Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Genetic modifiers as relevant biological variables of eye disorders.

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Q39290939-7895EA5A-B2D2-4026-8DFC-EFB066325157

P2860

Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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P1476

Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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P2093

Bo I Li

http://www.w3.org/2001/XMLSchema#string

James H Millonig

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Myka R Ababon

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Paul G Matteson

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Vikas Nanda

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Yong Lin

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P2860

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

Inorganic pyrophosphate generation and disposition in pathophysiology

The ciliary G-protein-coupled receptor Gpr161 negatively regulates the Sonic hedgehog pathway via cAMP signaling

The membrane- and soluble-protein helix-helix interactome: similar geometry via different interactions.

The inorganic pyrophosphate transporter ANK preserves the differentiated phenotype of articular chondrocyte.

Mouse models of congenital cataract.

Evaluation of methods for the prediction of membrane spanning regions.

Congenital cataract causing mutants of αA-crystallin/sHSP form aggregates and aggresomes degraded through ubiquitin-proteasome pathway.

Cadherin-6 mediates axon-target matching in a non-image-forming visual circuit.

Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

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e0170724

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scholarly article

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10.1371/JOURNAL.PONE.0170724

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English

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P478

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2017-01-30T00:00:00Z

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28135291

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P921

birth defect

P932

5279759

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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P2860

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Congenital Cataract in Gpr161vl/vl Mice Is Modified by Proximal Chromosome 15.

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932