B.S. Shastry - Concepedia

Author

B.S. Shastry

Oakland University

Also Known As

B S Shastry, B SHASTRY, B Shastry, B. S. Shastry, B. Shastry, B.S. Shastry, BS Shastry

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Oakland University Washington University in St. Louis Smith-Kettlewell Eye Research Institute Beaumont Hospital, Royal Oak

About

B.S. Shastry is an author at Oakland University specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	1.2K
2	Natural Sciences	4	4	1.1K
3	Molecular Biology	3	3	1K
4	Biology	2	2	142
5	Cell Biology	1	1	110

B.S. Shastry

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
Specific interaction of a purified transcription factor with an internal control region of 5S RNA genes David R. Engelke, Siok‐Bian Ng, B.S. Shastry, Cell Specific InteractionGeneticsRna Binding ProteinsPurified Transcription FactorRna Biology	1980	776
The binding of a transcription factor to deletion mutants of a 5S ribosomal RNA gene Shigeru Sakonju, Donald D. Brown, David R. Engelke, Cell Ribosomal Rna GeneTranscriptional RegulationNatural SciencesGeneticsRna Binding Proteins	1981	195
Multiple factors involved in the transcription of class III genes in Xenopus laevis. B.S. Shastry, S Y Ng, Robert G. Roeder Journal of Biological Chemistry	1982	176
Altered levels of a 5 S gene-specific transcription factor (TFIIIA) during oogenesis and embryonic development of Xenopus laevis. B.S. Shastry, Barry M. Honda, Robert G. Roeder Journal of Biological Chemistry Xenopus LaevisOocyteGeneticsMolecular GeneticsReproductive Biology	1984	110
Insertion and deletion mutations in the dinucleotide repeat region of the Norrie disease gene in patients with advanced retinopathy of prematurity Miina Hiraoka, Daniel M. Berinstein, Michael T. Trese, Journal of Human Genetics Ocular DiseaseOphthalmologyGenetic DisorderGeneticsDeletion Mutations	2001	79
A Colombian family with X-linked juvenile retinoschisis with three affected females: Finding of a frameshift mutation Roberto Mendoza‐Londono, Kelaginamane Hiriyanna, Eve L. Bingham, Ophthalmic Genetics Mendelian DisorderGenetic DisorderGeneticsEvolutionary BiologyX-linked Juvenile Retinoschisis	1999	39
Multiple forms of DNA-dependent RNA polymerases in Xenopus laevis. Rapid purification and structural and immunological properties. David R. Engelke, B.S. Shastry, Robert G. Roeder Journal of Biological Chemistry BiologyXenopus LaevisXenopus Laevis OvariesMolecular Biological MethodNatural Sciences	1983	32
Norrie Disease and Exudative Vitreoretinopathy in Families with Affected Female Carriers B.S. Shastry, Miki Hiraoka, D.C. Trese, European Journal of Ophthalmology	1999	30
Assessment of the Contribution of Insulin-like Growth Factor I Receptor 3174 G→A Polymorphism to the Progression of Advanced Retinopathy of Prematurity B.S. Shastry European Journal of Ophthalmology	2007	20
Cosegregation of two unlinked mutant alleles in some cases of autosomal dominant familial exudative vitreoretinopathy B.S. Shastry, Michael T. Trese European Journal of Human Genetics Unlinked Mutant AllelesMendelian DisorderGenetic DisorderGeneticsPathology	2003	15

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