Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state - Wikidata - wikimedia - TriplyDB

Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state

Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state

http://www.wikidata.org/entity/Q35946576

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The Structure of the Cataract-Causing P23T Mutant of Human γD-Crystallin Exhibits Distinctive Local Conformational and Dynamic Changes † , ‡Interplay of interlocus gene conversion and crossover in segmental duplications under a neutral scenario.Cat-Map: putting cataract on the map A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family.A novel mutation in γD-crystallin associated with autosomal dominant congenital cataract in a Chinese family The βγ-crystallins: native state stability and pathways to aggregation.Crystalline cataract caused by a heterozygous missense mutation in γD-crystallin (CRYGD).Fast multi-blind modification search through tandem mass spectrometry Novel mutations in CRYGD are associated with congenital cataracts in Chinese families.Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts.The human crystallin gene families Congenital cataracts and their molecular genetics A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea Founder heterozygous P23T CRYGD mutation associated with cerulean (and coralliform) cataract in 2 Saudi families.A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract A nonsense mutation of γD-crystallin associated with congenital nuclear and posterior polar cataract in a Chinese family.Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.Cuckoo search epistasis: a new method for exploring significant genetic interactions.Sodium 4-phenylbutyrate ameliorates the effects of cataract-causing mutant gammaD-crystallin in cultured cells.Discovery of proteomic code with mRNA assisted protein folding.A missense mutation in CRYGD linked with autosomal dominant congenital cataract of aculeiform type.

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P2860

Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state

http://www.wikidata.org/entity/Q35946576

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Conversion and compensatory ev ...... YGD gene to an ancestral state

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Conversion and compensatory ev ...... YGD gene to an ancestral state

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Conversion and compensatory ev ...... YGD gene to an ancestral state

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Conversion and compensatory ev ...... YGD gene to an ancestral state

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Conversion and compensatory ev ...... YGD gene to an ancestral state

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Anastasia P Grigorenko

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Evgeny I Rogaev

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Evgeny K Ginter

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Fyodor A Kondrashov

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Olga V Plotnikova

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Peter K Vlasov

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P2860

Progressive juvenile-onset punctate cataracts caused by mutation of the gammaD-crystallin gene

Novel mutations in the gamma-crystallin genes cause autosomal dominant congenital cataracts

Gamma-D crystallin gene (CRYGD) mutation causes autosomal dominant congenital cerulean cataracts

Gamma-crystallins of the human eye lens: expression analysis of five members of the gene family

A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD

The UCSC Genome Browser Database: update 2006

A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2

The gamma-crystallins and human cataracts: a puzzle made clearer

MUSCLE: multiple sequence alignment with high accuracy and high throughput

Structural and evolutionary relationships among five members of the human gamma-crystallin gene family

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10.1086/518616

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