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 *

296 related articles for article (PubMed ID: 29761634)

  • 1. Extracephalic manifestations of nonchromosomal, nonsyndromic holoprosencephaly.
    Martinez AF; Kruszka PS; Muenke M
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):246-257. PubMed ID: 29761634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Modeling the complex etiology of holoprosencephaly in mice.
    Hong M; Krauss RS
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):140-150. PubMed ID: 29749693
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cdon mutation and fetal ethanol exposure synergize to produce midline signaling defects and holoprosencephaly spectrum disorders in mice.
    Hong M; Krauss RS
    PLoS Genet; 2012; 8(10):e1002999. PubMed ID: 23071453
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Loss of Tgif function causes holoprosencephaly by disrupting the SHH signaling pathway.
    Taniguchi K; Anderson AE; Sutherland AE; Wotton D
    PLoS Genet; 2012; 8(2):e1002524. PubMed ID: 22383895
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects.
    Dennis JF; Kurosaka H; Iulianella A; Pace J; Thomas N; Beckham S; Williams T; Trainor PA
    PLoS Genet; 2012; 8(10):e1002927. PubMed ID: 23055936
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Holoprosencephaly: recommendations for diagnosis and management.
    Kauvar EF; Muenke M
    Curr Opin Pediatr; 2010 Dec; 22(6):687-95. PubMed ID: 20859208
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functions of TGIF homeodomain proteins and their roles in normal brain development and holoprosencephaly.
    Wotton D; Taniguchi K
    Am J Med Genet C Semin Med Genet; 2018 Jun; 178(2):128-139. PubMed ID: 29749689
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
    Nanni L; Ming JE; Bocian M; Steinhaus K; Bianchi DW; Die-Smulders C; Giannotti A; Imaizumi K; Jones KL; Campo MD; Martin RA; Meinecke P; Pierpont ME; Robin NH; Young ID; Roessler E; Muenke M
    Hum Mol Genet; 1999 Dec; 8(13):2479-88. PubMed ID: 10556296
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF-β, hedgehog, and FGF signaling.
    Roessler E; Hu P; Marino J; Hong S; Hart R; Berger S; Martinez A; Abe Y; Kruszka P; Thomas JW; Mullikin JC; ; Wang Y; Wong WSW; Niederhuber JE; Solomon BD; Richieri-Costa A; Ribeiro-Bicudo LA; Muenke M
    Hum Mutat; 2018 Oct; 39(10):1416-1427. PubMed ID: 29992659
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Rescue of holoprosencephaly in fetal alcohol-exposed Cdon mutant mice by reduced gene dosage of Ptch1.
    Hong M; Krauss RS
    PLoS One; 2013; 8(11):e79269. PubMed ID: 24244464
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sonic Hedgehog mutations are not a common cause of congenital hypopituitarism in the absence of complex midline cerebral defects.
    Paulo SS; Fernandes-Rosa FL; Turatti W; Coeli-Lacchini FB; Martinelli CE; Nakiri GS; Moreira AC; Santos AC; de Castro M; Antonini SR
    Clin Endocrinol (Oxf); 2015 Apr; 82(4):562-9. PubMed ID: 25056824
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pituitary stalk interruption syndrome and isolated pituitary hypoplasia may be caused by mutations in holoprosencephaly-related genes.
    Tatsi C; Sertedaki A; Voutetakis A; Valavani E; Magiakou MA; Kanaka-Gantenbein C; Chrousos GP; Dacou-Voutetakis C
    J Clin Endocrinol Metab; 2013 Apr; 98(4):E779-84. PubMed ID: 23476075
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Boc modifies the holoprosencephaly spectrum of Cdo mutant mice.
    Zhang W; Hong M; Bae GU; Kang JS; Krauss RS
    Dis Model Mech; 2011 May; 4(3):368-80. PubMed ID: 21183473
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly.
    Odent S; Atti-Bitach T; Blayau M; Mathieu M; Aug J; Delezo de AL; Gall JY; Le Marec B; Munnich A; David V; Vekemans M
    Hum Mol Genet; 1999 Sep; 8(9):1683-9. PubMed ID: 10441331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ectopic sonic hedgehog signaling impairs telencephalic dorsal midline development: implication for human holoprosencephaly.
    Huang X; Litingtung Y; Chiang C
    Hum Mol Genet; 2007 Jun; 16(12):1454-68. PubMed ID: 17468181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Human germline hedgehog pathway mutations predispose to fatty liver.
    Guillen-Sacoto MJ; Martinez AF; Abe Y; Kruszka P; Weiss K; Everson JL; Bataller R; Kleiner DE; Ward JM; Sulik KK; Lipinski RJ; Solomon BD; Muenke M
    J Hepatol; 2017 Oct; 67(4):809-817. PubMed ID: 28645738
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Zic2-associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation.
    Warr N; Powles-Glover N; Chappell A; Robson J; Norris D; Arkell RM
    Hum Mol Genet; 2008 Oct; 17(19):2986-96. PubMed ID: 18617531
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genetic approaches to understanding brain development: holoprosencephaly as a model.
    Muenke M; Cohen MM
    Ment Retard Dev Disabil Res Rev; 2000; 6(1):15-21. PubMed ID: 10899793
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog.
    Seppala M; Depew MJ; Martinelli DC; Fan CM; Sharpe PT; Cobourne MT
    J Clin Invest; 2007 Jun; 117(6):1575-84. PubMed ID: 17525797
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Holoprosencephaly: from Homer to Hedgehog.
    Ming JE; Muenke M
    Clin Genet; 1998 Mar; 53(3):155-63. PubMed ID: 9630065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.