Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
about
Increased expression of MERTK is associated with a unique form of canine retinopathyHuman iPSC derived disease model of MERTK-associated retinitis pigmentosaA novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa.A non-stop S-antigen gene mutation is associated with late onset hereditary retinal degeneration in dogs.Preclinical potency and safety studies of an AAV2-mediated gene therapy vector for the treatment of MERTK associated retinitis pigmentosa.Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations.Rescue of the MERTK phagocytic defect in a human iPSC disease model using translational read-through inducing drugs.TAM receptor tyrosine kinases as emerging targets of innate immune checkpoint blockade for cancer therapy.Otx2-Genetically Modified Retinal Pigment Epithelial Cells Rescue Photoreceptors after Transplantation.Gene therapy and genome surgery in the retina.GAS6/TAM Pathway Signaling in Hemostasis and Thrombosis.
P2860
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P2860
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@en
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@nl
type
label
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@en
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@nl
prefLabel
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@en
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@nl
P2093
P356
P1476
Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.
@en
P2093
Béatrice Bocquet
Christian P Hamel
Estèle Lafont
Isabelle Meunier
Mohamed Ksantini
P304
P356
10.5301/EJO.5000096
P577
2012-07-01T00:00:00Z