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Doberať si legenda slnečnica fluck adn pandey nature genetics 2004 diera výpad aktivácia

Investigating the Secretome | Circulation: Cardiovascular Genetics
Investigating the Secretome | Circulation: Cardiovascular Genetics

Genomic spectra of biliary tract cancer | Nature Genetics
Genomic spectra of biliary tract cancer | Nature Genetics

Identification and Prioritization of PET Neuroimaging Targets for  Microglial Phenotypes Associated with Microglial Activity in Alzheimer's  Disease | ACS Chemical Neuroscience
Identification and Prioritization of PET Neuroimaging Targets for Microglial Phenotypes Associated with Microglial Activity in Alzheimer's Disease | ACS Chemical Neuroscience

Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic  Scholar
Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic Scholar

Pathogens | Free Full-Text | A Landscape of CRISPR/Cas Technique for  Emerging Viral Disease Diagnostics and Therapeutics: Progress and Prospects
Pathogens | Free Full-Text | A Landscape of CRISPR/Cas Technique for Emerging Viral Disease Diagnostics and Therapeutics: Progress and Prospects

Genetics of Osteoporosis – topic of research paper in Biological sciences.  Download scholarly article PDF and read for free on CyberLeninka open  science hub.
Genetics of Osteoporosis – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.

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]

PDF) Identification and characterization of cytosolic malate dehydrogenase  from the liver fluke Fasciola gigantica
PDF) Identification and characterization of cytosolic malate dehydrogenase from the liver fluke Fasciola gigantica

P450 oxidoreductase deficiency - a new form of congenital adrenal  hyperplasia. | Semantic Scholar
P450 oxidoreductase deficiency - a new form of congenital adrenal hyperplasia. | Semantic Scholar

Fine mapping analysis confirms and strengthens linkage of four chromosomal  regions in familial hypospadias | European Journal of Human Genetics
Fine mapping analysis confirms and strengthens linkage of four chromosomal regions in familial hypospadias | European Journal of Human Genetics

Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A  and PBRM1 in intrahepatic cholangiocarcinomas | Nature Genetics
Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas | Nature Genetics

Exome sequencing identifies distinct mutational patterns in liver fluke–related  and non-infection-related bile duct cancers | Nature Genetics
Exome sequencing identifies distinct mutational patterns in liver fluke–related and non-infection-related bile duct cancers | Nature Genetics

Mutant P450 oxidoreductase causes disordered steroidogenesis with and  without Antley-Bixler syndrome | Nature Genetics
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome | Nature Genetics

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
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

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
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

PDF) P450 oxidoreductase deficiency: a new disorder of steroidogenesis  affecting all microsomal P450 enzymes | Amit Pandey - Academia.edu
PDF) P450 oxidoreductase deficiency: a new disorder of steroidogenesis affecting all microsomal P450 enzymes | Amit Pandey - Academia.edu

Frontiers | A CYPome-wide study reveals new potential players in the  pathogenesis of Parkinson's disease
Frontiers | A CYPome-wide study reveals new potential players in the pathogenesis of Parkinson's disease

Phosphoproteome Analysis of Drosophila melanogaster Embryos | Journal of  Proteome Research
Phosphoproteome Analysis of Drosophila melanogaster Embryos | Journal of Proteome Research

Frontiers | Low-Input High-Molecular-Weight DNA Extraction for Long-Read  Sequencing From Plants of Diverse Families
Frontiers | Low-Input High-Molecular-Weight DNA Extraction for Long-Read Sequencing From Plants of Diverse Families

PDF) Human P450 Oxidoreductase Deficiency
PDF) Human P450 Oxidoreductase Deficiency

EMQN best practice guidelines for molecular genetic testing and reporting  of 21-hydroxylase deficiency | European Journal of Human Genetics
EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency | European Journal of Human Genetics

PDF) Loss of multiple enzyme activities due to the human genetic variation  P284T in NADPH cytochrome P450 oxidoreductase
PDF) Loss of multiple enzyme activities due to the human genetic variation P284T in NADPH cytochrome P450 oxidoreductase

Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic  Scholar
Genetic and Clinical Features of P450 Oxidoreductase Deficiency | Semantic Scholar

Drug Metabolism: A Half-Century Plus of Progress, Continued Needs, and New  Opportunities | Drug Metabolism & Disposition
Drug Metabolism: A Half-Century Plus of Progress, Continued Needs, and New Opportunities | Drug Metabolism & Disposition

Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD  Phenotype | PLOS ONE
Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype | PLOS ONE