Transcription factors in dysmorphology

Repression of oxidative phosphorylation by NR2F2, MTERF3 and GDF15 in human skin under high-glucose stress.

Redox biology·2025

Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting.

BMC health services research·2023

Real-world data in oncology: a questionnaire-based analysis of the academic research landscape examining the policies and experiences of the cancer cooperative groups.

ESMO open·2023

Re-focusing on Agnathia-Otocephaly complex.

Clinical oral investigations·2020

Mitochondrial functions and rare diseases.

Molecular aspects of medicine·2020

Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.

The British journal of dermatology·2018

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1-Related Noonan Syndrome.

Clinical genetics·2026

Chorea-Acanthocytosis Without Acanthocytosis: Sensory Neuronopathy and Epilepsy as Prominent Features From a Novel VPS13A Variant.

Clinical genetics·2026

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

Clinical genetics·2026

Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation.

Clinical genetics·2026

Novel Germline ELP1 Splice-Acceptor Variant in NF1-Negative Optic Pathway Glioma: Expanding the Clinical Spectrum Associated With ELP1 Variation.

Clinical genetics·2026

Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.

Clinical genetics·2026

BAMBI acts as a molecular switch to determine cell fate of C2C12 myoblasts.

Journal of molecular endocrinology·2026

BRCA1-derived peptide constructs exhibit sequence-dependent features compatible with modulation of the p53-MDM2 axis.

Molecular biology reports·2026

Biological mechanisms and applications of photobiomodulation in wound care.

British journal of nursing (Mark Allen Publishing)·2026

Microvascular decompression through an anterior transpetrosal approach for trigeminal neuralgia caused by persistent primitive trigeminal artery variant traversing Meckel's cave: A case report.

Surgical neurology international·2026

Effect of neurotrophin-3 on bone healing in distraction osteogenesis.

Nagoya journal of medical science·2026

Substrate-selective mTORC1 regulation and gene dosage-dependent tissue divergence in Birt-Hogg-Dubé syndrome.

Frontiers in oncology·2026

Related Experiment Videos

Transcription factors in dysmorphology

Related Concept Videos

Repression of oxidative phosphorylation by NR2F2, MTERF3 and GDF15 in human skin under high-glucose stress.

Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting.

Real-world data in oncology: a questionnaire-based analysis of the academic research landscape examining the policies and experiences of the cancer cooperative groups.

Re-focusing on Agnathia-Otocephaly complex.

Mitochondrial functions and rare diseases.

Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1-Related Noonan Syndrome.

Chorea-Acanthocytosis Without Acanthocytosis: Sensory Neuronopathy and Epilepsy as Prominent Features From a Novel VPS13A Variant.

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

Expanding the Phenotypic and Functional Evidence for KCNK3 as a Neurodevelopmental Disorder Gene: A New Chinese Case and Drosophila Validation.

Novel Germline ELP1 Splice-Acceptor Variant in NF1-Negative Optic Pathway Glioma: Expanding the Clinical Spectrum Associated With ELP1 Variation.

Clinical and Molecular Characterization of a RASopathy Cohort From Türkiye and an AMMECR1-Related Noonan Syndrome-Mimicking Phenotype.

BAMBI acts as a molecular switch to determine cell fate of C2C12 myoblasts.

BRCA1-derived peptide constructs exhibit sequence-dependent features compatible with modulation of the p53-MDM2 axis.

Biological mechanisms and applications of photobiomodulation in wound care.

Microvascular decompression through an anterior transpetrosal approach for trigeminal neuralgia caused by persistent primitive trigeminal artery variant traversing Meckel's cave: A case report.

Effect of neurotrophin-3 on bone healing in distraction osteogenesis.

Substrate-selective mTORC1 regulation and gene dosage-dependent tissue divergence in Birt-Hogg-Dubé syndrome.

Related Experiment Videos

Transcription factors in dysmorphology

Related Concept Videos

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