T. P. Molchanova - Concepedia

Author

T. P. Molchanova

Augusta University ORCID

Also Known As

Molchanova, T., T P Molchanova, T. Molchanova, T. P. MOLCHANOVA, T. P. Molchanova, T.P. Molchanova, Tatiana Molchanova

Publications

833

Citations

H-Index

Concepts

All Affiliations

Augusta University Biotechnology Institute Pennsylvania State University

About

T. P. Molchanova is an author at Augusta University specializing in medicine, hematology, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	11	351
2	Natural Sciences	4	4	116
3	Biochemistry	4	4	122
4	Health Sciences	2	2	80
5	Public Health	1	1	72

T. P. Molchanova

Publications

721

Citations

H-Index

Page 1

	Year	Citations
Hb adana or α<sub>2</sub>59(E8)Gly→Aspβ<sub>2</sub>, A severely unstable α<sub>1</sub>‐globin variant, observed in combination with the ‐(α)20.5 KB α‐thal‐1 deletion in two Turkish patients Mehmet Akif Çürük, Aleksandar Dimovski, E. Baysal, American Journal of Hematology	1993	76
The differences in quantities of α2‐and α1‐globin gene variants in heterozygotes T. P. Molchanova, D. D. Pobedimskaya, T. H. J. Huisman British Journal of Haematology Phenotypic VariationGeneticsHuman PolymorphismMolecular BiologyPathology	1994	72
Access to a Syllabus of Human Hemoglobin Variants (1996) Via the World Wide Web Ross C. Hardison, David H.K. Chui, Caspar Riemer, Hemoglobin ImmunohematologyGeneticsMolecular BiologyDisease Gene IdentificationGenomics	1998	64
Structure and Calcium-Binding Studies of a Recoverin Mutant (E85Q) in an Allosteric Intermediate State James B. Ames, Nobuko Hamasaki, T. P. Molchanova Biochemistry Molecular BiologyCellular PhysiologyProtein X-ray CrystallographyRecoverin MutantRetinal Rod Cells	2002	62
A simplified procedure for sequencing amplified DNA containing the α2- or α1-Globin gene T. P. Molchanova, D. D. Pobedimskaya, Yu. V. Postnikov Hemoglobin Amplified DnaDna SequencingMedicineGeneticsNext-generation Sequencing	1994	37
Fission Yeast Homolog of Neuronal Calcium Sensor-1 (Ncs1p) Regulates Sporulation and Confers Calcium Tolerance Nobuko Hamasaki‐Katagiri, T. P. Molchanova, Kazuyo Takeda, Journal of Biological Chemistry	2004	35
An electronic database of human hemoglobin variants on the World Wide Web. David H.K. Chui, Ross C. Hardison, Cathy Riemer, PubMed	1998	33
Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia D. D. Pobedimskaya, T. P. Molchanova, Sara Streichman, American Journal of Hematology	1994	28
A New Abnormal Hemoglobin: Hb Mozhaisk β92 (FB)HISARG V. A. Spivak, T. P. Molchanova, Yu. V. Postnikov, Hemoglobin Russian BoyBiochemistryMedicineNatural SciencesHeme Degradation	1982	27
β‐thalassemia alleles and unstable hemoglobin types among russian pediatric patients Mehmet A. Cürük, T. P. Molchanova, Yu. V. Postnikov, American Journal of Hematology	1994	27

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