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1  preventing the formation of a male-specific coelomic blood vessel and the production of steroids.
2 rom the mesonephros into the gonad to form a coelomic blood vessel.
3 cells that normally come to fill most of the coelomic cavities failed to develop.
4 n epithelial gut, and that excretory organs, coelomic cavities, and nerve cords evolved after xenacoe
5 of B cells that express CD5, are abundant in coelomic cavities, and often produce autoantibodies, has
6 , organized gonads, excretory structures and coelomic cavities.
7       Most internal organs are situated in a coelomic cavity and are covered by a mesothelium.
8  Suppression of TWIST1 function in the right coelomic cavity caused a severe disruption of the villou
9 demonstrate that homing of B1 cells into the coelomic cavity is not a requirement for generating prot
10 anting preganglionic quail hindguts into the coelomic cavity of chick embryos.
11        B1a and B1b cells are enriched in the coelomic cavity, contribute to T-cell-independent (TI) a
12  which, similar to the heart, is housed in a coelomic cavity.
13                           In normal embryos, coelomic cells expressing Wt1, GATA-4, RALDH2 and RXRalp
14                                     However, coelomic cells lining the liver of Wt1-null embryos show
15 in pigment cells of the embryonic and in the coelomic cells of the adult - both cell-types having imm
16 thelial cells migrate and reaggregate in the coelomic domain to form the major testicular artery.
17 64 glycoproteins isolated from the oocyte or coelomic egg envelopes exhibited sperm binding activity,
18 se proteins are part of the intact oocyte or coelomic egg envelopes, they are not accessible to eithe
19 ertilized oviposited eggs, not to oocytes or coelomic eggs.
20 phorectomy significantly reduced the risk of coelomic epithelial cancer (hazard ratio, 0.04; 95 perce
21 rophylactic oophorectomy reduces the risk of coelomic epithelial cancer and breast cancer in women wi
22                                In XX gonads, coelomic epithelial cells also migrated into the gonad,
23 cted at the plasma membrane in proliferating coelomic epithelial cells and in the nucleus in Sertoli
24                  In XY gonads, the migrating coelomic epithelial cells became Sertoli cells, as well
25                                    After the coelomic epithelial cells migrate into the gonad, there
26  stages, corresponding to 11.5-11.7 dpc, the coelomic epithelial cells no longer became Sertoli cells
27  stages, corresponding to 11.2-11.4 dpc, the coelomic epithelial cells of both sexes migrated into th
28 s surrounding the tube and, most externally, coelomic epithelial cells.
29 ly gonadogenesis, proliferating cells in the coelomic epithelium (CE) give rise to most of the somati
30  to Sertoli cells has its origins within the coelomic epithelium (CE) of the genital ridge, but from
31 procedure reduces the risk of cancers of the coelomic epithelium and breast in women who carry such m
32 erved in SF1-negative cells at and below the coelomic epithelium and did not give rise to Sertoli cel
33 ed to the Sertoli precursors and LHX9 to the coelomic epithelium and interstitium.
34 n was observed initially in the cells of the coelomic epithelium and occurred in two distinct stages.
35 titial/stromal compartment of the gonad: the coelomic epithelium and specialized cells along the gona
36    The SLC lineage is closely related to the coelomic epithelium and specified as early as E10.5, mak
37 e endometrium and uterus also arise from the coelomic epithelium and the Mullerian ducts.
38  discontinuous, suggesting that cells in the coelomic epithelium at this stage might move inward.
39  in ovo, labelling at indifferent stages the coelomic epithelium by electroporation with a lacZ repor
40  were 3betaHSD-negative, indicating that the coelomic epithelium contributes only to non-steroidogeni
41  show that the posthepatic mesenchymal plate coelomic epithelium gives rise to a mesenchyme that popu
42 d the basement membrane layer underlying the coelomic epithelium had thickened to form the tunica alb
43 ll Mullerian duct components derive from the coelomic epithelium in both species.
44 ell as a reduction in genes expressed in the coelomic epithelium including the putative PGC chemo-att
45  duct and also the view of a tube forming by coelomic epithelium invagination along the mesonephros.
46       Taken together, our data show that the coelomic epithelium is a source of Sertoli cells as well
47 that the basement membrane barrier under the coelomic epithelium is discontinuous, suggesting that ce
48 t1 expression in cells delaminating from the coelomic epithelium is essential for the expansion of th
49 n increase in cell proliferation in the male coelomic epithelium is the earliest identified effect of
50 xpressing cells are initially present in the coelomic epithelium of both male and female urogenital r
51 ify a label-retaining cell population in the coelomic epithelium of the adult mouse ovary as candidat
52  findings strengthen the hypothesis that the coelomic epithelium of the anlage is a pluripotent tissu
53 utative somatic stem/progenitor cells of the coelomic epithelium of the mouse ovary.
54 ectively form a large group encompassing the coelomic epithelium of the regenerating anlage and mesen
55 ls from a cell population originating in the coelomic epithelium overlying the nascent gonad that als
56 elial-to-mesenchymal transition (EMT) of the coelomic epithelium specifically within the presumptive
57 that ovarian epithelial tumours arise in the coelomic epithelium that covers the ovarian surface, it
58                          This ability of the coelomic epithelium to give rise to Sertoli cells was de
59 the transition of MISRII expression from the coelomic epithelium to the mesenchyme and Mullerian duct
60 e adrenal primordium arises from adrenogenic coelomic epithelium via an epithelial-to-mesenchymal tra
61 test this possibility directly, cells of the coelomic epithelium were labeled using the fluorescent l
62 duct is known to form by invagination of the coelomic epithelium, but the mechanism for its elongatio
63       Vegetal plate descendents comprise the coelomic epithelium, circumesophageal muscle, basal cell
64 f the ovarian and cervical epithelium is the coelomic epithelium, the same tissue that regresses unde
65 ese cells support correct development of the coelomic epithelium, the target of PGC migration.
66 s earlier and increases predominantly in the coelomic epithelium, whereas Alk3 expression appears lat
67 ising earlier and more anteriorly within the coelomic epithelium.
68 pture and regenerative repair of the ovarian coelomic epithelium.
69 mal cells derived from local delamination of coelomic epithelium.
70  tubules, the mesonephric mesenchyme, or the coelomic epithelium.
71 ext, we have identified the heat inactivated coelomic fluid (HI-CF) of the earthworm, Perionyx excava
72  exposure experiments using tissue extracts, coelomic fluid and effluent water from wasting sunflower
73 g both (59)Fe overlay assays of MYP enriched coelomic fluid and immunoprecipitation of native iron-bo
74 Chelation experiments on R. pachyptila whole-coelomic fluid and purified hemoglobins reveal a role fo
75 human RNA-seq data to proteomic data for the coelomic fluid bathing the yolk sac.
76             The lectin was purified from the coelomic fluid by affinity chromatography on a GlcNAc-de
77 ay conclude that the As concentration in the coelomic fluid can be used as an index of As availabilit
78 in both the whole earthworm's body (AsE) and coelomic fluid extracts (AsF).
79 ht to be a defense mechanism against loss of coelomic fluid if the body wall is punctured, and it may
80         We conclude that AML-1 purified from coelomic fluid is encoded by AML-1b and represents a nov
81                         Within minutes after coelomic fluid is removed from the body cavity, a massiv
82 indicating that the As sequestrated into the coelomic fluid may reflect the total body concentration.
83 pectenicida strain FHCF-3, cultured from the coelomic fluid of a diseased sunflower sea star, caused
84                             Lysenin from the coelomic fluid of the earthworm Eisenia fetida belongs t
85         Deep sequencing of diseased sea star coelomic fluid samples from experiments and field outbre
86 ns, resulting in approximately 10% increased coelomic fluid serotonin, a pharmacological effect.
87 he vascular blood, V1 and V2, and one in the coelomic fluid, C1.
88 oprecipitation of native iron-bound MYP from coelomic fluid, support this classification.
89 d micronutrients, many of which are found in coelomic fluid.
90              We showed that the A. japonicus coelomic fluids plus antibiotics induce 100-fold more pe
91 c-induced V. splendidus persister cells, the coelomic fluids-induced persister cells have five resusc
92                             Furthermore, the coelomic fluids-induced persister cells showed similar p
93 er cells for both the antibiotic-induced and coelomic fluids-induced persister cells.
94  the process of infection due to exposure to coelomic fluids.
95 more readily in the presence of A. japonicus coelomic fluids.
96 was examined in muscleless limbs produced by coelomic grafting of early limb buds and (2) muscle deve
97                              Using rat-chick coelomic grafts, neural tube cultures, and gut explants,
98  or skin laceration, subcutaneous injection, coelomic injection, or via co-housing with an infected g
99 ted from the ectoderm and sequestered to the coelomic linings during myotome extension.
100  the archenteron (which includes presumptive coelomic mesoderm as well as presumptive endoderm) from
101 dult skeleton) fail to form, indicating that coelomic mesoderm, endoderm, or both are required for in
102 n intrinsic origin of mesothelial cells to a coelomic organ and provide a novel mechanism for the gen
103      Mesothelium is the surface layer of all coelomic organs and is crucial for the generation of the
104 erved mechanism in blood vessel formation to coelomic organs, and have major implications for our und
105 fic to the heart or applies broadly to other coelomic organs.
106 s to the development of blood vessels in all coelomic organs.
107 elomocyte adhesion is mediated by amassin, a coelomic plasma protein with a relative molecular mass (
108  the major contributor to the adult, but how coelomic pouch cells (CPCs) are specified during embryog
109    A third signal, Hedgehog, is required for coelomic pouch morphogenesis and institution of laterali
110 strulation and are then enriched in the left coelomic pouch of larvae.
111 scription factors asymmetrically in the left coelomic pouch only, which launch the pathway that event
112 micromeres, and later only expressed in that coelomic pouch which gives rise to the mesoderm of the v
113              These include cells in the left coelomic pouch, which forms the adult rudiment in the em
114 those left-sided structures, called the left coelomic pouch.
115 ockdown of foxY results in a failure to form coelomic pouches and disrupts the expression of virtuall
116 the creation of two sets of fully functional coelomic pouches and imaginal rudiments, and sex determi
117                          In sea urchins, the coelomic pouches are the major contributor to the adult,
118 The migration of the small micromeres to the coelomic pouches in the sea urchin embryo provides an ex
119 n of late mesodermal derivatives such as the coelomic pouches to which the small micromeres contribut
120 ar cells, randomized left-right asymmetry of coelomic pouches, and disorganized circumesophageal musc
121 on of small micromeres to the left and right coelomic pouches.
122 a division and are not incorporated into the coelomic pouches.
123 the earthworm Eisenia fetida using E. fetida coelomic proteins (EfCP) as a native repertoire and feta
124 embryos, but contribute significantly to the coelomic sacs of the larvae, from which the major tissue
125 the sea urchin embryo contribute only to the coelomic sacs, which produce major components of the adu
126 ttachment structure with a long pedicle with coelomic space.
127  surface of the gonad, are restricted to the coelomic surface of Dax1-deficient testis.
128 in the peritubular space and extend from the coelomic surface to the dorsal surface of the gonad, are
129                     Epidermis and mesodermal coelomic tissue produce distinct putative posterior stem
130               During the conversion from the coelomic to the vitelline envelope, the gp69/64 sperm re
131 Wnt4 in the embryonic testis did not inhibit coelomic vessel formation but vascular pattern was affec
132 enin, including formation of testis-specific coelomic vessel, appearance of androgen-producing adrena
133 e, which includes the development of a large coelomic vessel, develops coincident with expression of

 
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