These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 13679026)

  • 1. Organization of the mouse Zfhx1b gene encoding the two-handed zinc finger repressor Smad-interacting protein-1.
    Nelles L; Van de Putte T; van Grunsven L; Huylebroeck D; Verschueren K
    Genomics; 2003 Oct; 82(4):460-9. PubMed ID: 13679026
    [TBL] [Abstract][Full Text] [Related]  

  • 2. New mode of DNA binding of multi-zinc finger transcription factors: deltaEF1 family members bind with two hands to two target sites.
    Remacle JE; Kraft H; Lerchner W; Wuytens G; Collart C; Verschueren K; Smith JC; Huylebroeck D
    EMBO J; 1999 Sep; 18(18):5073-84. PubMed ID: 10487759
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Zfhx1a and Zfhx1b mRNAs have non-overlapping expression domains during chick and mouse midgestation limb development.
    Tylzanowski P; De Valck D; Maes V; Peeters J; Luyten FP
    Gene Expr Patterns; 2003 Mar; 3(1):39-42. PubMed ID: 12609600
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SIP1 (Smad interacting protein 1) and deltaEF1 (delta-crystallin enhancer binding factor) are structurally similar transcriptional repressors.
    van Grunsven LA; Schellens A; Huylebroeck D; Verschueren K
    J Bone Joint Surg Am; 2001; 83-A Suppl 1(Pt 1):S40-7. PubMed ID: 11263664
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5'-CACCT sequences in candidate target genes.
    Verschueren K; Remacle JE; Collart C; Kraft H; Baker BS; Tylzanowski P; Nelles L; Wuytens G; Su MT; Bodmer R; Smith JC; Huylebroeck D
    J Biol Chem; 1999 Jul; 274(29):20489-98. PubMed ID: 10400677
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome.
    Van de Putte T; Maruhashi M; Francis A; Nelles L; Kondoh H; Huylebroeck D; Higashi Y
    Am J Hum Genet; 2003 Feb; 72(2):465-70. PubMed ID: 12522767
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Interaction between Smad-interacting protein-1 and the corepressor C-terminal binding protein is dispensable for transcriptional repression of E-cadherin.
    van Grunsven LA; Michiels C; Van de Putte T; Nelles L; Wuytens G; Verschueren K; Huylebroeck D
    J Biol Chem; 2003 Jul; 278(28):26135-45. PubMed ID: 12714599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Integrative genomic analyses of ZEB2: Transcriptional regulation of ZEB2 based on SMADs, ETS1, HIF1alpha, POU/OCT, and NF-kappaB.
    Katoh M; Katoh M
    Int J Oncol; 2009 Jun; 34(6):1737-42. PubMed ID: 19424592
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Organization of the gene encoding transcriptional repressor deltaEF1 and cross-species conservation of its domains.
    Sekido R; Takagi T; Okanami M; Moribe H; Yamamura M; Higashi Y; Kondoh H
    Gene; 1996 Sep; 173(2):227-32. PubMed ID: 8964504
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features.
    Yamada K; Yamada Y; Nomura N; Miura K; Wakako R; Hayakawa C; Matsumoto A; Kumagai T; Yoshimura I; Miyazaki S; Kato K; Sonta S; Ono H; Yamanaka T; Nagaya M; Wakamatsu N
    Am J Hum Genet; 2001 Dec; 69(6):1178-85. PubMed ID: 11592033
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation.
    Miquelajauregui A; Van de Putte T; Polyakov A; Nityanandam A; Boppana S; Seuntjens E; Karabinos A; Higashi Y; Huylebroeck D; Tarabykin V
    Proc Natl Acad Sci U S A; 2007 Jul; 104(31):12919-24. PubMed ID: 17644613
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The zinc finger transcription factor ZFHX1A is linked to cell proliferation by Rb-E2F1.
    Liu Y; Costantino ME; Montoya-Durango D; Higashi Y; Darling DS; Dean DC
    Biochem J; 2007 Nov; 408(1):79-85. PubMed ID: 17655524
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.
    Garavelli L; Donadio A; Zanacca C; Banchini G; Della Giustina E; Bertani G; Albertini G; Del Rossi C; Zweier C; Rauch A; Zollino M; Neri G
    Am J Med Genet A; 2003 Feb; 116A(4):385-8. PubMed ID: 12522797
    [No Abstract]   [Full Text] [Related]  

  • 14. The Tgif2 gene contains a retained intron within the coding sequence.
    Melhuish TA; Wotton D
    BMC Mol Biol; 2006 Jan; 7():2. PubMed ID: 16436215
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Generation of the floxed allele of the SIP1 (Smad-interacting protein 1) gene for Cre-mediated conditional knockout in the mouse.
    Higashi Y; Maruhashi M; Nelles L; Van de Putte T; Verschueren K; Miyoshi T; Yoshimoto A; Kondoh H; Huylebroeck D
    Genesis; 2002 Feb; 32(2):82-4. PubMed ID: 11857784
    [No Abstract]   [Full Text] [Related]  

  • 16. Ocular coloboma and high myopia with Hirschsprung disease associated with a novel ZFHX1B missense mutation and trisomy 21.
    Gregory-Evans CY; Vieira H; Dalton R; Adams GG; Salt A; Gregory-Evans K
    Am J Med Genet A; 2004 Nov; 131(1):86-90. PubMed ID: 15384097
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease.
    Cacheux V; Dastot-Le Moal F; Kääriäinen H; Bondurand N; Rintala R; Boissier B; Wilson M; Mowat D; Goossens M
    Hum Mol Genet; 2001 Jul; 10(14):1503-10. PubMed ID: 11448942
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mechanism of biogenesis and potential function of the two alternatively spliced mRNAs encoded by the murine Msx3 gene.
    Matsui H; Takahashi T; Raghow R
    Mol Cell Biochem; 2004 Dec; 267(1-2):1-11. PubMed ID: 15663180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Distinct organization of the candidate tumor suppressor gene RFP2 in human and mouse: multiple mRNA isoforms in both species- and human-specific antisense transcript RFP2OS.
    Baranova A; Hammarsund M; Ivanov D; Skoblov M; Sangfelt O; Corcoran M; Borodina T; Makeeva N; Pestova A; Tyazhelova T; Nazarenko S; Gorreta F; Alsheddi T; Schlauch K; Nikitin E; Kapanadze B; Shagin D; Poltaraus A; Ivanovich Vorobiev A; Zabarovsky E; Lukianov S; Chandhoke V; Ibbotson R; Oscier D; Einhorn S; Grander D; Yankovsky N
    Gene; 2003 Dec; 321():103-12. PubMed ID: 14636997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneurons.
    McKinsey GL; Lindtner S; Trzcinski B; Visel A; Pennacchio LA; Huylebroeck D; Higashi Y; Rubenstein JL
    Neuron; 2013 Jan; 77(1):83-98. PubMed ID: 23312518
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.