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 *

161 related articles for article (PubMed ID: 24336072)

  • 21. CABLES1 Deficiency Impairs Quiescence and Stress Responses of Hematopoietic Stem Cells in Intrinsic and Extrinsic Manners.
    He L; Beghi F; Baral V; Dépond M; Zhang Y; Joulin V; Rueda BR; Gonin P; Foudi A; Wittner M; Louache F
    Stem Cell Reports; 2019 Aug; 13(2):274-290. PubMed ID: 31327733
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Structural abnormalities of corpus callosum and cortical axonal tracts accompanied by decreased anxiety-like behavior and lowered sociability in spock3- mutant mice.
    Yamamoto A; Uchiyama K; Nara T; Nishimura N; Hayasaka M; Hanaoka K; Yamamoto T
    Dev Neurosci; 2014; 36(5):381-95. PubMed ID: 25138526
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Defects in neural guidepost structures and failure to remove leptomeningeal cells from the septal midline behind the interhemispheric fusion defects in Netrin1 deficient mice.
    Hakanen J; Salminen M
    Int J Dev Neurosci; 2015 Dec; 47(Pt B):206-15. PubMed ID: 26397040
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A homozygous deleterious CDK10 mutation in a patient with agenesis of corpus callosum, retinopathy, and deafness.
    Guen VJ; Edvardson S; Fraenkel ND; Fattal-Valevski A; Jalas C; Anteby I; Shaag A; Dor T; Gillis D; Kerem E; Lees JA; Colas P; Elpeleg O
    Am J Med Genet A; 2018 Jan; 176(1):92-98. PubMed ID: 29130579
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Transit defect of potassium-chloride Co-transporter 3 is a major pathogenic mechanism in hereditary motor and sensory neuropathy with agenesis of the corpus callosum.
    Salin-Cantegrel A; Rivière JB; Shekarabi M; Rasheed S; Dacal S; Laganière J; Gaudet R; Rochefort D; Lesca G; Gaspar C; Dion PA; Lapointe JY; Rouleau GA
    J Biol Chem; 2011 Aug; 286(32):28456-65. PubMed ID: 21628467
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A familial Sonic Hedgehog (SHH) stop-gain mutation associated with agenesis of the corpus callosum, mild intellectual disability and facial dysmorphism.
    Yi X; Yuan X; Xie H; Chen X; Zhu Y
    Brain Dev; 2020 Nov; 42(10):771-774. PubMed ID: 32703609
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Agenesis of the corpus callosum with Probst bundles owing to haploinsufficiency for a gene in an 8 cM region of 6q25.
    Pirola B; Bortotto L; Giglio S; Piovan E; Janes A; Guerrini R; Zuffardi O
    J Med Genet; 1998 Dec; 35(12):1031-3. PubMed ID: 9863602
    [TBL] [Abstract][Full Text] [Related]  

  • 28. High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44.
    Ballif BC; Rosenfeld JA; Traylor R; Theisen A; Bader PI; Ladda RL; Sell SL; Steinraths M; Surti U; McGuire M; Williams S; Farrell SA; Filiano J; Schnur RE; Coffey LB; Tervo RC; Stroud T; Marble M; Netzloff M; Hanson K; Aylsworth AS; Bamforth JS; Babu D; Niyazov DM; Ravnan JB; Schultz RA; Lamb AN; Torchia BS; Bejjani BA; Shaffer LG
    Hum Genet; 2012 Jan; 131(1):145-56. PubMed ID: 21800092
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mice homozygous for a modified beta-amyloid precursor protein (beta APP) gene show impaired behavior and high incidence of agenesis of the corpus callosum.
    Müller U; Cristina N; Li ZW; Wolfer DP; Lipp HP; Rülicke T; Brandner S; Aguzzi A; Weissman C
    Ann N Y Acad Sci; 1996 Jan; 777():65-73. PubMed ID: 8624128
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Haploinsufficiency of ZNF238 is associated with corpus callosum abnormalities in 1q44 deletions.
    Perlman SJ; Kulkarni S; Manwaring L; Shinawi M
    Am J Med Genet A; 2013 Apr; 161A(4):711-6. PubMed ID: 23494996
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Agenesis of the corpus callosum and autism: a comprehensive comparison.
    Paul LK; Corsello C; Kennedy DP; Adolphs R
    Brain; 2014 Jun; 137(Pt 6):1813-29. PubMed ID: 24771497
    [TBL] [Abstract][Full Text] [Related]  

  • 32. VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
    Slavotinek AM; Chao R; Vacik T; Yahyavi M; Abouzeid H; Bardakjian T; Schneider A; Shaw G; Sherr EH; Lemke G; Youssef M; Schorderet DF
    Hum Mutat; 2012 Feb; 33(2):364-8. PubMed ID: 22095910
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Agenesis of the corpus callosum: a clinical approach to diagnosis.
    Palmer EE; Mowat D
    Am J Med Genet C Semin Med Genet; 2014 Jun; 166C(2):184-97. PubMed ID: 24866859
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Deficiency of the chromatin regulator BRPF1 causes abnormal brain development.
    You L; Zou J; Zhao H; Bertos NR; Park M; Wang E; Yang XJ
    J Biol Chem; 2015 Mar; 290(11):7114-29. PubMed ID: 25568313
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Low-level expression of EPG5 leads to an attenuated Vici syndrome phenotype.
    Waldrop MA; Gumienny F; Boue D; de Los Reyes E; Shell R; Weiss RB; Flanigan KM
    Am J Med Genet A; 2018 May; 176(5):1207-1211. PubMed ID: 29681093
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Loss-of-function variants in
    Heide S; Argilli E; Valence S; Boutaud L; Roux N; Mignot C; Nava C; Keren B; Giraudat K; Faudet A; Gerasimenko A; Garel C; Blondiaux E; Rastetter A; Grevent D; Le C; Mackenzie L; Richards L; Attié-Bitach T; Depienne C; Sherr E; Héron D
    J Med Genet; 2024 Feb; 61(3):244-249. PubMed ID: 37857482
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel heterozygous loss-of-function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature.
    Sagi-Dain L; Kurolap A; Ilivitzki A; Mory A; Paperna T; ; Kedar R; Gonzaga-Jauregui C; Peleg A; Baris Feldman H
    Am J Med Genet A; 2020 Jan; 182(1):205-212. PubMed ID: 31697046
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The Prenatal Morphomechanic Impact of Agenesis of the Corpus Callosum on Human Brain Structure and Asymmetry.
    Schwartz E; Diogo MC; Glatter S; Seidl R; Brugger PC; Gruber GM; Kiss H; Nenning KH; ; Langs G; Prayer D; Kasprian G
    Cereb Cortex; 2021 Jul; 31(9):4024-4037. PubMed ID: 33872347
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
    Edwards TJ; Sherr EH; Barkovich AJ; Richards LJ
    Brain; 2014 Jun; 137(Pt 6):1579-613. PubMed ID: 24477430
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PlexinA1 is crucial for the midline crossing of callosal axons during corpus callosum development in BALB/cAJ mice.
    Hossain MM; Tsuzuki T; Sakakibara K; Imaizumi F; Ikegaya A; Inagaki M; Takahashi I; Ito T; Takamatsu H; Kumanogoh A; Negishi T; Yukawa K
    PLoS One; 2019; 14(8):e0221440. PubMed ID: 31430342
    [TBL] [Abstract][Full Text] [Related]  

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