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carbonic anhydrase Ⅱ deficiency相关文献:
Carbonic Anhydrase VA Deficiency.
van Karnebeek C, Häberle J.
2015 Apr 2 [updated 2021 Aug 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID:25834911
Carbonic anhydrase II deficiency.
Whyte MP.
Bone. 2023 Apr;169:116684. doi: 10.1016/j.bone.2023.116684. Epub 2023 Jan 27.
PMID:36709914
Primate-conserved carbonic anhydrase IV and murine-restricted LY6C1 enable blood-brain barrier crossing by engineered viral vectors.
Shay TF, Sullivan EE, Ding X, Chen X, Ravindra Kumar S, Goertsen D, Brown D, Crosby A, Vielmetter J, Borsos M, Wolfe DA, Lam AW, Gradinaru V.
Sci Adv. 2023 Apr 21;9(16):eadg6618. doi: 10.1126/sciadv.adg6618. Epub 2023 Apr 19.
PMID:37075114
Squalene Epoxidase Induces Nonalcoholic Steatohepatitis Via Binding to Carbonic Anhydrase III and is a Therapeutic Target.
Liu D, Wong CC, Zhou Y, Li C, Chen H, Ji F, Go MYY, Wang F, Su H, Wei H, Cai Z, Wong N, Wong VWS, Yu J.
Gastroenterology. 2021 Jun;160(7):2467-2482.e3. doi: 10.1053/j.gastro.2021.02.051. Epub 2021 Feb 27.
PMID:33647280
Gastric carbonic anhydrase IX deficiency: At base, it is all about acid.
Akiba Y, Kaunitz JD.
Acta Physiol (Oxf). 2018 Apr;222(4):e13047. doi: 10.1111/apha.13047. Epub 2018 Feb 21.
PMID:29389066
Carbonic anhydrase.
Maren TH.
N Engl J Med. 1985 Jul 18;313(3):179-81. doi: 10.1056/NEJM198507183130309.
PMID:3925338
Carbonic Anhydrase II Activators in Osteopetrosis Treatment: A Review.
Alkhayal Z, Shinwari Z, Gaafar A, Alaiya A.
Curr Issues Mol Biol. 2023 Feb 6;45(2):1373-1386. doi: 10.3390/cimb45020089.
PMID:36826034
Acetazolamide and sulfonamide allergy: a not so simple story.
Kelly TE, Hackett PH.
High Alt Med Biol. 2010 Winter;11(4):319-23. doi: 10.1089/ham.2010.1051.
PMID:21190500
Anti-carbonic anhydrase antibodies in iron deficiency anemia.
Menteşe A, Erkut N, Sümer A, Us Altay D, Alver A, Sönmez M.
Hematology. 2015 Jul;20(6):363-7. doi: 10.1179/1607845414Y.0000000204. Epub 2014 Oct 6.
PMID:25283602
Carbonic anhydrase II deficiency syndrome with amelogenesis imperfecta linked to a homozygous CA2 deletion.
Leite LDR, Resende KKM, Rosa LDS, Mazzeu JF, de Oliveira LC, Scher MDCSD, Acevedo AC, Yamaguti PM.
Intractable Rare Dis Res. 2023 Aug;12(3):202-205. doi: 10.5582/irdr.2023.01033.
PMID:37662627
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