BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

538 related articles for article (PubMed ID: 16155112)

  • 21. Proper developmental control of human globin genes reproduced by transgenic mice containing a 160-kb BAC carrying the human beta-globin locus.
    Huang Y; Liu DP; Wu L; Li TC; Wu M; Feng DX; Liang CC
    Blood Cells Mol Dis; 2000 Dec; 26(6):598-610. PubMed ID: 11358351
    [TBL] [Abstract][Full Text] [Related]  

  • 22. An embryonic-specific repressor element located 3' to the Agamma-globin gene influences transcription of the human beta-globin locus in transgenic mice.
    Katsantoni EZ; de Krom M; Kong-a-San J; Imam AM; Grosveld F; Anagnou NP; Strouboulis J
    Exp Hematol; 2004 Feb; 32(2):224-33. PubMed ID: 15102485
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Chicken alpha-globin switching depends on autonomous silencing of the embryonic pi globin gene by epigenetics mechanisms.
    Rincón-Arano H; Guerrero G; Valdes-Quezada C; Recillas-Targa F
    J Cell Biochem; 2009 Oct; 108(3):675-87. PubMed ID: 19693775
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The role of the -50 region of the human gamma-globin gene in switching.
    Ristaldi MS; Drabek D; Gribnau J; Poddie D; Yannoutsous N; Cao A; Grosveld F; Imam AM
    EMBO J; 2001 Sep; 20(18):5242-9. PubMed ID: 11566887
    [TBL] [Abstract][Full Text] [Related]  

  • 25. DNase I hypersensitivity and epsilon-globin transcriptional enhancement are separable in locus control region (LCR) HS1 mutant human beta-globin YAC transgenic mice.
    Shimotsuma M; Okamura E; Matsuzaki H; Fukamizu A; Tanimoto K
    J Biol Chem; 2010 May; 285(19):14495-503. PubMed ID: 20231293
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Sequences located 3' to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal A gamma-globin gene in transgenic mice.
    Anagnou NP; Perez-Stable C; Gelinas R; Costantini F; Liapaki K; Constantopoulou M; Kosteas T; Moschonas NK; Stamatoyannopoulos G
    J Biol Chem; 1995 Apr; 270(17):10256-63. PubMed ID: 7537267
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hypersensitive site 2 specifies a unique function within the human beta-globin locus control region to stimulate globin gene transcription.
    Bungert J; Tanimoto K; Patel S; Liu Q; Fear M; Engel JD
    Mol Cell Biol; 1999 Apr; 19(4):3062-72. PubMed ID: 10082573
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A major role for the TATA box in recruitment of chromatin modifying complexes to a globin gene promoter.
    Gui CY; Dean A
    Proc Natl Acad Sci U S A; 2003 Jun; 100(12):7009-14. PubMed ID: 12773626
    [TBL] [Abstract][Full Text] [Related]  

  • 29. beta-YAC transgenic mice for studying LCR function.
    Peterson KR; Navas PA; Stamatoyannopoulos G
    Ann N Y Acad Sci; 1998 Jun; 850():28-37. PubMed ID: 9668524
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cluster specific regulation pattern of upstream regulatory elements in human alpha- and beta-globin gene clusters.
    Tang Y; Huang Y; Shen W; Liu G; Wang Z; Tang XB; Feng DX; Liu DP; Liang CC
    Exp Cell Res; 2008 Jan; 314(1):115-22. PubMed ID: 17996867
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome architecture of the human beta-globin locus affects developmental regulation of gene expression.
    Harju S; Navas PA; Stamatoyannopoulos G; Peterson KR
    Mol Cell Biol; 2005 Oct; 25(20):8765-78. PubMed ID: 16199858
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control region.
    Starck J; Sarkar R; Romana M; Bhargava A; Scarpa AL; Tanaka M; Chamberlain JW; Weissman SM; Forget BG
    Blood; 1994 Sep; 84(5):1656-65. PubMed ID: 7520781
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human fetal-to-adult globin gene switching in transgenic mice: persistent expression of the G gamma-globin gene in the Japanese HPFH.
    Katsube T; Tojo H; Sakaguchi T; Fukumaki Y
    Biochem Biophys Res Commun; 1993 Jul; 194(1):246-52. PubMed ID: 7687430
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Persistent gamma-globin expression in adult transgenic mice is mediated by HPFH-2, HPFH-3, and HPFH-6 breakpoint sequences.
    Katsantoni EZ; Langeveld A; Wai AW; Drabek D; Grosveld F; Anagnou NP; Strouboulis J
    Blood; 2003 Nov; 102(9):3412-9. PubMed ID: 12855570
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Partial repression of human gamma-globin genes by LCR element HS3 when linked to beta-globin genes and LCR element HS2 in MEL cells.
    Stoeckert CJ; Cheng H
    Am J Hematol; 1996 Mar; 51(3):220-8. PubMed ID: 8619403
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Original Research: Generation of non-deletional hereditary persistence of fetal hemoglobin β-globin locus yeast artificial chromosome transgenic mouse models: -175 Black HPFH and -195 Brazilian HPFH.
    Braghini CA; Costa FC; Fedosyuk H; Neades RY; Novikova LV; Parker MP; Winefield RD; Peterson KR
    Exp Biol Med (Maywood); 2016 Apr; 241(7):697-705. PubMed ID: 26946532
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients.
    Di Marzo R; Acuto S; Calzolari R; Maggio A
    Exp Hematol; 2005 Nov; 33(11):1363-70. PubMed ID: 16263421
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chromatin structure of the LCR in the human β-globin locus transcribing the adult δ- and β-globin genes.
    Kim S; Kim YW; Shim SH; Kim CG; Kim A
    Int J Biochem Cell Biol; 2012 Mar; 44(3):505-13. PubMed ID: 22178075
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A large upstream region is not necessary for gene expression or hypersensitive site formation at the mouse beta -globin locus.
    Farrell CM; Grinberg A; Huang SP; Chen D; Pichel JG; Westphal H; Felsenfeld G
    Proc Natl Acad Sci U S A; 2000 Dec; 97(26):14554-9. PubMed ID: 11121056
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A single point mutation is the cause of the Greek form of hereditary persistence of fetal haemoglobin.
    Berry M; Grosveld F; Dillon N
    Nature; 1992 Aug; 358(6386):499-502. PubMed ID: 1379347
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 27.