ライフサイエンスコーパス: HMG protein

1 me by expression of a heterologous mammalian HMG protein.

2 ined from analogous 12-RSS complexes lacking HMG protein.

3 roid hormone receptors and the architectural HMG proteins.

4 correlated positively with the synthesis of HMG proteins.

5 rion than previously published work with the HMG proteins.

6 ins the founding members of a third group of HMG proteins.

7 iated with chromatin, such as nucleolins and HMG proteins.

8 non-histone chromosomal high-mobility group (HMG) proteins.

9 g to the superfamily of high mobility group (HMG) proteins.

10 tors, including several high mobility group (HMG) proteins.

11 al properties common to high-mobility-group (HMG) proteins.

12 that the mitochondrial high mobility group (HMG) protein, Abf2p, of Saccharomyces cerevisiae influen

13 amino acids are normally conserved in human HMG proteins and 27 are conserved in the human Sox sub-f

14 Unbalanced growth would alter the amounts of HMG proteins and H1 histone, thus changing transcription

15 namic and competitive interactions involving HMG proteins and H1, and perhaps other structural protei

16 Further identification of serine ADPr on HMG proteins and hundreds of other targets indicates tha

17 contains similarity to DNA sequence-specific HMG proteins and is shown to bind specific satellite seq

18 lustering of architectural elements, such as HMG proteins and linker histone subtypes into distinct d

19 ts factors, and an A/T hook domain, found in HMG proteins and various other nuclear factors.

20 One is Rox1, an HMG protein, and the second, originally designated Rox7,

21 HMG proteins are architectural proteins that bind to DNA

22 Numerous natural variants in HMG proteins are associated with disease phenotypes.

23 A total of 33 amino acids in HMG proteins are known to have natural variants in disea

24 High-mobility group (HMG) proteins are architectural factors that have been s

25 Histone H1 and the high-mobility group (HMG) proteins are chromatin binding proteins that regula

26 The high mobility group (HMG) proteins are important modulators of chromatin stru

27 High mobility group (HMG) proteins are nuclear proteins believed to significa

28 High mobility group (HMG) proteins are thought to facilitate assembly of high

29 on factor A (TFAM) is a high-mobility group (HMG) protein at the nexus of mitochondrial DNA (mtDNA) r

30 es with homology to the high mobility group (HMG) protein-binding consensus sequence.

31 in DMSA, and 4) inhibition of expression of HMG proteins by antisense HMGI-C RNA in EL4 cells causes

32 High mobility group (HMG) proteins concentrate in the nucleus, interacting wi

33 and decreases nucleosomal access, while the HMG proteins decrease the compactness of the chromatin f

34 ggest that, in response to IFN treatment, an HMG protein-dependent complex involving multiple regulat

35 Of the three HMG proteins examined, HMG-1, HMG-2, and HMG-I(Y), the p

36 erium-derived HIV-1 integrase (IN), and host HMG protein family members.

37 arce1/BAF-57 is also the first member of the HMG protein family that was reported to contain a kinesi

38 Abf2p is a high mobility group (HMG) protein found in yeast mitochondria that is require

39 tural homology with the high mobility group (HMG) proteins from eukaryotic organisms.

40 One family of HMG proteins, HMG-I/Y, is known to facilitate the initia

41 were identified as the high-mobility group (HMG) protein, HMG-I, and its splicing variant, HMG-Y.

42 The high-mobility group (HMG) proteins HMG1, HMG2 and HMG2a are relatively abunda

43 n number AF022465), proposed to encode a new HMG protein, HMG4, is also likely to encode an HMG2a, ba

44 Amphoterin is an HMG protein (HMGB1) that has been shown to have extranuc

45 Oct-1 and Oct-2 and the high mobility group (HMG) protein HMGI(Y) bind to regulatory elements present

46 n of the nuclear matrix high mobility group (HMG) proteins HMGI(Y) when tested in three human prostat

47 nals utilized the same complement of RAG and HMG proteins, I compared the RAG protein stoichiometries

48 We propose that the abundance of HMG proteins in eukaryotic nuclei provides an environmen

49 e we study the spatial organization of these HMG proteins in the nucleus and the distribution of nucl

50 ntegration and examine the role of different HMG proteins in the reaction.

51 , a transcriptional coactivator of LEF-1/TCF HMG proteins in the Wnt/Wg signaling pathway.

52 coding for the abundant high-mobility-group (HMG) proteins in humans.

53 e presence of the ATTGTT core (recognized by HMG proteins) in the AR2 sequence suggests that an HMG p

54 Saccharomyces cerevisiae encodes 10 HMG proteins, including Hmo1, which is important for max

55 chondria (TFAM), a dual high-mobility group (HMG) protein involved in maintenance and compaction of t

56 on interference experiments suggest that the HMG protein is positioned 5' of the nonamer in 23-RSS co

57 The DNA binding domain of HMG proteins is known to be important in many diseases,

58 An additional effect of HMG proteins is to stimulate coupled cleavage greatly wh

59 by overexpression of POP-1, a TCF/LEF class HMG protein known to act downstream of the Wnt signaling

60 This role has been proposed for the HMG proteins LEF-1 and TCF-1.

61 oteins) in the AR2 sequence suggests that an HMG protein may activate through AR2.

62 in many diseases, with the Sox sub-family of HMG proteins of particular significance.

63 haromyces pombe, where the nucleocytoplasmic HMG protein Oxs1 acts cooperatively with Pap1 to regulat

64 .a. HMGI/Y) family of 'high mobility group' (HMG) proteins participate in a wide variety of nuclear p

65 Thus, HMG protein plays the dual role of bringing critical ele

66 HMG protein SON-1 and the sequence specific HMG protein POP-1 might both act in the Wnt responding c

67 The sequence nonspecific HMG protein SON-1 and the sequence specific HMG protein

68 e lymphocyte-restricted High Mobility Group (HMG) protein, SOX4.

69 l ways, including the recruitment of a yeast HMG protein that is required for the normally robust lev

70 The C. albicans clone also encoded an HMG protein that was capable of repression of a hypoxic

71 rrant cell growth and strengthen the link of HMG proteins to oncogenesis.

72 living cells, each of the three families of HMG proteins weakens the binding of H1 to nucleosomes by

73 o very high non-specific interactions of the HMG proteins with a carboxymethyl-dextran matrix, a nove

74 The interaction of HMG proteins with chromatin is dynamic.

75 e linker histone H1 and high-mobility-group (HMG) proteins with nucleosomes leads to changes in chrom