Genetic malformations of the human cerebral cortex

Achievement of Target Gain Larger than Unity in an Inertial Fusion Experiment.

Physical review letters·2024

Improved filters for angular filter refractometry.

The Review of scientific instruments·2024

Measurement of Magnetic Cavitation Driven by Heat Flow in a Plasma.

Physical review letters·2023

Nonlinear ablative Rayleigh-Taylor instability: Increased growth due to self-generated magnetic fields.

Physical review. E·2023

X-ray imaging and radiation transport effects on cylindrical implosions.

The Review of scientific instruments·2022

Increased Ion Temperature and Neutron Yield Observed in Magnetized Indirectly Driven D_{2}-Filled Capsule Implosions on the National Ignition Facility.

Physical review letters·2022

Divergent somatic mutation patterns among human cerebellar neuron types.

Neuron·2026

Subtypes of neurons in the cerebellar cortex.

Neuron·2026

Temporal changes in metabolism guide oligodendrocyte precursor cell dynamics in aging and multiple sclerosis.

Neuron·2026

Early-life stress alters H3K4me1 in VTA to prime stress sensitivity.

Neuron·2026

Inferring brain-wide interactions using data-constrained recurrent neural network models.

Neuron·2026

Deep learning-based control of electrically evoked activity in human visual cortex.

Neuron·2026

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Frontiers in genetics·2026

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

Frontiers in pediatrics·2026

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Epilepsia·2026

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Seizure·2026

Related Experiment Videos

Genetic malformations of the human cerebral cortex

Related Concept Videos

Achievement of Target Gain Larger than Unity in an Inertial Fusion Experiment.

Improved filters for angular filter refractometry.

Measurement of Magnetic Cavitation Driven by Heat Flow in a Plasma.

Nonlinear ablative Rayleigh-Taylor instability: Increased growth due to self-generated magnetic fields.

X-ray imaging and radiation transport effects on cylindrical implosions.

Increased Ion Temperature and Neutron Yield Observed in Magnetized Indirectly Driven D_{2}-Filled Capsule Implosions on the National Ignition Facility.

Divergent somatic mutation patterns among human cerebellar neuron types.

Subtypes of neurons in the cerebellar cortex.

Temporal changes in metabolism guide oligodendrocyte precursor cell dynamics in aging and multiple sclerosis.

Early-life stress alters H3K4me1 in VTA to prime stress sensitivity.

Inferring brain-wide interactions using data-constrained recurrent neural network models.

Deep learning-based control of electrically evoked activity in human visual cortex.

Case Report: First case of paternal mosaicism in Snijders Blok-Fisher syndrome.

Recognizing KBG syndrome in pediatric practice: a case series highlighting phenotypic variability and diagnostic clues.

[Association analysis between dystrophin gene polymorphism and non-syndromic cleft lip with or without cleft palate].

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Developmental pathways to autism in tuberous sclerosis complex: Evidence from a longitudinal cohort.

Homozygous missense variants in CACNB4 underlie autosomal recessive epilepsy in two unrelated Pakistani consanguineous families.

Related Experiment Videos

Genetic malformations of the human cerebral cortex

Related Concept Videos

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