Membrane‐enriched solute carrier family 2 member 1 (SLC2A1/GLUT1) in psoriatic keratinocytes confers sensitivity to 2‐deoxy‐D‐glucose (2‐DG) treatment
Sign Up to like & getrecommendations! Published in 2019 at "Experimental Dermatology"
DOI: 10.1111/exd.13850
Abstract: Psoriasis is a common chronic disease with accelerated epidermal cell growth. Solute carrier family 2 member 1 (SLC2A1), also named GLUT1, transports glucose and its analogues into cells. With elevated membrane‐bound GLUT1, psoriatic keratinocytes uptake… read more here.
Keywords: family member; member slc2a1; solute carrier; glut1 psoriatic ... See more keywords
Solute carrier family 11 member 1 genetic polymorphisms rs17235409 and rs3731865 associate with susceptibility to extremity post‐traumatic osteomyelitis in a Chinese Han population
Sign Up to like & getrecommendations! Published in 2023 at "International Journal of Immunogenetics"
DOI: 10.1111/iji.12620
Abstract: Genetic variations in the solute carrier family 11 member 1 (SLC11A1) gene have been implicated in developing inflammatory disorders. However, it is still unclear whether such polymorphisms contribute to the pathogenesis of post‐traumatic osteomyelitis (PTOM).… read more here.
Keywords: solute carrier; rs17235409 rs3731865; carrier family; ptom ... See more keywords
Comprehensive Analysis and Validation of Solute Carrier Family 25 (SLC25) and Its Correlation with Immune Infiltration in Pan-Cancer
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DOI: 10.1155/2022/4009354
Abstract: As the largest gene family functioning in protein transport among human solute carriers, the SLC25 family (mitochondrial carrier family) can participate in development of cancer. However, a comprehensive exploration for the exactly roles of SLC… read more here.
Keywords: family; validation; slc25 family; carrier family ... See more keywords
Maternal Primary Carnitine Deficiency and a Novel Solute Carrier Family 22 Member 5 (SLC22A5) Mutation
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DOI: 10.1177/23247096211019543
Abstract: Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder caused by loss of function mutations in the solute carrier family 22 member 5 (SLC22A5) gene that encodes a high-affinity sodium-ion–dependent organic cation transporter protein… read more here.
Keywords: carnitine deficiency; solute carrier; carrier family; primary carnitine ... See more keywords
Solute Carrier Family 7 Member 11 (SLC7A11) is a Potential Prognostic Biomarker in Uterine Corpus Endometrial Carcinoma
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DOI: 10.2147/ijgm.s398351
Abstract: Background Uterine corpus endometrial carcinoma (UCEC) is a common type of gynecological cancers, second only to cervical cancer in incidence. Thus, it is necessary to develop effective therapies and identify biomarkers for its prognosis. Solute… read more here.
Keywords: solute carrier; endometrial carcinoma; uterine corpus; carrier family ... See more keywords
Emerging Roles in the Biogenesis of Cytochrome c Oxidase for Members of the Mitochondrial Carrier Family
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DOI: 10.3389/fcell.2019.00003
Abstract: The mitochondrial carrier family (MCF) is a group of transport proteins that are mostly localized to the inner mitochondrial membrane where they facilitate the movement of various solutes across the membrane. Although these carriers represent… read more here.
Keywords: cytochrome oxidase; family; mitochondrial carrier; carrier ... See more keywords