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1 ving four compartments: anterior epithelium (germinative and central anterior zones), recruitment zon
2                                   The sheath/germinative and papilla/germinative cell implants repeat
3 ells located near the ventricular surface in germinative areas of the developing central nervous syst
4 ratinocyte differentiation while maintaining germinative capability could be due to inhibition of Not
5                     Importantly, the reduced germinative capacity and inability to utilize glucose ob
6           The sheath/germinative and papilla/germinative cell implants repeatedly induced giant vibri
7  high levels of apolipoprotein E mRNA in the germinative cell layer of the sebaceous gland and in epi
8  lasting damage or halt proliferation of the germinative cells.
9 anoemulsion showed a negligible influence on germinative energy of barley, while still efficiently el
10                             Hence, the adult germinative epidermal cells enable non-inductive adult d
11 cle bulb was found both in the proliferating germinative epithelial cells and in the terminally diffe
12 is transiently upregulated during early post-germinative growth and leaf senescence.
13  role in activating the promoter during post-germinative growth are located more than 1,200 bp upstre
14 eedlings increased from 18 h to 72 h of post-germinative growth in the dark, although somewhat later
15      By inhibiting seed germination and post-germinative growth through the PYR1/PYL/RCAR ABA recepto
16 catabolism during germination and early post-germinative growth was unaltered in the acx1-1 mutant, b
17 nanases are involved in germination and post-germinative growth, with LeMAN2 being associated with en
18 ion of ABA led to phenotypic changes in post-germinative growth.
19 PAPPA2 for the dermal papilla, FOXM1 for the germinative hair matrix, APOD for the connective tissue
20 migration of neurons arising from the deeper germinative layers of the mammalian brain.
21 en difficult to recapitulate the features of germinative LECs in vitro.
22 ral retina is spatially recapitulated at the germinative margin.
23     During anagen, cell proliferation in the germinative matrix of the hair follicle gives rise to th
24 s expressed in the companion layer and upper germinative matrix region of the hair follicle, the medu
25 e latter case expression was confined to the germinative neuroepithelium of three sharply delimited r
26     Thus in the present study, hair follicle germinative, outer root sheath or skin basal epidermal c
27 teriorly from a singular tissue: the neck or germinative region (GR).
28 ions the central (Dc) zone possesses its own germinative region in the dorsal proliferative zone.
29 ed to mediate to various degrees the proline germinative response while also influencing germination
30 functional importance in the proline-induced germinative response.
31 nchors a subset of LDs to the PM during post-germinative seedling growth in Arabidopsis.
32 ering CO2 and light conditions), during post-germinative seedling growth.
33 Mill.) endosperm during germination and post-germinative seedling growth.
34 red by other cerebellar lineages and whether germinative sites different from the PWM originate inhib
35 ation of CR cells have demonstrated multiple germinative sources for CR cells on the edges of the dev
36 d amino acid sequence similarity with a post-germinative tomato mannanase (LeMAN1).
37 ession from the ABI3::TPS1 transgene in post-germinative tps1 seedlings results in severe growth arre
38  elements were found to be required for post-germinative, vascular expression and guard cell/trichome
39 tively cycling cells exists primarily in the germinative zone and represents the transit amplifying c
40               The BrdU-labeling index in the germinative zone declined from approximately 3.5% at 1 m
41 ounting BrdU-labeled and total nuclei in the germinative zone in flatmounts of lens epithelia.
42 eral region, an area referred to as the lens germinative zone in which most active cell division occu
43 ssumed that these cells are generated in the germinative zone of the earliest cortical neuroepitheliu
44 iary body, the ocular tissues closest to the germinative zone of the lens, a region where most prolif
45 in D1 and survivin, are downregulated in the germinative zone of the MAPK1-deficient lens.
46 ommitted daughter cells delaminate from this germinative zone.
47 ficient to restore cell proliferation in the germinative zone.
48         Interneurons are born in subcortical germinative zones and tangentially migrate in multiple s
49 ma-aminobutyric acid neurons, born in remote germinative zones in the ventral forebrain (telencephalo
50                  Sox2 expression persists in germinative zones of the adult rodent brain, but Sox3 ex
51 enesis suggest that neurons migrate from the germinative zones through the white matter to the cortex
52 three neuronal populations to form displaced germinative zones within the developing brain may reflec
53 tly labeled LRCs, located in the central and germinative zones, cycle more frequently than the heavil
54       The cerebellar primordium contains two germinative zones, the rhombic lip (RL) and the ventricu
55 led cells were found in both the central and germinative zones.