Intragenic mapping of the Neurospora pyrimidine-3 locus by functional deletions

Correlating pulmonary embolism severity with short term mortality to risk stratify for outpatient management.

Acute medicine·2020

Hypoxic changes to the urothelium as a bystander of end-stage bladder disease.

Journal of pediatric urology·2019

Late ascended testes: is non-orthotopic gubernacular insertion a confirmation of an alternative embryological etiology?

Journal of pediatric urology·2018

Respiratory disease and sero-epidemiology of respiratory pathogens in the working horses of Ethiopia.

Equine veterinary journal·2018

Modified tubularized incised plate urethroplasty in distal hypospadias repair: Stepwise technique with validated functional and cosmetic outcome.

Journal of pediatric urology·2016

Global minimally invasive pyeloplasty study in children: Results from the Pediatric Urology Expert Group of the European Association of Urology Young Academic Urologists working party.

Journal of pediatric urology·2016

A multigene family in Calothrix sp. PCC 7601 encodes phycocyanin, the major component of the cyanobacterial light-harvesting antenna

Molecular & general genetics : MGG·2017

Mutants of Schizosaccharomyces pombe which sporulate in the haploid state.

Molecular & general genetics : MGG·2015

The chloroplast genomes of conifers lack one of the rRNA-encoding inverted repeats.

Molecular & general genetics : MGG·2014

Multiple mutant analysis of recombination in yeast.

Molecular & general genetics : MGG·2012

Intergenic suppression of spoO phenotypes by the Bacillus subtilis mutation rvtA.

Molecular & general genetics : MGG·2010

Expression of the seqA gene is negatively modulated by the HU protein in Escherichia coli.

Molecular & general genetics : MGG·2001

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Clinical laboratory·2026

Audiological Features in Pendred Syndrome: A Scoping Review.

The journal of international advanced otology·2026

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Journal of blood medicine·2026

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Journal of molecular neuroscience : MN·2026

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Frontiers in endocrinology·2026

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Frontiers in psychiatry·2026

Related Experiment Videos

Intragenic mapping of the Neurospora pyrimidine-3 locus by functional deletions

Related Concept Videos

Correlating pulmonary embolism severity with short term mortality to risk stratify for outpatient management.

Hypoxic changes to the urothelium as a bystander of end-stage bladder disease.

Late ascended testes: is non-orthotopic gubernacular insertion a confirmation of an alternative embryological etiology?

Respiratory disease and sero-epidemiology of respiratory pathogens in the working horses of Ethiopia.

Modified tubularized incised plate urethroplasty in distal hypospadias repair: Stepwise technique with validated functional and cosmetic outcome.

Global minimally invasive pyeloplasty study in children: Results from the Pediatric Urology Expert Group of the European Association of Urology Young Academic Urologists working party.

A multigene family in Calothrix sp. PCC 7601 encodes phycocyanin, the major component of the cyanobacterial light-harvesting antenna

Mutants of Schizosaccharomyces pombe which sporulate in the haploid state.

The chloroplast genomes of conifers lack one of the rRNA-encoding inverted repeats.

Multiple mutant analysis of recombination in yeast.

Intergenic suppression of spoO phenotypes by the Bacillus subtilis mutation rvtA.

Expression of the seqA gene is negatively modulated by the HU protein in Escherichia coli.

A Normal Phenotype Case of a Small Supernumerary Marker Chromosome Chimeric Carrier with 12p11.21p11.21 Duplication.

Audiological Features in Pendred Syndrome: A Scoping Review.

Synergistic Interaction Between PEAR1-FGB and the Dominant Role of ABCB1 in Thrombosis Risk: A SHAP and MDR-Based Study in Vietnamese Pedigrees.

Mitochondrial Function-Related Genes in Sleep Disorders: A Multi-Omics Mendelian Randomization Study.

Xp21 contiguous gene deletion syndrome presenting as congenital adrenal hypoplasia: molecular diagnosis and clinical re-evaluation of a pedigree.

Multi-trait GWAS identifies pleiotropic loci shared between early pregnancy bleeding and psychiatric traits.

Related Experiment Videos

Intragenic mapping of the Neurospora pyrimidine-3 locus by functional deletions

Related Concept Videos

Related Articles