SLC4A11 抗体
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Latest Publications for our SLC4A11 抗体
: "SLC4A11 mutations in Fuchs endothelial corneal dystrophy." in: Human molecular genetics, Vol. 17, Issue 5, pp. 656-66, (2008) (PubMed).: "Identification of mutations in the SLC4A11 gene in patients with recessive congenital hereditary endothelial dystrophy." in: Archives of ophthalmology (Chicago, Ill. : 1960), Vol. 126, Issue 5, pp. 700-8, (2008) (PubMed).
: "Autosomal recessive corneal endothelial dystrophy (CHED2) is associated with mutations in SLC4A11." in: Journal of medical genetics, Vol. 44, Issue 1, pp. 64-8, (2007) (PubMed).
: "Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy." in: Journal of medical genetics, Vol. 44, Issue 5, pp. 322-6, (2007) (PubMed).
: "Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)." in: Nature genetics, Vol. 38, Issue 7, pp. 755-7, (2006) (PubMed).
: "NaBC1 is a ubiquitous electrogenic Na+ -coupled borate transporter essential for cellular boron homeostasis and cell growth and proliferation." in: Molecular cell, Vol. 16, Issue 3, pp. 331-41, (2004) (PubMed).
: "Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney." in: Biochemical and biophysical research communications, Vol. 282, Issue 5, pp. 1103-9, (2001) (PubMed).
Aliases for SLC4A11 抗体
solute carrier family 4 member 11 (Slc4a11) 抗体solute carrier family 4 member 11 (SLC4A11) 抗体
solute carrier family 4 member 11 L homeolog (slc4a11.L) 抗体
solute carrier family 4 member 11 (slc4a11) 抗体
solute carrier family 4, sodium borate transporter, member 11 (slc4a11) 抗体
solute carrier family 4, sodium bicarbonate transporter-like, member 11 (Slc4a11) 抗体
AI503023 抗体
BTR1 抗体
CDPD1 抗体
CHED2 抗体
dJ794I6.2 抗体
NaBC1 抗体
NABC1 抗体
si:dkey-12j14.4 抗体