Roles of the imprinted gene lgf2 and paternal duplication of distal chromosome 7 in the perinatal abnormalities of androgenetic mouse chimeras

Development

Volumn 124, Issue 23, 1997, Pages 4897-4904

  McLaughlin, K John ^a   Kochanowski, Helga ^a   Solter, Davor ^a   Schwarzkopf, Georg ^b   Szabó, Piroska E ^c   Mann, Jeffrey R ^c  

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

^b UNIVERSITY OF FREIBURG   (Germany)

^c CITY OF HOPE NATIONAL MEDICAL CENTER   (United States)

Author keywords

Androgenetic; Beckwith Wiedemann syndrome; Chimera; Growth factor 2; Imprinting; Insulin like; Mouse

Indexed keywords

MITOGENIC AGENT; SOMATOMEDIN B;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHIMERA; CHROMOSOME 7; DEVELOPMENTAL GENETICS; EMBRYO; EMBRYO DEVELOPMENT; GENE DUPLICATION; GENE MUTATION; GENOME IMPRINTING; MOUSE; NONHUMAN; OOCYTE; PERINATAL DEATH; PRIORITY JOURNAL; RIB CARTILAGE; SKELETON MALFORMATION; STEM CELL;

ANIMALS; CARTILAGE; CHIMERA; CHROMOSOMES; EMBRYO; FEMALE; FETAL DEATH; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENOMIC IMPRINTING; INSULIN-LIKE GROWTH FACTOR II; MALE; MICE; MICE, INBRED C57BL; MICE, INBRED CBA; MICE, INBRED STRAINS; MULTIGENE FAMILY; RIBS; STEM CELLS;

ANIMALIA; RODENTIA; VERTEBRATA;

EID: 0031441067     PISSN: 09501991     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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