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Hmg20a - RPE65 null mutant model of Leber's congenital amaurosis
GEO DataSets Gene Profile neighbors Chromosome neighbors Homologene neighbors
Hmg20a - TGF-beta receptor type II knockdown effect on embryonic palatal tissue
Hmg20a - Transcription factor Sp3 deficiency effect on the embryonic heart
Hmg20a - Homeobox Dlx1/2 mutations effect on embryonic telencephalon
Hmg20a - Pubertal mammary gland development
Hmg20a - Rod-derived cone viability factor deficiency effect on the retina
Hmg20a - D-3-phosphoglycerate dehydrogenase deficiency effect on the embryonic head
Hmg20a - p300 genetic reduction model of Rubinstein-Taybi syndrome: hippocampus
Hmg20a - Homeobox Lim1 mutant nephron-deficient kidneys
Hmg20a - Polycomb group protein Ezh2 deficiency effect on lymph node T cells
Hmg20a - SIRT1 deficiency effect on the brain
Hmg20a - Aquaporin-11 deficiency effect on the kidney
Hmg20a - Morphine effect on the striatum
Hmg20a - Retinoic acid effect on CD4+ T cells from spleen/lymph nodes
Hmg20a - Estrogen effect on estrogen receptors alpha and beta single knockouts: aorta
Hmg20a - SOD1-G93A transgenic model of amyotrophic lateral sclerosis: oculomotor nucleus
Hmg20a - All-trans retinoic acid effect on retinoic acid receptor α-deficient F9 teratocarcinoma cells
Hmg20a - Aged, lupus-prone MRL/Faslpr model: splenic CD4 T cells
Hmg20a - Skeletal muscle synaptic region
Hmg20a - Furin deficiency effect on T-cells
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