Review on DKC1 (dyskeratosis congenita 1, dyskerin), with data on DNA, on the protein encoded, and where the gene is implicated
Review on CDT1 (chromatin licensing and DNA replication factor 1), with data on DNA, on the protein ...
We report the precise mapping and characterization of the genomic structure of the human homolog of ...
Review on CTSL1 (cathepsin L1), with data on DNA, on the protein encoded, and where the gene is impl...
Review on Dyskeratosis congenita (DKC), with data on clinics, and the genes involved
Dyskeratosis congenita (DKC) is a rare, heritable multisystem disorder which is mainly characterized...
Review on PKD1 (protein kinase D1), with data on DNA, on the protein encoded, and where the gene is ...
Review on DEK (DEK oncogene), with data on DNA, on the protein encoded, and where the gene is implic...
Review on CKS1B (CDC28 protein kinase regulatory subunit 1B), with data on DNA, on the protein encod...
Background: The human DKC1 gene is causative of X-linked dyskeratosis congenita (X-DC), a syndrome c...
SummaryDyskeratosis congenita is a rare inherited bone marrow–failure syndrome characterized by abno...
Review on DYRK1B (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B), with data on D...
Review on DAPK1 (death-associated protein kinase 1), with data on DNA, on the protein encoded, and w...
Mutations in the highly conserved human DKC1 gene cause the rare genetic disease X-linked recessive ...
Dyskeratosis congenita (DKC) is a rare and fatal congenital syndrome characterized by the triad of r...
Review on PKD1 (polycystic kidney disease 1 (autosomal dominant)), with data on DNA, on the protein ...
Review on CDT1 (chromatin licensing and DNA replication factor 1), with data on DNA, on the protein ...
We report the precise mapping and characterization of the genomic structure of the human homolog of ...
Review on CTSL1 (cathepsin L1), with data on DNA, on the protein encoded, and where the gene is impl...
Review on Dyskeratosis congenita (DKC), with data on clinics, and the genes involved
Dyskeratosis congenita (DKC) is a rare, heritable multisystem disorder which is mainly characterized...
Review on PKD1 (protein kinase D1), with data on DNA, on the protein encoded, and where the gene is ...
Review on DEK (DEK oncogene), with data on DNA, on the protein encoded, and where the gene is implic...
Review on CKS1B (CDC28 protein kinase regulatory subunit 1B), with data on DNA, on the protein encod...
Background: The human DKC1 gene is causative of X-linked dyskeratosis congenita (X-DC), a syndrome c...
SummaryDyskeratosis congenita is a rare inherited bone marrow–failure syndrome characterized by abno...
Review on DYRK1B (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1B), with data on D...
Review on DAPK1 (death-associated protein kinase 1), with data on DNA, on the protein encoded, and w...
Mutations in the highly conserved human DKC1 gene cause the rare genetic disease X-linked recessive ...
Dyskeratosis congenita (DKC) is a rare and fatal congenital syndrome characterized by the triad of r...
Review on PKD1 (polycystic kidney disease 1 (autosomal dominant)), with data on DNA, on the protein ...
Review on CDT1 (chromatin licensing and DNA replication factor 1), with data on DNA, on the protein ...
We report the precise mapping and characterization of the genomic structure of the human homolog of ...
Review on CTSL1 (cathepsin L1), with data on DNA, on the protein encoded, and where the gene is impl...
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