Difference between revisions of "BRCA1 interacting protein C-terminal helicase 1"

BRCA1 interacting protein C-terminal helicase 1 (view source)

138 bytes added , 4 November

no edit summary

48,868

edits

Revision as of 13:59, 8 September 2023 (view source) Michael (talk \| contribs) ← Older edit		Revision as of 05:22, 4 November 2024 (view source) Michael (talk \| contribs) Newer edit →
Line 1:		Line 1:
			[[Image: Serous carcinoma - fallopian tube -- intermed mag.jpg \| thumb \| right \| Serous carcinoma of the fallopian tube. [[H&E stain]].]]
	'''BRCA1 interacting protein C-terminal helicase 1''', abbreviated '''BRIP''', is a tumour suppressor gene that interacts with [[BRCA1]] to help repair double-strand DNA breaks.<ref>URL: [https://www.ncbi.nlm.nih.gov/gene/83990 https://www.ncbi.nlm.nih.gov/gene/83990]. Accessed on: 05 March 2020.</ref> <ref name=NBK1401>URL: [https://www.ncbi.nlm.nih.gov/books/NBK1401/ https://www.ncbi.nlm.nih.gov/books/NBK1401/]. Accessed on: 05 March 2020.</ref> It is a good example of a gene whose mutations cause clinical manifestations that can be dominant or recessive.		'''BRCA1 interacting protein C-terminal helicase 1''', abbreviated '''BRIP''', is a tumour suppressor gene that interacts with [[BRCA1]] to help repair double-strand DNA breaks.<ref>URL: [https://www.ncbi.nlm.nih.gov/gene/83990 https://www.ncbi.nlm.nih.gov/gene/83990]. Accessed on: 05 March 2020.</ref> <ref name=NBK1401>URL: [https://www.ncbi.nlm.nih.gov/books/NBK1401/ https://www.ncbi.nlm.nih.gov/books/NBK1401/]. Accessed on: 05 March 2020.</ref> It is a good example of a gene whose mutations cause clinical manifestations that can be dominant or recessive.