MiR-212 and miR-132 are dispensable for mouse mammary gland development

Nature Genetics

Volumn 46, Issue 8, 2014, Pages 802-804

  Kayo, Hiroyuki ^a   Kiga, Kotaro ^a   Fukuda Yuzawa, Yoko ^a   Hedlund, Sebastian ^a   Murakami, Kazuyoshi ^a   De La Rosa Velazquez, Inti A ^a   Kimura, Tokuhiro ^b   Shimoda, Kouji ^c   Tanabe, Masanobu ^c   Fukao, Taro ^a  

^a MAX PLANCK INSTITUTE OF IMMUNOBIOLOGY AND EPIGENETICS   (Germany)

^b YAMAGUCHI UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MICRORNA; MICRORNA 132; MICRORNA 212; NEOMYCIN; UNCLASSIFIED DRUG;

BREAST DEVELOPMENT; CELL POPULATION; EMBRYONIC STEM CELL; GENE LOCUS; GENETIC VARIABILITY; HOMOZYGOSITY; LETTER; MAMMARY GLAND; MAMMARY GLAND DEVELOPMENT; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; ANIMAL; CELL COMMUNICATION; EPITHELIUM CELL; FEMALE; GROWTH, DEVELOPMENT AND AGING; METABOLISM; PATHOLOGY; UDDER;

ANIMALS; CELL COMMUNICATION; EPITHELIAL CELLS; FEMALE; MAMMARY GLANDS, ANIMAL; MICRORNAS;

EID: 84905499604     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2990     Document Type: Letter

References (2)

1. Ucar, A. et al. Nat. Genet. 42, 1101-1108 (2010).
2. Wales, M.M. et al. Nat. Med. 1, 570-577 (1995).