1 e defects in the immune response but show no
embryologic abnormalities.
2 To integrate knowledge on the
embryologic and molecular basis of optic fissure closure
3 drome to postnatal onset as a consequence of
embryologic anomalies affecting pancreatic drainage post
4 These patterns of Tbx5 expression provide an
embryologic basis for the prevalence of atrial septal de
5 ogenicity, such groupings often lack a sound
embryologic basis, given the etiologic heterogeneity of
6 Hedgehog signaling mediates
embryologic development of the central nervous system an
7 Embryologic development of the dorsal mesenteries sugges
8 present in a pattern following the lines of
embryologic development of the ectoderm.
9 t in concert with other proteins to regulate
embryologic development of the fly.
10 or the regression of the vessel walls during
embryologic development), via anomalous or decompressing
11 This review article focuses on the
embryologic development, hemodynamics, and imaging featu
12 ons of chromatin at protein-coding genes, in
embryologic development, remain elusive.
13 e than primitive mesenchymal cells surviving
embryologic development, they differ from mesenchymal ce
14 These TSCs have access to
embryologic developmental programs, including the capaci
15 These findings further establish the
embryologic,
developmentally arrested, hemangioblast as
16 ly members have distinct roles in a range of
embryologic,
differentiation or response pathways (as in
17 Alternatively, vascular malformations are
embryologic errors in vasculogenesis.
18 The experimental manipulation of early
embryologic events, resulting in the misexpression of th
19 nt the activity of C1 protein to mediate two
embryologic functions of Dkk1: induction of chordal and
20 related to distinct smooth muscle cell (SMC)
embryologic lineages.
21 y be indicative of a previously unrecognized
embryologic malformation of the cochlear nerve.
22 on and classified according to a new imaging/
embryologic MCD classification system.
23 Lens induction is a classical
embryologic model to study cell fate determination.
24 been suspected on the basis of their common
embryologic origin and apparent parallel involvement in
25 h the left ventricle, the RV has a different
embryologic origin, undergoes a dramatic change during t
26 This study defines the aortic
embryologic origin-specific proteome in a validated iPSC
27 n their biology, genetics, metabolomics, and
embryologic origin.
28 cal presentation, differential diagnosis and
embryologic origin.
29 Accruing evidence indicates that the
embryologic origins of axial and appendicular muscles ar
30 rapidly progressing from the recognition of
embryologic origins to insight into the genetic basis fo
31 ially complex, with distinct pathologies and
embryologic origins.
32 tube closure of the spinal column during the
embryologic period.
33 microRNA (miRNA) expression patterns of many
embryologic,
physiologic, and oncogenic processes have b
34 l its developmental origin from two distinct
embryologic populations: the metanephric mesenchyme and
35 exible enough to be easily modified when new
embryologic processes are described or new malformations
36 Due to their
embryologic relationship with other urogenital organs, c
37 By examining serial
embryologic sections, Wilhelm His, Jr, showed that a con
38 n, the allantois frequently is overlooked in
embryologic studies.
39 s used molecular genetic, pharmacologic, and
embryologic techniques to study the biology of ARS in a