Biological actions and interactions of anosmin-1.

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Frontiers of Hormone Research

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1159/000312695PMID 20389087
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Novel Mechanisms of Fibroblast Growth Factor Receptor 1 Regulation by Extracellular Matrix Protein Anosmin-1*

  2009cited by this paper
• Decreased FGF8 signaling causes deficiency of gonadotropin-releasing hormone in humans and mice.

  2008cited by this paper
• Functional roles of N‐glycans in cell signaling and cell adhesion in cancer

  2008cited by this paper
• Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.

  2008cited by this paper
• Essential requirement for zebrafish anosmin-1a in the migration of the posterior lateral line primordium.

  2008cited by this paper
• Fibronectin type III (FN3) modules of the neuronal cell adhesion molecule L1 interact directly with the fibroblast growth factor (FGF) receptor.

  2008cited by this paper
• Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism.

  2007cited by this paper
• Localization of anosmin-1a and anosmin-1b in the inner ear and neuromasts of zebrafish.

  2007cited by this paper
• Diversity in Fibroblast Growth Factor Receptor 1 Regulation: Learning from the Investigation of Kallmann Syndrome

  2007cited by this paper
• C. elegans Kallmann syndrome protein KAL-1 interacts with syndecan and glypican to regulate neuronal cell migrations.

  2006cited by this paper
• Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2

  2006cited by this paper
• Anosmin-1 modulates the FGF-2-dependent migration of oligodendrocyte precursors in the developing optic nerve.

  2006cited by this paper
• Comprehensive analysis of HE4 expression in normal and malignant human tissues

  2006cited by this paper
• Functional dissection of the Drosophila Kallmann's syndrome protein DmKal-1

  2006cited by this paper
• Forebrain gonadotropin-releasing hormone neuronal development: insights from transgenic medaka and the relevance to X-linked Kallmann syndrome.

  2006cited by this paper
• Extended and flexible domain solution structure of the extracellular matrix protein anosmin-1 by X-ray scattering, analytical ultracentrifugation and constrained modelling.

  2005cited by this paper
• A role for foxd3 and sox10 in the differentiation of gonadotropin-releasing hormone (GnRH) cells in the zebrafish Danio rerio

  2005cited by this paper
• Molecular analysis of WFDC1/ps20 gene in prostate cancer

  2004cited by this paper
• Anosmin-1 Modulates Fibroblast Growth Factor Receptor 1 Signaling in Human Gonadotropin-Releasing Hormone Olfactory Neuroblasts through a Heparan Sulfate-Dependent Mechanism

  2004cited by this paper
• Differential sulfations and epimerization define heparan sulfate specificity in nervous system development.

  2004cited by this paper
• The transmembrane protein XFLRT3 forms a complex with FGF receptors and promotes FGF signalling

  2004cited by this paper
• Cross-talk of anosmin-1, the protein implicated in X-linked Kallmann's syndrome, with heparan sulphate and urokinase-type plasminogen activator.

  2004cited by this paper
• Embryonic expression pattern of the Drosophila Kallmann syndrome gene kal-1.

  2004cited by this paper
• Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or KAL2) in five families and 18 sporadic patients.

  2004cited by this paper
• The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons.

  2004cited by this paper
• Mammalian Brain Morphogenesis and Midline Axon Guidance Require Heparan Sulfate

  2003cited by this paper
• Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

  2003cited by this paper
• Structural basis for a direct interaction between FGFR1 and NCAM and evidence for a regulatory role of ATP.

  2003cited by this paper
• Identification of Sef, a novel modulator of FGF signalling

  2002cited by this paper
• The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism.

  2002cited by this paper
• Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons.

  2002cited by this paper
• Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1

  2002cited by this paper
• Molecular modelling and experimental studies of mutation and cell-adhesion sites in the fibronectin type III and whey acidic protein domains of human anosmin-1.

  2001cited by this paper
• Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization*

  2001cited by this paper
• Identification of an N-cadherin Motif That Can Interact with the Fibroblast Growth Factor Receptor and Is Required for Axonal Growth*

  2001cited by this paper
• The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.

  2001cited by this paper
• Disruption of gastrulation and heparan sulfate biosynthesis in EXT1-deficient mice.

  2000cited by this paper
• CAMs and axonal growth: a critical evaluation of the role of calcium and the MAPK cascade.

  2000cited by this paper
• Anosmin‐1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome‐linked Kallmann syndrome

  1999cited by this paper
• Gene expression pattern Characterization of the two zebra ® sh orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndrome

  1999cited by this paper
• Fibroblast growth factor receptor signalling is dictated by specific heparan sulphate saccharides.

  1999cited by this paper
• Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner.

  1998cited by this paper
• Molecular Cloning and Expression of ps20 Growth Inhibitor

  1998cited by this paper
• The fibronectin type III domain as a scaffold for novel binding proteins.

  1998cited by this paper
• Structural Modification of Fibroblast Growth Factor-binding Heparan Sulfate at a Determinative Stage of Neural Development*

  1998cited by this paper
• Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system.

  1996cited by this paper
• The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis.

  1996cited by this paper
• The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component.

  1996cited by this paper
• Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo.

  1994cited by this paper
• Urokinase‐type Plasminogen Activator Expression by Neurons and Oligodendrocytes During Process Outgrowth in Developing Rat Brain

  1993cited by this paper
• A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

  1991cited by this paper
• The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.

  1991cited by this paper
• The WDNM1 gene product is a novel member of the 'four-disulphide core' family of proteins.

  1991cited by this paper
• Identical twins discordant for Kallmann's syndrome.

  1990cited by this paper
• Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome.

  1989cited by this paper
• Edinburgh Research Explorer Expression of secretory leukocyte protease inhibitor and elafin in human fallopian tube and in an in-vitro model of Chlamydia trachomatis infection

  year unknowncited by this paper

• Signaling of Mitogenic and Metabolic Activities by Fibroblast Growth Factors

  2025cites this paper
• ANOS1 accelerates the progression of esophageal cancer identified by multi-omic approaches.

  2024cites this paper
• Olfactory bulb neurogenesis depending on signaling in the subventricular zone.

  2023cites this paper
• Interaction of Prokineticin Receptors with Accessory Proteins

  2023cites this paper
• A Simple Purification Method for Heat-Stable Recombinant Low Molecular Weight Proteins and Peptides Via GST-Fusion Products.

  2023cites this paper
• Simplification of the purification of heat stable recombinant low molecular weight proteins and peptides from GST-fusion products.

  2021cites this paper
• ANOS1 Gene

  2020cites this paper
• Prenatal Development of GnRH Neurons

  2018cites this paper
• Functional insights from proteome-wide structural modeling of Treponema pallidum subspecies pallidum, the causative agent of syphilis

  2018cites this paper
• Genetics of vesicoureteral reflux and congenital anomalies of the kidney and urinary tract

  2017cites this paper
• The role of whey acidic protein four-disulfide-core proteins in respiratory health and disease

  2017cites this paper
• Potential Biomarkers in Diagnosis of Human Gastric Cancer

  2016cites this paper
• Cell adhesion to anosmin via α5β1, α4β1, and α9β1 integrins

  2016cites this paper
• GnRH, anosmia and hypogonadotropic hypogonadism--where are we?

  2015cites this paper
• Mutation analyses in pedigrees and sporadic cases of ethnic Han Chinese Kallmann syndrome patients

  2015cites this paper
• Pathophysiology of Ovarian Function in the Human Female

  2015cites this paper
• Anosmin-1 contributes to brain tumor malignancy through integrin signal pathways

  2013cites this paper
• Síndrome de Kallmann - Revisión sistemática de la literatura

  2010cites this paper