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 *

118 related articles for article (PubMed ID: 18409201)

  • 1. No major role for the EMX2 gene in schizencephaly.
    Merello E; Swanson E; De Marco P; Akhter M; Striano P; Rossi A; Cama A; Leventer RJ; Guerrini R; Capra V; Dobyns WB
    Am J Med Genet A; 2008 May; 146A(9):1142-50. PubMed ID: 18409201
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comprehensive EMX2 genotyping of a large schizencephaly case series.
    Tietjen I; Bodell A; Apse K; Mendonza AM; Chang BS; Shaw GM; Barkovich AJ; Lammer EJ; Walsh CA
    Am J Med Genet A; 2007 Jun; 143A(12):1313-6. PubMed ID: 17506092
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly.
    Hehr U; Pineda-Alvarez DE; Uyanik G; Hu P; Zhou N; Hehr A; Schell-Apacik C; Altus C; Daumer-Haas C; Meiner A; Steuernagel P; Roessler E; Winkler J; Muenke M
    Hum Genet; 2010 Mar; 127(5):555-61. PubMed ID: 20157829
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Schizencephaly: surgical features and new molecular genetic results.
    Capra V; De Marco P; Moroni A; Faiella A; Brunelli S; Tortori-Donati P; Andreussi I; Boncinelli E; Cama A
    Eur J Pediatr Surg; 1996 Dec; 6 Suppl 1():27-9. PubMed ID: 9008816
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Schizencephaly: association with young maternal age, alcohol use, and lack of prenatal care.
    Dies KA; Bodell A; Hisama FM; Guo CY; Barry B; Chang BS; Barkovich AJ; Walsh CA
    J Child Neurol; 2013 Feb; 28(2):198-203. PubMed ID: 23266945
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort.
    Mellado C; Poduri A; Gleason D; Elhosary PC; Barry BJ; Partlow JN; Chang BS; Shaw GM; Barkovich AJ; Walsh CA
    Am J Med Genet A; 2010 Nov; 152A(11):2736-42. PubMed ID: 20949537
    [TBL] [Abstract][Full Text] [Related]  

  • 7. EMX2-independent familial schizencephaly: clinical and genetic analyses.
    Tietjen I; Erdogan F; Currier S; Apse K; Chang BS; Hill RS; Lee CK; Walsh CA
    Am J Med Genet A; 2005 Jun; 135(2):166-70. PubMed ID: 15887302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A number of schizencephaly patients including 2 brothers are heterozygous for germline mutations in the homeobox gene EMX2.
    Faiella A; Brunelli S; Granata T; D'Incerti L; Cardini R; Lenti C; Battaglia G; Boncinelli E
    Eur J Hum Genet; 1997; 5(4):186-90. PubMed ID: 9359037
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cytomegalovirus infection and schizencephaly: case reports.
    Iannetti P; Nigro G; Spalice A; Faiella A; Boncinelli E
    Ann Neurol; 1998 Jan; 43(1):123-7. PubMed ID: 9450779
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The same enhancer regulates the earliest Emx2 expression in caudal forebrain primordium, subsequent expression in dorsal telencephalon and later expression in the cortical ventricular zone.
    Suda Y; Kokura K; Kimura J; Kajikawa E; Inoue F; Aizawa S
    Development; 2010 Sep; 137(17):2939-49. PubMed ID: 20667915
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly.
    Yoneda Y; Haginoya K; Kato M; Osaka H; Yokochi K; Arai H; Kakita A; Yamamoto T; Otsuki Y; Shimizu S; Wada T; Koyama N; Mino Y; Kondo N; Takahashi S; Hirabayashi S; Takanashi J; Okumura A; Kumagai T; Hirai S; Nabetani M; Saitoh S; Hattori A; Yamasaki M; Kumakura A; Sugo Y; Nishiyama K; Miyatake S; Tsurusaki Y; Doi H; Miyake N; Matsumoto N; Saitsu H
    Ann Neurol; 2013 Jan; 73(1):48-57. PubMed ID: 23225343
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia.
    Jansen LA; Mirzaa GM; Ishak GE; O'Roak BJ; Hiatt JB; Roden WH; Gunter SA; Christian SL; Collins S; Adams C; Rivière JB; St-Onge J; Ojemann JG; Shendure J; Hevner RF; Dobyns WB
    Brain; 2015 Jun; 138(Pt 6):1613-28. PubMed ID: 25722288
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The role of cytomegalovirus in schizencephaly.
    Spalice A; Del Balzo F; Nicita F; Papetti L; Ursitti F; Iannetti P
    Am J Med Genet A; 2011 Jul; 155A(7):1768; author reply 1769. PubMed ID: 21638760
    [No Abstract]   [Full Text] [Related]  

  • 14. Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion.
    Liu S; Gao X; Qin Y; Liu W; Huang T; Ma J; Simpson JL; Chen ZJ
    Fertil Steril; 2015 Mar; 103(3):769-74.e2. PubMed ID: 25577462
    [TBL] [Abstract][Full Text] [Related]  

  • 15. DMRT5, DMRT3, and EMX2 Cooperatively Repress
    Desmaris E; Keruzore M; Saulnier A; Ratié L; Assimacopoulos S; De Clercq S; Nan X; Roychoudhury K; Qin S; Kricha S; Chevalier C; Lingner T; Henningfeld KA; Zarkower D; Mallamaci A; Theil T; Campbell K; Pieler T; Li M; Grove EA; Bellefroid EJ
    J Neurosci; 2018 Oct; 38(42):9105-9121. PubMed ID: 30143575
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Emx2 promotes symmetric cell divisions and a multipotential fate in precursors from the cerebral cortex.
    Heins N; Cremisi F; Malatesta P; Gangemi RM; Corte G; Price J; Goudreau G; Gruss P; Götz M
    Mol Cell Neurosci; 2001 Nov; 18(5):485-502. PubMed ID: 11922140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
    Guerrini R; Carrozzo R
    Seizure; 2002 Apr; 11 Suppl A():532-43; quiz 544-7. PubMed ID: 12185771
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Potential target genes of EMX2 include Odz/Ten-M and other gene families with implications for cortical patterning.
    Li H; Bishop KM; O'Leary DD
    Mol Cell Neurosci; 2006 Oct; 33(2):136-49. PubMed ID: 16919471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.
    Brunelli S; Faiella A; Capra V; Nigro V; Simeone A; Cama A; Boncinelli E
    Nat Genet; 1996 Jan; 12(1):94-6. PubMed ID: 8528262
    [No Abstract]   [Full Text] [Related]  

  • 20. Severe sex differentiation disorder in a boy with a 3.8 Mb 10q25.3-q26.12 microdeletion encompassing EMX2.
    Piard J; Mignot B; Arbez-Gindre F; Aubert D; Morel Y; Roze V; McElreavy K; Jonveaux P; Valduga M; Van Maldergem L
    Am J Med Genet A; 2014 Oct; 164A(10):2618-22. PubMed ID: 24975717
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.