FIGURE

Figure 1

ID
ZDB-FIG-240212-16
Publication
Napoli et al., 2024 - Developmental loss of NMDA receptors results in supernumerary forebrain neurons through delayed maturation of transit-amplifying neuroblasts
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Figure 1

grin1−/− fish do not show gross morphological changes in brain structure. (AF) Nissl stained 5-micron coronal sections of a 5 dpf wild-type (A, C, & E) and a grin1−/− (B, D, & F) fish at the anterior (A & B), mid (C & D) and posterior (E & F) forebrain. Measurement locations indicated in (C): yellow solid line, dorsoventral height measured at midline; dashed line, mediolateral width measured at widest aspect of the brain; and dotted line, hemispheric area. (GI) Box and whisker plots indicating median value, interquartile ranges, and maximum and minimum values, for coronal morphometric measurements of dorsoventral height (G), mediolateral width (H) and hemispheric area (I). In this and all subsequent figures, points represent individual values for each fish. (J & K) External brain size proxy measurements (J) and total area of fish measured in lateral view (K). Inset to (J): dorsal (upper) and lateral (lower) views with measurement locations indicated in red dashed line (optic tectum width, TeO), dotted line (eye diameter, ED), and solid line (eye to ear distance, EE). (l) Total hemispheric cell counts of 5 dpf fish performed on representative sections at anterior, mid, and posterior levels of the forebrain (A–F) in wild-type and grin1−/− fish. Significance (t-test) is indicated (*p < 0.05; ns, not significant). For specific sample sizes and statistical values see Table 2.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
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