Missense-Mutationen in Transkriptionsfaktoren - Wikidata - wikimedia - TriplyDB

Missense-Mutationen in Transkriptionsfaktoren

Missense-Mutationen in Transkriptionsfaktoren

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Missense-Mutationen in Transkriptionsfaktoren

http://www.wikidata.org/entity/Q56974756

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wetenschappelijk artikel

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наукова стаття, опублікована в березні 2015

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name

Missense-Mutationen in Transkriptionsfaktoren

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Missense-Mutationen in Transkriptionsfaktoren

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Missense-Mutationen in Transkriptionsfaktoren

@en

Missense-Mutationen in Transkriptionsfaktoren

@nl

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Missense-Mutationen in Transkriptionsfaktoren

@en

Missense-Mutationen in Transkriptionsfaktoren

@nl

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S11825-015-0034-6

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medizinische genetik

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Missense-Mutationen in Transkriptionsfaktoren

@en

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Identification of a dominant negative homeodomain mutation in Rieger syndrome

Dominant negative dimerization of a mutant homeodomain protein in Axenfeld-Rieger syndrome

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

Different TBX5 interactions in heart and limb defined by Holt-Oram syndrome mutations

Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation

Arrested development of embryonic red cell precursors in mouse embryos lacking transcription factor GATA-1

Distinct global shifts in genomic binding profiles of limb malformation-associated HOXD13 mutations

ChIP-seq: advantages and challenges of a maturing technology

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s11825-015-0034-6

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1-6

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scholarly article

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10.1007/S11825-015-0034-6

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1

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27

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Daniel M. Ibrahim

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2015-03-01T00:00:00Z

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