and Ligands Comprise Two Major Specificity Subclasses and Are Reciprocally Compartmentalized during Embryogenesis , 1996, Neuron.
[46] J. Ruiz,et al. Embryonic expression of eph signalling factors in Xenopus , 1996, Mechanisms of Development.
[47] D. Wilkinson,et al. Function of the Eph-related kinase rtk1 in patterning of the zebrafish forebrain , 1996, Nature.
[48] P. Leedman,et al. Thyroid Hormone Modulates the Interaction between Iron Regulatory Proteins and the Ferritin mRNA Iron-responsive Element (*) , 1996, The Journal of Biological Chemistry.
[49] A. Reith,et al. A juxtamembrane autophosphorylation site in the Eph family receptor tyrosine kinase, Sek, mediates high affinity interaction with p59fyn. , 1996, Oncogene.
[50] E. Pasquale,et al. B61, a ligand for the Eck receptor protein‐tyrosine kinase, exhibits neurotrophic activity in cultures of rat spinal cord neurons , 1996, Journal of neuroscience research.
[51] A. Reith,et al. Germ-line inactivation of the murine Eck receptor tyrosine kinase by gene trap retroviral insertion. , 1996, Oncogene.
[52] Salvador Martinez,et al. Midbrain development induced by FGF8 in the chick embryo , 1996, Nature.
[53] M. Goulding,et al. Expression of theTyro4/Mek4/Cek4Gene Specifically Marks a Subset of Embryonic Motor Neurons and Their Muscle Targets , 1996, Molecular and Cellular Neuroscience.
[54] A. Iwama,et al. The receptor tyrosine kinase, Cek8, is transiently expressed on subtypes of motoneurons in the spinal cord during development , 1996, Mechanisms of Development.
[55] Harukazu Nakamura,et al. A Role for Gradient en Expression in Positional Specification on the Optic Tectum , 1996, Neuron.
[56] D. Wilkinson,et al. Progressive spatial restriction of Sek-1 and Krox-20 gene expression during hindbrain segmentation. , 1996, Developmental biology.
[57] A. Boyd,et al. Embryonic stem cells express multiple Eph-subfamily receptor tyrosine kinases. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[58] Y. Barde,et al. Physiology of the neurotrophins. , 1996, Annual review of neuroscience.
[59] D. Hilton,et al. Molecular cloning of two novel transmembrane ligands for Eph-related kinases (LERKS) that are related to LERK-2. , 1996, Growth factors.
[60] M. Nieto,et al. Characterisation of Cek-11, a member of the EPH-receptor family in the chick embryo. , 1996, The International journal of developmental biology.
[61] Pasquale Eb,et al. Genomic organization and alternatively processed forms of Cek5, a receptor protein-tyrosine kinase of the Eph subfamily. , 1995 .
[62] E. Pasquale,et al. Polarized expression of the receptor protein tyrosine kinase Cek5 in the developing avian visual system. , 1995, Developmental biology.
[63] M. Bronner‐Fraser,et al. The receptor tyrosine kinase QEK5 mRNA is expressed in a gradient within the neural retina and the tectum. , 1995, Developmental biology.
[64] D. Wilkinson,et al. Expression of truncated Sek-1 receptor tyrosine kinase disrupts the segmental restriction of gene expression in the Xenopus and zebrafish hindbrain. , 1995, Development.
[65] A. Ullrich,et al. Cloning, characterization, and differential expression of MDK2 and MDK5, two novel receptor tyrosine kinases of the eck/eph family. , 1995, Oncogene.
[66] Scott E. Fraser,et al. Effects of brain-derived neurotrophic factor on optic axon branching and remodelling in vivo , 1995, Nature.
[67] Scales Jb,et al. Novel members of the eph receptor tyrosine kinase subfamily expressed during Xenopus development. , 1995 .
[68] N. Copeland,et al. Isolation of LERK-5: a ligand of the eph-related receptor tyrosine kinases. , 1995, Molecular immunology.
[69] S. Zipursky,et al. Neuronal target recognition , 1995, Cell.
[70] J. Biegel,et al. cDNA cloning, molecular characterization, and chromosomal localization of NET(EPHT2), a human EPH-related receptor protein-tyrosine kinase gene preferentially expressed in brain. , 1995, Genomics.
[71] J. Flanagan,et al. ELF-2, a new member of the Eph ligand family, is segmentally expressed in mouse embryos in the region of the hindbrain and newly forming somites , 1995, Molecular and cellular biology.
[72] M. Freeman,et al. Inhibition of Drosophila EGF receptor activation by the secreted protein Argos , 1995, Nature.
[73] A. Pandey,et al. Characterization of a Novel Src-like Adapter Protein That Associates with the Eck Receptor Tyrosine Kinase (*) , 1995, The Journal of Biological Chemistry.
[74] Jürgen Löschinger,et al. In vitro guidance of retinal ganglion cell axons by RAGS, a 25 kDa tectal protein related to ligands for Eph receptor tyrosine kinases , 1995, Cell.
[75] John G Flanagan,et al. Complementary gradients in expression and binding of ELF-1 and Mek4 in development of the topographic retinotectal projection map , 1995, Cell.
[76] M. Tessier-Lavigne,et al. Eph receptor tyrosine kinases, axon repulsion, and the development of topographic maps , 1995, Cell.
[77] S. Ziegler,et al. Embryo brain kinase: a novel gene of the eph/elk receptor tyrosine kinase family , 1995, Mechanisms of Development.
[78] C. Holt,et al. From tags to RAGS: Chemoaffinity finally has receptors and ligands , 1995, Neuron.
[79] R. Beddington,et al. Capturing genes encoding membrane and secreted proteins important for mouse development. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[80] A. Schnapp,et al. Membrane‐bound LERK2 ligand can signal through three different Eph‐related receptor tyrosine kinases. , 1995, The EMBO journal.
[81] M. Kirschner,et al. Molecular cloning of tyrosine kinases in the early Xenopus embryo: Identification of eck‐related genes expressed in cranial neural crest cells of the second (Hyoid) Arch , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.
[82] M. Tessier-Lavigne,et al. The axonal chemoattractant netrin-1 is also a chemorepellent for trochlear motor axons , 1995, Cell.
[83] F. Hefti,et al. Cloning of AL-1, a ligand for an Eph-related tyrosine kinase receptor involved in axon bundle formation , 1995, Neuron.
[84] A. Pandey,et al. Role of B61, the ligand for the Eck receptor tyrosine kinase, in TNF-alpha-induced angiogenesis. , 1995, Science.
[85] N. Ip,et al. Identification of full-length and truncated forms of Ehk-3, a novel member of the Eph receptor tyrosine kinase family. , 1995, Oncogene.
[86] P. Robbins,et al. The Retinoblastoma Susceptibility Gene Product Represses Transcription When Directly Bound to the Promoter (*) , 1995, The Journal of Biological Chemistry.
[87] H. Kung,et al. Expression of an amphibian homolog of the Eph family of receptor tyrosine kinases is developmentally regulated. , 1995, Oncogene.
[88] A. Goddard,et al. Molecular cloning of a ligand for the EPH-related receptor protein-tyrosine kinase Htk. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[89] R. Lindberg,et al. cDNA cloning and tissue distribution of five human EPH-like receptor protein-tyrosine kinases. , 1995, Oncogene.
[90] A. Pandey,et al. cDNA Cloning and Characterization of a Cek7 Receptor Protein-tyrosine Kinase Ligand That Is Identical to the Ligand (ELF-1) for the Mek-4 and Sek Receptor Protein-tyrosine Kinases (*) , 1995, The Journal of Biological Chemistry.
[91] D. Hilt,et al. Molecular cloning of TOPAP: A topographically graded protein in the developing chick visual system , 1995, Neuron.
[92] S. Srinivasan,et al. Ligands for the receptor tyrosine kinases hek and elk: isolation of cDNAs encoding a family of proteins. , 1995, Oncogene.
[93] A. Ullrich,et al. Identification of alternatively spliced mRNAs encoding variants of MDK1, a novel receptor tyrosine kinase expressed in the murine nervous system. , 1995, Oncogene.
[94] D D O'Leary,et al. Mechanisms and molecules controlling the development of retinal maps. , 1995, Perspectives on developmental neurobiology.
[95] E. Pasquale,et al. Genomic organization and alternatively processed forms of Cek5, a receptor protein-tyrosine kinase of the Eph subfamily. , 1995, Oncogene.
[96] C. Renaud,et al. Novel members of the eph receptor tyrosine kinase subfamily expressed during Xenopus development. , 1995, Oncogene.
[97] T. Jessell,et al. Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes , 1994, Cell.
[98] A. Pandey,et al. Activation of the Eck receptor protein tyrosine kinase stimulates phosphatidylinositol 3-kinase activity. , 1994, The Journal of biological chemistry.
[99] T Pawson,et al. Ligands for EPH-related receptor tyrosine kinases that require membrane attachment or clustering for activity. , 1994, Science.
[100] Stephen W. Wilson,et al. Regulatory gene expression boundaries demarcate sites of neuronal differentiation in the embryonic zebrafish forebrain , 1994, Neuron.
[101] E. Pasquale,et al. Characterization of the expression of the Cek8 receptor-type tyrosine kinase during development and in tumor cell lines. , 1994, Oncogene.
[102] J. Schlessinger,et al. Regulation of signal transduction and signal diversity by receptor oligomerization. , 1994, Trends in biochemical sciences.
[103] A. Pandey,et al. cDNA cloning and characterization of a ligand for the Cek5 receptor protein-tyrosine kinase. , 1994, The Journal of biological chemistry.
[104] J. Rubenstein,et al. The embryonic vertebrate forebrain: the prosomeric model. , 1994, Science.
[105] M. Verderame,et al. Identification of a complete Cek7 receptor protein tyrosine kinase coding sequence and cDNAs of alternatively spliced transcripts. , 1994, Gene.
[106] J. Flanagan,et al. Identification and cloning of ELF-1, a developmentally expressed ligand for the Mek4 and Sek receptor tyrosine kinases , 1994, Cell.
[107] J. Flanagan,et al. Transmembrane kit ligand cleavage does not require a signal in the cytoplasmic domain and occurs at a site dependent on spacing from the membrane. , 1994, Molecular biology of the cell.
[108] D. O'Leary,et al. Control of topographic retinal axon branching by inhibitory membrane-bound molecules. , 1994, Science.
[109] T. Pawson,et al. Molecular characterization of a family of ligands for eph‐related tyrosine kinase receptors. , 1994, The EMBO journal.
[110] L. Cantley,et al. A neu acquaintance for ErbB3 and ErbB4: A role for receptor heterodimerization in growth signaling , 1994, Cell.
[111] H Sugimura,et al. Overexpression of ERK, an EPH family receptor protein tyrosine kinase, in various human tumors. , 1994, Cancer research.
[112] T. Sargent,et al. Pagliaccio, a member of the Eph family of receptor tyrosine kinase genes, has localized expression in a subset of neural crest and neural tissues in Xenopus laevis embryos , 1994, Mechanisms of Development.
[113] A. Reith,et al. The Eck receptor tyrosine kinase is implicated in pattern formation during gastrulation, hindbrain segmentation and limb development. , 1994, Oncogene.
[114] Y. Barde,et al. Expression of the BDNF gene in the developing visual system of the chick. , 1994, Development.
[115] D. Goeddel,et al. Cloning and characterization of HTK, a novel transmembrane tyrosine kinase of the EPH subfamily. , 1994, The Journal of biological chemistry.
[116] R. Derynck,et al. Association of the transmembrane TGF-alpha precursor with a protein kinase complex , 1994, The Journal of cell biology.
[117] B. Barres,et al. Control of oligodendrocyte number in the developing rat optic nerve , 1994, Neuron.
[118] E. Robertson,et al. The expression of the receptor-protein tyrosine kinase gene, eck, is highly restricted during early mouse development , 1994, Mechanisms of Development.
[119] A. Andres,et al. Expression of two novel eph-related receptor protein tyrosine kinases in mammary gland development and carcinogenesis. , 1994, Oncogene.
[120] Yosef Yarden,et al. B61 is a ligand for the ECK receptor protein-tyrosine kinase , 1994, Nature.
[121] S. Fraser,et al. BDNF in the development of the visual system of Xenopus , 1994, Neuron.
[122] T. Pawson,et al. Immunolocalization of the Nuk receptor tyrosine kinase suggests roles in segmental patterning of the brain and axonogenesis. , 1994, Oncogene.
[123] W. Gullick,et al. eph, the largest known family of putative growth factor receptors. , 1994, British Journal of Cancer.
[124] Stephen W. Wilson,et al. Spatially regulated expression of three receptor tyrosine kinase genes during gastrulation in the zebrafish. , 1994, Development.
[125] C. Cepko,et al. Asymmetric expression of a novel homeobox gene in vertebrate sensory organs , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[126] G. Rubin,et al. Determination of neuronal cell fate: lessons from the R7 neuron of Drosophila. , 1994, Annual review of neuroscience.
[127] L. F. Kromer,et al. Isolation and characterization of Bsk, a growth factor receptor‐like tyrosine kinase associated with the limbic system , 1994, Journal of neuroscience research.
[128] D. Wilkinson,et al. Several receptor tyrosine kinase genes of the Eph family are segmentally expressed in the developing hindbrain , 1994, Mechanisms of development.
[129] T. Hunter,et al. Receptor protein-tyrosine kinases and their signal transduction pathways. , 1994, Annual review of cell biology.
[130] C. Goodman,et al. The semaphorin genes encode a family of transmembrane and secreted growth cone guidance molecules , 1993, Cell.
[131] S. Schneider-Maunoury,et al. Disruption of Krox-20 results in alteration of rhombomeres 3 and 5 in the developing hindbrain , 1993, Cell.
[132] G. Yancopoulos,et al. Ehk-1 and Ehk-2: two novel members of the Eph receptor-like tyrosine kinase family with distinctive structures and neuronal expression. , 1993, Oncogene.
[133] P. Swiatek,et al. Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20. , 1993, Genes & development.
[134] D. Raible,et al. Collapsin: A protein in brain that induces the collapse and paralysis of neuronal growth cones , 1993, Cell.
[135] C. Holt,et al. Position, guidance, and mapping in the developing visual system. , 1993, Journal of neurobiology.
[136] K. Grzeschik,et al. PCR mediated detection of a new human receptor-tyrosine-kinase, HEK 2. , 1993, Oncogene.
[137] A. Graham,et al. Even-numbered rhombomeres control the apoptotic elimination of neural crest cells from odd-numbered rhombomeres in the chick hindbrain. , 1993, Development.
[138] Pasquale Eb,et al. Five novel avian Eph-related tyrosine kinases are differentially expressed. , 1993 .
[139] S. Fraser,et al. Segmental migration of the hindbrain neural crest does not arise from its segmental generation. , 1993, Development.
[140] C. Stern,et al. Segmental organization of embryonic diencephalon , 1993, Nature.
[141] J. Sanes. Topographic maps and molecular gradients , 1993, Current Opinion in Neurobiology.
[142] R. Krumlauf,et al. The zinc finger gene Krox20 regulates HoxB2 (Hox2.8) during hindbrain segmentation , 1993, Cell.
[143] J. Massagué,et al. Membrane-anchored growth factors. , 1993, Annual review of biochemistry.
[144] E. Pasquale,et al. Five novel avian Eph-related tyrosine kinases are differentially expressed. , 1993, Oncogene.
[145] J. Massagué,et al. The cytoplasmic carboxy-terminal amino acid specifies cleavage of membrane TGFα into soluble growth factor , 1992, Cell.
[146] D. Wilkinson,et al. A receptor protein tyrosine kinase implicated in the segmental patterning of the hindbrain and mesoderm. , 1992, Development.
[147] D. Williams,et al. Developmental abnormalities in Steel17H mice result from a splicing defect in the steel factor cytoplasmic tail. , 1992, Genes & development.
[148] T. Deerinck,et al. Cek5, a membrane receptor-type tyrosine kinase, is in neurons of the embryonic and postnatal avian brain , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[149] L. D. Ward,et al. Isolation and characterization of a novel receptor-type protein tyrosine kinase (hek) from a human pre-B cell line. , 1992, The Journal of biological chemistry.
[150] S. Fraser. Patterning of retinotectal connections in the vertebrate visual system , 1992, Current Opinion in Neurobiology.
[151] C. Nüsslein-Volhard,et al. The origin of pattern and polarity in the Drosophila embryo , 1992, Cell.
[152] D. Wilkinson,et al. An Eph-related receptor protein tyrosine kinase gene segmentally expressed in the developing mouse hindbrain. , 1992, Oncogene.
[153] S. Subramani,et al. Identification of a new eph-related receptor tyrosine kinase gene from mouse and chicken that is developmentally regulated and encodes at least two forms of the receptor. , 1991, The New biologist.
[154] M. Kirschner,et al. Expression of a dominant negative mutant of the FGF receptor disrupts mesoderm formation in xenopus embryos , 1991, Cell.
[155] E. Pasquale. Identification of chicken embryo kinase 5, a developmentally regulated receptor-type tyrosine kinase of the Eph family. , 1991, Cell regulation.
[156] J. Chan,et al. eek and erk, new members of the eph subclass of receptor protein-tyrosine kinases. , 1991, Oncogene.
[157] D. Williams,et al. Steel-Dickie mutation encodes a c-kit ligand lacking transmembrane and cytoplasmic domains. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[158] H. Ueno,et al. Inhibition of PDGF beta receptor signal transduction by coexpression of a truncated receptor , 1991, Science.
[159] SC McLoon,et al. A monoclonal antibody that distinguishes between temporal and nasal retinal axons , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[160] G. Lemke,et al. An extended family of protein-tyrosine kinase genes differentially expressed in the vertebrate nervous system , 1991, Neuron.
[161] P. Leder,et al. Transmembrane form of the kit ligand growth factor is determined by alternative splicing and is missing in the SId mutant , 1991, Cell.
[162] M. Bronner‐Fraser,et al. Effects of mesodermal tissues on avian neural crest cell migration. , 1991, Developmental biology.
[163] Karthryn W. Tonsey,et al. Cells and cell‐interactions that guide motor axons in the developing chick embryo , 1991 .
[164] Kathryn W. Tosney. Cells and cell-interactions that guide motor axons in the developing chick embryo. , 1991, BioEssays : news and reviews in molecular, cellular and developmental biology.
[165] S. Hanks,et al. Protein kinase catalytic domain sequence database: identification of conserved features of primary structure and classification of family members. , 1991, Methods in enzymology.
[166] T. Hunter,et al. cDNA cloning and characterization of eck, an epithelial cell receptor protein-tyrosine kinase in the eph/elk family of protein kinases , 1990, Molecular and cellular biology.
[167] Edward C. Cox,et al. Biochemical characterization of a putative axonal guidance molecule of the chick visual system , 1990, Neuron.
[168] V. Dixit,et al. A novel immediate-early response gene of endothelium is induced by cytokines and encodes a secreted protein , 1990, Molecular and cellular biology.
[169] T. Allsopp,et al. A common denominator of growth cone guidance and collapse? , 1990, Trends in Neurosciences.
[170] P. Leder,et al. The kit ligand: A cell surface molecule altered in steel mutant fibroblasts , 1990, Cell.
[171] I. Stamenkovic,et al. CD44 is the principal cell surface receptor for hyaluronate , 1990, Cell.
[172] Edward C. Cox,et al. Axonal guidance in the chick visual system: Posterior tectal membanes induce collapse of growth cones from the temporal retina , 1990, Neuron.
[173] D. O'Leary,et al. Inaccuracies in initial growth and arborization of chick retinotectal axons followed by course corrections and axon remodeling to develop topographic order , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[174] S. Singer,et al. Identification of a developmentally regulated protein-tyrosine kinase by using anti-phosphotyrosine antibodies to screen a cDNA expression library. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[175] T. Pawson,et al. Novel protein-tyrosine kinase cDNAs related to fps/fes and eph cloned using anti-phosphotyrosine antibody. , 1988, Oncogene.
[176] H. Hirai,et al. A novel putative tyrosine kinase receptor encoded by the eph gene. , 1987, Science.
[177] S. Henke-Fahle,et al. Avoidance of posterior tectal membranes by temporal retinal axons. , 1987, Development.
[178] Alfred Gierer,et al. Directional cues for growing axons forming the retinotectal projection , 1987 .
[179] R. Levi‐montalcini. The nerve growth factor: thirty‐five years later. , 1987, The EMBO journal.
[180] M. Catsicas,et al. Long-distance intraretinal connections in birds , 1987, Nature.
[181] S. Cohen,et al. Epidermal growth factor , 1972, The Journal of investigative dermatology.
[182] A. Ullrich,et al. Epidermal growth factor: Is the precursor a receptor? , 1985, Nature.
[183] R. Keynes,et al. Segmentation in the vertebrate nervous system , 1984, Nature.
[184] Uli Schwarz,et al. Preferential adhesion of tectal membranes to anterior embryonic chick retina neurites , 1981, Nature.
[185] M Nirenberg,et al. A topographic gradient of molecules in retina can be used to identify neuron position. , 1981, Proceedings of the National Academy of Sciences of the United States of America.
[186] R. Hunt,et al. Retinotectal specificity: models and experiments in search of a mapping function. , 1980, Annual review of neuroscience.
[187] K. Rock,et al. A gradient of adhesive specificity in developing avian retina. , 1976, Proceedings of the National Academy of Sciences of the United States of America.
[188] R. Sperry. CHEMOAFFINITY IN THE ORDERLY GROWTH OF NERVE FIBER PATTERNS AND CONNECTIONS. , 1963, Proceedings of the National Academy of Sciences of the United States of America.
[189] R. Sperry. Visuomotor coordination in the newt (triturus viridescens) after regeneration of the optic nerve , 1943 .