Neuron derived neurotrophic factor

Neuron derived neurotrophic factor (NDNF) is a secreted protein that, in humans, is located on chromosome 4.[5] This protein helps in the growth, survival, migration, and differentiation of neurons.[6] To assist with migration, NDNF shows neuro-repulsive effects on GnRH neurons. Loss of function (LoF) in the NDNF gene has been shown to be a cause of a disease known as congenital hypogonadotropic hypogonadism, which can have associated cleft lip and cleft palate.[7] A preliminary study has shown that knock-down of ndnf reduces development of the ethmoid plate, which is homologous to the human palate.[8][9]
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000173376 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000049001 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "NDNF neuron derived neurotrophic factor [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlm.nih.gov. Retrieved 2023-05-12.
- ^ Kuang XL, Zhao XM, Xu HF, Shi YY, Deng JB, Sun GT (October 2010). "Spatio-temporal expression of a novel neuron-derived neurotrophic factor (NDNF) in mouse brains during development". BMC Neuroscience. 11 (1): 137. doi:10.1186/1471-2202-11-137. PMC 2984559. PMID 20969804.
- ^ Messina A, Pulli K, Santini S, Acierno J, Känsäkoski J, Cassatella D, et al. (January 2020). "Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism". American Journal of Human Genetics. 106 (1): 58–70. doi:10.1016/j.ajhg.2019.12.003. PMC 7042563. PMID 31883645.
- ^ Swartz ME, Sheehan-Rooney K, Dixon MJ, Eberhart JK (September 2011). "Examination of a palatogenic gene program in zebrafish". Developmental Dynamics. 240 (9): 2204–2220. doi:10.1002/dvdy.22713. PMC 3202344. PMID 22016187.
- ^ Melvin VS, Feng W, Hernandez-Lagunas L, Artinger KB, Williams T (July 2013). "A morpholino-based screen to identify novel genes involved in craniofacial morphogenesis". Developmental Dynamics. 242 (7): 817–831. doi:10.1002/dvdy.23969. PMC 4027977. PMID 23559552.
Further reading
- Utine GE, Aktas D (2006). "Mosaicism for terminal deletion of 4q". Genetic Counseling. 17 (2): 205–209. PMID 16970039.
- Kalsi G, Kuo PH, Aliev F, Alexander J, McMichael O, Patterson DG, et al. (June 2010). "A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts". Human Molecular Genetics. 19 (12): 2497–2506. doi:10.1093/hmg/ddq112. PMC 2876884. PMID 20332099.
- Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Molecular Medicine. 16 (7–8): 247–253. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
Content Disclaimer
Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.
- The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
- There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
- It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
- Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
- Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.