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Typical pantothenate kinase-associated neurodegeneration caused by compound heterozygous mutations in
PANK2
gene in a Chinese patient: a case report and literature review.
Not available
S-EPMC10175671
|
biostudies-literature
Cite
Case Report: Complete Maternal Uniparental Disomy of Chromosome 2 With a Novel
UNC80
Splicing Variant c.5609-4G> A in a Chinese Patient With Infantile Hypotonia With Psychomotor Retardation and Characteristic Facies 2.
Not available
S-EPMC8476880
|
biostudies-literature
Cite
The association between ADAM12 gene polymorphisms and osteoarthritis: an updated meta-analysis.
Not available
S-EPMC9974398
|
biostudies-literature
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A
GATA3
gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature review.
Not available
S-EPMC10485837
|
biostudies-literature
Cite
Novel HPD mutation p.A244V compound with p.T219M causing tyrosinemia type III in a Chinese girl and review of the genotype-phenotype spectrum.
Not available
S-EPMC10767433
|
biostudies-literature
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Association between
OPG
polymorphisms and osteoporosis risk: An updated meta-analysis.
Not available
S-EPMC9682267
|
biostudies-literature
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Correlation between vascular endothelial growth factor A gene polymorphisms and tendon and ligament injury risk: a systematic review and meta-analysis.
Not available
S-EPMC10845593
|
biostudies-literature
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Human umbilical cord mesenchymal stem cell-derived extracellular vesicles harboring IGF-1 improve ovarian function of mice with premature ovarian insufficiency through the Nrf2/HO-1 pathway.
Not available
S-EPMC11566650
|
biostudies-literature
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RNA helicase DDX5-induced circPHF14 promotes gastric cancer cell progression.
Not available
S-EPMC10120908
|
biostudies-literature
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Discovery of Novel 2,4-Dianilinopyrimidine Derivatives Containing 4-(Morpholinomethyl)phenyl and N-Substituted Benzamides as Potential FAK Inhibitors and Anticancer Agents.
Not available
S-EPMC8304610
|
biostudies-literature
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