Jochen Graw mainly focuses on Genetics, Gene, Crystallin, Cataracts and Mutation. His is doing research in Mutant, Allele, Eye development, PAX6 and Locus, both of which are found in Genetics. His work is dedicated to discovering how Mutant, Exon are connected with Gene cluster and other disciplines.
His Crystallin research is multidisciplinary, relying on both Molecular biology, Lens and Human genetics. His Cataracts study combines topics in areas such as Threshold dose, Radiation therapy, Human studies and Ionizing radiation. His work carried out in the field of Mutation brings together such families of science as Multiple endocrine neoplasia and Promoter.
Jochen Graw mainly investigates Genetics, Gene, Molecular biology, Mutant and Mutation. His study in Exon, Candidate gene, Allele, Cataracts and Phenotype is done as part of Genetics. Gene and Crystallin are frequently intertwined in his study.
As a member of one scientific family, Jochen Graw mostly works in the field of Molecular biology, focusing on PAX6 and, on occasion, Eye development. The concepts of his Mutant study are interwoven with issues in Gene cluster, Lens and Cell biology. His Mutation research includes themes of Heterozygote advantage, Gene expression and Coding region.
Jochen Graw focuses on Genetics, Mutant, Cataracts, Ionizing radiation and Cell biology. His Mutant study is concerned with the larger field of Gene. Jochen Graw interconnects Intellectual disability and Immune system in the investigation of issues within Gene.
The various areas that Jochen Graw examines in his Cataracts study include Optical coherence tomography, Bioinformatics and Glaucoma. Jochen Graw has included themes like Scheimpflug principle, Ophthalmology, Lens, Radiation protection and Low dose in his Ionizing radiation study. His research in Cell biology intersects with topics in Microphthalmia, Retinal, Transcription factor, Eye development and Crystallin.
His primary areas of study are Genetics, Cell biology, Gene, Ionizing radiation and Cataracts. His studies in Mutation, Mutant, HMGN, Nucleosome and Chromatin are all subfields of Genetics research. His Mutant research is multidisciplinary, incorporating elements of Pleiotropy, Human genome, Lens fiber cell differentiation and ERCC2.
His Cell biology research incorporates elements of Microphthalmia, Transcription factor, Eye development, Induced pluripotent stem cell and Regulation of gene expression. The Ionizing radiation study which covers Radiation protection that intersects with Lens, Bone marrow, Human studies and Bioinformatics. Jochen Graw works mostly in the field of Cataracts, limiting it down to topics relating to Diabetes mellitus and, in certain cases, Internal medicine, Optometry, Cross-sectional study and Glaucoma, as a part of the same area of interest.
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A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice
Wolfgang Enard;Sabine Gehre;Kurt Hammerschmidt;Sabine M. Hölter.
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans.
Natalia S. Pellegata;Leticia Quintanilla-Martinez;Heide Siggelkow;Elenore Samson.
Proceedings of the National Academy of Sciences of the United States of America (2006)
A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains
Michelle M Simon;Simon Greenaway;Jacqueline K White;Helmut Fuchs.
Genome Biology (2013)
Radiation cataractogenesis: a review of recent studies.
E. A. Ainsbury;S. D. Bouffler;W. Dörr;J. Graw.
Radiation Research (2009)
Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3.
Marten P. Smidt;Simone M. Smits;Hans Bouwmeester;Frank P. T. Hamers.
Genetics of crystallins: cataract and beyond.
Experimental Eye Research (2009)
Rapamycin extends murine lifespan but has limited effects on aging
Frauke Neff;Diana Flores-Dominguez;Devon P. Ryan;Marion Horsch.
Journal of Clinical Investigation (2013)
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice
Elena V. Semina;Jeffrey C. Murray;Rebecca Reiter;Ronald F. Hrstka.
Human Molecular Genetics (2000)
The genetic and molecular basis of congenital eye defects
Nature Reviews Genetics (2003)
Haemophilia A: from mutation analysis to new therapies
Jochen Graw;Hans-Hermann Brackmann;Johannes Oldenburg;Reinhard Schneppenheim.
Nature Reviews Genetics (2005)
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