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Unknown
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Genomics
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Homo sapiens
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EGA
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Illumina HumanCNV370, Illumina HumanHap 300 v2 Duo, Taqman and sequencing, Illumina Human660W-Quad
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Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
Not available
S-EPMC9145262
|
biostudies-literature
Cite
Co-culture of human fibroblasts, smooth muscle and endothelial cells promotes osteopontin induction in hypoxia.
Not available
S-EPMC7077551
|
biostudies-literature
Cite
Spironolactone metabolite concentrations in decompensated heart failure: insights from the ATHENA-HF trial.
Not available
S-EPMC7958586
|
biostudies-literature
Cite
Females present higher dose-adjusted drug concentrations of metoprolol and allopurinol/oxypurinol than males.
Not available
S-EPMC10175982
|
biostudies-literature
Cite
A Genome-Wide Association Study of Oxypurinol Concentrations in Patients Treated with Allopurinol
Not available
S-EPMC11204675
|
biostudies-literature
Cite
Circulating tumor DNA as a non-invasive substitute to metastasis biopsy for tumor genotyping and personalized medicine in a prospective trial across all tumor types.
Not available
S-EPMC5528781
|
biostudies-literature
Cite
Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness.
Not available
S-EPMC4121477
|
biostudies-literature
Cite
5' Region Large Genomic Rearrangements in the
BRCA1
Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.
Not available
S-EPMC8268747
|
biostudies-literature
Cite
MELARISK_SNP_MITF_geno
Genotypes at MITF E318K variant
EGAD00000000122
|
EGA
Cite
MELARISK_MITF_geno
Genotypes at MITF E318K variant
EGAD00000000121
|
EGA
Cite
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