Topic: Base Sequence
Journal: Human Molecular Genetics
Documents
A list of abstracts that contain a topic of "Base Sequence" and a journal name of "Human Molecular Genetics".
Acquisition of the Wobble Modification in Mitochondrial Trnaleu(Cun) Bearing the G12300a Mutation Suppresses the Melas Molecular Defect.
PMID: 16446307
A Common Haplotype of the Annexin A5 (Anxa5) Gene Promoter is Associated with Recurrent Pregnancy Loss.
PMID: 17339269
In-frame Deletion in a Novel Centrosomal/Ciliary Protein Cep290/Nphp6 Perturbs Its Interaction with Rpgr and Results in Early-onset Retinal Degeneration in the Rd16 Mouse.
PMID: 16632484
The Molecular Basis for Tissue Specificity of the Oxidative Phosphorylation Deficiencies in Patients with Mutations in the Mitochondrial Translation Factor Efg1.
PMID: 16632485
Identification of the Transcription Factor Arntl2 As a Candidate Gene for the Type 1 Diabetes Locus Idd6.
PMID: 16893914
Deletion of the Triplet Repeat Encoding Polyglutamine Within the Mouse Huntington's Disease Gene Results in Subtle Behavioral/Motor Phenotypes in Vivo and Elevated Levels of Atp with Cellular Senescence in Vitro.
PMID: 16403806
Unexpected Mosaicism of R201h-gnas1 Mutant-bearing Cells in the Testes Underlie Macro-orchidism Without Sexual Precocity in Mccune-albright Syndrome.
PMID: 17101633
Myc-containing Double Minutes in Hematologic Malignancies: Evidence in Favor of the Episome Model and Exclusion of Myc As the Target Gene.
PMID: 16452126