145 related articles for article (PubMed ID: 38534384)
1. Analyses of Conditional Knockout Mice for
Hamada N; Nishijo T; Iwamoto I; Shifman S; Nagata KI
Cells; 2024 Mar; 13(6):. PubMed ID: 38534384
[TBL] [Abstract][Full Text] [Related]
2. Pathogenic POGZ mutation causes impaired cortical development and reversible autism-like phenotypes.
Matsumura K; Seiriki K; Okada S; Nagase M; Ayabe S; Yamada I; Furuse T; Shibuya H; Yasuda Y; Yamamori H; Fujimoto M; Nagayasu K; Yamamoto K; Kitagawa K; Miura H; Gotoda-Nishimura N; Igarashi H; Hayashida M; Baba M; Kondo M; Hasebe S; Ueshima K; Kasai A; Ago Y; Hayata-Takano A; Shintani N; Iguchi T; Sato M; Yamaguchi S; Tamura M; Wakana S; Yoshiki A; Watabe AM; Okano H; Takuma K; Hashimoto R; Hashimoto H; Nakazawa T
Nat Commun; 2020 Feb; 11(1):859. PubMed ID: 32103003
[TBL] [Abstract][Full Text] [Related]
3. Expression Analyses of POGZ, A Responsible Gene for Neurodevelopmental Disorders, during Mouse Brain Development.
Ibaraki K; Hamada N; Iwamoto I; Ito H; Kawamura N; Morishita R; Tabata H; Nagata KI
Dev Neurosci; 2019; 41(1-2):139-148. PubMed ID: 31430754
[TBL] [Abstract][Full Text] [Related]
4. A convergent mechanism of high risk factors ADNP and POGZ in neurodevelopmental disorders.
Conrow-Graham M; Williams JB; Martin J; Zhong P; Cao Q; Rein B; Yan Z
Brain; 2022 Sep; 145(9):3250-3263. PubMed ID: 35775424
[TBL] [Abstract][Full Text] [Related]
5. Exploring the molecular pathways linking sleep phenotypes and
Marquezini BP; Moysés-Oliveira M; Kloster A; Cunha L; Deconto TB; Mosini AC; Guerreiro P; Paschalidis M; Adami LNG; Andersen ML; Tufik S
J Med Genet; 2024 May; 61(6):586-589. PubMed ID: 38350721
[TBL] [Abstract][Full Text] [Related]
6. Loss of POGZ alters neural differentiation of human embryonic stem cells.
Deng L; Mojica-Perez SP; Azaria RD; Schultz M; Parent JM; Niu W
Mol Cell Neurosci; 2022 May; 120():103727. PubMed ID: 35367590
[TBL] [Abstract][Full Text] [Related]
7. Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes.
Markenscoff-Papadimitriou E; Binyameen F; Whalen S; Price J; Lim K; Ypsilanti AR; Catta-Preta R; Pai EL; Mu X; Xu D; Pollard KS; Nord AS; State MW; Rubenstein JL
Cell Rep; 2021 Dec; 37(10):110089. PubMed ID: 34879283
[TBL] [Abstract][Full Text] [Related]
8. Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.
Stessman HAF; Willemsen MH; Fenckova M; Penn O; Hoischen A; Xiong B; Wang T; Hoekzema K; Vives L; Vogel I; Brunner HG; van der Burgt I; Ockeloen CW; Schuurs-Hoeijmakers JH; Klein Wassink-Ruiter JS; Stumpel C; Stevens SJC; Vles HS; Marcelis CM; van Bokhoven H; Cantagrel V; Colleaux L; Nicouleau M; Lyonnet S; Bernier RA; Gerdts J; Coe BP; Romano C; Alberti A; Grillo L; Scuderi C; Nordenskjöld M; Kvarnung M; Guo H; Xia K; Piton A; Gerard B; Genevieve D; Delobel B; Lehalle D; Perrin L; Prieur F; Thevenon J; Gecz J; Shaw M; Pfundt R; Keren B; Jacquette A; Schenck A; Eichler EE; Kleefstra T
Am J Hum Genet; 2016 Mar; 98(3):541-552. PubMed ID: 26942287
[TBL] [Abstract][Full Text] [Related]
9. Intranasal oxytocin administration ameliorates social behavioral deficits in a POGZ
Kitagawa K; Matsumura K; Baba M; Kondo M; Takemoto T; Nagayasu K; Ago Y; Seiriki K; Hayata-Takano A; Kasai A; Takuma K; Hashimoto R; Hashimoto H; Nakazawa T
Mol Brain; 2021 Mar; 14(1):56. PubMed ID: 33726803
[TBL] [Abstract][Full Text] [Related]
10. Pogz deficiency leads to transcription dysregulation and impaired cerebellar activity underlying autism-like behavior in mice.
Suliman-Lavie R; Title B; Cohen Y; Hamada N; Tal M; Tal N; Monderer-Rothkoff G; Gudmundsdottir B; Gudmundsson KO; Keller JR; Huang GJ; Nagata KI; Yarom Y; Shifman S
Nat Commun; 2020 Nov; 11(1):5836. PubMed ID: 33203851
[TBL] [Abstract][Full Text] [Related]
11. Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Garde A; Cornaton J; Sorlin A; Moutton S; Nicolas C; Juif C; Geneviève D; Perrin L; Khau-Van-Kien P; Smol T; Vincent-Delorme C; Isidor B; Cogné B; Afenjar A; Keren B; Coubes C; Prieur F; Toutain A; Trousselet Y; Bourgouin S; Gonin-Olympiade C; Giraudat K; Piton A; Gérard B; Odent S; Tessier F; Lemasson L; Heide S; Gelineau AC; Sarret C; Miret A; Schaefer E; Piard J; Mathevet R; Boucon M; Bruel AL; Mau-Them FT; Chevarin M; Vitobello A; Philippe C; Thauvin-Robinet C; Faivre L
Clin Genet; 2021 Mar; 99(3):407-417. PubMed ID: 33277917
[TBL] [Abstract][Full Text] [Related]
12. POGZ truncating alleles cause syndromic intellectual disability.
White J; Beck CR; Harel T; Posey JE; Jhangiani SN; Tang S; Farwell KD; Powis Z; Mendelsohn NJ; Baker JA; Pollack L; Mason KJ; Wierenga KJ; Arrington DK; Hall M; Psychogios A; Fairbrother L; Walkiewicz M; Person RE; Niu Z; Zhang J; Rosenfeld JA; Muzny DM; Eng C; Beaudet AL; Lupski JR; Boerwinkle E; Gibbs RA; Yang Y; Xia F; Sutton VR
Genome Med; 2016 Jan; 8(1):3. PubMed ID: 26739615
[TBL] [Abstract][Full Text] [Related]
13. A novel de novo POGZ mutation in a patient with intellectual disability.
Tan B; Zou Y; Zhang Y; Zhang R; Ou J; Shen Y; Zhao J; Luo X; Guo J; Zeng L; Hu Y; Zheng Y; Pan Q; Liang D; Wu L
J Hum Genet; 2016 Apr; 61(4):357-9. PubMed ID: 26763879
[TBL] [Abstract][Full Text] [Related]
14. De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly.
Ye Y; Cho MT; Retterer K; Alexander N; Ben-Omran T; Al-Mureikhi M; Cristian I; Wheeler PG; Crain C; Zand D; Weinstein V; Vernon HJ; McClellan R; Krishnamurthy V; Vitazka P; Millan F; Chung WK
Cold Spring Harb Mol Case Stud; 2015 Oct; 1(1):a000455. PubMed ID: 27148570
[TBL] [Abstract][Full Text] [Related]
15. White-Sutton syndrome and congenital heart disease: case report and literature review.
Duan J; Ye Y; Liao J; Chen L; Zhao X; Liu C; Wen J
BMC Pediatr; 2023 Apr; 23(1):158. PubMed ID: 37016333
[TBL] [Abstract][Full Text] [Related]
16. CDKL5 deficiency in forebrain glutamatergic neurons results in recurrent spontaneous seizures.
Wang HT; Zhu ZA; Li YY; Lou SS; Yang G; Feng X; Xu W; Huang ZL; Cheng X; Xiong ZQ
Epilepsia; 2021 Feb; 62(2):517-528. PubMed ID: 33400301
[TBL] [Abstract][Full Text] [Related]
17. Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.
Nagy D; Verheyen S; Wigby KM; Borovikov A; Sharkov A; Slegesky V; Larson A; Fagerberg C; Brasch-Andersen C; Kibæk M; Bader I; Hernan R; High FA; Chung WK; Schieving JH; Behunova J; Smogavec M; Laccone F; Witsch-Baumgartner M; Zobel J; Duba HC; Weis D
Genes (Basel); 2022 Jan; 13(1):. PubMed ID: 35052493
[No Abstract] [Full Text] [Related]
18. SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
El Chehadeh S; Han KA; Kim D; Jang G; Bakhtiari S; Lim D; Kim HY; Kim J; Kim H; Wynn J; Chung WK; Vitiello G; Cutcutache I; Page M; Gecz J; Harper K; Han AR; Kim HM; Wessels M; Bayat A; Jaén AF; Selicorni A; Maitz S; de Brouwer APM; Silfhout AV; Armstrong M; Symonds J; Küry S; Isidor B; Cogné B; Nizon M; Feger C; Muller J; Torti E; Grange DK; Willems M; Kruer MC; Ko J; Piton A; Um JW
Nat Commun; 2022 Jul; 13(1):4112. PubMed ID: 35840571
[TBL] [Abstract][Full Text] [Related]
19. POGZ suppresses 2C transcriptional program and retrotransposable elements.
Sun X; Zhang T; Tong B; Cheng L; Jiang W; Sun Y
Cell Rep; 2023 Aug; 42(8):112867. PubMed ID: 37494184
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
