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 *

180 related articles for article (PubMed ID: 17216607)

  • 21. [Progress of study on the transcription factor SALL4].
    Lin J; Ji RB; Qian J
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2011 Jun; 19(3):820-3. PubMed ID: 21729579
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Okihiro syndrome is caused by SALL4 mutations.
    Kohlhase J; Heinrich M; Schubert L; Liebers M; Kispert A; Laccone F; Turnpenny P; Winter RM; Reardon W
    Hum Mol Genet; 2002 Nov; 11(23):2979-87. PubMed ID: 12393809
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Thalidomide promotes degradation of SALL4, a transcription factor implicated in Duane Radial Ray syndrome.
    Donovan KA; An J; Nowak RP; Yuan JC; Fink EC; Berry BC; Ebert BL; Fischer ES
    Elife; 2018 Aug; 7():. PubMed ID: 30067223
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Sall1, sall2, and sall4 are required for neural tube closure in mice.
    Böhm J; Buck A; Borozdin W; Mannan AU; Matysiak-Scholze U; Adham I; Schulz-Schaeffer W; Floss T; Wurst W; Kohlhase J; Barrionuevo F
    Am J Pathol; 2008 Nov; 173(5):1455-63. PubMed ID: 18818376
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical and molecular genetic findings in isolated sporadic Duane syndrome].
    Wabbels BK; Kohlhase J; Lorenz B
    Klin Monbl Augenheilkd; 2004 Oct; 221(10):849-53. PubMed ID: 15499520
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Diversified clinical presentations associated with a novel sal-like 4 gene mutation in a Chinese pedigree with Duane retraction syndrome.
    Yang MM; Ho M; Lau HH; Tam PO; Young AL; Pang CP; Yip WW; Chen L
    Mol Vis; 2013; 19():986-94. PubMed ID: 23687435
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of the SALL4 gene in patients with Duane retraction syndrome in a South Indian population.
    Arya LK; Kumar AB; Shetty S; Perumalsamy V; Sundaresan P
    Ophthalmic Genet; 2011 Sep; 32(3):156-7. PubMed ID: 21405998
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Novel frameshift mutations in SALL4 in two Chinese families with Okihiro syndrome].
    Bai Y; Wu QH; Li FZ; Sun Y; Wang L; Jiao ZH; Kong XD
    Zhonghua Yi Xue Za Zhi; 2023 Jul; 103(26):2006-2010. PubMed ID: 37438083
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Magnetic resonance imaging of innervational and extraocular muscle abnormalities in Duane-radial ray syndrome.
    Demer JL; Clark RA; Lim KH; Engle EC
    Invest Ophthalmol Vis Sci; 2007 Dec; 48(12):5505-11. PubMed ID: 18055799
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Murine inner cell mass-derived lineages depend on Sall4 function.
    Elling U; Klasen C; Eisenberger T; Anlag K; Treier M
    Proc Natl Acad Sci U S A; 2006 Oct; 103(44):16319-24. PubMed ID: 17060609
    [TBL] [Abstract][Full Text] [Related]  

  • 31. SALL4: engine of cell stemness.
    Xiong J
    Curr Gene Ther; 2014; 14(5):400-11. PubMed ID: 25174577
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Functional and clinical significance of SALL4 in breast cancer.
    Dirican E; Akkiprik M
    Tumour Biol; 2016 Sep; 37(9):11701-11709. PubMed ID: 27444278
    [TBL] [Abstract][Full Text] [Related]  

  • 33. SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism.
    Borozdin W; Boehm D; Leipoldt M; Wilhelm C; Reardon W; Clayton-Smith J; Becker K; Mühlendyck H; Winter R; Giray O; Silan F; Kohlhase J
    J Med Genet; 2004 Sep; 41(9):e113. PubMed ID: 15342710
    [No Abstract]   [Full Text] [Related]  

  • 34. Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new families.
    Becker K; Beales PL; Calver DM; Matthijs G; Mohammed SN
    J Med Genet; 2002 Jan; 39(1):68-71. PubMed ID: 11826030
    [No Abstract]   [Full Text] [Related]  

  • 35. SALL4 controls cell fate in response to DNA base composition.
    Pantier R; Chhatbar K; Quante T; Skourti-Stathaki K; Cholewa-Waclaw J; Alston G; Alexander-Howden B; Lee HY; Cook AG; Spruijt CG; Vermeulen M; Selfridge J; Bird A
    Mol Cell; 2021 Feb; 81(4):845-858.e8. PubMed ID: 33406384
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The association of an epibulbar dermoid and Duane syndrome in a patient with a SALL1 mutation (Townes-Brocks Syndrome).
    Barry JS; Reddy MA
    Ophthalmic Genet; 2008 Dec; 29(4):177-80. PubMed ID: 19005989
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Stemness-related factor Sall4 interacts with transcription factors Oct-3/4 and Sox2 and occupies Oct-Sox elements in mouse embryonic stem cells.
    Tanimura N; Saito M; Ebisuya M; Nishida E; Ishikawa F
    J Biol Chem; 2013 Feb; 288(7):5027-38. PubMed ID: 23269686
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Cooperative and antagonistic interactions between Sall4 and Tbx5 pattern the mouse limb and heart.
    Koshiba-Takeuchi K; Takeuchi JK; Arruda EP; Kathiriya IS; Mo R; Hui CC; Srivastava D; Bruneau BG
    Nat Genet; 2006 Feb; 38(2):175-83. PubMed ID: 16380715
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Normal embryonic development and neonatal digit regeneration in mice overexpressing a stem cell factor, Sall4.
    Chen KQ; Anderson A; Kawakami H; Kim J; Barrett J; Kawakami Y
    PLoS One; 2022; 17(4):e0267273. PubMed ID: 35482646
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Structural studies of SALL family protein zinc finger cluster domains in complex with DNA reveal preferential binding to an AATA tetranucleotide motif.
    Ru W; Koga T; Wang X; Guo Q; Gearhart MD; Zhao S; Murphy M; Kawakami H; Corcoran D; Zhang J; Zhu Z; Yao X; Kawakami Y; Xu C
    J Biol Chem; 2022 Dec; 298(12):102607. PubMed ID: 36257403
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.