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1  adult mice, including dramatically from mid-phalangeal amputation.
2 e-mapped population, pillar, Deiters', inner phalangeal and border cells had equal capacity to regene
3 ose-response relationship between both 2D:4D phalangeal and metacarpal length ratios and the risk of
4                                    The 2D:4D phalangeal and metacarpal length ratios were measured se
5 measured in capillaries of the dorsal middle phalangeal area of the finger in six subjects using a re
6 nerates is the distal region of the terminal phalangeal bone that is associated with the nail organ.
7 lls of the connective tissue surrounding the phalangeal bones of regeneration competent (P3) and inco
8 ly from all australopiths, but also from the phalangeal bones of the penecontemporaneous and geograph
9 mproper segmentations of many metacarpal and phalangeal bones.
10 tes, and glial cells adjacent to IHCs [inner phalangeal cells (IPCs)] in whole-mount preparations of
11  ablated inner border cells (IBCs) and inner phalangeal cells (IPhCs), the two types of supporting ce
12 AV2.7m8 infects inner pillar cells and inner phalangeal cells with high efficiency.
13 hair cell area (i.e., inner border and inner phalangeal cells) and outer hair cell area (i.e., Deiter
14  transients, markers of the SC subtype inner phalangeal cells, and survive in the mature cochlea.
15 e intermediate cells of the SV, in the inner phalangeal cells, Hensen's, Deiters' and pillar cells, i
16 iv) cytoplasmic attraction of adjacent inner phalangeal cells, which envelop IHCs.
17 y ectopic hair cells at the expense of inner phalangeal cells.
18  inner hair cells and their associated inner phalangeal cells.
19 d duplications of inner hair cells and inner phalangeal cells.
20 We also detected Tbc1d24 expression in mouse phalangeal chondrocytes and calvaria, which suggests a r
21                                          The phalangeal cortical structure demonstrates diversity in
22            Here, we investigate the internal phalangeal cortical structure of the nearly complete Aus
23 mportant implication of this finding is that phalangeal curvature among fossil hominins is evidently
24 ds produced by lifetime arboreal activities, phalangeal curvature appears to be shaped largely by gen
25     We show that the degree of hand and foot phalangeal curvature in this individual is indistinguish
26                        Here, we describe the phalangeal curvature of a chimpanzee who was raised duri
27 ent fossil hominins also exhibit substantial phalangeal curvature, which, too, has been interpreted a
28 including more severe carpal, metacarpal and phalangeal defects.
29 ds to amputations at the level of the second phalangeal element (P2) of neonatal digits, and the hind
30 more proximal location, e.g. the subterminal phalangeal element (P2), fails to regenerate.
31 mputated at a proximal level of the terminal phalangeal element (P3).
32 in the extensor tendons and ligaments of the phalangeal elements of the limb.
33 is corroborated by the formation of only two phalangeal elements which are unique to digit one on the
34 t: six metatarsal fractures and one proximal phalangeal fracture.
35  the hands: six metacarpal and nine proximal phalangeal fractures.
36           This molecular reversal eliminates phalangeal joint spaces, and consequently, Short digits
37     Aspiration of his first right metatarsal phalangeal joint was performed and fungal hyphae were ob
38 tterning defects with longitudinally shifted phalangeal joints and impaired chondrogenesis.
39                                              Phalangeal lengths were most similar to those of Gorilla
40  digit segments as compared to the ancestral phalangeal pattern of mammaliaforms and extant mammals.
41 limb are morphologically similar in terms of phalangeal pattern, it has been suggested that self-orga
42 ndicates that BMP signaling is necessary for phalangeal prechondrogenic cells to differentiate into c
43 progenitors, which arise in conjunction with phalangeal precursors at the digit tip.
44 s by fusion of the proximal and intermediate phalangeal precursors, a developmental process for which
45 ided by the outer hair cell and Deiters cell phalangeal process.
46 cell, the Deiters cell, and the Deiters cell phalangeal process.
47 ies that the RL mosaic, comprised of OHC and phalangeal-process tops joined together by adhesion mole
48 rangement of the outer hair cells (OHCs) and phalangeal processes of the Deiters cells serves to crea
49 ution of outer pillar cell and Deiters' cell phalangeal processes that are not corrected during the p
50            The elongation of the midfoot and phalangeal reduction in Ar. ramidus relative to the Afri
51 cells and chondrocyte differentiation in the phalangeal region are markedly reduced.
52 er to four, a deformed posterior metatarsal, phalangeal soft tissue fusion as well as the absence of
53                                 Tricho-rhino-phalangeal syndrome (TRPS) is an autosomal dominant cran
54  of the hair, face, and digits, tricho-rhino-phalangeal syndrome (TRPS) types I (MIM 190350) and III
55         Moreover, patients with tricho-rhino-phalangeal syndrome frequently present with low bone mas
56 genic GATA transcription factor tricho-rhino-phalangeal syndrome I (TRPS1).
57 line from a patient with BO and tricho-rhino-phalangeal syndrome I that involves a chromosome 8q rear
58                          TRPS1 (tricho-rhino-phalangeal syndrome) is a unique GATA-type transcription
59  gene are responsible for human tricho-rhino-phalangeal syndrome, which is characterized by skeletal
60              Involvement of the tricho-rhino-phalangeal syndrome-1 factor, which also binds a GATA se
61 licated in dominantly inherited tricho-rhino-phalangeal (TRP) syndromes.
62                          Although in general phalangeal variations fall within a range of nearly equa
63       Even in the context of this exception, phalangeal variations observed in nature are a small sub