BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 37106788)

  • 21. Expression analyses of WAC, a responsible gene for neurodevelopmental disorders, during mouse brain development.
    Nishikawa M; Matsuki T; Hamada N; Nakayama A; Ito H; Nagata KI
    Med Mol Morphol; 2023 Dec; 56(4):266-273. PubMed ID: 37402055
    [TBL] [Abstract][Full Text] [Related]  

  • 22. De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila.
    Lugtenberg D; Reijnders MR; Fenckova M; Bijlsma EK; Bernier R; van Bon BW; Smeets E; Vulto-van Silfhout AT; Bosch D; Eichler EE; Mefford HC; Carvill GL; Bongers EM; Schuurs-Hoeijmakers JH; Ruivenkamp CA; Santen GW; van den Maagdenberg AM; Peeters-Scholte CM; Kuenen S; Verstreken P; Pfundt R; Yntema HG; de Vries PF; Veltman JA; Hoischen A; Gilissen C; de Vries BB; Schenck A; Kleefstra T; Vissers LE
    Eur J Hum Genet; 2016 Aug; 24(8):1145-53. PubMed ID: 26757981
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The histone H2B ubiquitination regulator Wac is essential for plasma cell differentiation.
    Li Y; Ruan GX; Chen W; Huang H; Zhang R; Wang J; Ouyang Y; Zhu Z; Meng L; Wang R; Huo J; Xu S; Ou X
    FEBS Lett; 2023 Jul; 597(13):1748-1760. PubMed ID: 37171241
    [TBL] [Abstract][Full Text] [Related]  

  • 24. WAC, a functional partner of RNF20/40, regulates histone H2B ubiquitination and gene transcription.
    Zhang F; Yu X
    Mol Cell; 2011 Feb; 41(4):384-97. PubMed ID: 21329877
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A de novo 10p11.23-p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders.
    Abdelhedi F; El Khattabi L; Essid N; Viot G; Letessier D; Lebbar A; Dupont JM
    Am J Med Genet A; 2016 Jul; 170(7):1912-7. PubMed ID: 27119754
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The wac gene product of bacteriophage T4 contains coiled-coil structural patterns.
    Sobolev BN; Mesyanzhinov VV
    J Biomol Struct Dyn; 1991 Apr; 8(5):953-65. PubMed ID: 1878168
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular diversity and phenotypic pleiotropy of ancient genomic regulatory loci derived from human endogenous retrovirus type H (HERVH) promoter LTR7 and HERVK promoter LTR5_Hs and their contemporary impacts on pathophysiology of Modern Humans.
    Glinsky GV
    Mol Genet Genomics; 2022 Nov; 297(6):1711-1740. PubMed ID: 36121513
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Fibritin encoded by bacteriophage T4 gene wac has a parallel triple-stranded alpha-helical coiled-coil structure.
    Efimov VP; Nepluev IV; Sobolev BN; Zurabishvili TG; Schulthess T; Lustig A; Engel J; Haener M; Aebi U; Venyaminov SYu
    J Mol Biol; 1994 Sep; 242(4):470-86. PubMed ID: 7932704
    [TBL] [Abstract][Full Text] [Related]  

  • 29. LncRNA WAC-AS1 expression in human tumors correlates with immune infiltration and affects prognosis.
    Wang Y; Gong H; Cao Y
    Hereditas; 2023 May; 160(1):26. PubMed ID: 37248547
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A Human
    Wundrach D; Martinetti LE; Stafford AM; Bilinovich SM; Angara K; Prokop JW; Crandall SR; Vogt D
    Front Mol Neurosci; 2020; 13():573409. PubMed ID: 33071758
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome-wide analysis of the WW domain-containing protein genes in silkworm and their expansion in eukaryotes.
    Meng G; Dai F; Tong X; Li N; Ding X; Song J; Lu C
    Mol Genet Genomics; 2015 Jun; 290(3):807-24. PubMed ID: 25424044
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Baculovirus FP25K Localization: Role of the Coiled-Coil Domain.
    Garretson TA; McCoy JC; Cheng XW
    J Virol; 2016 Nov; 90(21):9582-9597. PubMed ID: 27512078
    [TBL] [Abstract][Full Text] [Related]  

  • 33. De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype.
    Chilton I; Okur V; Vitiello G; Selicorni A; Mariani M; Goldenberg A; Husson T; Campion D; Lichtenbelt KD; van Gassen K; Steinraths M; Rice J; Roeder ER; Littlejohn RO; Srour M; Sebire G; Accogli A; Héron D; Heide S; Nava C; Depienne C; Larson A; Niyazov D; Azage M; Hoganson G; Burton J; Rush ET; Jenkins JL; Saunders CJ; Thiffault I; Alaimo JT; Fleischer J; Groepper D; Gripp KW; Chung WK
    Am J Med Genet A; 2020 May; 182(5):962-973. PubMed ID: 32031333
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations.
    Chen CA; Bosch DG; Cho MT; Rosenfeld JA; Shinawi M; Lewis RA; Mann J; Jayakar P; Payne K; Walsh L; Moss T; Schreiber A; Schoonveld C; Monaghan KG; Elmslie F; Douglas G; Boonstra FN; Millan F; Cremers FP; McKnight D; Richard G; Juusola J; Kendall F; Ramsey K; Anyane-Yeboa K; Malkin E; Chung WK; Niyazov D; Pascual JM; Walkiewicz M; Veluchamy V; Li C; Hisama FM; de Vries BB; Schaaf C
    Genet Med; 2016 Nov; 18(11):1143-1150. PubMed ID: 26986877
    [TBL] [Abstract][Full Text] [Related]  

  • 35. WAC, a novel GBM tumor suppressor, induces GBM cell apoptosis and promotes autophagy.
    Wang Y; Zhang S; Sun Q; Yuan F; Zhao L; Ye Z; Li Y; Wang R; Jiang H; Hu P; Tian D; Liu B
    Med Oncol; 2021 Sep; 38(11):132. PubMed ID: 34581882
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Wac: a new Augmin subunit required for chromosome alignment but not for acentrosomal microtubule assembly in female meiosis.
    Meireles AM; Fisher KH; Colombié N; Wakefield JG; Ohkura H
    J Cell Biol; 2009 Mar; 184(6):777-84. PubMed ID: 19289792
    [TBL] [Abstract][Full Text] [Related]  

  • 37. H2B ubiquitination: Conserved molecular mechanism, diverse physiologic functions of the E3 ligase during meiosis.
    Wang L; Cao C; Wang F; Zhao J; Li W
    Nucleus; 2017 Sep; 8(5):461-468. PubMed ID: 28628358
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Rapid progression of aortic stenosis in a 3-month-old infant with bicuspid aortic valve and DeSanto-Shinawi syndrome.
    Takajo D; Katato G; Aggarwal S
    Ann Pediatr Cardiol; 2021; 14(2):208-210. PubMed ID: 34103862
    [TBL] [Abstract][Full Text] [Related]  

  • 39. VCIP135 deubiquitinase and its binding protein, WAC, in p97ATPase-mediated membrane fusion.
    Totsukawa G; Kaneko Y; Uchiyama K; Toh H; Tamura K; Kondo H
    EMBO J; 2011 Aug; 30(17):3581-93. PubMed ID: 21811234
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Pathogenic variants in
    Granadillo JL; P A Stegmann A; Guo H; Xia K; Angle B; Bontempo K; Ranells JD; Newkirk P; Costin C; Viront J; Stumpel CT; Sinnema M; Panis B; Pfundt R; Krapels IPC; Klaassens M; Nicolai J; Li J; Jiang Y; Marco E; Canton A; Latronico AC; Montenegro L; Leheup B; Bonnet C; M Amudhavalli S; Lawson CE; McWalter K; Telegrafi A; Pearson R; Kvarnung M; Wang X; Bi W; Rosenfeld JA; Shinawi M
    J Med Genet; 2020 Oct; 57(10):717-724. PubMed ID: 32152250
    [TBL] [Abstract][Full Text] [Related]  

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