Chromosome structure deficiencies in MCPH1 syndrome.

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The human Cranio Facial Development Protein 1 (Cfdp1) gene encodes a protein required for the maintenance of higher-order chromatin organization.MCPH1, mutated in primary microcephaly, is required for efficient chromosome alignment during mitosis.

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Chromosome structure deficiencies in MCPH1 syndrome.

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http://www.wikidata.org/entity/Q41928351

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Chromosome structure deficiencies in MCPH1 syndrome.

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Item

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Chromosome structure deficiencies in MCPH1 syndrome.

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Chromosome structure deficiencies in MCPH1 syndrome.

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Chromosome structure deficiencies in MCPH1 syndrome.

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A Sánchez

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H Neitzel

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J A Marchal

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M Arroyo

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M Trimborn

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T Hirano

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Differential contributions of condensin I and condensin II to mitotic chromosome architecture in vertebrate cells

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

Precocious sister chromatid separation (PSCS) in Cornelia de Lange syndrome

Mutation in PHC1 implicates chromatin remodeling in primary microcephaly pathogenesis

Autosomal Recessive Primary Microcephaly (MCPH): clinical manifestations, genetic heterogeneity and mutation continuum

Dual recognition of phosphoserine and phosphotyrosine in histone variant H2A.X by DNA damage response protein MCPH1

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s00412-015-0512-2

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491-501

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scholarly article

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10.1007/S00412-015-0512-2

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124

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2015-04-07T00:00:00Z

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Chromosome structure deficiencies in MCPH1 syndrome.

about

P2860

P2860

Chromosome structure deficiencies in MCPH1 syndrome.

description

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P698