A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1

Environmental and occupational factors in the aetiopathogenesis of systemic sclerosis: insights from a large multinational patient survey.

Scandinavian journal of rheumatology·2026

Contribution of new imaging sequences to the diagnosis of multiple sclerosis.

Revue neurologique·2026

Some Like it Hot: Efficiency of the Type III Secretion System has Multiple Thermosensitive Behaviours in the Pseudomonas syringae Complex.

Molecular plant pathology·2025

Re-treatment with panitumumab followed by regorafenib versus the reverse sequence in chemorefractory metastatic colorectal cancer patients with RAS and BRAF wild-type circulating tumor DNA: the PARERE study by GONO.

Annals of oncology : official journal of the European Society for Medical Oncology·2025

Impact of age and sex on the efficacy and safety of ramucirumab plus paclitaxel as switch maintenance versus continuation of first-line oxaliplatin-based chemotherapy: a subgroup analysis of the ARMANI phase III trial.

ESMO open·2025

Clinical relevance and methodological approach for the assessment of drug-drug interactions in cancer patients: a position statement from the Italian Association of Medical Oncology (AIOM) and the Italian Society of Pharmacology (SIF).

ESMO open·2025

VPS13C regulates triglyceride homeostasis and adipocyte differentiation.

Human molecular genetics·2026

Gene regulatory behaviors of mutant CRX proteins demonstrated with late-stage human retinal organoids.

Human molecular genetics·2026

Modeling patient variants of Cnot1 and Cdc42bpb results in distinct forms of congenital diaphragmatic hernia in mice.

Human molecular genetics·2026

DUOXA2-mediated thyroid hormone synthesis is indispensable for postnatal maturation of auditory function.

Human molecular genetics·2026

Parkinson's disease-associated LRRK2 risk variant, G2385R, enhances Rab substrate phosphorylation and impairs neuronal integrity.

Human molecular genetics·2026

Pleiotropy and eQTL analysis identify shared genetic architecture of lipid traits in African-ancestry populations.

Human molecular genetics·2026

Delayed diagnosis of familial glucocorticoid deficiency type 4 in a child with epilepsy: a case report and literature review.

Journal of pediatric endocrinology & metabolism : JPEM·2026

[Low-frequency trisomy 21 mosaicism diagnosed following conflicting prenatal testing].

Ugeskrift for laeger·2026

Rare Xq23 Microdeletion Involving the DCX and PAK3 Genes Presenting With Lissencephaly, Agenesis of the Corpus Callosum, and Intractable Epilepsy: A Case Report.

Cureus·2026

Reduced insulin/IGF-1 signaling extends reproductive span through somatic gonadal collagen-mediated maintenance of oocyte and embryo quality in Caenorhabditis elegans.

Cell communication and signaling : CCS·2026

Lipid requirements for brain development and function: what we can learn from Drosophila melanogaster.

Genome·2026

Genetically proxied sex hormones, Sjögren's disease, and broad dry eye disease: A bidirectional two-sample mendelian randomization study.

Science progress·2026

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A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1

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Environmental and occupational factors in the aetiopathogenesis of systemic sclerosis: insights from a large multinational patient survey.

Contribution of new imaging sequences to the diagnosis of multiple sclerosis.

Some Like it Hot: Efficiency of the Type III Secretion System has Multiple Thermosensitive Behaviours in the Pseudomonas syringae Complex.

Re-treatment with panitumumab followed by regorafenib versus the reverse sequence in chemorefractory metastatic colorectal cancer patients with RAS and BRAF wild-type circulating tumor DNA: the PARERE study by GONO.

Impact of age and sex on the efficacy and safety of ramucirumab plus paclitaxel as switch maintenance versus continuation of first-line oxaliplatin-based chemotherapy: a subgroup analysis of the ARMANI phase III trial.

Clinical relevance and methodological approach for the assessment of drug-drug interactions in cancer patients: a position statement from the Italian Association of Medical Oncology (AIOM) and the Italian Society of Pharmacology (SIF).

VPS13C regulates triglyceride homeostasis and adipocyte differentiation.

Gene regulatory behaviors of mutant CRX proteins demonstrated with late-stage human retinal organoids.

Modeling patient variants of Cnot1 and Cdc42bpb results in distinct forms of congenital diaphragmatic hernia in mice.

DUOXA2-mediated thyroid hormone synthesis is indispensable for postnatal maturation of auditory function.

Parkinson's disease-associated LRRK2 risk variant, G2385R, enhances Rab substrate phosphorylation and impairs neuronal integrity.

Pleiotropy and eQTL analysis identify shared genetic architecture of lipid traits in African-ancestry populations.

Delayed diagnosis of familial glucocorticoid deficiency type 4 in a child with epilepsy: a case report and literature review.

[Low-frequency trisomy 21 mosaicism diagnosed following conflicting prenatal testing].

Rare Xq23 Microdeletion Involving the DCX and PAK3 Genes Presenting With Lissencephaly, Agenesis of the Corpus Callosum, and Intractable Epilepsy: A Case Report.

Reduced insulin/IGF-1 signaling extends reproductive span through somatic gonadal collagen-mediated maintenance of oocyte and embryo quality in Caenorhabditis elegans.

Lipid requirements for brain development and function: what we can learn from Drosophila melanogaster.

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Related Experiment Videos

A dinucleotide repeat polymorphism (D9S202) in the Friedreich's ataxia region on chromosome 9q13-q21.1

Related Concept Videos

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