Genetics of Osteoporosis – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Identification of a self‐sufficient cytochrome P450 monooxygenase from Cupriavidus pinatubonensis JMP134 involved in 2‐hydroxyphenylacetic acid catabolism, via homogentisate pathway - Donoso - 2021 - Microbial Biotechnology - Wiley Online Library
EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics
Frontiers | Low-Input High-Molecular-Weight DNA Extraction for Long-Read Sequencing From Plants of Diverse Families
Identification and Prioritization of PET Neuroimaging Targets for Microglial Phenotypes Associated with Microglial Activity in Alzheimer's Disease | ACS Chemical Neuroscience
Proteogenomic studies in epithelial ovarian cancer: established knowledge and future needs | Biomarkers in Medicine
Efficient Incorporation of Protein Flexibility and Dynamics into Molecular Docking Simulations | Biochemistry
Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas | Nature Genetics
PDF) Differential effects on human cytochromes P450 by CRISPR/Cas9-induced genetic knockout of cytochrome P450 reductase and cytochrome b5 in HepaRG cells
PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase
High-quality reference genome of Fasciola gigantica: Insights into the genomic signatures of transposon-mediated evolution and specific parasitic adaption in tropical regions | PLOS Neglected Tropical Diseases
Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic Scholar
Animals | Free Full-Text | One Health and Cattle Genetic Resources: Mining More than 500 Cattle Genomes to Identify Variants in Candidate Genes Potentially Affecting Coronavirus Infections
Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype | PLOS ONE
Frontiers | A CYPome-wide study reveals new potential players in the pathogenesis of Parkinson's disease
Amit V Pandey – Group Leader – University of Bern | LinkedIn
A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics | European Journal of Human Genetics
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia. | Semantic Scholar
PDF) Human P450 Oxidoreductase Deficiency
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome | Nature Genetics
Differential effects on human cytochromes P450 by CRISPR/Cas9-induced genetic knockout of cytochrome P450 reductase and cytochrome b5 in HepaRG cells | Scientific Reports
Biology | Free Full-Text | Effects of the Density of Invasive Lantana camara Plants on the Biodiversity of Large and Small Mammals in the Groenkloof Nature Reserve (GNR) in South Africa
Pathogens | Free Full-Text | A Landscape of CRISPR/Cas Technique for Emerging Viral Disease Diagnostics and Therapeutics: Progress and Prospects
Phosphoproteome Analysis of Drosophila melanogaster Embryos | Journal of Proteome Research
Incorporating marine macrophytes in plant–soil feedbacks: Emerging evidence and opportunities to advance the field - Piercey - 2021 - Journal of Ecology - Wiley Online Library
IJMS | Free Full-Text | Variants of STAR, AMH and ZFPM2/FOG2 May Contribute towards the Broad Phenotype Observed in 46,XY DSD Patients with Heterozygous Variants of NR5A1
