190 related articles for article (PubMed ID: 38238293)
1. Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning.
Abad C; Robayo MC; Muñiz-Moreno MDM; Bernardi MT; Otero MG; Kosanovic C; Griswold AJ; Pierson TM; Walz K; Young JI
Transl Psychiatry; 2024 Jan; 14(1):33. PubMed ID: 38238293
[TBL] [Abstract][Full Text] [Related]
2. GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder.
Shieh C; Jones N; Vanle B; Au M; Huang AY; Silva APG; Lee H; Douine ED; Otero MG; Choi A; Grand K; Taff IP; Delgado MR; Hajianpour MJ; Seeley A; Rohena L; Vernon H; Gripp KW; Vergano SA; Mahida S; Naidu S; Sousa AB; Wain KE; Challman TD; Beek G; Basel D; Ranells J; Smith R; Yusupov R; Freckmann ML; Ohden L; Davis-Keppen L; Chitayat D; Dowling JJ; Finkel R; Dauber A; Spillmann R; Pena LDM; ; Metcalfe K; Splitt M; Lachlan K; McKee SA; Hurst J; Fitzpatrick DR; Morton JEV; Cox H; Venkateswaran S; Young JI; Marsh ED; Nelson SF; Martinez JA; Graham JM; Kini U; Mackay JP; Pierson TM
Genet Med; 2020 May; 22(5):878-888. PubMed ID: 31949314
[TBL] [Abstract][Full Text] [Related]
3. Intellectual disability due to monoallelic variant in GATAD2B and mosaicism in unaffected parent.
Rabin R; Millan F; Cabrera-Luque J; Pappas J
Am J Med Genet A; 2018 Dec; 176(12):2907-2910. PubMed ID: 30346093
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND).
Vera G; Sorlin A; Delplancq G; Lecoquierre F; Brasseur-Daudruy M; Petit F; Smol T; Ziegler A; Bonneau D; Colin E; Mercier S; Cogné B; Bézieau S; Edery P; Lesca G; Chatron N; Sabatier I; Duban-Bedu B; Colson C; Piton A; Durand B; Capri Y; Perrin L; Wiesener A; Zweier C; Maroofian R; Carroll CJ; Galehdari H; Mazaheri N; Callewaert B; Giulianno F; Zaafrane-Khachnaoui K; Buchert-Lo R; Haack T; Magg J; Rieß A; Blandfort M; Waldmüller S; Horber V; Leonardi E; Polli R; Turolla L; Murgia A; Frebourg T; Lebre AS; Nicolas G; Saugier-Veber P; Guerrot AM
Eur J Med Genet; 2020 Oct; 63(10):104004. PubMed ID: 32688057
[TBL] [Abstract][Full Text] [Related]
5. The NuRD complex and macrocephaly associated neurodevelopmental disorders.
Pierson TM; Otero MG; Grand K; Choi A; Graham JM; Young JI; Mackay JP
Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):548-556. PubMed ID: 31737996
[TBL] [Abstract][Full Text] [Related]
6. GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila.
Willemsen MH; Nijhof B; Fenckova M; Nillesen WM; Bongers EM; Castells-Nobau A; Asztalos L; Viragh E; van Bon BW; Tezel E; Veltman JA; Brunner HG; de Vries BB; de Ligt J; Yntema HG; van Bokhoven H; Isidor B; Le Caignec C; Lorino E; Asztalos Z; Koolen DA; Vissers LE; Schenck A; Kleefstra T
J Med Genet; 2013 Aug; 50(8):507-14. PubMed ID: 23644463
[TBL] [Abstract][Full Text] [Related]
7. A novel mutation in the GATAD2B gene associated with severe intellectual disability.
Ueda K; Yanagi K; Kaname T; Okamoto N
Brain Dev; 2019 Mar; 41(3):276-279. PubMed ID: 30482549
[TBL] [Abstract][Full Text] [Related]
8. GATAD2B-related intellectual disability due to parental mosaicism and review of literature.
Kaur P; Mishra S; Rajesh SM; Girisha KM; Shukla A
Clin Dysmorphol; 2019 Oct; 28(4):190-194. PubMed ID: 31205050
[TBL] [Abstract][Full Text] [Related]
9. Tissue-specific DNase I footprint analysis confirms the association of
Nikam V; Shaik Mohammad N
J Genet; 2021; 100():. PubMed ID: 34470925
[TBL] [Abstract][Full Text] [Related]
10. Novel GATAD2B loss-of-function mutations cause intellectual disability in two unrelated cases.
Luo X; Zou Y; Tan B; Zhang Y; Guo J; Zeng L; Zhang R; Tan H; Wei X; Hu Y; Zheng Y; Liang D; Wu L
J Hum Genet; 2017 Apr; 62(4):513-516. PubMed ID: 28077840
[TBL] [Abstract][Full Text] [Related]
11. Establishment of a CRISPR/Cas9-mediated GATAD2B homozygous knockout human embryonic stem cell line.
Wang B; Zhu S; Deng Y; Sai X; Chen Z; Liu J; Li G; Liu N; Chen J; Yu C; Sun T; Zhu P
Stem Cell Res; 2021 Dec; 57():102590. PubMed ID: 34749018
[TBL] [Abstract][Full Text] [Related]
12. Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Machol K; Rousseau J; Ehresmann S; Garcia T; Nguyen TTM; Spillmann RC; Sullivan JA; Shashi V; Jiang YH; Stong N; Fiala E; Willing M; Pfundt R; Kleefstra T; Cho MT; McLaughlin H; Rosello Piera M; Orellana C; Martínez F; Caro-Llopis A; Monfort S; Roscioli T; Nixon CY; Buckley MF; Turner A; Jones WD; van Hasselt PM; Hofstede FC; van Gassen KLI; Brooks AS; van Slegtenhorst MA; Lachlan K; Sebastian J; Madan-Khetarpal S; Sonal D; Sakkubai N; Thevenon J; Faivre L; Maurel A; Petrovski S; Krantz ID; Tarpinian JM; Rosenfeld JA; Lee BH; ; Campeau PM
Am J Hum Genet; 2019 Jan; 104(1):164-178. PubMed ID: 30580808
[TBL] [Abstract][Full Text] [Related]
13. The transcriptional repressor GATAD2B mediates progesterone receptor suppression of myometrial contractile gene expression.
Chen CC; Montalbano AP; Hussain I; Lee WR; Mendelson CR
J Biol Chem; 2017 Jul; 292(30):12560-12576. PubMed ID: 28576827
[TBL] [Abstract][Full Text] [Related]
14. 1q21.3 deletion involving GATAD2B: An emerging recurrent microdeletion syndrome.
Tim-Aroon T; Jinawath N; Thammachote W; Sinpitak P; Limrungsikul A; Khongkhatithum C; Wattanasirichaigoon D
Am J Med Genet A; 2017 Mar; 173(3):766-770. PubMed ID: 28211977
[TBL] [Abstract][Full Text] [Related]
15. Integrative RNA profiling of TBEV-infected neurons and astrocytes reveals potential pathogenic effectors.
Selinger M; Věchtová P; Tykalová H; Ošlejšková P; Rumlová M; Štěrba J; Grubhoffer L
Comput Struct Biotechnol J; 2022; 20():2759-2777. PubMed ID: 35685361
[TBL] [Abstract][Full Text] [Related]
16. BCL11B functionally associates with the NuRD complex in T lymphocytes to repress targeted promoter.
Cismasiu VB; Adamo K; Gecewicz J; Duque J; Lin Q; Avram D
Oncogene; 2005 Oct; 24(45):6753-64. PubMed ID: 16091750
[TBL] [Abstract][Full Text] [Related]
17. ZMYND8 Co-localizes with NuRD on Target Genes and Regulates Poly(ADP-Ribose)-Dependent Recruitment of GATAD2A/NuRD to Sites of DNA Damage.
Spruijt CG; Luijsterburg MS; Menafra R; Lindeboom RG; Jansen PW; Edupuganti RR; Baltissen MP; Wiegant WW; Voelker-Albert MC; Matarese F; Mensinga A; Poser I; Vos HR; Stunnenberg HG; van Attikum H; Vermeulen M
Cell Rep; 2016 Oct; 17(3):783-798. PubMed ID: 27732854
[TBL] [Abstract][Full Text] [Related]
18. BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
Dias C; Estruch SB; Graham SA; McRae J; Sawiak SJ; Hurst JA; Joss SK; Holder SE; Morton JE; Turner C; Thevenon J; Mellul K; Sánchez-Andrade G; Ibarra-Soria X; Deriziotis P; Santos RF; Lee SC; Faivre L; Kleefstra T; Liu P; Hurles ME; ; Fisher SE; Logan DW
Am J Hum Genet; 2016 Aug; 99(2):253-74. PubMed ID: 27453576
[TBL] [Abstract][Full Text] [Related]
19.
Werren EA; Guxholli A; Jones N; Wagner M; Hannibal I; Granadillo JL; Tyndall AV; Moccia A; Kuehl R; Levandoski KM; Day-Salvatore DL; Wheeler M; ; Chong JX; Bamshad MJ; Innes AM; Pierson TM; Mackay JP; Bielas SL; Martin DM
HGG Adv; 2023 Jul; 4(3):100198. PubMed ID: 37181331
[TBL] [Abstract][Full Text] [Related]
20. De Novo Mutations in CHD4, an ATP-Dependent Chromatin Remodeler Gene, Cause an Intellectual Disability Syndrome with Distinctive Dysmorphisms.
Weiss K; Terhal PA; Cohen L; Bruccoleri M; Irving M; Martinez AF; Rosenfeld JA; Machol K; Yang Y; Liu P; Walkiewicz M; Beuten J; Gomez-Ospina N; Haude K; Fong CT; Enns GM; Bernstein JA; Fan J; Gotway G; Ghorbani M; ; van Gassen K; Monroe GR; van Haaften G; Basel-Vanagaite L; Yang XJ; Campeau PM; Muenke M
Am J Hum Genet; 2016 Oct; 99(4):934-941. PubMed ID: 27616479
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
