Editorial for the Molecular Mechanisms in Neurodevelopmental Disorders Special Issue

被引:0
作者
Madrigal, Irene [1 ,2 ]
机构
[1] Hosp Clin Barcelona, Biochem & Mol Genet, Barcelona 08036, Spain
[2] Fundacio Recerca Clin Barcelona Inst Invest Biomed, Barcelona 08036, Spain
关键词
MATERNAL IMMUNE ACTIVATION;
D O I
10.3390/genes14091762
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页数:3
相关论文
共 11 条
  • [1] Maternal Immunological Adaptation During Normal Pregnancy
    Abu-Raya, Bahaa
    Michalski, Christina
    Sadarangani, Manish
    Lavoie, Pascal M.
    [J]. FRONTIERS IN IMMUNOLOGY, 2020, 11
  • [2] Genes Participating in the Ensheathment of Neurons Are Affected by Postnatal Stress and Maternal Immune Activation in the Pituitary Gland
    Alsegehy, Samah
    Southey, Bruce R.
    Rund, Laurie
    Johnson, Rodney W.
    Rodriguez-Zas, Sandra L.
    [J]. GENES, 2023, 14 (05)
  • [3] Zeb2 DNA-Binding Sites in Neuroprogenitor Cells Reveal Autoregulation and Affirm Neurodevelopmental Defects, Including in Mowat-Wilson Syndrome
    Birkhoff, Judith C. C.
    Korporaal, Anne L. L.
    Brouwer, Rutger W. W.
    Nowosad, Karol
    Milazzo, Claudia
    Mouratidou, Lidia
    van den Hout, Mirjam C. G. N.
    van IJcken, Wilfred F. J.
    Huylebroeck, Danny
    Conidi, Andrea
    [J]. GENES, 2023, 14 (03)
  • [4] Haploinsufficiency as a Foreground Pathomechanism of Poirer-Bienvenu Syndrome and Novel Insights Underlying the Phenotypic Continuum of CSNK2B-Associated Disorders
    Di Stazio, Mariateresa
    Zanus, Caterina
    Faletra, Flavio
    Pesaresi, Alessia
    Ziccardi, Ilaria
    Morgan, Anna
    Girotto, Giorgia
    Costa, Paola
    Carrozzi, Marco
    d'Adamo, Adamo P.
    Musante, Luciana
    [J]. GENES, 2023, 14 (02)
  • [5] Maternal immune activation as an epidemiological risk factor for neurodevelopmental disorders: Considerations of timing, severity, individual differences, and sex in human and rodent studies
    Hall, Mary Beth
    Willis, Daria E.
    Rodriguez, Elina L.
    Schwarz, Jaclyn M.
    [J]. FRONTIERS IN NEUROSCIENCE, 2023, 17
  • [6] Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders
    Isabel Alvarez-Mora, Maria
    Rodriguez-Revenga, Laia
    Jodar, Meritxell
    Potrony, Miriam
    Sanchez, Aurora
    Badenas, Celia
    Oriola, Josep
    Villanueva-Canas, Jose Luis
    Munoz, Esteban
    Valldeoriola, Francesc
    Camara, Ana
    Compta, Yaroslau
    Carreno, Mar
    Jose Marti, Maria
    Sanchez-Valle, Raquel
    Madrigal, Irene
    [J]. GENES, 2023, 14 (04)
  • [7] Clinical and molecular analysis of Mowat-Wilson syndrome associated with ZFHX1B mutations and deletions at 2q22-q24.1
    Ishihara, N
    Yamada, K
    Yamada, Y
    Miura, K
    Kato, J
    Kuwabara, N
    Hara, Y
    Kobayashi, Y
    Hoshino, K
    Nomura, Y
    Mimaki, M
    Ohya, K
    Matsushima, M
    Nitta, H
    Tanaka, K
    Segawa, M
    Ohki, T
    Ezoe, T
    Kumagai, T
    Onuma, A
    Kuroda, T
    Yoneda, M
    Yamanaka, T
    Saeki, M
    Segawa, M
    Saji, T
    Nagaya, M
    Wakamatsu, N
    [J]. JOURNAL OF MEDICAL GENETICS, 2004, 41 (05) : 387 - 393
  • [8] Mowat-Wilson syndrome
    Mowat, DR
    Wilson, MJ
    Goossens, M
    [J]. JOURNAL OF MEDICAL GENETICS, 2003, 40 (05) : 305 - 310
  • [9] High Performance of a Dominant/X-Linked Gene Panel in Patients with Neurodevelopmental Disorders
    Spataro, Nino
    Trujillo-Quintero, Juan Pablo
    Manso, Carmen
    Gabau, Elisabeth
    Capdevila, Nuria
    Martinez-Glez, Victor
    Berenguer-Llergo, Antoni
    Reyes, Sara
    Brunet, Anna
    Baena, Neus
    Guitart, Miriam
    Ruiz, Anna
    [J]. GENES, 2023, 14 (03)
  • [10] Atypical Mowat-Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex
    Verstappen, Griet
    van Grunsven, Leo A.
    Michiels, Christine
    Van de Putte, Tom
    Souopgui, Jacob
    Van Damme, Jozef
    Bellefroid, Eric
    Vandekerckhove, Joel
    Huylebroeck, Danny
    [J]. HUMAN MOLECULAR GENETICS, 2008, 17 (08) : 1175 - 1183