Catherine B. Talmadge

Author

University of Nebraska Medical Center

Also Known As

C B Talmadge, C Talmadge, C. Talmadge, C.B. Talmadge, Catherine B. Talmadge, Catherine Talmadge, Talmadge, Catherine B.

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

University of Nebraska Medical Center Boys Town National Research Hospital Harvard University National Cancer Institute University of California, Irvine

About

Catherine B. Talmadge is an author at University of Nebraska Medical Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	1.6K
2	Cell Biology	6	6	1.3K
3	Natural Sciences	3	3	928
4	Molecular Biology	2	2	95
5	Health Sciences	1	1	12

Catherine B. Talmadge

Publications

1.7K

Citations

H-Index

Page 1

	Year	Citations
The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors Keith D. Robertson, É. Uzvölgyi, Gangning Liang, Nucleic Acids Research Histone ModificationsEpigenetic ChangeGeneticsDna MethylationCancer Biology	1999	833
Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa James D. Eudy, Michael D. Weston, Su-Fang Yao, Science Molecular PhysiologyDevelopmental BiologyMarkers Afm268zd1Genetic DisorderExtracellular Matrix Motifs	1998	391
Isolation of a Gene Encoding a Novel Member of the Nuclear Receptor Superfamily from the Critical Region of Usher Syndrome Type IIa at 1q41 James D. Eudy, Sufang Yao, Michael D. Weston, Genomics Molecular PhysiologySignal TransductionNuclear Receptor SuperfamilyCritical RegionGenetic Disorder	1998	133
Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip Soraya Beiraghi, Ming Zhou, Catherine B. Talmadge, Gene Developmental BiologyNovel GeneNatural SciencesGeneticsMolecular Biology	2003	73
Isolation of a Novel Human Homologue of the Gene Coding for Echinoderm Microtubule-Associated Protein (EMAP) from the Usher Syndrome Type 1a Locus at 14q32 James D. Eudy, Manling Ma-Edmonds, Sufang Yao, Genomics Developmental BiologyGenetic DisorderGeneticsProtein GeneticsEchinoderm Microtubule-associated Protein	1997	46
The Genomic Structure of the Gene Defective in Usher Syndrome Type Ib (MYO7A) Philip M. Kelley, Mike D. Weston, Zheng‐Yi Chen, Genomics	1997	44
Transfer of Sensitivity to Tumor Promoters by Transfection of DNA from Sensitive into Insensitive Mouse JB6 Epidermal Cells Nancy H. Colburn, Catherine B. Talmadge, Thomas D. Gindhart Molecular and Cellular Biology	1983	30
The Construction of a Yeast Artificial Chromosome (YAC) Contig in the Vicinity of the Usher Syndrome Type IIa (USH2A) Gene in 1q41 János Sümegi, Ji-Yi Wang, DongKai Zhen, Genomics ChromatinYeast Artificial ChromosomeDevelopmental BiologyGenetic DisorderGenetics	1996	25
Identification of the Mouse and Rat Orthologs of the Gene Mutated in Usher Syndrome Type IIA and the Cellular Source of USH2A mRNA in Retina, a Target Tissue of the Disease Dali Huang, James D. Eudy, É. Uzvölgyi, Genomics Knockout MouseUsh2a MrnaDevelopmental BiologyMolecular NeuroscienceSignal Transduction	2002	22
Transfer of Sensitivity to Tumor Promoters by Transfection of DNA from Sensitive into Insensitive Mouse JB6 Epidermal Cells Nancy H. Colburn, Catherine B. Talmadge, Thomas D. Gindhart Molecular and Cellular Biology Molecular BiologyGene DeliveryCancer BiologyCell SpecializationTumor Biology	1983	22

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