The control of gene function in cell differentiation and in embryogenesis

Transition from pediatric to adult care in patients with Turner syndrome in Italy: a consensus statement by the TRAMITI project.

Journal of endocrinological investigation·2024

Additional booster doses in patients with chronic lymphocytic leukemia induce humoral and cellular immune responses to SARS-CoV-2 similar to natural infection regardless ongoing treatments: A study by ERIC, the European Research Initiative on CLL.

American journal of hematology·2024

Multicentric Italian case-control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome.

Journal of endocrinological investigation·2023

New insights into the comorbid conditions of Turner syndrome: results from a long-term monocentric cohort study.

Journal of endocrinological investigation·2022

Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.

Journal of endocrinological investigation·2021

Is there any gender difference in epidemiology, clinical presentation and co-morbidities of non-functioning pituitary adenomas? A prospective survey of a National Referral Center and review of the literature.

Journal of endocrinological investigation·2020

Studies on the incorporation of the sodium channel of lobster nerve into soybean liposomes.

Advances in cytopharmacology·1979

Electrophysiological studies on the effects of the neurotoxin apamin on cultured neurons.

Advances in cytopharmacology·1979

Biochemical studies on the ionic channel of Torpedo acetylcholine receptor.

Advances in cytopharmacology·1979

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Frontiers in genetics·2026

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Frontiers in genetics·2026

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Developmental biology·2026

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Journal of neural transmission (Vienna, Austria : 1996)·2026

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

The Plant journal : for cell and molecular biology·2026

Low-Level Viremia and Spatial Heterogeneity Among Individuals on Dolutegravir-Based Antiretroviral Therapy in Botswana: A Nationwide Study (2016-2022).

The Journal of infectious diseases·2026

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The control of gene function in cell differentiation and in embryogenesis

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Transition from pediatric to adult care in patients with Turner syndrome in Italy: a consensus statement by the TRAMITI project.

Additional booster doses in patients with chronic lymphocytic leukemia induce humoral and cellular immune responses to SARS-CoV-2 similar to natural infection regardless ongoing treatments: A study by ERIC, the European Research Initiative on CLL.

Multicentric Italian case-control study on 25OH vitamin D levels in children and adolescents with Prader-Willi syndrome.

New insights into the comorbid conditions of Turner syndrome: results from a long-term monocentric cohort study.

Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.

Is there any gender difference in epidemiology, clinical presentation and co-morbidities of non-functioning pituitary adenomas? A prospective survey of a National Referral Center and review of the literature.

Studies on the incorporation of the sodium channel of lobster nerve into soybean liposomes.

Electrophysiological studies on the effects of the neurotoxin apamin on cultured neurons.

Biochemical studies on the ionic channel of Torpedo acetylcholine receptor.

Preimplantation genetic testing and prenatal diagnosis of TANGO2 deficiency disorder with biallelic pathogenic variants using single-nucleotide polymorphism-based haplotyping and gap-polymerase chain reaction.

Clinical and genetic features of syndromic craniosynostosis in 18 Chinese probands: novel candidate genes and phenotypes of known pathogenic genes.

Notch-Regulated Hematopoiesis in Drosophila: Parallels and Contrasts with Vertebrate Blood Development.

Serotonin deficiency caused by inactivation of Tph2 in mice leads to widespread sex-dependent changes in cerebral oxidative metabolic activity.

Haplotype-resolved genome assembly of a male Dioscorea alata cultivar reveals the structure and evolution of young sex chromosomes.

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