BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

159 related articles for article (PubMed ID: 27409069)

  • 1. Increased bone turnover, osteoporosis, progressive tibial bowing, fractures, and scoliosis in a patient with a final-exon SATB2 frameshift mutation.
    Boone PM; Chan YM; Hunter JV; Pottkotter LE; Davino NA; Yang Y; Beuten J; Bacino CA
    Am J Med Genet A; 2016 Nov; 170(11):3028-3032. PubMed ID: 27409069
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype and phenotype in 12 additional individuals with SATB2-associated syndrome.
    Zarate YA; Kalsner L; Basinger A; Jones JR; Li C; Szybowska M; Xu ZL; Vergano S; Caffrey AR; Gonzalez CV; Dubbs H; Zackai E; Millan F; Telegrafi A; Baskin B; Person R; Fish JL; Everman DB
    Clin Genet; 2017 Oct; 92(4):423-429. PubMed ID: 28139846
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SATB2-associated syndrome in patients from Japan: Linguistic profiles.
    Yamada M; Uehara T; Suzuki H; Takenouchi T; Yoshihashi H; Suzumura H; Mizuno S; Kosaki K
    Am J Med Genet A; 2019 Jun; 179(6):896-899. PubMed ID: 30848049
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome.
    Liedén A; Kvarnung M; Nilssson D; Sahlin E; Lundberg ES
    Am J Med Genet A; 2014 Dec; 164A(12):3083-7. PubMed ID: 25251319
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.
    Leoyklang P; Suphapeetiporn K; Siriwan P; Desudchit T; Chaowanapanja P; Gahl WA; Shotelersuk V
    Hum Mutat; 2007 Jul; 28(7):732-8. PubMed ID: 17377962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SATB2-associated syndrome: Mechanisms, phenotype, and practical recommendations.
    Zarate YA; Fish JL
    Am J Med Genet A; 2017 Feb; 173(2):327-337. PubMed ID: 27774744
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Bone health and SATB2-associated syndrome.
    Zarate YA; Steinraths M; Matthews A; Smith WE; Sun A; Wilson LC; Brain C; Allgove J; Jacobs B; Fish JL; Powell CM; Wasserman WW; van Karnebeek CD; Wakeling EL; Ma NS
    Clin Genet; 2018 Mar; 93(3):588-594. PubMed ID: 28787087
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.
    Zarate YA; Perry H; Ben-Omran T; Sellars EA; Stein Q; Almureikhi M; Simmons K; Klein O; Fish J; Feingold M; Douglas J; Kruer MC; Si Y; Mao R; McKnight D; Gibellini F; Retterer K; Slavotinek A
    Am J Med Genet A; 2015 May; 167A(5):1026-32. PubMed ID: 25885067
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients.
    Mouillé M; Rio M; Breton S; Piketty ML; Afenjar A; Amiel J; Capri Y; Goldenberg A; Francannet C; Michot C; Mignot C; Perrin L; Quelin C; Van Gils J; Barcia G; Pingault V; Maruani G; Koumakis E; Cormier-Daire V
    Orphanet J Rare Dis; 2022 Mar; 17(1):100. PubMed ID: 35241104
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Patients with SATB2-associated syndrome exhibiting multiple odontomas.
    Kikuiri T; Mishima H; Imura H; Suzuki S; Matsuzawa Y; Nakamura T; Fukumoto S; Yoshimura Y; Watanabe S; Kinoshita A; Yamada T; Shindoh M; Sugita Y; Maeda H; Yawaka Y; Mikoya T; Natsume N; Yoshiura KI
    Am J Med Genet A; 2018 Dec; 176(12):2614-2622. PubMed ID: 30575289
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SATB2-associated syndrome presenting with Rett-like phenotypes.
    Lee JS; Yoo Y; Lim BC; Kim KJ; Choi M; Chae JH
    Clin Genet; 2016 Jun; 89(6):728-32. PubMed ID: 26596517
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Further delineation of the SATB2 phenotype.
    Döcker D; Schubach M; Menzel M; Munz M; Spaich C; Biskup S; Bartholdi D
    Eur J Hum Genet; 2014 Aug; 22(8):1034-9. PubMed ID: 24301056
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bone health in SATB2-associated syndrome: Results from a large prospective cohort and recommendations for surveillance.
    Zarate YA; Bosanko K; Andres A; Fish JL
    Am J Med Genet A; 2024 Feb; 194(2):203-210. PubMed ID: 37786328
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis of SATB2 gene mutation in a child with Glass syndrome].
    Lin M; Yao R; Lu J; Chen W; Xu Y; Li G; Yu T; Qing Y; Jin X; Wang J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jul; 36(7):712-715. PubMed ID: 31302918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SATB2-Associated Syndrome: a Case Report of a De Novo Nonsense Mutation in SATB2 from China and Review of Literature.
    Lv HY; Zheng RJ; Wang QL; Ren PS; Jin LH; Gu XL; Li LX
    Clin Lab; 2018 Apr; 64(4):627-637. PubMed ID: 29739092
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular consequences of disease-associated de novo mutations in SATB2.
    Bengani H; Handley M; Alvi M; Ibitoye R; Lees M; Lynch SA; Lam W; Fannemel M; Nordgren A; Malmgren H; Kvarnung M; Mehta S; McKee S; Whiteford M; Stewart F; Connell F; Clayton-Smith J; Mansour S; Mohammed S; Fryer A; Morton J; ; Grozeva D; Asam T; Moore D; Sifrim A; McRae J; Hurles ME; Firth HV; Raymond FL; Kini U; Nellåker C; Ddd Study ; FitzPatrick DR
    Genet Med; 2017 Aug; 19(8):900-908. PubMed ID: 28151491
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dental Follicle Cells Participate in Tooth Eruption via the RUNX2-MiR-31-SATB2 Loop.
    Ge J; Guo S; Fu Y; Zhou P; Zhang P; Du Y; Li M; Cheng J; Jiang H
    J Dent Res; 2015 Jul; 94(7):936-44. PubMed ID: 25818585
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Natural history and genotype-phenotype correlations in 72 individuals with SATB2-associated syndrome.
    Zarate YA; Smith-Hicks CL; Greene C; Abbott MA; Siu VM; Calhoun ARUL; Pandya A; Li C; Sellars EA; Kaylor J; Bosanko K; Kalsner L; Basinger A; Slavotinek AM; Perry H; Saenz M; Szybowska M; Wilson LC; Kumar A; Brain C; Balasubramanian M; Dubbs H; Ortiz-Gonzalez XR; Zackai E; Stein Q; Powell CM; Schrier Vergano S; Britt A; Sun A; Smith W; Bebin EM; Picker J; Kirby A; Pinz H; Bombei H; Mahida S; Cohen JS; Fatemi A; Vernon HJ; McClellan R; Fleming LR; Knyszek B; Steinraths M; Velasco Gonzalez C; Beck AE; Golden-Grant KL; Egense A; Parikh A; Raimondi C; Angle B; Allen W; Schott S; Algrabli A; Robin NH; Ray JW; Everman DB; Gambello MJ; Chung WK
    Am J Med Genet A; 2018 Apr; 176(4):925-935. PubMed ID: 29436146
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Estrogen regulates stemness and senescence of bone marrow stromal cells to prevent osteoporosis via ERβ-SATB2 pathway.
    Wu G; Xu R; Zhang P; Xiao T; Fu Y; Zhang Y; Du Y; Ye J; Cheng J; Jiang H
    J Cell Physiol; 2018 May; 233(5):4194-4204. PubMed ID: 29030963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of the first intragenic SATB2 duplication in a girl with intellectual disability, nearly absent speech and suspected hypodontia.
    Kaiser AS; Maas B; Wolff A; Sutter C; Janssen JW; Hinderhofer K; Moog U
    Eur J Hum Genet; 2015 May; 23(5):704-7. PubMed ID: 25118029
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.