The formins: Connecting embryonic pattern formation and hypofertility in the mouse

Annals of the New York Academy of Sciences

Volumn 1038, Issue , 2004, Pages 75-79

  Leder, Philip ^a  

^a HARVARD MEDICAL SCHOOL   (United States)

Author keywords

Chromosome; Fertility; Formin; Spindle body

Indexed keywords

AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME SEGREGATION; CONFERENCE PAPER; EMBRYO PATTERN FORMATION; FORMIN GENE; GENE; GENE FUNCTION; GENE LOCUS; GENE MUTATION; HYPOFERTILITY; INFERTILITY; KIDNEY AGENESIS; KNOCKOUT MOUSE; LIMB MALFORMATION; MOUSE; NONHUMAN; PHENOTYPE; TRANSGENIC MOUSE;

MUS MUSCULUS;

EID: 17744365408     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1196/annals.1315.013     Document Type: Conference Paper

References (3)

1. LEADER, B. & P. LEDER. 2000. Formin 2, a novel formin homology protein of the cappucino subfamily, is highly expressed in the developing and adult central nervous system. Mech. Dev. 93: 221-231.
2. LEADER, B. , H. LIM, M.J. CARABATSOS, et al. 2002. Formin-2, polyploidy, hypofertility, and the positioning of the meiotic spindle in mouse oocytes. Nature Cell Biol. 4:921-928.
3. WOYCHIK, R.P., R.L. MAAS, R. ZELLER, et al. 1990. The formins of proteins deduced from the alternative transcripts of the limb deformity gene. Nature 346: 858-853.