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1 the progression from normal to preneoplastic mammary tissue.
2 , cyclooxygenase-2 (COX-2), and aromatase in mammary tissue.
3 athways emanating from gp130 are utilized in mammary tissue.
4 ressed in the Golgi, is induced in lactating mammary tissue.
5 d significantly in non-neoplastic WAP-CRD-BP mammary tissue.
6 s obtained in Cx32-null mice and in Cx43KI32 mammary tissue.
7 clones with approximately 6000 obtained from mammary tissue.
8 is the only isoform detected in normal human mammary tissue.
9 ifferentiation, were compared with wild-type mammary tissue.
10 te to mediate the effects of beta-catenin in mammary tissue.
11 and protein are readily detectable in normal mammary tissue.
12 he lowest uptake in benign tumors and normal mammary tissue.
13 observed in DeltaE3 beta-catenin transgenic mammary tissue.
14 antly higher than in aged-matched, wild-type mammary tissue.
15 arched for genes preferentially expressed in mammary tissue.
16 promoter is restricted to liver, muscle, and mammary tissue.
17 r showed wild-type infection of lymphoid and mammary tissue.
18 l growth factor (EGF), can activate Stat5 in mammary tissue.
19 of 1500 duplicated genes isolated from mouse mammary tissue.
20 n important role in the normal remodeling of mammary tissue.
21 ng mice, but not in nonpregnant/virgin mouse mammary tissue.
22 ry human breast cancers compared with benign mammary tissue.
23 c delay of involution occurred in Stat3 null mammary tissue.
24 that genistein acts as an estrogen in normal mammary tissue.
25 nomic sequence specifically expressed in the mammary tissue.
26 that are needed for infection of adolescent mammary tissue.
27 ssess higher telomerase activity than normal mammary tissue.
28 ts in structurally and functionally impaired mammary tissue.
29 les, including colonic contents, plasma, and mammary tissue.
30 al enhancers and promoter elements unique to mammary tissue.
31 immunoreactivity of glandular epithelium in mammary tissue.
32 hydroxylated in comparison to non-neoplastic mammary tissue.
33 e of the udder for directed elution into the mammary tissue.
34 enesis collected directly from fresh ex vivo mammary tissue.
35 ypes have been identified in mouse and human mammary tissue.
36 ributors to tumorigenesis in BRCA1-deficient mammary tissue.
37 d the 'responsible' isoforms using data from mammary tissue.
38 enes Adfp, Fabp4, and Pdhk4 in preneoplastic mammary tissue.
39 in vivo disposition in rat serum, liver, and mammary tissue.
40 ersus luminal-like breast tumors and healthy mammary tissue.
41 f insulin and IGF-I receptors in transformed mammary tissue.
42 E form that typically is expressed in normal mammary tissue.
43 rvival of five cell lines derived from human mammary tissue.
44 ediated matrix degradation and remodeling of mammary tissue.
45 ells compared with cells derived from normal mammary tissue.
46 OX-2 expression in both normal and malignant mammary tissues.
47 e results in loss of Ramp3 expression in non-mammary tissues.
48 a-catenin signaling pathways in premalignant mammary tissues.
49 of Ptc1 transcripts was observed in Shh-null mammary tissues.
50 and activity of p53 were examined in normal mammary tissues.
51 plifications were found in any preneoplastic mammary tissues.
52 mmary tumors induced by MNU and non-involved mammary tissues.
53 ive breast cancer cases compared with normal mammary tissues.
54 es via long-term propagation of normal human mammary tissues.
55 ncy and involution cycle in rodent and human mammary tissues.
56 trix and induces precancerous lesions in the mammary tissues.
58 ccurs in vivo during the involution of mouse mammary tissues, a morphogenic process requiring cellula
61 zed mRNA in both bovine and murine lactating mammary tissue and associates with microsomal membranes
62 expression was low or undetectable in normal mammary tissue and benign lesions, approximately two-thi
64 substantial fraction of the stroma of normal mammary tissue and breast tumors, undergo transcriptiona
65 (SERM), which acts as an antiestrogen in the mammary tissue and displays estrogenic activity in other
66 skin and tongue epithelia, adipose, lung and mammary tissue and has been found upregulated in several
67 LGD1069 inhibits the expression of COX-2 in mammary tissue and in normal human mammary epithelial ce
69 ggering an intense influx of leukocytes into mammary tissue and increased concentrations of IL-6, IL-
70 Stra6 mRNA was also observed in hyperplastic mammary tissue and mammary gland tumors from transgenic
71 th genes are most highly expressed in normal mammary tissue and mammary tumors from several transgeni
72 omparison of Ets factor expression in normal mammary tissue and mammary tumors identified significant
73 uberculosis also has been reported to infect mammary tissue and milk, and we showed that M. avium sub
74 ereas GATA5 is minimally expressed in normal mammary tissue and more strongly expressed in two breast
77 mammary tissue but were also found in virgin mammary tissue and, interestingly, spleen and thymus.
78 we show that GPR109A is expressed in normal mammary tissue and, irrespective of the hormone receptor
79 east carcinomas, adjacent tissues and normal mammary tissues and bladder transitional cell carcinomas
80 in situ cancers growing within primary human mammary tissues and is also required for metastasis in v
81 Pten altered the steady-state biology of the mammary tissues and the expression profiles of genes inv
82 otein expression levels compared with normal mammary tissues and there is an inverse correlation betw
84 ivo effects of hCG on Cx26 expression in rat mammary tissues and used its effect on the expressions o
85 Kcs abundance and activity, most markedly in mammary tissue, and are both radiosensitive and suscepti
86 have fewer blood vessels, less blood in the mammary tissue, and impaired alveolar coverage of the fa
89 cript is present in both virgin and pregnant mammary tissue, and SMC synthesis is induced rapidly in
90 ial, strong mitogenic effect in the fat-rich mammary tissues, and this effect was not observed with E
91 g mice, therefore, alterations to the distal mammary tissue are mediated by the systemic host respons
92 ith compliances comparable to that of normal mammary tissue, are protective against EMT, whereas stif
94 e ITAM mutation in Env infected lymphoid and mammary tissue at the same level as wild-type MMTV and w
95 e., trimethylated histone H3 at K4) marks in mammary tissues at early and midpregnancy and at parturi
96 nic mice exhibit alveolar hyperplasia in the mammary tissue but do not develop spontaneous mammary tu
97 induced during pregnancy was low in immature mammary tissue but increased with epithelial differentia
98 nt kinase inhibitor, was expressed in normal mammary tissue but was not detected in the mammary carci
99 transcripts were not restricted to lactating mammary tissue but were also found in virgin mammary tis
100 breast epithelial cells and in normal human mammary tissue, but at lower levels in various breast ca
101 mice decreased lipid synthesis in lactating mammary tissue, but the mechanism of S14's action is unk
102 ry epithelial cells were found in the normal mammary tissue, but the resulting mammary tumors were al
103 expression was absent or very low in normal mammary tissue, but was high in 44% of primary breast ca
104 t and maintenance of female reproductive and mammary tissues, but is also involved in maintenance of
105 ids from normal, benign as well as malignant mammary tissues can be propagated from the same animal t
106 of BRCA1 function in cell lines derived from mammary tissue caused rapid amplification and fragmentat
107 astitis is an inflammatory disease affecting mammary tissues caused by bacterial infection that negat
110 3,4-Q (200 nmol) at four mammary glands, the mammary tissue contained 2.3 micromol 4-OHE2-1(alpha, be
113 erized by amplification of the EGFR ErbB2 in mammary tissue, correlates with a marked up-regulation o
114 is high in SCs/CSCs from human/mouse primary mammary tissues, correlates with the basal-like breast c
118 aturated fatty acid, is essential for normal mammary tissue development, at least in part because it
123 rrelation was observed between leukocyte and mammary tissue DNA methylation for most of the analyzed
124 Methylation levels observed in leukocyte and mammary tissue DNA were close to the 50% expected for mo
127 and human IGF binding protein-3 (IGFBP-3) to mammary tissue during late pregnancy and throughout lact
130 of two STAT proteins, Stat5a and Stat5b, in mammary tissue during pregnancy suggests an active role
132 , we find that HDR is particularly robust in mammary tissue during puberty and pregnancy, accounting
133 r expression is maintained in the transgenic mammary tissue even without circulating ovarian estrogen
135 on of LBH, mice exhibit pronounced delays in mammary tissue expansion during puberty and pregnancy, a
136 uman breast cancers, in contrast with normal mammary tissue, express the intracellular tyrosine kinas
137 NA for the protein is most abundant in human mammary tissue followed by kidney and testis, with lower
139 elution, fulvestrant was found to penetrate mammary tissue forming a concentration gradient beyond 1
140 uration (10 weeks) with syngeneic Trp53-null mammary tissue fragments and monitored for one year.
141 from cryopreserved mammary tissue, in which mammary tissue fragments were isolated and embedded into
142 om virgin transgenic rats but is detected in mammary tissue from certain lines of mid-pregnant transg
143 profiles of mammary tumors and preneoplastic mammary tissue from MMTV-Neu transgenic mice to expressi
145 reduction of Cav-1 expression as compared to mammary tissue from normal FVB/N mice, suggesting that i
147 than 8 kb and are specifically expressed in mammary tissue from pregnant and lactating mice from the
149 This approach allowed for the growth of mammary tissue from the injected cells and transient act
150 pression profiling of parous and nulliparous mammary tissue from these four strains yielded a common
151 tomics, and flow cytometry, we identify that mammary tissue from UTI-bearing mice displays collagen d
152 rbonic anhydrase III, is highly expressed in mammary tissue from virgin and pregnant mice and in gene
153 of the transgenic mRNAs is not detectable in mammary tissue from virgin transgenic rats but is detect
154 erential ras gene expression was examined in mammary tissue from virgin, pregnant, and lactating rats
155 l because it was differentially expressed in mammary tissues from BALB/c-Trp53(+/-) and C57BL/6-Trp53
157 A were observed between the undifferentiated mammary tissues from wild-type and mutant mice, indicati
165 These findings suggest that loss of Mnt in mammary tissue has similarities to Myc overexpression.
167 icant role for stromal TGF-beta signaling in mammary tissue homeostasis and mammary tumor progression
168 Hsp72 KO mice, expression of Her2 instead of mammary tissue hyperplasia led to suppression of duct de
170 gate the effects of GH/IGF-I augmentation on mammary tissue in a model relevant to aging humans, we t
171 we demonstrate that when placed adjacent to mammary tissue in the 7,12-dimethylbenz[a]anthracene-ind
173 mor cells in tumors developing directly from mammary tissue in transgenic models, we have evaluated t
175 e first cells that migrated intensely to the mammary tissue, in line with an early production of CXCL
176 nced phosphorylation of IR/IGF-IR and Akt in mammary tissue, in the context of three different mouse
177 ammary organoids (EqMaOs) from cryopreserved mammary tissue, in which mammary tissue fragments were i
178 hat were preferentially expressed in MK-PTEN mammary tissue, including the IGF-binding protein-5 (Igf
179 shared TCR clonotypes between intestinal and mammary tissues, including intriguing public TCR familie
180 elium, as transplantation of EphA2-deficient mammary tissue into wild-type recipient stroma recapitul
181 remic C3H/HeN females, even though the I/LnJ mammary tissue is not refractory to MMTV infection.
183 e mammary tumorigenesis, whereas the role of mammary tissue macrophages (MTMs) remains incompletely u
186 essentially the entire Ets family in normal mammary tissue, mammary-related cell lines, and mammary
188 -/2-hydroxyestradiol formation in neoplastic mammary tissue may therefore provide a useful marker of
189 e of demarcation between necrotic and viable mammary tissue (mean lesion volume, 14.24 cm(3); largest
192 t did not affect total fat deposition in the mammary tissue nor the extent of epithelial invasion int
193 with a TIMP1 neutralizing antibody, restores mammary tissue normal homeostasis, thus providing eviden
194 R2) were analyzed in DNA from leukocytes and mammary tissue (normal, benign diseases, or malignant tu
195 to explore the bovine transcriptome from the mammary tissue of 12 Chinese Holstein cows with 6 extrem
196 ur in focal patches of histologically normal mammary tissue of a substantial fraction of healthy, can
204 Eighteen RF treatments were performed in the mammary tissue of three domestic swine under ultrasonogr
206 phosphorylation of Akt and cyclin D1 in the mammary tissue of transgenic mice vulnerable to carcinog
208 c mice, loss of Pak1 prolonged survival, and mammary tissues of such mice showed loss of beta-catenin
213 rget (colon) and nontarget (liver, lung, and mammary tissues) organs of female CD rats injected with
214 rograms promote stemness and thereby support mammary tissue outgrowth and tumors of basal origin.
217 ivery systems to control release and prolong mammary tissue persistence of a lipophilic metal complex
219 the rapid ductal clearance of CPX, prolongs mammary tissue persistence, improves efficacy against DC
220 t in the non-lactating period could help the mammary tissue prevent issues with inflammation and udde
222 a majority of breast tumors, but not normal mammary tissue, promotes breast carcinoma cell prolifera
224 latory feature that is actively regulated in mammary tissues, providing evidence that variants in thi
226 capacity, Maspin could potentially regulate mammary tissue remodeling occurring under normal and pat
231 that CrbpI loss disrupts atRA homeostasis in mammary tissue, resulting in microenvironmental defects
232 ession of the placental gene and IAPs in the mammary tissues, RT-PCR showed that LTR sequences are ab
233 proliferation antigen Ki67 were evaluated in mammary tissue sections at approximately d 7 and d 14 of
236 was characterized by active histone marks in mammary tissue, STAT5 binding and expression during preg
237 ry breast tumors but never in matched normal mammary tissues, suggesting a contribution of Syk(S) to
238 mBTEB2 transcript is found at high levels in mammary tissue taken from a transgenic mouse overexpress
240 in specific to liver, adipose, and lactating mammary tissues that functions to activate genes encodin
241 osure expression signature in both blood and mammary tissues that is predictive for poor survival amo
242 e results in elevated expression of Ramp3 in mammary tissue through augmented promoter-enhancer inter
243 ion of int-5/aromatase appears to predispose mammary tissue to preneoplastic changes, which may, in t
246 ata demonstrate that the genetic response of mammary tissue varies significantly between 129S1 and C5
247 iogenic regulatory genes in COX-2 transgenic mammary tissue was also potently inhibited by indomethac
248 idered a tumor suppressor gene and Cx26-null mammary tissue was evaluated after five pregnancies.
249 ce that received premalignant AIB3(+/-)/PyMT mammary tissue was much faster than in nude mice that re
250 sdifferentiation, the expression of genes in mammary tissue was profiled in the absence and presence
251 K2alpha, dnGSK3beta and Cyclin D1 transgenic mammary tissues was similar to that in DeltaE3 beta-cate
252 he molecular consequences of Shh deletion in mammary tissue, we compared mRNA levels of patched 1, a
253 rate the physiological role of VEGF(165)b in mammary tissue, we generated transgenic (TG) mice expres
255 tion due to obesity enhanced fibrosis within mammary tissue, we utilized a high-fat diet model of obe
257 markably, 88% of estrogen-regulated genes in mammary tissue were mediated through neutrophils, which
261 nd low RON expression was observed in normal mammary tissue whereas high RON and low or undetectable
262 received transplants of premalignant WT/PyMT mammary tissue, which indicated that the accelerated tum
263 fects were due to massive cell senescence in mammary tissue, which was associated with upregulation o
264 agents antagonize the effects of estrogen on mammary tissue while mimicking the actions of estrogen o
265 Sec amounts were reduced by more than 70% in mammary tissue with either transgene, while in skin and
267 benefits of human milk, models of secretory mammary tissue would offer opportunities to study factor