X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
mutation (7) 7
index medicus (6) 6
genetics (5) 5
humans (5) 5
life sciences (5) 5
eye diseases (4) 4
female (4) 4
genetic aspects (4) 4
genetic structures (4) 4
genetics & heredity (4) 4
male (4) 4
retina (4) 4
sense organs (4) 4
analysis (3) 3
blindness (3) 3
genotyping (3) 3
human health and pathology (3) 3
pedigree (3) 3
phenotype (3) 3
phenotypes (3) 3
retinitis pigmentosa - genetics (3) 3
retinitis-pigmentosa (3) 3
[ sdv.gen ] life sciences [q-bio]/genetics (2) 2
[ sdv.mhep.os ] life sciences [q-bio]/human health and pathology/sensory organs (2) 2
acuity (2) 2
alpha-subunit (2) 2
animals (2) 2
color vision (2) 2
cone-rod dystrophy (2) 2
deoxyribonucleic acid--dna (2) 2
disease (2) 2
dna sequencing (2) 2
dystrophy (2) 2
electroretinography (2) 2
fundus autofluorescence (2) 2
genes (2) 2
genes, recessive (2) 2
genetic research (2) 2
genotype & phenotype (2) 2
genotype-phenotype correlation (2) 2
genotypes (2) 2
human genetics (2) 2
medicine (2) 2
medicine, research & experimental (2) 2
mutations (2) 2
next-generation sequencing (2) 2
nucleotide sequencing (2) 2
photoreceptors (2) 2
protein (2) 2
recessive retinitis-pigmentosa (2) 2
research (2) 2
retinal degeneration (2) 2
retinitis pigmentosa (2) 2
sensory organs (2) 2
[ sdv.gen.gh ] life sciences [q-bio]/genetics/human genetics (1) 1
[ sdv.mhep ] life sciences [q-bio]/human health and pathology (1) 1
abca4 (1) 1
abca4 abcr gene (1) 1
abridged index medicus (1) 1
adult (1) 1
alleles (1) 1
amino acid sequence (1) 1
article (1) 1
article subject (1) 1
autosomal-recessive cone (1) 1
base sequence (1) 1
beta-subunit (1) 1
binocular vision (1) 1
biochemistry & molecular biology (1) 1
biology (1) 1
biotechnology & applied microbiology (1) 1
blood mononuclear-cells (1) 1
c-mer tyrosine kinase - genetics (1) 1
care and treatment (1) 1
cell cycle proteins - genetics (1) 1
cgmp-phosphodiesterase (1) 1
channel (1) 1
chemistry (1) 1
chemistry, multidisciplinary (1) 1
ciliogenesis (1) 1
ciliopathies (1) 1
codon, nonsense (1) 1
cohort studies (1) 1
cone dystrophy (1) 1
congenital diseases (1) 1
congenital stationary night blindness (1) 1
core (1) 1
deep-intronic variants (1) 1
defects (1) 1
diagnosis (1) 1
digestive system diseases (1) 1
dna copy number variations (1) 1
dna microarrays (1) 1
dominant cone (1) 1
dominant retinitis-pigmentosa (1) 1
dynamics (1) 1
electroretinogram (1) 1
electroretinograms (1) 1
epithelium (1) 1
exome (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 4180 - 8
Hepatitis C virus (HCV) genotype and subtype (1a/1b) identification is needed to tailor anti-HCV therapy. Currently available methods accurately identify the... 
CORE | SUBTYPES | MULTIDISCIPLINARY SCIENCES | HCV GENOTYPE | PATTERNS | INFECTION | IDENTIFICATION | TIME PCR ASSAY | Performance evaluation | Genotype & phenotype | Hepatitis | Genotyping | Genomes | Phylogeny | Hepatitis C | Genotypes
Journal Article
Journal Article
Clinical Genetics, ISSN 0009-9163, 06/2016, Volume 89, Issue 6, pp. 690 - 699
Congenital stationary night blindness ( CSNB ) is a clinically and genetically heterogeneous retinal disorder which represents rod photoreceptor dysfunction or... 
SLC24A1 | high‐throughput sequencing | congenital stationary night blindness | humans | Congenital stationary night blindness | High-throughput sequencing | Humans | RHODOPSIN GENE | ALPHA-SUBUNIT | CHANNEL | PATHOGENIC MECHANISMS | ROD TRANSDUCIN | GENETICS & HEREDITY | MISSENSE MUTATION | ELECTRORETINOGRAM | CONE DYSTROPHY | NA/CA-K EXCHANGER | NA+/CA2+-K+ EXCHANGERS | high-throughput sequencing | Eye Diseases, Hereditary - diagnosis | Family Health | Male | Sodium-Calcium Exchanger - genetics | Base Sequence | Myopia - diagnosis | Female | Genetic Diseases, X-Linked - genetics | High-Throughput Nucleotide Sequencing - methods | Night Blindness - genetics | Genetic Diseases, X-Linked - physiopathology | Electroretinography | Amino Acid Sequence | Genetic Predisposition to Disease - genetics | Eye Diseases, Hereditary - physiopathology | Night Blindness - diagnosis | Genes, Recessive | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Myopia - genetics | Sequence Homology, Amino Acid | Homozygote | Exome - genetics | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Mutation | Analysis | Genomics | Genetic disorders | Retina | Photoreceptors | Eye diseases | Congenital diseases | Blindness | Index Medicus | Life Sciences | Human health and pathology | Genetics
Journal Article
Journal of Antimicrobial Chemotherapy, ISSN 0305-7453, 2018, Volume 73, Issue 11, pp. 3122 - 3128
Background: Standard genotypic tests performed on HIV DNA from patients on suppressive ART, with previous resistance-associated mutations (RAMs) detected in... 
INFECTIOUS DISEASES | GENOTYPIC TEST | RESERVOIR | MICROBIOLOGY | BLOOD MONONUCLEAR-CELLS | LONG-TERM HAART | THERAPY | IMMUNODEFICIENCY-VIRUS TYPE-1 | DYNAMICS | PHARMACOLOGY & PHARMACY | MUTATIONS | PROVIRAL DNA | PROTEASE
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.