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 *

128 related articles for article (PubMed ID: 29887954)

  • 41. Prenatal diagnosis of fetal skeletal dysplasia using targeted next-generation sequencing: an analysis of 30 cases.
    Liu Y; Wang L; Yang YK; Liang Y; Zhang TJ; Liang N; Yang LM; Li SJ; Shan D; Wu QQ
    Diagn Pathol; 2019 Jul; 14(1):76. PubMed ID: 31299979
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review.
    Hsueh SJ; Lee NC; Yang SH; Lin HI; Lin CH
    BMC Neurol; 2017 Jan; 17(1):2. PubMed ID: 28056872
    [TBL] [Abstract][Full Text] [Related]  

  • 43. microRNA-31 inhibition partially ameliorates the deficiency of bone marrow stromal cells from cleidocranial dysplasia.
    Xu L; Fu Y; Zhu W; Xu R; Zhang J; Zhang P; Cheng J; Jiang H
    J Cell Biochem; 2019 Jun; 120(6):9472-9486. PubMed ID: 30506733
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Bcl-2-associated athanogene-1 (BAG-1): a transcriptional regulator mediating chondrocyte survival and differentiation during endochondral ossification.
    Tare RS; Townsend PA; Packham GK; Inglis S; Oreffo RO
    Bone; 2008 Jan; 42(1):113-28. PubMed ID: 17950682
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.
    Krakow D; Robertson SP; King LM; Morgan T; Sebald ET; Bertolotto C; Wachsmann-Hogiu S; Acuna D; Shapiro SS; Takafuta T; Aftimos S; Kim CA; Firth H; Steiner CE; Cormier-Daire V; Superti-Furga A; Bonafe L; Graham JM; Grix A; Bacino CA; Allanson J; Bialer MG; Lachman RS; Rimoin DL; Cohn DH
    Nat Genet; 2004 Apr; 36(4):405-10. PubMed ID: 14991055
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation.
    Rickels MR; Zhang X; Mumm S; Whyte MP
    J Bone Miner Res; 2005 May; 20(5):878-85. PubMed ID: 15824861
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Dexamethasone inhibits insulin-induced chondrogenesis of ATDC5 cells by preventing PI3K-Akt signaling and DNA binding of Runx2.
    Fujita T; Fukuyama R; Enomoto H; Komori T
    J Cell Biochem; 2004 Oct; 93(2):374-83. PubMed ID: 15368363
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome.
    Carapito R; Goldenberg A; Paul N; Pichot A; David A; Hamel A; Dumant-Forest C; Leroux J; Ory B; Isidor B; Bahram S
    Eur J Hum Genet; 2016 Dec; 24(12):1746-1751. PubMed ID: 27381093
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Identification of Filamin-A and -B as potential biomarkers for prostate cancer.
    Narain NR; Diers AR; Lee A; Lao S; Chan JY; Schofield S; Andreazi J; Ouro-Djobo R; Jimenez JJ; Friss T; Tanna N; Dalvi A; Wang S; Bunch D; Sun Y; Wu W; Thapa K; Gesta S; Rodrigues LO; Akmaev VR; Vishnudas VK; Sarangarajan R
    Future Sci OA; 2017 Mar; 3(1):FSO161. PubMed ID: 28344825
    [TBL] [Abstract][Full Text] [Related]  

  • 50. GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome.
    Patel N; Shamseldin HE; Sakati N; Khan AO; Softa A; Al-Fadhli FM; Hashem M; Abdulwahab FM; Alshidi T; Alomar R; Alobeid E; Wakil SM; Colak D; Alkuraya FS
    Am J Hum Genet; 2017 May; 100(5):831-836. PubMed ID: 28475863
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Differential effect of BMP4 on NIH/3T3 and C2C12 cells: implications for endochondral bone formation.
    Li G; Peng H; Corsi K; Usas A; Olshanski A; Huard J
    J Bone Miner Res; 2005 Sep; 20(9):1611-23. PubMed ID: 16059633
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Differential expressions of BMP family genes during chondrogenic differentiation of mouse ATDC5 cells.
    Akiyama H; Shukunami C; Nakamura T; Hiraki Y
    Cell Struct Funct; 2000 Jun; 25(3):195-204. PubMed ID: 10984103
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Type and level of RMRP functional impairment predicts phenotype in the cartilage hair hypoplasia-anauxetic dysplasia spectrum.
    Thiel CT; Mortier G; Kaitila I; Reis A; Rauch A
    Am J Hum Genet; 2007 Sep; 81(3):519-29. PubMed ID: 17701897
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Aloe-Emodin Induces Chondrogenic Differentiation of ATDC5 Cells via MAP Kinases and BMP-2 Signaling Pathways.
    Yang M; Li L; Heo SM; Soh Y
    Biomol Ther (Seoul); 2016 Jul; 24(4):395-401. PubMed ID: 27350340
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Molecular basis for the treatment of achondroplasia.
    Yamanaka Y; Ueda K; Seino Y; Tanaka H
    Horm Res; 2003; 60 Suppl 3():60-4. PubMed ID: 14671399
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Different mutations in PDE4D associated with developmental disorders with mirror phenotypes.
    Lindstrand A; Grigelioniene G; Nilsson D; Pettersson M; Hofmeister W; Anderlid BM; Kant SG; Ruivenkamp CA; Gustavsson P; Valta H; Geiberger S; Topa A; Lagerstedt-Robinson K; Taylan F; Wincent J; Laurell T; Pekkinen M; Nordenskjöld M; Mäkitie O; Nordgren A
    J Med Genet; 2014 Jan; 51(1):45-54. PubMed ID: 24203977
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Sphenoid bone hypoplasia is a skeletal phenotype of cleidocranial dysplasia in a mouse model and patients.
    Mitomo K; Matsunaga S; Kitamura K; Nakamura T; Saito A; Komori T; Muramatsu T; Yamaguchi A
    Bone; 2019 Mar; 120():176-186. PubMed ID: 30391578
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Effects of transforming growth factor-beta signaling on chondrogenesis in mouse chondrogenic EC cells, ATDC5.
    Kawai J; Akiyama H; Shigeno C; Ito H; Konishi J; Nakamura T
    Eur J Cell Biol; 1999 Oct; 78(10):707-14. PubMed ID: 10569243
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Genotoxicity of 1,3-butadiene and its epoxy intermediates.
    Walker VE; Walker DM; Meng Q; McDonald JD; Scott BR; Seilkop SK; Claffey DJ; Upton PB; Powley MW; Swenberg JA; Henderson RF;
    Res Rep Health Eff Inst; 2009 Aug; (144):3-79. PubMed ID: 20017413
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
    Fan P; Zhao YM; Zhang D; Liao Y; Yang KQ; Tian T; Lou Y; Luo F; Ma WJ; Zhang HM; Song L; Cai J; Liu YX; Zhou XL
    Am J Hypertens; 2019 Jul; 32(8):752-758. PubMed ID: 30977777
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.