Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype | PLOS ONE
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Drug Metabolism: A Half-Century Plus of Progress, Continued Needs, and New Opportunities | Drug Metabolism & Disposition
Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas | Nature Genetics
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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
PDF) Oligogenic Causes of Human Differences of Sex Development: Facing the Challenge of Genetic Complexity
Incorporating marine macrophytes in plant–soil feedbacks: Emerging evidence and opportunities to advance the field - Piercey - 2021 - Journal of Ecology - Wiley Online Library
Proteogenomic studies in epithelial ovarian cancer: established knowledge and future needs | Biomarkers in Medicine
Phosphoproteome Analysis of Drosophila melanogaster Embryos | Journal of Proteome Research
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
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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
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
PDF) P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymes | Amit Pandey - Academia.edu
Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic Scholar
Investigating the Secretome | Circulation: Cardiovascular Genetics
Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation | Cell Death & Disease
Genetics of Osteoporosis – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics | European Journal of Human Genetics
Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias | European Journal of Human Genetics
![Genome resequencing clarifies phylogeny and reveals patterns of selection in the toxicogenomics model Pimephales promelas [PeerJ]](https://dfzljdn9uc3pi.cloudfront.net/2022/13954/1/fig-2-full.png "Genome resequencing clarifies phylogeny and reveals patterns of selection in the toxicogenomics model Pimephales promelas [PeerJ]")
Genome resequencing clarifies phylogeny and reveals patterns of selection in the toxicogenomics model Pimephales promelas [PeerJ]
Pathogens | Free Full-Text | A Landscape of CRISPR/Cas Technique for Emerging Viral Disease Diagnostics and Therapeutics: Progress and Prospects
Exome sequencing identifies distinct mutational patterns in liver fluke–related and non-infection-related bile duct cancers | Nature Genetics
Efficient Incorporation of Protein Flexibility and Dynamics into Molecular Docking Simulations | Biochemistry
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
