1986 - Member of the National Academy of Sciences
1963 - Fellow of the American Association for the Advancement of Science (AAAS)
Liane B. Russell mainly investigates Genetics, Locus, Molecular biology, Gene and Cell biology. Genetics is closely attributed to Radiation induced in her research. Her biological study spans a wide range of topics, including Internal medicine, Allele, Gene mapping and Chromosome 7.
Her research integrates issues of Antigen and Gene mutation in her study of Molecular biology. Her study in the fields of Genetically modified mouse, Transgene and GABRA5 under the domain of Gene overlaps with other disciplines such as Beta-3 adrenergic receptor. Her Cell biology study combines topics in areas such as Melanosome transport, Synaptonemal complex and Anatomy.
Her primary areas of investigation include Genetics, Locus, Molecular biology, Gene and Mutant. Her is doing research in Allele, Mutation rate, Phenotype, Gene mutation and Point mutation, both of which are found in Genetics. Her Mutation rate study integrates concerns from other disciplines, such as Andrology and Ratón.
Her Locus research is multidisciplinary, incorporating elements of Genetic analysis, Mutation frequency, Germline, Complementation and Gene mapping. Her research investigates the connection between Molecular biology and topics such as X chromosome that intersect with problems in Chromosomal translocation. Liane B. Russell frequently studies issues relating to DNA and Gene.
Liane B. Russell mostly deals with Genetics, Molecular biology, Gene, Locus and Allele. Genetics is represented through her Mutagenesis, Mutation, Germline, Meiosis and Germ cell research. The Molecular biology study combines topics in areas such as Mutant, Ethylnitrosourea, Point mutation, Ratón and Exon.
Her work on Chromosome 7, GATA1 and Genetic linkage as part of general Gene study is frequently linked to Bone morphogenetic protein 5, bridging the gap between disciplines. Her Locus research incorporates themes from Germline mutation, Phenotype, Complementation, Gene mutation and Genotype. Her work in the fields of Compound heterozygosity overlaps with other areas such as Unconventional Myosin-Va.
Her scientific interests lie mostly in Genetics, Locus, Gene, Molecular biology and Chromosome 7. Her research ties Myosin and Genetics together. Her research in Locus intersects with topics in Gene mutation, Allele and Genotype.
In general Gene study, her work on Cloning, Gene product and Positional cloning often relates to the realm of Bone morphogenetic protein 5, thereby connecting several areas of interest. Her Molecular biology study combines topics from a wide range of disciplines, such as Phenotype and Immunology, Antigen. Liane B. Russell works mostly in the field of Chromosome 7, limiting it down to concerns involving GABRA5 and, occasionally, Chromosome 15 and Angelman syndrome.
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The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily
David M. Kingsley;Adrienne E. Bland;Janet M. Grubber;Paul C. Marker.
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
Karen B. Avraham;Tama Hasson;Karen P. Steel;David M. Kingsley.
Nature Genetics (1995)
Disruption of the nuclear hormone receptor RORα in staggerer mice
Bruce A. Hamilton;Wayne N. Frankel;Anne W. Kerrebrock;Trevor L. Hawkins.
A Mutation in Rab27a causes the vesicle transport defects observed in ashen mice
Scott M. Wilson;Richard Yip;Deborah A. Swing;T. Norene O'Sullivan.
Proceedings of the National Academy of Sciences of the United States of America (2000)
X-linked lymphoreticular disease in the scurfy (sf) mutant mouse.
Virginia L. Godfrey;J. E. Wilkinson;Liane B. Russell.
American Journal of Pathology (1991)
Radiation dose rate and mutation frequency.
W. L. Russell;Liane Brauch Russell;Elizabeth M. Kelly.
THE Y-CHROMOSOME AS THE BEARER OF MALE DETERMINING FACTORS IN THE MOUSE.
W. J. Welshons;Liane Brauch Russell.
Proceedings of the National Academy of Sciences of the United States of America (1959)
An analysis of the changing radiation response of the developing mouse embryo.
Liane Brauch Russell;W. L. Russell.
Journal of Cellular and Comparative Physiology (1954)
Mammalian X-Chromosome Action: Inactivation Limited in Spread and in Region of Origin
Liane Brauch Russell.
X‐ray induced developmental abnormalities in the mouse and their use in the analysis of embryological patterns. I. External and gross visceral changes
Liane Brauch Russell.
Journal of Experimental Zoology (1950)
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