Observations on the regulation of uricase activity during development of Drosophila melanogaster

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Clinical genetics·2016

Unresolved questions regarding human hereditary deafness.

Oral diseases·2016

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Clinical genetics·2009

Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.

Clinical genetics·2009

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

Clinical genetics·2008

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.

Clinical genetics·2008

Genetic Association of VDR Polymorphism with Diabetic Foot Ulcers in Type 2 Diabetes: Evidence from Kerala, India.

Biochemical genetics·2026

Viral Infection of Cumulus Cells Impairs the Developmental Competence of Ovulated Mouse Oocytes.

Biochemical genetics·2026

TRPV4 is Associated with a Marfan Syndrome-Related Mechanosensitive Gene Program in Aortic Smooth Muscle Cells.

Biochemical genetics·2026

Integrated Proteomics and Metabolomics Analysis Reveals Regulatory Mechanisms Underlying Flower Bud Development in Camellia drupifera.

Biochemical genetics·2026

Secretory Carrier Membrane Protein 3 Knockdown Attenuates Hypoxic Pulmonary Hypertension Potentially Involving WW Domain-Containing E3 Ubiquitin Protein Ligase 1.

Biochemical genetics·2026

Mitogenomic Architecture and Phylogenetic Insights Shed Light on the Matrilineal Evolution of the Mahseer Fish Neolissochilus sumatranus (Cyprinidae: Torinae) in Southeast Asia.

Biochemical genetics·2026

Reaction-based cryo-EM resolves the continuous conformational spectrum of CTP synthase catalysis.

Proceedings of the National Academy of Sciences of the United States of America·2026

Exploring a FRET-driven ratiometric probe based on perovskite quantum dots and a rhodamine derivative for Cu2+ sensing in environmental water samples.

The Analyst·2026

Fixed drug eruption to propofol: Case series and clinical implications.

Allergologie select·2026

An Unusual Presentation of Right fifth Flexor Digitorum Profundus Tendon Zone 3 Rupture Following Jersey Finger Mechanism Injury.

Journal of orthopaedic case reports·2026

Human iPSC-derived 2D cortical neurons and 3D cortical organoids show fetal brain proteomic similarity and distinct phosphoproteomic profiles.

Frontiers in bioengineering and biotechnology·2026

Postoperative Day 2 C-reactive Protein Identifies Patients at Low Risk of Anastomotic Leakage After Colon Cancer Resection.

Annals of surgery·2026

Related Experiment Videos

Observations on the regulation of uricase activity during development of Drosophila melanogaster

Related Concept Videos

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

Unresolved questions regarding human hereditary deafness.

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2-q15.

Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.

USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.

A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.

Genetic Association of VDR Polymorphism with Diabetic Foot Ulcers in Type 2 Diabetes: Evidence from Kerala, India.

Viral Infection of Cumulus Cells Impairs the Developmental Competence of Ovulated Mouse Oocytes.

TRPV4 is Associated with a Marfan Syndrome-Related Mechanosensitive Gene Program in Aortic Smooth Muscle Cells.

Integrated Proteomics and Metabolomics Analysis Reveals Regulatory Mechanisms Underlying Flower Bud Development in Camellia drupifera.

Secretory Carrier Membrane Protein 3 Knockdown Attenuates Hypoxic Pulmonary Hypertension Potentially Involving WW Domain-Containing E3 Ubiquitin Protein Ligase 1.

Mitogenomic Architecture and Phylogenetic Insights Shed Light on the Matrilineal Evolution of the Mahseer Fish Neolissochilus sumatranus (Cyprinidae: Torinae) in Southeast Asia.

Reaction-based cryo-EM resolves the continuous conformational spectrum of CTP synthase catalysis.

Exploring a FRET-driven ratiometric probe based on perovskite quantum dots and a rhodamine derivative for Cu2+ sensing in environmental water samples.

Fixed drug eruption to propofol: Case series and clinical implications.

An Unusual Presentation of Right fifth Flexor Digitorum Profundus Tendon Zone 3 Rupture Following Jersey Finger Mechanism Injury.

Human iPSC-derived 2D cortical neurons and 3D cortical organoids show fetal brain proteomic similarity and distinct phosphoproteomic profiles.

Postoperative Day 2 C-reactive Protein Identifies Patients at Low Risk of Anastomotic Leakage After Colon Cancer Resection.

Related Experiment Videos

Observations on the regulation of uricase activity during development of Drosophila melanogaster

Related Concept Videos

Related Articles