[Schizophrenia and heredity. Apropos of distortions of methods and finalities]

Complete nucleotide sequence of the genomic RNA of a French isolate of Pepino mosaic virus (PepMV). Brief report.

Archives of virology·2002

The influence of long emersion on biota, ammonium fluxes and nitrification in intertidal sediments of Marennes-Oléron Bay, France.

Marine environmental research·2002

Inositol hexakisphosphate-mediated regulation of glutamate receptors in rat brain sections.

Hippocampus·2002

Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10.

Human molecular genetics·2001

DNA vaccine protection against challenge with simian/human immunodeficiency virus 89.6 in rhesus macaques.

Developments in biologicals·2001

On the evolutionary conservation of the cell death pathway: mitochondrial release of an apoptosis-inducing factor during Dictyostelium discoideum cell death.

Molecular biology of the cell·2001

[Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].

Journal de genetique humaine·1989

[Genetic mapping of chromosome X: known localizations].

Journal de genetique humaine·1989

[Animal models of gene therapy].

Journal de genetique humaine·1989

[Frontonasal dysplasia or the median cleft face syndrome: a case report].

Journal de genetique humaine·1989

[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].

Journal de genetique humaine·1989

[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].

Journal de genetique humaine·1989

Differentiating β-Thalassaemia From Iron Deficiency: Performance and Cut-Off Dependency of More Than 40 Red Cell Discrimination Indices in a Large German Cohort.

International journal of laboratory hematology·2026

A multi-omics Mendelian randomization study identifies putatively causal genes and pathways for Alzheimer's disease associated with reactive astrocytes.

Journal of Alzheimer's disease : JAD·2026

Integrative Genomic and Transcriptomic Analysis Reveals Hypothesis-Generating Candidate Genes for Nephrolithiasis Susceptibility in Primary Hyperoxaluria.

Nephrology (Carlton, Vic.)·2026

Perceptions of and willingness to participate in genomics research among a U.S. sample.

Frontiers in genetics·2026

Identification of Potential Key Biomarkers for Comorbid Depression and Obesity Through Integrated Bioinformatics Analysis and Experimental Verification.

Journal of inflammation research·2026

Isocitrate Dehydrogenase (IDH)-Wildtype Glioblastoma With an Unusual EWSR1::RAD51B Gene Fusion: A Case Report and Review of the Literature.

Cureus·2026

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[Schizophrenia and heredity. Apropos of distortions of methods and finalities]

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Complete nucleotide sequence of the genomic RNA of a French isolate of Pepino mosaic virus (PepMV). Brief report.

The influence of long emersion on biota, ammonium fluxes and nitrification in intertidal sediments of Marennes-Oléron Bay, France.

Inositol hexakisphosphate-mediated regulation of glutamate receptors in rat brain sections.

Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10.

DNA vaccine protection against challenge with simian/human immunodeficiency virus 89.6 in rhesus macaques.

On the evolutionary conservation of the cell death pathway: mitochondrial release of an apoptosis-inducing factor during Dictyostelium discoideum cell death.

[Ultrasonic prenatal diagnosis of the Jarcho-Levin syndrome].

[Genetic mapping of chromosome X: known localizations].

[Animal models of gene therapy].

[Frontonasal dysplasia or the median cleft face syndrome: a case report].

[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis].

[F.G. syndrome: a rare and/or extremely polymorphic syndrome?].

Differentiating β-Thalassaemia From Iron Deficiency: Performance and Cut-Off Dependency of More Than 40 Red Cell Discrimination Indices in a Large German Cohort.

A multi-omics Mendelian randomization study identifies putatively causal genes and pathways for Alzheimer's disease associated with reactive astrocytes.

Integrative Genomic and Transcriptomic Analysis Reveals Hypothesis-Generating Candidate Genes for Nephrolithiasis Susceptibility in Primary Hyperoxaluria.

Perceptions of and willingness to participate in genomics research among a U.S. sample.

Identification of Potential Key Biomarkers for Comorbid Depression and Obesity Through Integrated Bioinformatics Analysis and Experimental Verification.

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