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Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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SEMA3C

Introduction

Semaphorin-3C is a protein that in humans is encoded by the SEMA3C gene.[1][2][3]

References

References

  1. ↑ Püschel AW, Adams RH, Betz H (May 1995). “Murine semaphorin D/collapsin is a member of a diverse gene family and creates domains inhibitory for axonal extension”. Neuron. 14 (5): 941–8. doi:10.1016/0896-6273(95)90332-1. PMID 7748561.
  2. ↑ Mangasser-Stephan K, Dooley S, Welter C, Mutschler W, Hanselmann RG (May 1997). “Identification of human semaphorin E gene expression in rheumatoid synovial cells by mRNA differential display”. Biochemical and Biophysical Research Communications. 234 (1): 153–6. doi:10.1006/bbrc.1997.6607. PMID 9168980.
  3. ↑ “Entrez Gene: SEMA3C sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C”.
Further reading

Further reading

  • Robertson NG, Khetarpal U, Gutiérrez-Espeleta GA, Bieber FR, Morton CC (September 1994). “Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening”. Genomics. 23 (1): 42–50. doi:10.1006/geno.1994.1457. PMID 7829101.
  • Bonaldo MF, Lennon G, Soares MB (September 1996). “Normalization and subtraction: two approaches to facilitate gene discovery”. Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
  • Chen H, Chédotal A, He Z, Goodman CS, Tessier-Lavigne M (September 1997). “Neuropilin-2, a novel member of the neuropilin family, is a high affinity receptor for the semaphorins Sema E and Sema IV but not Sema III”. Neuron. 19 (3): 547–59. doi:10.1016/S0896-6273(00)80371-2. PMID 9331348.
  • Yamada T, Endo R, Gotoh M, Hirohashi S (December 1997). “Identification of semaphorin E as a non-MDR drug resistance gene of human cancers”. Proceedings of the National Academy of Sciences of the United States of America. 94 (26): 14713–8. doi:10.1073/pnas.94.26.14713. PMC 25101. PMID 9405678.
  • Galani E, Sgouros J, Petropoulou C, Janinis J, Aravantinos G, Dionysiou-Asteriou D, Skarlos D, Gonos E (2002). “Correlation of MDR-1, nm23-H1 and H Sema E gene expression with histopathological findings and clinical outcome in ovarian and breast cancer patients”. Anticancer Research. 22 (4): 2275–80. PMID 12174914.
  • Rieger J, Wick W, Weller M (June 2003). “Human malignant glioma cells express semaphorins and their receptors, neuropilins and plexins”. Glia. 42 (4): 379–89. doi:10.1002/glia.10210. PMID 12730958.
  • Miller LE, Weidler C, Falk W, Angele P, Schaumburger J, Schölmerich J, Straub RH (April 2004). “Increased prevalence of semaphorin 3C, a repellent of sympathetic nerve fibers, in the synovial tissue of patients with rheumatoid arthritis”. Arthritis and Rheumatism. 50 (4): 1156–63. doi:10.1002/art.20110. PMID 15077297.
  • Beckers J, Herrmann F, Rieger S, Drobyshev AL, Horsch M, Hrabé de Angelis M, Seliger B (April 2005). “Identification and validation of novel ERBB2 (HER2, NEU) targets including genes involved in angiogenesis”. International Journal of Cancer. 114 (4): 590–7. doi:10.1002/ijc.20798. PMID 15609325.
  • Herman JG, Meadows GG (May 2007). “Increased class 3 semaphorin expression modulates the invasive and adhesive properties of prostate cancer cells”. International Journal of Oncology. 30 (5): 1231–8. doi:10.3892/ijo.30.5.1231. PMID 17390026.