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Temporal BMP4 effects on mouse embryonic and extraembryonic development

• Authors : Hadas, R.; Rubinstein, H.; Mittnenzweig, M.

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The extended analogy of extraembryonic development in insects and amniotes

• Authors : Panfilio, Kristen A. A.; Chuva de Sousa Lopes, Susana Marina

Subjects: Biology and Life Sciences; Medicine and Health Sciences; extraembryonic development

• Source: PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES ; ISSN: 0962-8436 ; ISSN: 1471-2970

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Epithelial reorganization events during late extraembryonic development in a hemimetabolous insect

• Authors : Panfilio, Kristen A.; Roth, Siegfried

Subjects: ddc:570; doc-type:article

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The transcription factor GATA6 is essential for early extraembryonic development

• Authors : Koutsourakis, M (Manousos); Langeveld, JCM; Patient, R

Subjects: dk/atira/pure/keywords/researchprograms/AFL001000/EMCMGC021302; article; article

• Source: Koutsourakis , M , Langeveld , JCM , Patient , R , Beddington , R & Grosveld , F 1998 , ' The transcription factor GATA6 is essential for early extraembryonic

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The transcription factor GATA6 is essential for early extraembryonic development

• Authors : Koutsourakis, M. (Manousos); Langeveld, A. (An); Patient, R. (Roger)

Subjects: Gene Expression Regulation, Developmental; Animals; Blastocyst/metabolism

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Extraembryonic development in insects and the acrobatics of blastokinesis

• Authors : Panfilio, Kristen A.

• Source: Developmental Biology ; volume 313, issue 2, page 471-491 ; ISSN 0012-1606

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The transcription factor GATA6 is essential for early extraembryonic development

• Authors : Koutsourakis, M; Langeveld, A; Patient, R

Subjects: Journal Articles

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The Nf2 tumor suppressor gene product is essential for extraembryonic development immediately prior to gastrulation.

• Authors : McClatchey, A I; Saotome, I; Ramesh, V

Subjects: Research Papers

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Figure 4—figure supplement 2. Timeline to outline reported features of extraembryonic development in the context of M. abdita embryonic staging. ; Definition and duration of developmental stages are as previously reported (Wotton et al., 2014). Universal landmarks of fly development (onset of germband extension, onset of germband retraction and end of germband retraction) are shown as observed in vivo and in quantified SPIM recordings. Hallmarks of amnion and serosa development are shown in this context as reported in main text Figures 1–3, stars indicate time points of amnion/serosa disjunction (a, anterior; l, lateral; p, posterior).

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Figure 1—figure supplement 1. Quantitative analyses of cell measures in M.abdita embryos fixed at subsequent stages of development. ; (A) Model of early extraembryonic development in M. abdita without distinction of amnion and serosa (extraembryonic tissue labeled in black). (B–Db’) Global embryonic view of fixed embryos stained for Phallacidin to outline actin cytoskeleton (B–D), with close-up views (Ba-Db) and three dimensional volume renderings (Ba’-Db’) of embryonic (Ba-a’, Ca-a’, Da-a’) and extraembryonic cells (Bb-b’, Cb-b’, Db-b’). (E–G) Collective quantitative analysis of apical cell area (E), apical cell circularity (F) and relative cell height (G). Apical circularity (c) was defined as c = 1 for a perfect circle and c < 1 for angular shapes with c = 4 π area/perimeter2 (Thomas and Wieschaus, 2004). Unless indicated otherwise, embryos and close-ups are shown with anterior left and dorsal up. Presumptive embryonic cells and corresponding quantifications are shaded grey, presumptive extraembryonic cells and corresponding quantification are in black. Scale bars, 10 µm.

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