H H Dahl
University of Melbourne(AU)
Publications by Year
Research Areas
Metabolism and Genetic Disorders, Mitochondrial Function and Pathology, Biochemical Acid Research Studies, Biochemical and Molecular Research, Folate and B Vitamins Research
Most-Cited Works
- → Leigh syndrome: Clinical features and biochemical and DNA abnormalities(1996)777 cited
- → A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment(2005)338 cited
- → The construction of cosmid libraries which can be used to transform eukaryotic cells(1982)316 cited
- → Respiratory chain complex I deficiency(1999)265 cited
- → The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA.(1987)142 cited
- → Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis(2013)128 cited
- → Mitochondrial DNA mutations at nucleotide 8993 show a lack of tissue‐ or age‐related variation(1999)111 cited
- → Characterization of the Polypeptide Composition of Human Factor VIII:C and the Nucleotide Sequence and Expression of the Human Kidney cDNA(1985)104 cited
- → Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites.(1986)89 cited
- → Structure and expression of a cloned β°thalassaemic globin gene(1981)85 cited