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1 ulating expression of growth factors such as insulin-like growth factor II.
2 LD1) pathway that controls the production of insulin-like growth factor II, an autocrine inducer of d
3 more, the cranial nerve 3/4-restricted genes insulin-like growth factor II and guanine deaminase prot
4 ssion of positive growth regulators, such as insulin-like growth factor II and the insulin-like growt
5 utant ES cells are deficient in secretion of insulin-like growth factor II and their defect can be co
6 e VO2peak, REE, and interactions of sex with insulin-like growth factor-II and insulin for whole-body
8 nt binding protein (CRD-BP), binds to c-myc, insulin-like growth factor II, and beta-actin mRNAs, and
9 centrations of insulin-like growth factor-I, insulin-like growth factor-II, and insulin-like growth f
10 centrations of insulin-like growth factor-I, insulin-like growth factor-II, and insulin-like growth f
12 growth factor, insulin-like growth factor 1, insulin-like growth factor II, basic fibroblast growth f
13 pendent mannose 6-phosphate receptor and the insulin-like growth factor II/cation-independent mannose
14 annose 6-phosphate receptor (CD-MPR) and the insulin-like growth factor II/cation-independent mannose
15 s, the cation-dependent MPR (CD-MPR) and the insulin-like growth factor II/cation-independent MPR, ca
16 t growth factor, and nerve growth factor and insulin-like growth factor II, either alone or in variou
17 We present evidence that SYT-SSX1 induces insulin-like growth factor II expression in fibroblast c
18 analysis of loss of imprinting (LOI) of the insulin-like growth factor II gene (IGF2) in tumours.
23 LOI), an epigenetic alteration affecting the insulin-like growth factor II gene (IGF2), is found in n
24 use model of loss of imprinting (LOI) of the insulin-like growth factor II gene (Igf2), which shows a
28 ve described loss of imprinting (LOI) of the insulin-like growth factor-II gene (IGF2), leading to bi
33 rest identified differential localization of insulin-like growth factor II, guanine deaminase, periph
34 loci and the genes coding for p53, p57, and insulin-like growth factor II, have been reported in adr
35 differentiation medium and are defective in insulin like growth factor-II (IGF-II) secretion, an aut
36 -6, tumor necrosis factor alpha (TNF-alpha), insulin-like growth factor II (IGF II), and parathyroid
38 etal bovine serum and carries mature 7.5-kDa insulin-like growth factor II (IGF-II) and at least 12 d
40 de (ANP), relaxin, glucagon, proinsulin, and insulin-like growth factor II (IGF-II) bind to and are d
43 ancer (insulinoma) cells that do not produce insulin-like growth factor II (IGF-II) grow slowly in pu
44 studies showed that a bilateral injection of insulin-like growth factor II (IGF-II) into the dorsal h
49 In this study, the short-term effects of insulin-like growth factor II (IGF-II) on extraocular mu
50 with IL-3 alone or with both IL-3 and either insulin-like growth factor II (IGF-II) or stem cell grow
52 a systemic administration of the polypeptide insulin-like growth factor II (IGF-II) reverses all thes
53 st the effects of systemic administration of insulin-like growth factor II (IGF-II), a polypeptide th
54 six imprinted genes within this domain: (a) insulin-like growth factor II (IGF-II), an important aut
55 rising insulin-like growth factor I (IGF-I), insulin-like growth factor II (IGF-II), and their bindin
56 ression of another known PLAGL2 target gene, insulin-like growth factor II (IGF-II), was greatly dimi
57 depends on the interaction of a fragment of insulin-like growth factor II (IGF-II), with the IGF-II
65 We report that, in the rat, administering insulin-like growth factor II (IGF-II, also known as IGF
70 n-regulated in prostate cancer, up-regulates insulin-like growth factor-II (IGF-II) mRNA and protein
75 tors (augmenter of liver regeneration [ALR], insulin-like growth factor-II [IGF-II], and hepatocyte g
76 imprinted genes; these include the gene for insulin-like growth factor II (IGF2) and H19, which show
80 med comparative evolutionary analyses of the insulin-like growth factor II (IGF2) gene in teleost fis
81 thesize that loss of imprinting (LOI) of the insulin-like growth factor II (IGF2) gene is associated
83 demethylation of repeated sequences, loss of insulin-like growth factor II (IGF2) imprinting, abrogat
87 ted diet during E11-17 have higher levels of insulin-like growth factor II (IGF2) mRNA and protein in
89 eptors (M6P/IGF2R) bind and target exogenous insulin-like growth factor II (IGF2) to the prelysosomes
90 has been particularly true for the imprinted Insulin-like Growth Factor II (IGF2), a key regulator of
91 singly, LOI of LIT1 was not linked to LOI of insulin-like growth factor II (IGF2), which was found in
93 f the normally silent maternal allele of the insulin-like growth factor-II (IGF2) gene, silencing of
94 R1; myoblast determination protein 1, MYOD1; insulin-like growth factor II, IGF2; tumor suppressor ca
97 otein of recombinant NAGLU and a fragment of insulin-like growth factor II (IGFII) was prepared for e
98 2 myoblasts by controlling the expression of insulin-like growth factor-II in a kinase-independent ma
99 Vesamicol did not have any effect on EGF or insulin-like growth factor-II-induced growth of human BA
101 rocess of characterizing mannose 6-phosphate/insulin-like growth factor II (M-6-P/IGF-II) receptor bi
102 ytoplasmic domain of the mannose 6-phosphate/insulin-like growth factor-II (Man-6-P/IGF-II) receptor.
103 in-regulatable aminopeptidase, receptors for insulin-like growth factor-II/Man-6-phosphate and transf
107 erminants of carbohydrate recognition by the insulin-like growth factor II/mannose 6-phosphate recept
108 6-phosphate (Man-6-P) binding domains of the insulin-like growth factor II/mannose 6-phosphate recept
110 lated and nonbiotinylated populations of the insulin-like growth factor-II/mannose 6-phosphate recept
111 e 6-phosphate (Man-6-P) binding sites of the insulin-like growth factor-II/mannose 6-phosphate recept
112 oluble forms of the human cation-independent insulin-like growth factor-II/mannose 6-phosphate recept
114 distinct cell surface recycling pathways for insulin-like growth factor-II/mannose 6-phosphate recept
115 ), the cation-dependent MPR (CD-MPR) and the insulin-like growth factor II/MPR (IGF-II/MPR), recogniz
117 d Igf2bp1, a VICKZ (Vg1 RNA binding protein, Insulin-like growth factor II mRNA binding protein 1, Co
122 ding latent transforming growth factor-beta, insulin-like growth factor-II, plasminogen, and urokinas
123 nic effects of insulin-like growth factor I, insulin-like growth factor II, platelet-derived growth f
124 so identified several growth factors such as insulin-like growth factor-II, platelet-derived growth f
125 shing mTOR activity, which in turn decreased insulin-like growth factor II production and autocrine s
126 levels of transcription of an Sp1-dependent insulin-like growth factor II promoter construct in MCF-
128 antagomir-352 up-regulated the expression of insulin-like growth factor II receptor (IGF2R), which ma
131 The cation-independent mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGF-II recep
132 EG binds directly to the mannose-6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) depen
134 f lysosomal enzymes, the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) plays
136 c acid (RA) binds to the mannose-6-phosphate/insulin-like growth factor II receptor (M6P/IGF2R) with
137 , we have identified the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGFIIR) as a
138 n the trafficking of the mannose 6-phosphate/insulin-like growth factor II receptor (Man-6-P/IGF-II r
139 or (uPAR) binding by the mannose 6-phosphate/insulin-like growth factor II receptor (Man-6-P/IGF2R) i
140 of chemotherapy; (c) the mannose 6-phosphate/insulin-like growth factor II receptor and the TGF-beta
141 ated by isolation of the mannose 6-phosphate/insulin-like growth factor II receptor and the transform
142 urine cation-independent mannose 6-phosphate/insulin-like growth factor II receptor cytoplasmic domai
143 ted short tandem repeat polymorphisms of the insulin-like growth factor II receptor gene (IGF2R) in o
144 in their coding sequences, such as BAX, the insulin-like growth factor II receptor IGFIIR, and even
145 a possible role for the mannose 6-phosphate/insulin-like growth factor II receptor in GUS transport
146 zation of TGF-beta1, the mannose 6-phosphate/insulin-like growth factor II receptor, the TGF-beta typ
148 y the induction by KSHV of the expression of insulin-like growth factor-II receptor (IGF-IIR), a mann
151 nalytes (leptin, prolactin, osteopontin, and insulin-like growth factor-II), that can discriminate be
152 r, is particularly striking and includes the insulin-like growth factor II, the cisplatin resistance-
153 ting (GILT) tag, which contains a portion of insulin-like growth factor II, to create an active, chim
154 of the nutrient- and stress-sensing insulin/insulin-like growth factor (IIS)/TOR signalling network,
156 trations of insulin-like growth factor-I and insulin-like growth factor-II were low and remained low
157 This autoantigen binds to mRNA encoding insulin-like growth factor II, which has been found to b
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