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Development (Cambridge, England)|April 18, 2002
Semaphorin 1a and semaphorin 1b are required for correct epidermal cell positioning and adhesion during morphogenesis in C. elegansVal E Ginzburg, Peter J Roy, Joseph G CulottiDevelopment (Cambridge, England)|April 18, 2002
Fgf3 and Fgf8 are required together for formation of the otic placode and vesicleHabib Maroon, Jennifer Walshe, Radma Mahmood, et al.Development (Cambridge, England)|April 18, 2002
The C. elegans LAR-like receptor tyrosine phosphatase PTP-3 and the VAB-1 Eph receptor tyrosine kinase have partly redundant functions in morphogenesisRobert J Harrington, Michael J Gutch, Michael O Hengartner, et al.Development (Cambridge, England)|April 1, 1995
Cell dispersion patterns in different cortical regions studied with an X-inactivated transgenic markerS S Tan, B Faulkner-Jones, S J Breen, et al.Development (Cambridge, England)|April 1, 1995
Identifying tumor suppressors in genetic mosaics: the Drosophila lats gene encodes a putative protein kinaseT Xu, W Wang, S Zhang, et al.Development (Cambridge, England)|April 1, 1995
Vascular endothelial cell lineage-specific promoter in transgenic miceT M Schlaeger, Y Qin, Y Fujiwara, et al.Development (Cambridge, England)|April 1, 1995
Scleraxis: a basic helix-loop-helix protein that prefigures skeletal formation during mouse embryogenesisP Cserjesi, D Brown, K L Ligon, et al.Development (Cambridge, England)|April 1, 1995
The limbic system-associated membrane protein (LAMP) selectively mediates interactions with specific central neuron populationsV Zhukareva, P LevittDevelopment (Cambridge, England)|April 1, 1995
Control of proliferation activation in quiescent neuroblasts of the Drosophila central nervous systemS DattaDevelopment (Cambridge, England)|April 1, 1995
An analysis of the response to gut induction in the C. elegans embryoB GoldsteinPageof 1,629