Structural anomalies of the X chromosome and inactivation center

Beyond sense-specific processing: decoding texture in the brain from touch and sonified movement.

iScience·2023

The synthetic molecule stauprimide impairs cell growth and migration in triple-negative breast cancer.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie·2022

Sensitization to Vitis vinifera Pollen in a Wine Production Area: Identification of the Allergens Involved.

Journal of investigational allergology & clinical immunology·2022

Histopathological and virological features of lung, heart and liver percutaneous tissue core biopsy in patients with COVID-19: A clinicopathological case series.

The Malaysian journal of pathology·2022

[Evaluation of the validity of Ag PANBIO-COVID19 in the diagnosis of SARS-CoV-2 infection in asymptomatic or mildly infected patients].

Revista espanola de quimioterapia : publicacion oficial de la Sociedad Espanola de Quimioterapia·2021

The impact of movement sonification on haptic perception changes with aging.

Scientific reports·2021

Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Human genetics·2026

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

Human genetics·2026

Integrating genetic, historical, and demographic evidence to reconstruct Argentina's matrilineal ancestry.

Human genetics·2026

Expected costs and benefits of genetic counselling and germline genetic testing in metastatic prostate cancer.

Human genetics·2026

From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

Human genetics·2026

Genomic characterization of historical Jinlingnan individuals: insights into genetic continuity and trans-Eurasian signals in eastern China.

Human genetics·2026

A robustness-first cross-disease framework supports a candidate shared microbial redox axis and disease-specific metabolic divergence in colorectal cancer, Crohn's disease, and liver cirrhosis.

mSystems·2026

Novel TCOF1 Frameshift Variant and Phenotypic Heterogeneity in a Chinese Family With Treacher Collins Syndrome.

Molecular genetics & genomic medicine·2026

Estrogen insensitivity syndrome: the 'Upside Down' of ESR1 mutations.

The Journal of endocrinology·2026

Development of a lethal adult mouse model of Coxsackievirus B1 infection for antiviral research.

iScience·2026

SCLC TumorMiner: A genomics platform for small cell lung cancer precision oncology.

iScience·2026

[The unbearable versatility of endocrine aging].

Problemy endokrinologii·2026

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Structural anomalies of the X chromosome and inactivation center

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Beyond sense-specific processing: decoding texture in the brain from touch and sonified movement.

The synthetic molecule stauprimide impairs cell growth and migration in triple-negative breast cancer.

Sensitization to Vitis vinifera Pollen in a Wine Production Area: Identification of the Allergens Involved.

Histopathological and virological features of lung, heart and liver percutaneous tissue core biopsy in patients with COVID-19: A clinicopathological case series.

[Evaluation of the validity of Ag PANBIO-COVID19 in the diagnosis of SARS-CoV-2 infection in asymptomatic or mildly infected patients].

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Optical genome mapping improves structural variant detection and characterization in syndromic and neurogenetic disorders.

Development of RS1-specific ACMG/AMP variant classification criteria with pilot variant curation.

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From targeted SCN1A analysis to whole exome sequencing: clinical utility and novel genetic findings in a Hungarian paediatric epilepsy cohort.

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Structural anomalies of the X chromosome and inactivation center

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