1996 - Member of the National Academy of Sciences
His scientific interests lie mostly in Genetics, Retinitis pigmentosa, Gene, Mutation and Molecular biology. As part of his studies on Genetics, he often connects relevant areas like Rhodopsin. He has researched Rhodopsin in several fields, including Congenital stationary night blindness, Mutant and Transversion.
His Retinitis pigmentosa research integrates issues from Retinal degeneration, Missense mutation, Electroretinography and Visual phototransduction. His Molecular biology research includes elements of Retina and Exon. Thaddeus P. Dryja has included themes like Chromosome 13, Cancer research, Germline mutation and Somatic cell in his Retinoblastoma study.
His primary areas of study are Genetics, Retinitis pigmentosa, Gene, Molecular biology and Mutation. His study involves Allele, Locus, Missense mutation, Exon and Retinoblastoma, a branch of Genetics. The study incorporates disciplines such as Chromosome 13, Cancer research, DNA and Retinoblastoma gene in addition to Retinoblastoma.
His Retinitis pigmentosa study integrates concerns from other disciplines, such as Retinal degeneration, Rhodopsin and Electroretinography. His Rhodopsin research is multidisciplinary, relying on both Retina and Mutant. Molecular biology is frequently linked to Gene mutation in his study.
His primary scientific interests are in Pathology, Ophthalmology, Gene, Retina and Pharmacology. His studies deal with areas such as Hyaluronic acid, Dermal Fillers, PAX8 and Eyelid as well as Pathology. His work carried out in the field of Ophthalmology brings together such families of science as Animal model, Psychiatry and Age related.
His Gene study contributes to a more complete understanding of Genetics. Thaddeus P. Dryja interconnects Complement system, Viral vector, Nucleic acid and Cancer research in the investigation of issues within Retina. He combines subjects such as Antibody, Neutralizing antibody and Bioinformatics with his study of Pharmacology.
His primary areas of investigation include Gene, Genetics, Internal medicine, Antibody and Psoriasis. His Gene research is multidisciplinary, incorporating perspectives in Retina, Nucleic acid and Virology. His work is connected to Retinitis pigmentosa, Linkage disequilibrium, Haplotype, Single-nucleotide polymorphism and Minor allele frequency, as a part of Genetics.
His work deals with themes such as Sensorineural hearing loss and Mutation, Frameshift mutation, Exon, which intersect with Retinitis pigmentosa. His Antibody research includes themes of Receptor, Retinal, Pharmacology and Peptide. His Psoriasis research is multidisciplinary, incorporating elements of Rheumatoid arthritis, Uveitis and Rheumatology.
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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
Stephen H. Friend;Stephen H. Friend;Rene Bernards;Snezna Rogelj;Robert A. Weinberg.
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
W. K. Cavenee;W. K. Cavenee;T. P. Dryja;R. A. Phillips;William F Benedict.
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
Thaddeus P. Dryja;Terri L. McGee;Elias Reichel;Lauri B. Hahn.
Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
Kazuto Kajiwara;Eliot L. Berson;Thaddeus P. Dryja.
Effects of AIN457, a Fully Human Antibody to Interleukin-17A, on Psoriasis, Rheumatoid Arthritis, and Uveitis
Wolfgang Hueber;Dhavalkumar D Patel;Thaddeus Dryja;Andrew M Wright.
Science Translational Medicine (2010)
Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa
Margaret E. McLaughlin;Michael A. Sandberg;Eliot L. Berson;Thaddeus P. Dryja.
Nature Genetics (1993)
Frequent inactivation of the retinoblastoma anti-oncogene is restricted to a subset of human tumor cells.
Jonathan M. Horowitz;Sang Ho Park;Emil Bogenmann;Jeng Chung Cheng;Jeng Chung Cheng.
Proceedings of the National Academy of Sciences of the United States of America (1990)
Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
Kazuto Kajiwara;Lauri B. Hahn;Shizuo Mukai;Gabriel H. Travis.
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor gene.
T Sakai;J Toguchida;N Ohtani;D W Yandell.
American Journal of Human Genetics (1991)
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis
Hiroyuki Morimura;Gerald A. Fishman;Sandeep A. Grover;Anne B. Fulton.
Proceedings of the National Academy of Sciences of the United States of America (1998)
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