Two novel polymorphisms, c1086T>C and c1798C>T, in the MADH4/DPC4 gene

Avoidable general anesthesia for nonobstetric surgery during pregnancy: a retrospective cohort pilot study (2011-2020).

International journal of obstetric anesthesia·2024

Ischemic injury of the upper gastrointestinal tract after out-of-hospital cardiac arrest: a prospective, multicenter study.

Critical care (London, England)·2022

[Hepatopulmonary syndrome: Prevalence, pathophysiology and clinical implications].

Revue des maladies respiratoires·2022

Antitumor activity of ipatasertib combined with chemotherapy: results from a phase Ib study in solid tumors.

Annals of oncology : official journal of the European Society for Medical Oncology·2020

Vaccinia-based oncolytic immunotherapy Pexastimogene Devacirepvec in patients with advanced hepatocellular carcinoma after sorafenib failure: a randomized multicenter Phase IIb trial (TRAVERSE).

Oncoimmunology·2019

How Artificial Intelligence Can Improve Our Understanding of the Genes Associated with Endometriosis: Natural Language Processing of the PubMed Database.

BioMed research international·2018

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Human mutation·2026

Mutation-Immune Crosstalk Contextualizes CAF-Associated ARPC1A Programs and Cisplatin Response in Gastric Cancer.

Human mutation·2026

Identification of Novel Pathogenic Variants in Familial Adenomatous Polyposis Through Whole Genome Sequencing.

Human mutation·2026

A Pathogenic ANK1 c.5096G>A Mutation Disrupting the Ankyrin-1/β-Spectrin Interaction in Hereditary Spherocytosis.

Human mutation·2026

A Novel Splice Variant in the COL1A1 Gene Leads to Exon 46 Skipping and Osteogenesis Imperfecta.

Human mutation·2026

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Human mutation·2026

Genetic and stochastic basis of phenotypic discordance in 16p11.2 mouse model deletion.

bioRxiv : the preprint server for biology·2026

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

Clinical genetics·2026

DNA Methylation Profiling in IDH-Mutant Gliomas: Biological Evolution, Molecular Grading and Clinical Implementation.

Neuropathology and applied neurobiology·2026

Multiomic Single-Nucleus Profiling Reveals Cell-Type-Specific Epigenetic and Transcriptional Dysregulation in Major Depressive Disorder Brain.

The international journal of neuropsychopharmacology·2026

Serum Isthmin-1 in Gestational Diabetes Mellitus: A Case-Control Study Providing Preliminary Evidence of Elevated Levels and Association With Insulin Resistance.

Medical science monitor : international medical journal of experimental and clinical research·2026

Genomic structural equation modeling reveals novel genetic loci and pathways in panvascular disease.

Medicine·2026

Related Experiment Videos

Two novel polymorphisms, c1086T>C and c1798C>T, in the MADH4/DPC4 gene

Related Concept Videos

Avoidable general anesthesia for nonobstetric surgery during pregnancy: a retrospective cohort pilot study (2011-2020).

Ischemic injury of the upper gastrointestinal tract after out-of-hospital cardiac arrest: a prospective, multicenter study.

[Hepatopulmonary syndrome: Prevalence, pathophysiology and clinical implications].

Antitumor activity of ipatasertib combined with chemotherapy: results from a phase Ib study in solid tumors.

Vaccinia-based oncolytic immunotherapy Pexastimogene Devacirepvec in patients with advanced hepatocellular carcinoma after sorafenib failure: a randomized multicenter Phase IIb trial (TRAVERSE).

How Artificial Intelligence Can Improve Our Understanding of the Genes Associated with Endometriosis: Natural Language Processing of the PubMed Database.

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Mutation-Immune Crosstalk Contextualizes CAF-Associated ARPC1A Programs and Cisplatin Response in Gastric Cancer.

Identification of Novel Pathogenic Variants in Familial Adenomatous Polyposis Through Whole Genome Sequencing.

A Pathogenic ANK1 c.5096G>A Mutation Disrupting the Ankyrin-1/β-Spectrin Interaction in Hereditary Spherocytosis.

A Novel Splice Variant in the COL1A1 Gene Leads to Exon 46 Skipping and Osteogenesis Imperfecta.

Two Unrelated Families With Noncoding Duplications Upstream of MSX2 Refine the Critical Regulatory Region Likely Involved in Cranial Bone Development and a Cleidocranial Dysplasia-Like Phenotype.

Genetic and stochastic basis of phenotypic discordance in 16p11.2 mouse model deletion.

Genetics in Heterotaxy: A Case Series and Literature Review on DNAH9, PKD1L1, MMP21, and GDF1.

DNA Methylation Profiling in IDH-Mutant Gliomas: Biological Evolution, Molecular Grading and Clinical Implementation.

Multiomic Single-Nucleus Profiling Reveals Cell-Type-Specific Epigenetic and Transcriptional Dysregulation in Major Depressive Disorder Brain.

Serum Isthmin-1 in Gestational Diabetes Mellitus: A Case-Control Study Providing Preliminary Evidence of Elevated Levels and Association With Insulin Resistance.

Genomic structural equation modeling reveals novel genetic loci and pathways in panvascular disease.

Related Experiment Videos

Two novel polymorphisms, c1086T>C and c1798C>T, in the MADH4/DPC4 gene

Related Concept Videos

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