[The place of genetics in digestive pathology]

Mannose transporter of Escherichia coli. Backbone assignments and secondary structure of the IIA domain of the IIABMan subunit.

Biochemistry·1994

Synaptonemal complex studies in male mice treated with cyproterone acetate or with testosterone.

Mutation research·1993

Increased sister chromatid exchanges and tumor markers in workers exposed to elemental chromium-, cobalt- and nickel-containing dusts.

Mutation research·1993

Synaptonemal complex alterations in X-irradiated and in oestrogen-treated mice: a comparative study.

Mutation research·1992

Effect of estradiol treatment on male mice synaptonemal complexes: difference of sensitivity between neonates and adults.

Genetica·1992

Experimental diabetes impairs rat embryo development during the preimplantation period.

Diabetologia·1990

Silent Fungus, Sudden Crisis: Gastrointestinal Bleeding due to Disseminated Histoplasmosis.

Acta gastro-enterologica Belgica·2026

Acute oesophageal necrosis following ethyl-induced emesis: A Case Report.

Acta gastro-enterologica Belgica·2026

Conservative Management of Omental Infarction Using Only Analgesia.

Acta gastro-enterologica Belgica·2026

Angor abdominalis caused by a pancreatic arteriovenous malformation: a case report.

Acta gastro-enterologica Belgica·2026

Gastric Trichobezoars in Children and Adolescents: A Single-Center Case Series.

Acta gastro-enterologica Belgica·2026

Therapeutic challenges in the multidisciplinary approach of liver transplant-associated biliary tract complications in Roux-en-Y gastric bypass patients.

Acta gastro-enterologica Belgica·2026

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Related Experiment Videos

[The place of genetics in digestive pathology]

Related Concept Videos

Mannose transporter of Escherichia coli. Backbone assignments and secondary structure of the IIA domain of the IIABMan subunit.

Synaptonemal complex studies in male mice treated with cyproterone acetate or with testosterone.

Increased sister chromatid exchanges and tumor markers in workers exposed to elemental chromium-, cobalt- and nickel-containing dusts.

Synaptonemal complex alterations in X-irradiated and in oestrogen-treated mice: a comparative study.

Effect of estradiol treatment on male mice synaptonemal complexes: difference of sensitivity between neonates and adults.

Experimental diabetes impairs rat embryo development during the preimplantation period.

Silent Fungus, Sudden Crisis: Gastrointestinal Bleeding due to Disseminated Histoplasmosis.

Acute oesophageal necrosis following ethyl-induced emesis: A Case Report.

Conservative Management of Omental Infarction Using Only Analgesia.

Angor abdominalis caused by a pancreatic arteriovenous malformation: a case report.

Gastric Trichobezoars in Children and Adolescents: A Single-Center Case Series.

Therapeutic challenges in the multidisciplinary approach of liver transplant-associated biliary tract complications in Roux-en-Y gastric bypass patients.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

Related Experiment Videos

[The place of genetics in digestive pathology]

Related Concept Videos

Related Articles