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1 e expression of CNTF, was involved in glioma growth regulation.
2 ts, including genes with known roles in cell growth regulation.
3 mor development and may reveal mechanisms of growth regulation.
4 text for studying in vivo mechanisms of cell growth regulation.
5  controlled, and how it participates in cell growth regulation.
6 hat potentially challenges present models of growth regulation.
7  dual positive and negative roles for FAK in growth regulation.
8 appropriate cells, can substitute for NF1 in growth regulation.
9 tigated the role of endogenous MBP-1 in cell growth regulation.
10 has been reported regarding TIMP-1's role in growth regulation.
11 ation, and Fat and Merlin act in parallel in growth regulation.
12 veries of the function of mTOR in cancer and growth regulation.
13 ular mechanism of signal integration in cell growth regulation.
14 ion that is critical for an understanding of growth regulation.
15 te roles for the APC/C-CBP/p300 complexes in growth regulation.
16  hairs, exposing a mechanistic view of plant growth regulation.
17  for integrating the stress signals into the growth regulation.
18 sion but does not modulate TGF-beta-mediated growth regulation.
19 main of UHRF1 as a functional determinant of growth regulation.
20  ligands as well as lysosomal biogenesis and growth regulation.
21 ificant number of which are involved in cell growth regulation.
22 ggesting a biological role of PCGEM1 in cell growth regulation.
23 ir the functions of the Hippo pathway in eye growth regulation.
24 xpands the role of the NF1 gene in astrocyte growth regulation.
25 sting a function for T-cadherin in astrocyte growth regulation.
26 r encompasses many different aspects of cell growth regulation.
27 are only weakly active in restoring seedling growth regulation.
28 amined the role of T-cadherin in astrocytoma growth regulation.
29 dy, we investigated the role of Brd4 in cell growth regulation.
30 sting a possible role of IkappaBalpha in the growth regulation.
31 tial biological role in prostate cancer cell growth regulation.
32 heir gene products have an important role in growth regulation.
33 anscriptional modulation, apoptosis and cell growth regulation.
34 ll elongation, consistent with their role in growth regulation.
35 onal interaction of MIP-2A and MBP-1 in cell growth regulation.
36 antiviral defense, immune response, and cell growth regulation.
37 localization, transcriptional activation, or growth regulation.
38 otein links together 2 important pathways of growth regulation.
39 g a potential role for NF-kappaB in negative growth regulation.
40 es may offer a dynamic process of filopodial growth regulation.
41 ety of gene products with a role or roles in growth regulation.
42 suppress inflammation, immunomodulation, and growth regulation.
43  domains that play an important role in cell growth regulation.
44  be indispensable for TGF-beta-mediated cell growth regulation.
45 genes whose protein products are involved in growth regulation.
46 n of QSCN6 and discuss its potential role in growth regulation.
47 to a human protein, Quiescin Q6, involved in growth regulation.
48  processes including signal transduction and growth regulation.
49 ctors argues for a potential role of PA26 in growth regulation.
50 provides new tools for studies of organismal growth regulation.
51 rs will be subject to multiple mechanisms of growth regulation.
52  a rate-determining factor for p53-dependent growth regulation.
53 logy domain, plays an important role in cell growth regulation.
54 est that BRCA2 has an important role in cell growth regulation.
55 ies identify a novel function for TR in cell growth regulation.
56 as been linked to both positive and negative growth regulation.
57 self can serve as a second messenger of cell growth regulation.
58 of development, transcriptional control, and growth regulation.
59 tor, suggesting a role for this gene in cell growth regulation.
60 ion of merlin proteins defective in negative growth regulation.
61 o mechanisms of transcription initiation and growth regulation.
62 duction pathways that contribute to aberrant growth regulation.
63 A response pathway that is important in cell growth regulation.
64 and nucleus, primary sites of chemotaxis and growth regulation.
65 able for B cell survival, proliferation, and growth regulation.
66 ll, promoters that contain E2F sites display growth regulation.
67 mprinting and the role of imprinted genes in growth regulation.
68  signaling pathways involved in FGF-mediated growth regulation.
69 d another more complex, involving aspects of growth regulation.
70 ing the importance of chromatin dynamics for growth regulation.
71 ses, hematopoietic differentiation, and cell growth regulation.
72 eferential splicing of genes associated with growth regulation.
73  STAT3 and STAT5, which are involved in cell growth regulation.
74 l walls, where it plays an important role in growth regulation.
75 receptor is primarily responsible for muscle growth regulation.
76 tly uncovered new connections to filamentous growth regulation.
77 or a role of the peripheral retina in ocular growth regulation.
78 ing the fundamental role of GAs in secondary growth regulation.
79 entified a role for UPR transducers in organ growth regulation.
80 ndependent of temperature, may underpin this growth regulation.
81 link between innate immune response and cell growth regulation.
82 erating in liver regeneration and hepatocyte growth regulation.
83 exerts a strong influence on sugar-dependent growth regulation.
84 monal and light-signaling pathways for plant growth regulation.
85 unique set of genes associated with synaptic growth regulation.
86 flammation, wound healing, angiogenesis, and growth regulation.
87 hat YAP is a major effector of Merlin/NF2 in growth regulation.
88 nd HCF-1C, is critical for the BAP1-mediated growth regulation.
89 ce for the importance of this GTPase in cell growth regulation.
90  of growth pathways plays a critical role in growth regulation.
91 specific cellular gene promoters involved in growth regulation.
92 and Rho-regulated signaling pathways in cell growth regulation.
93 lish whether these may play a role in ocular growth regulation across species.
94 nges is suggestive of a role for BMP2 in eye growth regulation, although the diffuse ocular expressio
95  identify a novel function for IP6K2 in cell growth regulation and apoptosis.
96  children exhibit abnormalities in astrocyte growth regulation and are prone to the development of br
97 heat shock protein with implications in cell growth regulation and cancer progression, thus opening u
98 aglandin synthesis, has been associated with growth regulation and carcinogenesis in several systems.
99 tropic effects on cellular genes involved in growth regulation and cell cycle control.
100 se genes should enhance our understanding of growth regulation and cellular aging.
101 ional regulators, which are involved in cell growth regulation and cellular senescence.
102            The role of endogenous nSMase2 in growth regulation and ceramide metabolism was investigat
103 - and phytochrome-dependent, tissue-specific growth regulation and confirmed the roles of three such
104 gen may result in the abrogation of negative growth regulation and contribute to the development of h
105  factors and an oncogene that contributes to growth regulation and development of mammary and other t
106 w they interact with growth hormones to link growth regulation and development to cause changes in le
107 operative mechanism that could contribute to growth regulation and developmental plasticity in organs
108  in cellular signal transduction, apoptosis, growth regulation and differentiation.
109 y accumulate mutations, some of which affect growth regulation and drive successive waves of clonal e
110 epithelial cells and restore epithelial cell growth regulation and epithelial integrity that are alte
111 g of the role of the epidermal cell walls in growth regulation and establish a new role for DEK1 in p
112 lular signalling mechanisms that can lead to growth regulation and even programmed cell death in resp
113 between the retinoid and IGF systems in cell growth regulation and explain why loss of RARbeta might
114 ygen intermediates play a role in tumor cell growth regulation and expression of the inducible COX, C
115  therefore potentially useful for studies of growth regulation and for gene therapy when growth inhib
116 ltiple biological responses involved in cell growth regulation and immune activation.
117 isms are likely to have an important role in growth regulation and in the induction of cell death by
118 nocarcinomas may indicate a role for CDX1 in growth regulation and in the maintenance of the differen
119 FERM domain-binding motif is responsible for growth regulation and induction of Hippo target gene exp
120  family of proteins plays important roles in growth regulation and is implicated in tumorigenesis.
121                  Rho also has a role in cell growth regulation and is required for cell transformatio
122 ha12 and Galpha13 coupled receptor, promotes growth regulation and local confinement of germinal cent
123 F1 gene product, neurofibromin, to astrocyte growth regulation and NF1-associated astrocytoma formati
124 ments each domain was tested for its role in growth regulation and organization of epithelial structu
125  a critical role for GATA-1 in megakaryocyte growth regulation and platelet biogenesis, and illustrat
126 erived hepatocytes were responsive to normal growth regulation and proliferated at the same rate as t
127 orm S1P, which plays important roles in cell growth regulation and protection from apoptosis.
128  demonstrate the importance of BAF57 in cell growth regulation and provide a novel link between hSWI/
129 eptibility, and tumor-related alterations of growth regulation and signal transduction pathways.
130 r, those responsible for Cdc42-mediated cell growth regulation and transformation are still being det
131 eptor (IGF-IR) plays a critical role in cell growth regulation and transformation.
132 lycans, play crucial roles in morphogenesis, growth regulation and tumor suppression.
133 anscription factors have been linked to cell growth regulation and tumorigenesis in a number of syste
134    However, the mechanisms of BRCA1-mediated growth regulation and tumour suppression remain unknown.
135 pathways, lifespan extension, cell cycle and growth regulation, and circadian rhythms.
136  model system in which to study adult tissue growth regulation, and demonstrated a role of the insuli
137 ty, in the hematopoietic system, in cellular growth regulation, and for many other cellular processes
138 eir receptors also function in angiogenesis, growth regulation, and HIV-1 pathogenesis--effects that
139 enesis that likely contribute to cell cycle, growth regulation, and longevity pathways to which MRPL1
140 ding in recombinant protein production, cell growth regulation, and medium formulation.
141 involved in adhesion, molecular trafficking, growth regulation, and migration of oligodendrocytes and
142 bility to study the genetics of development, growth regulation, and physiology in the same organ.
143 nally show that AAK1 contributes to dendrite growth regulation, and Rabin8 regulates spine developmen
144 sh a critical role for SAFB1 in development, growth regulation, and reproduction.
145 of BMP signaling in adrenocortical carcinoma growth regulation, and the discovery that ERCC1 expressi
146 ointed to genomic regions likely involved in growth regulation, and three of them were individually v
147  architecture, signaling cascades related to growth regulation, and transcription factors directly in
148 n vivo, including antiviral activities, cell growth regulation, and tumorigenesis.
149 sses, including inflammation, wound healing, growth regulation, angiogenesis, and tumorigenesis.
150 sses, including inflammation, wound healing, growth regulation, angiogenesis, and tumorigenesis.
151 portant role in inflammation, wound healing, growth regulation, angiogenesis, and tumorigenesis.
152 n implicated in cellular events such as cell-growth regulation, antiviral defense, and development of
153 ays an important role in responses involving growth regulation, apoptosis, and hypoxic stress.
154 important biological functions, such as cell growth regulation, apoptosis, and migration.
155 l protein that plays essential roles in cell growth regulation, apoptosis, transcriptional regulation
156 es have suggested the role of PMEPA1 in cell growth regulation as noted by androgen induction of PMEP
157 ions are often associated with dysfunctional growth regulation, as is demonstrated in several transge
158 ing but suggest its involvement in mast cell growth regulation based on the inhibition of cell prolif
159 ually diverse regulator of multiple steps in growth regulation because it also directly regulates c-m
160 gested a potentially broader role for MIF in growth regulation because of its ability to antagonize p
161 for function, PDZ2 and PDZ3 are required for growth regulation but not for epithelial structure, and
162 de receptor and has been implicated in plant growth regulation, but little is known about its molecul
163                            The modulation of growth regulation by autocrine TGF-alpha was associated
164                           Here, we show that growth regulation by BON1 is mediated through defense re
165  or the decreased responsiveness to negative growth regulation by Ca2+ in vitro.
166                                         Cell growth regulation by CM and TRAIL was associated with th
167 n cytoskeletal remodeling, also mediate cell growth regulation by coupling cell shape to the cell-cyc
168 ther elucidate the mechanism of differential growth regulation by EGCG, we have investigated the role
169                                              Growth Regulation by Estrogen in Breast cancer (GREB1) w
170 0-epi analogues interrupt IL-1beta autocrine growth regulation by inhibiting IL-1beta production and
171 g of EphA2 has been implicated in epithelial growth regulation by inhibiting the extracellular signal
172 rapamycin (TOR) plays a central role in cell growth regulation by integrating signals from growth fac
173 These data indicate that SOX9 contributes to growth regulation by mac25 via inhibition of cell growth
174 networks to formulate a systems view of root growth regulation by multiple hormones.
175 o family GTPases can both contribute to cell growth regulation by p19Arf and p53 and cooperate with p
176  central transcription network that mediates growth regulation by several hormonal and environmental
177 es, highlighting many unexpected features of growth regulation by the insect fat tissue.
178 fects on growth of AMP-dependent kinase, the growth regulation by the mTOR pathways, and the bioenerg
179 rc, may play a critical role in hypertrophic growth regulation by their association with cytoskeletal
180 in signal transduction processes involved in growth regulation, cell transformation, cell migration,
181 le in developmental processes such as tissue growth regulation, cell-cell recognition, and cell migra
182 how that HBI1, as a component of the central growth regulation circuit, functions as a major node of
183            Our results demonstrate a central growth-regulation circuit that integrates hormonal, envi
184 isms by which NS5A exerts its effect on cell growth regulation contributing to hepatitis C virus-medi
185 cooperate with additional factors to achieve growth regulation could be relieved by bringing the E2F1
186 transcripts that encode proteins involved in growth regulation, damage repair and stress responses, p
187                    Consistent with a role in growth regulation, DeltaNp63alpha-c-Rel complexes bind a
188 nal effect mutant medea (mea) shows aberrant growth regulation during embryogenesis in Arabidopsis th
189 g endosome as a key compartment for synaptic growth regulation during neurodegenerative processes.
190 a, is critical to our understanding of their growth regulation during the first steps of spermatogene
191 ework for delineating the molecular basis of growth regulation, expression of the transformed phenoty
192 er, and REDD1-/- cells are defective in cell growth regulation following ATP depletion.
193 se observations suggest a novel mechanism of growth regulation for T-cadherin involving p21(CIP1/WAF1
194  upstream of mTOR complex 1 (mTORC1) in cell growth regulation, for their potential involvement in my
195        An essential role for Cdc42Hs in cell growth regulation has been suggested by the finding that
196 ating the flexibility that leads to aberrant growth regulation have not been well described.
197 In this study, to characterize cell size and growth regulation in a multicellular context, we develop
198 AT2 are, in a complementary way, involved in growth regulation in Arabidopsis.
199 ulation that aids our basic understanding of growth regulation in birds.
200 at control proliferation is a key feature of growth regulation in developing tissues.
201 rgent interactions of network components and growth regulation in each species.
202 ter may be a result of intersex conflict for growth regulation in early mammalian development and cou
203  PTPRJ/DEP-1 has been implicated in negative growth regulation in endothelial cells, where its expres
204 eases, suggesting a possible role in hepatic growth regulation in pathologic states.
205 ), indicating that LKB1 plays a role in cell growth regulation in response to cellular energy levels.
206 complex formation, gene expression, and cell growth regulation in response to stimulation with type I
207  (NF1) gene has been implicated in astrocyte growth regulation in several studies.
208 s, suggesting that AMOG may be important for growth regulation in the brain.
209 tribution of mTor signaling to Pten-mediated growth regulation in the mammalian nervous system, we tr
210 e erbB family of growth factor receptors and growth regulation in these cells.
211 re we have examined a role of SCC-S2 in cell growth regulation in vitro and in vivo.
212 but a molecular mechanism that links them to growth regulation in vivo has been lacking.
213 hree BLP receptor subtypes may contribute to growth regulation in vivo.
214 ew of recent advances in understanding shoot growth regulation in water-limiting conditions.
215 ss" genes may create opportunities for plant growth regulation, in suppressing propagation of weeds a
216 on of multiple signaling kinases involved in growth regulation, including ErbB2, Raf-1, and Akt.
217   Several cellular polypeptides critical for growth regulation interact with DNA tumor virus oncoprot
218                                         Cell growth regulation is also a critical component of the me
219               The p66(Shc) signaling in cell growth regulation is apparently mediated by extracellula
220                   Perturbation of hepatocyte growth regulation is associated with a number of liver d
221       Here we show that ouabain-induced cell growth regulation is intrinsically coupled to changes in
222 ce for a physiological role for Ing4 in cell-growth regulation is lacking.
223 mour derived cDNA, and therefore the altered growth regulation is not associated with mutations withi
224 mbryogenesis, but the molecular mechanism of growth regulation is not well understood.
225                                              Growth regulation is particularly important in the postn
226 In contrast to its developmental importance, growth regulation is poorly understood in plants.
227  A major downstream target of auxin-mediated growth regulation is the cell wall, which is a determina
228 h the mechanism by which mutant BRCA1 alters growth regulation is unknown, the COOH terminus of BRCA1
229                         Our knowledge of PCA growth regulation lags behind that of other cancers, suc
230 gnaling may be useful to circumvent negative growth regulation limiting plant productivity.
231  important insights into the role of Ku80 in growth regulation, lymphocyte development, and DNA repai
232 embers with proven functional roles in plant growth regulation, morphogenesis, disease resistance, an
233 despite its potential significance for plant growth regulation, mRNA trafficking remains poorly under
234      In this study, the role of activin A in growth regulation of breast cancer cells was investigate
235            We demonstrated that E2F-mediated growth regulation of dhfr transcription requires activat
236 -beta induces accumulation of p27 for normal growth regulation of EECs.
237  direct role of COX-2-mediated PGE(2) in the growth regulation of human cholangiocarcinoma cells.
238 cular mechanisms of PPARgamma ligands in the growth regulation of human cholangiocarcinoma cells.
239 cation, requires precise pre- and post-natal growth regulation of individual calvarial elements.
240  cellular p38 MAPK signaling participates in growth regulation of malignant cholangiocytes.
241 otooncogene plays a key role in the abnormal growth regulation of melanoma cells.
242 icates their role in paracrine and autocrine growth regulation of melanomas.
243 e describe the role of IL-8 in the autocrine growth regulation of MMs.
244        Thus, p27 may be a central target for growth regulation of normal endometrium and in the patho
245 s study, we examine the role of Cdc37 in the growth regulation of normal prostate epithelial cells us
246 the absence of any significant change in the growth regulation of PC12 cells by NGF.
247      To understand the mechanism of negative growth regulation of prostate cancer cells by EGCG we un
248 late the complex AR signaling and subsequent growth regulation of prostate cancer cells.
249                                         Cell growth regulation of Runx2 is also observed in primary c
250 ) signaling pathway participates in negative growth regulation of the mammary gland.
251  most bacteria is governed by spatiotemporal growth regulation of the peptidoglycan cell wall layer.
252                              In studying the growth regulation of these tumors, we recently discovere
253 ta suggest that ROCK is also involved in the growth regulation of tumor cells.
254 in neurological function, regulation of cell growth, regulation of metabolism, and several genes know
255 required for bud formation during vegetative growth, regulation of the activity or amount of one or m
256 a coli shifts from exponential to stationary growth, regulation of transcription is achieved in large
257 gesting a role for Wnt-10b in patterning and growth-regulation of the mammary gland.
258 at may play a role in myeloid cell signaling growth regulation pathways that are responsive to diacyl
259    However, the mechanisms of SRC-3-mediated growth regulation remain unclear.
260                        Understanding neurite growth regulation remains a seminal problem in neurobiol
261 ests that PTEN and NF1 (neurofibromin) glial growth regulation requires TSC/Rheb (Ras homolog enriche
262  pleiotropic effects of yeast PKA, including growth regulation, response to stress and carbohydrate s
263 that OH-POX plays a role analogous to POX in growth regulation, ROS generation, and activation of the
264      Here we characterize larval NMJ growth, growth regulation, structure, and function in a developm
265 Met co-regulated many genes involved in cell growth regulation such as oncogenes, growth factors, tra
266 t transcription factors involved in cellular growth regulation, such as ribosomal RNA transcription,
267 cation of this glioma-associated molecule in growth regulation suggest a potentially important role f
268 play a bigger biological role in tumour cell growth regulation than MIF's enzymatic activity.
269 ule as nucleolin, a protein involved in cell growth regulation that can be cell surface-expressed.
270  Here, we describe a novel property of tumor growth regulation that is neither species nor tumor-type
271 stic understanding of a novel mode of hyphal growth regulation that may be widely employed.
272             In addition to a general role in growth regulation, the importance of cic in regulating c
273 ion heterogeneity, novel mechanisms of glial growth regulation, the neurochemical bases for attention
274 mportant functions in glucose metabolism and growth regulation, this gene may play a central role in
275 utes to neoplastic development by inhibiting growth regulation through effects on CD19 gene expressio
276 ctly inhibits the p21WAF1 induction and cell growth regulation through the IFN-gamma/STAT signaling p
277 se (RLK)/Pelle genes play roles ranging from growth regulation to defense response, and the dramatic
278        We found that the E2F element confers growth regulation to the dhfr promoter only when it is p
279                               Auxin-mediated growth regulation typically involves the establishment o
280 stems are thought to play important roles in growth regulation under stress conditions.
281 cade where transforming GPCRs cause aberrant growth regulation via activation of Rho family small GTP
282 y a role in the control of cell division and growth regulation, virus-glypican 5 interactions may als
283 e central role of AKT signaling in placental growth regulation was confirmed in Akt1 null mice, which
284  factors caused increased promoter activity, growth regulation was not observed, suggesting that a ge
285 inding of Myc-Max or USF is critical for cad growth regulation, we analyzed promoter constructs which
286 role of RpL17 in vascular smooth muscle cell growth regulation, we analyzed the relationship between
287 latory factor (IRF) family mediation of cell growth regulation, we established U937 cell lines stably
288 lipoxygenase (5-LO) pathway on breast cancer growth regulation, we exposed cells to insulinlike growt
289  To evaluate the role of PTEN in endometrial growth regulation, we expressed wild-type or mutant PTEN
290 evelopment and the mechanism of Id3-mediated growth regulation, we generated and analyzed Id3-deficie
291 thesis that the Notch pathway was coupled to growth regulation, we generated VSMC lines overexpressin
292 into the roles of members of this pathway in growth regulation, we inactivated AKT1, AKT2, or PDPK1 g
293 e effects of methyl jasmonate (MeJA) on leaf growth regulation were investigated in Arabidopsis (Arab
294 ophysical parameters potentially involved in growth regulation were studied at the single-cell level
295 atin remodeling, cell cycle progression, and growth regulation, were differentially methylated.
296  multilayered epithelium reflect a defect in growth regulation, which resulted from an imbalance betw
297 in receptor (INSR), which may play a role in growth regulation with its reciprocally imprinted ligand
298 direct observation of cellular mechanisms of growth regulation within the hair follicle and that has
299 ol to investigate the role of PKAc in larval growth regulation without concomitant changes in pattern
300 e forms of noncoding RNAs that contribute to growth regulation without expression of immunogenic prot

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