Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development

Remote assessment of the Penn computerised neurocognitive battery in individuals with 22q11.2 deletion syndrome.

Journal of intellectual disability research : JIDR·2024

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.

Molecular psychiatry·2017

Emergent, remitted and persistent psychosis-spectrum symptoms in 22q11.2 deletion syndrome.

Translational psychiatry·2017

Incidental radiologic findings in the 22q11.2 deletion syndrome.

AJNR. American journal of neuroradiology·2014

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.

Molecular psychiatry·2014

Expression of the chlorophyll-a/b-protein multigene family in pea (Pisum sativum L.) : Evidence for distinct developmental responses.

Planta·2013

Alternative splicing dynamics in pig tissues under soybean oil supplementation.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Development and validation of a high density SNP array for indigenous Indian pigs.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Integrative bioinformatics and machine learning reveal hub genes and immune signatures bridging type 2 diabetes mellitus, fracture susceptibility, and osteoblast differentiation dysfunction.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Genomic analysis of breed composition and population structure in Montana composite cattle.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Delayed diagnosis of familial glucocorticoid deficiency type 4 in a child with epilepsy: a case report and literature review.

Journal of pediatric endocrinology & metabolism : JPEM·2026

[Low-frequency trisomy 21 mosaicism diagnosed following conflicting prenatal testing].

Ugeskrift for laeger·2026

Rare Xq23 Microdeletion Involving the DCX and PAK3 Genes Presenting With Lissencephaly, Agenesis of the Corpus Callosum, and Intractable Epilepsy: A Case Report.

Cureus·2026

Reduced insulin/IGF-1 signaling extends reproductive span through somatic gonadal collagen-mediated maintenance of oocyte and embryo quality in Caenorhabditis elegans.

Cell communication and signaling : CCS·2026

Lipid requirements for brain development and function: what we can learn from Drosophila melanogaster.

Genome·2026

Genetically proxied sex hormones, Sjögren's disease, and broad dry eye disease: A bidirectional two-sample mendelian randomization study.

Science progress·2026

Related Experiment Videos

Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development

Related Concept Videos

Remote assessment of the Penn computerised neurocognitive battery in individuals with 22q11.2 deletion syndrome.

A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium.

Emergent, remitted and persistent psychosis-spectrum symptoms in 22q11.2 deletion syndrome.

Incidental radiologic findings in the 22q11.2 deletion syndrome.

Neurocognitive development in 22q11.2 deletion syndrome: comparison with youth having developmental delay and medical comorbidities.

Expression of the chlorophyll-a/b-protein multigene family in pea (Pisum sativum L.) : Evidence for distinct developmental responses.

Alternative splicing dynamics in pig tissues under soybean oil supplementation.

Development and validation of a high density SNP array for indigenous Indian pigs.

Integrative bioinformatics and machine learning reveal hub genes and immune signatures bridging type 2 diabetes mellitus, fracture susceptibility, and osteoblast differentiation dysfunction.

USP38 promotes breast cancer immune evasion and malignant progression by deubiquitinating and stabilizing PD-L1.

The role of impaired mitochondrial function in neurological manifestations of mitochondrial diseases.

Genomic analysis of breed composition and population structure in Montana composite cattle.

Delayed diagnosis of familial glucocorticoid deficiency type 4 in a child with epilepsy: a case report and literature review.

[Low-frequency trisomy 21 mosaicism diagnosed following conflicting prenatal testing].

Rare Xq23 Microdeletion Involving the DCX and PAK3 Genes Presenting With Lissencephaly, Agenesis of the Corpus Callosum, and Intractable Epilepsy: A Case Report.

Reduced insulin/IGF-1 signaling extends reproductive span through somatic gonadal collagen-mediated maintenance of oocyte and embryo quality in Caenorhabditis elegans.

Lipid requirements for brain development and function: what we can learn from Drosophila melanogaster.

Genetically proxied sex hormones, Sjögren's disease, and broad dry eye disease: A bidirectional two-sample mendelian randomization study.

Related Experiment Videos

Characterization of CDC45L: a gene in the 22q11.2 deletion region expressed during murine and human development

Related Concept Videos

Related Articles