VNTR at the DXYS14 locus

Fluorocholine (18F) and sodium fluoride (18F) PET/CT in the detection of prostate cancer: prospective comparison of diagnostic performance determined by masked reading.

The quarterly journal of nuclear medicine and molecular imaging : official publication of the Italian Association of Nuclear Medicine (AIMN) [and] the International Association of Radiopharmacology (IAR), [and] Section of the Society of...·2011

The advantages of combining low-density lipoproteins with glutamine for cryopreservation of canine semen.

Reproduction in domestic animals = Zuchthygiene·2008

Deficiency of the 5-hydroxytryptamine transporter gene leads to cardiac fibrosis and valvulopathy in mice.

Circulation·2005

Evaluation of the effect of nifedipine upon myocardial perfusion and contractility using cardiac magnetic resonance imaging and tissue Doppler echocardiography in systemic sclerosis.

Annals of the rheumatic diseases·2005

[Echocardiography in elderly patients].

Presse medicale (Paris, France : 1983)·2004

Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15.

Journal of neural transmission (Vienna, Austria : 1996)·2003

A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

Human molecular genetics·2026

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Human molecular genetics·2026

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

Human molecular genetics·2026

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

Human molecular genetics·2026

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Human molecular genetics·2026

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

Human molecular genetics·2026

EvoDiffMol: evolutionary diffusion framework for 3D molecular design with optimized properties.

Journal of cheminformatics·2026

Harnessing genetic, chemical, and transcriptomic analyses guided the selection of Cistus creticus subsp. creticus genotypes rich in labdane-type diterpenes.

Planta·2026

Metabolic profiling-based screening of potential hepatotoxic combinations in green tea components under non-specific reactive oxygen species-removal cellular conditions.

Food & function·2026

Sustainable pH sensing: repurposing the anthocyanin-rich extract from Dioscorea alata for green analytical chemistry.

RSC advances·2026

mRNA decapping proteins regulate EIN2-dependent ethylene signaling in arabidopsis.

Frontiers in plant science·2026

Correction: İnce et al. Controlled and Modified Atmospheres Combined with 1-MCP Improve Postharvest Quality and Suppress Botrytis cinerea in Cut Roses (Rosa hybrida L.). Plants 2026, 15, 1452.

Plants (Basel, Switzerland)·2026

Related Experiment Videos

VNTR at the DXYS14 locus

Related Concept Videos

Fluorocholine (18F) and sodium fluoride (18F) PET/CT in the detection of prostate cancer: prospective comparison of diagnostic performance determined by masked reading.

The advantages of combining low-density lipoproteins with glutamine for cryopreservation of canine semen.

Deficiency of the 5-hydroxytryptamine transporter gene leads to cardiac fibrosis and valvulopathy in mice.

Evaluation of the effect of nifedipine upon myocardial perfusion and contractility using cardiac magnetic resonance imaging and tissue Doppler echocardiography in systemic sclerosis.

[Echocardiography in elderly patients].

Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15.

A de novo TRPV4 variant c.2479C>G (p.Pro827Ala) in Spondylometaphyseal dysplasia Kozlowski type: identification and functional analysis.

SPEN deficiency contributes to the development of orofacial clefts in humans and mice.

Fetal myogenesis chromatin state and CpG from the open alliance markers and their intersection with adult muscle and gastrointestinal genetics.

The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

A functional framework in patient fibroblasts informs ATP7A variant pathogenicity and identifies p.Q990P as a novel cause of distal motor neuropathy.

Integrated multi-platform genetic profiling reveals dual molecular pathology in 46, XY disorders of sex development through NR5A1 Haploinsufficiency and maternal chromosome 15 UPD.

EvoDiffMol: evolutionary diffusion framework for 3D molecular design with optimized properties.

Harnessing genetic, chemical, and transcriptomic analyses guided the selection of Cistus creticus subsp. creticus genotypes rich in labdane-type diterpenes.

Metabolic profiling-based screening of potential hepatotoxic combinations in green tea components under non-specific reactive oxygen species-removal cellular conditions.

Sustainable pH sensing: repurposing the anthocyanin-rich extract from <i>Dioscorea alata</i> for green analytical chemistry.

mRNA decapping proteins regulate EIN2-dependent ethylene signaling in arabidopsis.

Correction: İnce et al. Controlled and Modified Atmospheres Combined with 1-MCP Improve Postharvest Quality and Suppress <i>Botrytis cinerea</i> in Cut Roses (<i>Rosa hybrida</i> L.). <i>Plants</i> 2026, <i>15</i>, 1452.

Related Experiment Videos

VNTR at the DXYS14 locus

Related Concept Videos

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