(Q37777429)

23 August 2017

1 reference

title

Hippocampus development and function: role of epigenetic factors and implications for cognitive disease (English)

1 reference

23 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20681996

16 June 2024

author name string

P. S. Lagali

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20681996

16 June 2024

C. P. Corcoran

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20681996

16 June 2024

D. J. Picketts

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20681996

16 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20681996

16 June 2024

publication date

1 October 2010

1 reference

full work available at URL

23 August 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1399-0004.2010.01503.x

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-0004.2010.01503.x

16 June 2024

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

16 June 2024

1 reference

23 August 2017

volume

78

1 reference

23 August 2017

issue

4

1 reference

23 August 2017

page(s)

321-333

1 reference

Targeted mutation of the DNA methyltransferase gene results in embryonic lethality

23 August 2017

cites work

1 reference

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Epigenetic control of neural precursor cell fate during development

15 July 2023

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Chromatin remodeling in neural stem cell differentiation

16 June 2024

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Epigenetic principles and mechanisms underlying nervous system functions in health and disease

16 June 2024

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The language of covalent histone modifications

16 June 2024

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Chromatin modifications and their function

16 June 2024

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Molecular and comparative genetics of mental retardation

16 June 2024

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The genetic landscape of intellectual disability arising from chromosome X.

16 June 2024

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X-linked intellectual disability: unique vulnerability of the male genome

16 June 2024

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Disruption of the epigenetic code: an emerging mechanism in mental retardation

16 June 2024

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Prolonged sojourn of developing pyramidal cells in the intermediate zone of the hippocampus and their settling in the stratum pyramidale

16 June 2024

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1 reference

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The mode of migration of neurons to the hippocampus: a Golgi and electron microscopic analysis in foetal rhesus monkey

16 June 2024

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1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The Establishment of GABAergic and Glutamatergic Synapses on CA1 Pyramidal Neurons is Sequential and Correlates with the Development of the Apical Dendrite

16 June 2024

13

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Time of neuron origin in the hippocampal region. An autoradiographic study in the mouse

16 June 2024

14

1 reference

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Hippocampal development in the rat: cytogenesis and morphogenesis examined with autoradiography and low-level X-irradiation

16 June 2024

15

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Cell migration from the ganglionic eminences is required for the development of hippocampal GABAergic interneurons

16 June 2024

16

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Early sequential formation of functional GABA(A) and glutamatergic synapses on CA1 interneurons of the rat foetal hippocampus

16 June 2024

17

1 reference

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Postnatal development of CA3 pyramidal neurons and their afferents in the Ammon's horn of rhesus monkeys

16 June 2024

18

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Development of the mossy fibers of the dentate gyrus: I. A light and electron microscopic study of the mossy fibers and their expansions.

16 June 2024

19

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Migration and distribution of two populations of hippocampal granule cell precursors during the perinatal and postnatal periods

16 June 2024

20

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Autoradiographic and histological evidence of postnatal hippocampal neurogenesis in rats

16 June 2024

21

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Epigenetics, hippocampal neurogenesis, and neuropsychiatric disorders: unraveling the genome to understand the mind.

16 June 2024

22

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The long-term potential of LTP

16 June 2024

23

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Long-Term Potentiation and Memory

16 June 2024

24

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Toward a molecular explanation for long-term potentiation.

16 June 2024

25

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

16 June 2024

LTP and LTD

26

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Beyond transcription factors: the role of chromatin modifying enzymes in regulating transcription required for memory

16 June 2024

27

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Regulation of chromatin structure in memory formation

16 June 2024

28

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Genomic DNA methylation: the mark and its mediators

16 June 2024

29

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Transient forebrain ischemia alters the mRNA expression of methyl DNA-binding factors in the adult rat hippocampus.

16 June 2024

30

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

A family of human zinc finger proteins that bind methylated DNA and repress transcription

16 June 2024

31

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons.

16 June 2024

34

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Conditional Dnmt1 deletion in dorsal forebrain disrupts development of somatosensory barrel cortex and thalamocortical long-term potentiation

16 June 2024

35

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation

16 June 2024

36

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Evidence that DNA (cytosine-5) methyltransferase regulates synaptic plasticity in the hippocampus.

16 June 2024

38

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Covalent modification of DNA regulates memory formation

16 June 2024

39

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Activity-dependent suppression of miniature neurotransmission through the regulation of DNA methylation.

16 June 2024

40

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Epigenetic regulation of BDNF gene transcription in the consolidation of fear memory

16 June 2024

41

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mice lacking methyl-CpG binding protein 1 have deficits in adult neurogenesis and hippocampal function

16 June 2024

42

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

16 June 2024

43

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

16 June 2024

44

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

16 June 2024

45

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

16 June 2024

46

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome

16 June 2024

48

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

16 June 2024

49

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

16 June 2024

50

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

16 June 2024

51

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

16 June 2024

52

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

16 June 2024

53

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

16 June 2024

54

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

16 June 2024

55

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

MeCP2-dependent transcriptional repression regulates excitatory neurotransmission

16 June 2024

56

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.

16 June 2024

57

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Histones: annotating chromatin

16 June 2024

58

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

ERK/MAPK regulates hippocampal histone phosphorylation following contextual fear conditioning

16 June 2024

59

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The nuclear kinase mitogen- and stress-activated protein kinase 1 regulates hippocampal chromatin remodeling in memory formation.

16 June 2024

60

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Protein phosphatase 1 regulates the histone code for long-term memory

16 June 2024

61

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

PolyADP-ribosylation is required for long-term memory formation in mammals

16 June 2024

62

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Histone methylation regulates memory formation.

16 June 2024

63

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Proper expression of the Gcn5 histone acetyltransferase is required for neural tube closure in mouse embryos.

16 June 2024

64

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Loss of Gcn5 acetyltransferase activity leads to neural tube closure defects and exencephaly in mouse embryos

16 June 2024

65

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Gene dosage-dependent embryonic development and proliferation defects in mice lacking the transcriptional integrator p300

16 June 2024

66

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Altered memory capacities and response to stress in p300/CBP-associated factor (PCAF) histone acetylase knockout mice

16 June 2024

68

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

CBP histone acetyltransferase activity is a critical component of memory consolidation

16 June 2024

69

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration.

16 June 2024

70

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis

16 June 2024

71

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

NSD1 is essential for early post-implantation development and has a catalytically active SET domain

16 June 2024

72

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Control of cognition and adaptive behavior by the GLP/G9a epigenetic suppressor complex

16 June 2024

73

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice.

16 June 2024

74

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome

16 June 2024

75

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The N-Myc-DLL3 cascade is suppressed by the ubiquitin ligase Huwe1 to inhibit proliferation and promote neurogenesis in the developing brain.

16 June 2024

76

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

16 June 2024

77

1 reference

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Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease

16 June 2024

78

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Differential role for CBP and p300 CREB-binding domain in motor skill learning.

16 June 2024

79

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Transgenic mice expressing an inhibitory truncated form of p300 exhibit long-term memory deficits.

16 June 2024

80

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Recovery of learning and memory is associated with chromatin remodelling

16 June 2024

81

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Histone deacetylases 1 and 2 form a developmental switch that controls excitatory synapse maturation and function

16 June 2024

82

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

HDAC2 negatively regulates memory formation and synaptic plasticity.

16 June 2024

83

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The biology of chromatin remodeling complexes

16 June 2024

84

1 reference

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Structure and function of SWI/SNF chromatin remodeling complexes and mechanistic implications for transcription

16 June 2024

85

1 reference

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Neuronal death resulting from targeted disruption of the Snf2 protein ATRX is mediated by p53.

16 June 2024

87

1 reference

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Loss of Chd7 function in gene-trapped reporter mice is embryonic lethal and associated with severe defects in multiple developing tissues.

16 June 2024

88

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome

16 June 2024

89

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Defective transcription-coupled repair in Cockayne syndrome B mice is associated with skin cancer predisposition

16 June 2024

90

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes

16 June 2024

91

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Brg1 is required for murine neural stem cell maintenance and gliogenesis

16 June 2024

92

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Geminin regulates neuronal differentiation by antagonizing Brg1 activity

16 June 2024

93

1 reference

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The SWI/SNF chromatin remodeling protein Brg1 is required for vertebrate neurogenesis and mediates transactivation of Ngn and NeuroD.

16 June 2024

94

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

An essential switch in subunit composition of a chromatin remodeling complex during neural development

16 June 2024

95

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Regulation of dendritic development by neuron-specific chromatin remodeling complexes

16 June 2024

96

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

16 June 2024

98

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

16 June 2024

99

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.

16 June 2024

100

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation

16 June 2024

101

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Cyclin-dependent kinase-like 5 binds and phosphorylates DNA methyltransferase 1.

16 June 2024

102

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

16 June 2024

103

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

16 June 2024

104

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

16 June 2024

106

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Proteomics analysis of Ring1B/Rnf2 interactors identifies a novel complex with the Fbxl10/Jhdm1B histone demethylase and the Bcl6 interacting corepressor

16 June 2024

107

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Transgenic mice expressing a truncated form of CREB-binding protein (CBP) exhibit deficits in hippocampal synaptic plasticity and memory storage.

16 June 2024

108

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Dendrite development regulated by CREST, a calcium-regulated transcriptional activator

16 June 2024

109

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

A calcium-dependent switch in a CREST-BRG1 complex regulates activity-dependent gene expression

16 June 2024

110

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Developmental regulation of Eed complex composition governs a switch in global histone modification in brain

16 June 2024

111

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Histone deacetylases 1 and 2 control the progression of neural precursors to neurons during brain development

16 June 2024

112

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation

16 June 2024

113

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Characterization of E3Histone, a novel testis ubiquitin protein ligase which ubiquitinates histones

16 June 2024

114

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Mediator links epigenetic silencing of neuronal gene expression with x-linked mental retardation

16 June 2024

115

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The human CDK8 subcomplex is a histone kinase that requires Med12 for activity and can function independently of mediator

16 June 2024

116

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

16 June 2024

117

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

The original Lujan syndrome family has a novel missense mutation (p.N1007S) in the MED12 gene

16 June 2024

118

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndrome

16 June 2024

119

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes

16 June 2024

120

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Haploinsufficiency of NSD1 causes Sotos syndrome

16 June 2024

121

1 reference

https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

p21-activated kinase 1 interacts with and phosphorylates histone H3 in breast cancer cells

16 June 2024

122

1 reference

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Regulation of hippocampal long-term potentiation by p21-activated protein kinase 1 (PAK1).

16 June 2024

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A GIT1/PIX/Rac/PAK signaling module regulates spine morphogenesis and synapse formation through MLC

16 June 2024

124

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Alteration of working memory but not in anxiety or stress response in p300/CBP associated factor (PCAF) histone acetylase knockout mice bred on a C57BL/6 background.

16 June 2024

125

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A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation

16 June 2024

126

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Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

16 June 2024

127

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Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndrome

16 June 2024

128

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Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior

16 June 2024

129

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Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3

16 June 2024

130

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Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

16 June 2024

131

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Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation

16 June 2024

132

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The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation.

16 June 2024

133

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Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly

16 June 2024

134

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Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome

16 June 2024

135

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Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation

16 June 2024

136

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https://api.crossref.org/works/10.1111/J.1399-0004.2010.01503.X

Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation

16 June 2024

137

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ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation

16 June 2024

138

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A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

16 June 2024

139

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16 June 2024

Identifiers

1 reference

23 August 2017

1 reference