Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion

Beyond sense-specific processing: decoding texture in the brain from touch and sonified movement.

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The impact of movement sonification on haptic perception changes with aging.

Scientific reports·2021

First Report of Fusarium Head Blight on Winter Wheat in the Grand Duchy of Luxembourg.

Plant disease·2019

First Report of Wheat Leaf Rust in the Grand Duchy of Luxembourg and the Progress of its Appearance over the 2003-2008 Period.

Plant disease·2019

First Report of the Nivalenol Chemotype of Fusarium graminearum Causing Head Blight of Wheat in the Grand Duchy of Luxembourg.

Plant disease·2019

[IHC, FISH, CISH, NGS in non-small cell lung cancer: What changes in the biomarker era?]

Revue de pneumologie clinique·2018

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

Clinical genetics·2026

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

Clinical genetics·2026

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Clinical genetics·2026

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

Clinical genetics·2026

Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

Clinical genetics·2026

Liquid Biopsy and Multi-Cancer Early Detection Tests for Cancer Screening: A Scoping Review.

Clinical genetics·2026

Type 1 diabetes SIRPG risk variants increase SIRPγ expression and CD47 loss enhances CD8+ T cell cytotoxicity.

NPJ autoimmunity·2026

Characterisation of the Novel HLA-DQB1*02:85:02 Allele by Sequencing-Based Typing.

HLA·2026

Clinical Epigenomics in Rare Diseases: Interpreting DNA Methylation Episignatures.

Molecular genetics & genomic medicine·2026

Maternal obesity imprints methylation marks in oocytes to drive intergenerational metabolic dysfunction.

Nature metabolism·2026

C. elegans CEH-43/DLX drives convergent astrocyte differentiation by sequential control of axon guidance and synaptic gene expression programs.

Genes & development·2026

Integrative genomics decoding DNA methylation-mediated genetic control of complex traits in pigs.

Journal of advanced research·2026

Related Experiment Videos

Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion

Related Concept Videos

Beyond sense-specific processing: decoding texture in the brain from touch and sonified movement.

The impact of movement sonification on haptic perception changes with aging.

First Report of Fusarium Head Blight on Winter Wheat in the Grand Duchy of Luxembourg.

First Report of Wheat Leaf Rust in the Grand Duchy of Luxembourg and the Progress of its Appearance over the 2003-2008 Period.

First Report of the Nivalenol Chemotype of Fusarium graminearum Causing Head Blight of Wheat in the Grand Duchy of Luxembourg.

[IHC, FISH, CISH, NGS in non-small cell lung cancer: What changes in the biomarker era?]

A Novel ACAN Missense Variant in the G1 Domain Causes Short Stature, Advanced Bone Age, and Osteochondritis Dissecans: A Case Report and Literature Review.

A De Novo ATP1A3 p.Arg995His Variant in a Patient With an Adult-Onset Primary Lateral Sclerosis-Like Syndrome.

A Homozygous Frameshift Variant in KHDC4 Is Associated With a Syndromic Inherited Retinal Disease in Humans.

Müllerian Duct Aplasia in a Girl With SMARCB1-Related Coffin-Siris Syndrome: A Rare Co-Occurring Anomaly.

Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

Liquid Biopsy and Multi-Cancer Early Detection Tests for Cancer Screening: A Scoping Review.

Type 1 diabetes SIRPG risk variants increase SIRPγ expression and CD47 loss enhances CD8+ T cell cytotoxicity.

Characterisation of the Novel HLA-DQB1*02:85:02 Allele by Sequencing-Based Typing.

Clinical Epigenomics in Rare Diseases: Interpreting DNA Methylation Episignatures.

Maternal obesity imprints methylation marks in oocytes to drive intergenerational metabolic dysfunction.

C. elegans CEH-43/DLX drives convergent astrocyte differentiation by sequential control of axon guidance and synaptic gene expression programs.

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Related Experiment Videos

Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletion

Related Concept Videos

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