COL4A6 is dispensable for autosomal recessive Alport syndrome

10.1038/srep29450

Saved in:

Bibliographic Details
Main Authors:	Murata, T, Katayama, K, Oohashi, T, Jahnukainen, T, Yonezawa, T, Sado, Y, Ishikawa, E, Nomura, S, Tryggvason, K, Ito, M
Other Authors:	DUKE-NUS MEDICAL SCHOOL
Format:	Article
Published:	Nature Publishing Group 2020
Subjects:	COL4A1 protein, human Col4a1 protein, mouse COL4A2 protein, human Col4a2 protein, mouse COL4A6 protein, human collagen type 4 peptide fragment adolescent animal C57BL mouse cross breeding female genetics glomerulus basement membrane homozygote human intron kidney knockout mouse male metabolism mouse mutation nephritis recessive gene Adolescent Animals Collagen Type IV Crosses, Genetic Female Genes, Recessive Glomerular Basement Membrane Homozygote Humans Introns Kidney Male Mice Mice, Inbred C57BL Mice, Knockout Mutation Nephritis, Hereditary Peptide Fragments
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/182453
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	National University of Singapore

id	sg-nus-scholar.10635-182453
record_format	dspace
spelling	sg-nus-scholar.10635-1824532024-11-10T02:50:15Z COL4A6 is dispensable for autosomal recessive Alport syndrome Murata, T Katayama, K Oohashi, T Jahnukainen, T Yonezawa, T Sado, Y Ishikawa, E Nomura, S Tryggvason, K Ito, M DUKE-NUS MEDICAL SCHOOL COL4A1 protein, human Col4a1 protein, mouse COL4A2 protein, human Col4a2 protein, mouse COL4A6 protein, human collagen type 4 peptide fragment adolescent animal C57BL mouse cross breeding female genetics glomerulus basement membrane homozygote human intron kidney knockout mouse male metabolism mouse mutation nephritis recessive gene Adolescent Animals Collagen Type IV Crosses, Genetic Female Genes, Recessive Glomerular Basement Membrane Homozygote Humans Introns Kidney Male Mice Mice, Inbred C57BL Mice, Knockout Mutation Nephritis, Hereditary Peptide Fragments 10.1038/srep29450 Scientific Reports 6 29450 2020-10-31T11:31:05Z 2020-10-31T11:31:05Z 2016 Article Murata, T, Katayama, K, Oohashi, T, Jahnukainen, T, Yonezawa, T, Sado, Y, Ishikawa, E, Nomura, S, Tryggvason, K, Ito, M (2016). COL4A6 is dispensable for autosomal recessive Alport syndrome. Scientific Reports 6 : 29450. ScholarBank@NUS Repository. https://doi.org/10.1038/srep29450 2045-2322 https://scholarbank.nus.edu.sg/handle/10635/182453 Attribution 4.0 International http://creativecommons.org/licenses/by/4.0/ Nature Publishing Group Unpaywall 20201031
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
topic	COL4A1 protein, human Col4a1 protein, mouse COL4A2 protein, human Col4a2 protein, mouse COL4A6 protein, human collagen type 4 peptide fragment adolescent animal C57BL mouse cross breeding female genetics glomerulus basement membrane homozygote human intron kidney knockout mouse male metabolism mouse mutation nephritis recessive gene Adolescent Animals Collagen Type IV Crosses, Genetic Female Genes, Recessive Glomerular Basement Membrane Homozygote Humans Introns Kidney Male Mice Mice, Inbred C57BL Mice, Knockout Mutation Nephritis, Hereditary Peptide Fragments
spellingShingle	COL4A1 protein, human Col4a1 protein, mouse COL4A2 protein, human Col4a2 protein, mouse COL4A6 protein, human collagen type 4 peptide fragment adolescent animal C57BL mouse cross breeding female genetics glomerulus basement membrane homozygote human intron kidney knockout mouse male metabolism mouse mutation nephritis recessive gene Adolescent Animals Collagen Type IV Crosses, Genetic Female Genes, Recessive Glomerular Basement Membrane Homozygote Humans Introns Kidney Male Mice Mice, Inbred C57BL Mice, Knockout Mutation Nephritis, Hereditary Peptide Fragments Murata, T Katayama, K Oohashi, T Jahnukainen, T Yonezawa, T Sado, Y Ishikawa, E Nomura, S Tryggvason, K Ito, M COL4A6 is dispensable for autosomal recessive Alport syndrome
description	10.1038/srep29450
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL Murata, T Katayama, K Oohashi, T Jahnukainen, T Yonezawa, T Sado, Y Ishikawa, E Nomura, S Tryggvason, K Ito, M
format	Article
author	Murata, T Katayama, K Oohashi, T Jahnukainen, T Yonezawa, T Sado, Y Ishikawa, E Nomura, S Tryggvason, K Ito, M
author_sort	Murata, T
title	COL4A6 is dispensable for autosomal recessive Alport syndrome
title_short	COL4A6 is dispensable for autosomal recessive Alport syndrome
title_full	COL4A6 is dispensable for autosomal recessive Alport syndrome
title_fullStr	COL4A6 is dispensable for autosomal recessive Alport syndrome
title_full_unstemmed	COL4A6 is dispensable for autosomal recessive Alport syndrome
title_sort	col4a6 is dispensable for autosomal recessive alport syndrome
publisher	Nature Publishing Group
publishDate	2020
url	https://scholarbank.nus.edu.sg/handle/10635/182453
_version_	1821208573277896704

COL4A6 is dispensable for autosomal recessive Alport syndrome

Similar Items