Paper · 10433902
Heparan sulfate proteoglycans are essential for FGF receptor signaling during Drosophila embryonic development.
Lin X and 3 others. Development, 1999. Cited by 298 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. Heparan sulfate proteoglycans are essential for FGF receptor signaling during Drosophila embryonic development. Papers, record 10433902. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/10433902
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- Heparan sulfate proteoglycans are essential for FGF receptor signaling during Drosophila embryonic development.
- PubMed
Topics18
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Drosophila | Major topic |
| Drosophila Proteins | Major topic |
| Fibroblast Growth Factors | Major topic |
| Heparan Sulfate Proteoglycans | Major topic |
| Protein-Tyrosine Kinases | Major topic |
| Receptors, Fibroblast Growth Factor | Major topic |
| Amidohydrolases | |
| Animals | |
| Gene Expression | |
| Genes, Insect | |
| Insect Proteins | |
| Mesoderm | |
| Mitogen-Activated Protein Kinases | |
| Mutation | |
| Phenotype | |
| Signal Transduction | |
| Sulfotransferases | |
| Trachea |
Source PubMed
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Trials0
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Comments and corrections0
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References0
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Cited by104
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 298 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 39,729,990 | Heparan sulfate regulates the fate decisions of human pluripotent stem cells. | Stem Cell Reports | 2025 | https://conductscience.org/library/papers/39729990 | PubMed |
| 37,750,089 | FGFR families: biological functions and therapeutic interventions in tumors. | MedComm (2020) | 2023 | https://conductscience.org/library/papers/37750089 | PubMed |
| 37,016,295 | The genetic basis of wing spots in Pieris canidia butterflies. | BMC Genomics | 2023 | https://conductscience.org/library/papers/37016295 | PubMed |
| 36,699,460 | Regulation of autophagy, lipid metabolism, and neurodegenerative pathology by heparan sulfate proteoglycans. | Front Genet | 2022 | https://conductscience.org/library/papers/36699460 | PubMed |
| 36,503,154 | Neuronal expression of ndst3 in early zebrafish development is responsive to Wnt signaling manipulation. | Gene Expr Patterns | 2023 | https://conductscience.org/library/papers/36503154 | PubMed |
| 35,648,312 | Therapeutic Potential of Skin Stem Cells and Cells of Skin Origin: Effects of Botanical Drugs Derived from Traditional Medicine. | Stem Cell Rev Rep | 2022 | https://conductscience.org/library/papers/35648312 | PubMed |
| 35,319,900 | Coreceptor functions of cell surface heparan sulfate proteoglycans. | Am J Physiol Cell Physiol | 2022 | https://conductscience.org/library/papers/35319900 | PubMed |
| 34,124,035 | In vivo Functional Genomics for Undiagnosed Patients: The Impact of Small GTPases Signaling Dysregulation at Pan-Embryo Developmental Scale. | Front Cell Dev Biol | 2021 | https://conductscience.org/library/papers/34124035 | PubMed |
| 32,664,575 | Cerebellar Morphology and Behavioral Profiles in Mice Lacking Heparan Sulfate Ndst Gene Function. | J Dev Biol | 2020 | https://conductscience.org/library/papers/32664575 | PubMed |
| 32,001,716 | Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy. | Nat Commun | 2020 | https://conductscience.org/library/papers/32001716 | PubMed |
1 to 10 of 104
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Data0
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Data dates
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- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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