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The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral follicles.

Molecular and cellular endocrinology·2017

Overweight and the feline gut microbiome - a pilot study.

Journal of animal physiology and animal nutrition·2015

Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.

Molecular and cellular endocrinology·2015

Evidence for induction of humoral and cytotoxic immune responses against devil facial tumor disease cells in Tasmanian devils (Sarcophilus harrisii) immunized with killed cell preparations.

Vaccine·2015

Effect of the FSH receptor single nucleotide polymorphisms (FSHR 307/680) on the follicular fluid hormone profile and the granulosa cell gene expression in human small antral follicles.

Molecular human reproduction·2014

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

Human molecular genetics·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

Human molecular genetics·2026

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Human molecular genetics·2026

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Human molecular genetics·2026

Congenital knee deformity: rare case report and unexpected finding in the delivery room.

AME case reports·2026

X-linked ARSL chondrodysplasia punctata: expanding the spectrum with a severe multisystem phenotype.

Case reports in perinatal medicine·2026

Phenytoin-induced drug rash with eosinophilia and systemic symptoms syndrome in a child: A rare but serious adverse drug reaction.

Indian journal of pharmacology·2026

Bilateral Papillary Traction due to Persistent Hyaloid Vessel Remnants in Aymé-Gripp Syndrome.

Case reports in ophthalmological medicine·2026

Coexisting PTEN and SDHB Mutations in a Pediatric Patient with PTEN Hamartoma Tumor Syndrome: a case report.

Frontiers in pediatrics·2026

Buccal Lobular Capillary Haemangioma in Children - A Case Report.

Annals of maxillofacial surgery·2026

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Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit

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miR-151a induces partial EMT by regulating E-cadherin in NSCLC cells.

The polymorphic insertion of the luteinizing hormone receptor "insLQ" show a negative association to LHR gene expression and to the follicular fluid hormonal profile in human small antral follicles.

Overweight and the feline gut microbiome - a pilot study.

Size matters: Associations between the androgen receptor CAG repeat length and the intrafollicular hormone milieu.

Evidence for induction of humoral and cytotoxic immune responses against devil facial tumor disease cells in Tasmanian devils (Sarcophilus harrisii) immunized with killed cell preparations.

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Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit

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