Search Results - "Efremov, G.D"

Morphological precursors of high-grade serous ovarian cancer by Novikov, F V, Efremov, G D

“…At the beginning of this century, there was a paradigm shift in understanding the histogenesis of high-grade serous carcinomas. The theory of the origin of…”
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P008 “Histoscanning” – in diagnosis of prostate cancer, results for implementation in transperineal biopsies by Apolikhin, O.I, Sivkov, A.V, Efremov, G.D, Keshishev, N.G, Koryakin, A.V

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P087 Average rates of chromogranin A in patients with various prostate diseases by Apolikhin, O.I, Sivkov, A.V, Keshishev, N.G, Kovchenko, G.A, Efremov, G.D, Sokov, D.G, Nikonova, L.M, Rabinovich, E.Z, Prohorov, S.A

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Stimulation of Structural and Functional Recovery of the Kidney in Rats with Postischemic Acute Renal Failure of Different Severity by Embryonic Protein-Peptide Complex Therapy by Kirpatovskii, V. I., Sivkov, A. V., Golovanov, S. A., Drozhzheva, V. V., Efremov, G. D., Samoilova, S. I.

“…In male rats, acute renal failure was simulated by clamping the vascular pedicle of the left kidney for 60 or 90 min and right-sided nephrectomy. In the…”
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Stimulation of Spermatogenesis and Synthesis of Testosterone by Allotransplantation of Neonatal Testicular Tissue under Tunica Albuginea of Cryptorchid Testis by Kirpatovskii, V. I., Efremov, G. D., Frolova, E. V., Kudryavtseva, L. V.

“…The abdominal type of cryptorchism was modeled on random-bred albino rats by replacing both testes from the scrotum into the abdominal cavity for 3 weeks;…”
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Detection of Rare Mutations by Routine Analysis of KRAS, NRAS, and BRAF Oncogenes by Mikhailenko, D. S., Efremov, G. D., Safronova, N. Yu, Strelnikov, V. V., Alekseev, B. Ya

“…Molecular genetic analysis of KRAS , NRAS , and BRAF genes was carried out in order to develop an optimal algorithm for detection of minor mutations. We…”
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Ischemia in Pelvic Organs as an Independent Pathogenic Factor in the Development of Benign Prostatic Hyperplasia and Urinary Bladder Dysfunction by Kirpatovskii, V. I., Mudraya, I. S., Mkrtchyan, K. G., Revenko, S. V., Efremov, G. D., Nadtochii, O. N., Kabanova, I. V.

“…Blood supply to the pelvic organs of outbred male rats was diminished by graduated constriction of the distal part of the inferior vena cava. Deficiency of…”
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Hb Jambol: a new hyperunstable hemoglobin causing severe hemolytic anemia by Efremov, G D, Simjanovska, L, Plaseska-Karanfilska, D, Stanojevic, E, Petkov, G H

“…We describe a new hyperunstable beta-chain variant due to a complex genomic rearrangement. The abnormal hemoglobin (Hb) was found as a de novo mutation in a…”
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An Alu insert as the cause of a severe form of hemophilia A by Sukarova, E, Dimovski, A J, Tchacarova, P, Petkov, G H, Efremov, G D

“…Alu sequences represent a specific human family of interspersed repetitive DNA, with a copy number in excess of 500,000 within the human genome. Alu repeats…”
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Reverse transcriptase/polymerase chain reaction analyses of hemodialysis ultrafiltrates and sera of hepatitis C virus positive patients by Simjanovska, L J, Porcu, K, Amitov, V, Efremov, G D, Polenakovic, M

“…The hepatitis C virus is a highly prevalent infection among chronic dialysis patients and represents one of the major problems of hemodialysis units. Hepatitis…”
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An Electronic Database of Human Hemoglobin Variants on the World Wide Web by Chui, David H.K., Hardison, Ross, Riemer, Cathy, Miller, Webb, Carver, M.F.H., Molchanova, T.P., Efremov, G.D., Huisman, Titus H.J.

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Macedonian (δβ)° Thalassemia Has the Same Molecular Basis as Turkish Inversion-Deletion (δβ) Thalassemia by Craig, J.E., Efremov, G.D., Fisher, C., Thein, S.L.

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Differential diagnosis of Hb EE and Hb E-beta(0)-thalassemia by protein and DNA analyses by Wong, S C, Aw, T C, Suri, R, Wong, C K, Plaseska, D, Efremov, G D

“…DNA analysis was used to confirm the Hb EE genotype and to differentiate from the possible genotype of Hb E-beta(0)-thalassemia in two Malay patients. The…”
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The 18- to 23-kb Deletion of the Macedonian δß-Thalassemia Includes the Entire δ and ß Globin Genes by Efremov, G.D., Nikolov, N., Hattori, Y., Bakioglu, I., Huisman, T.H.J.

“…Restriction endonuclease mapping analyses were made of DNA from a few members of a Macedonian family with hematological characteristics of δß-thalassemia, ie,…”
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Relative levels of alpha-, beta-, and gamma-mRNA from patients with severe and intermediate beta-thalassemia major by Smetanina, N S, Gu, L H, Schilirò, G, Di Cataldo, A, Testa, R, Jakovlevska, Z, Efremov, G D, Huisman, T H

“…We have determined the relative quantities of gamma- and beta-mRNAs and the alpha/beta-mRNA ratios in 37 patients with beta-thalassemia major with specific…”
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Beta-thalassemia due to a T----A mutation within the ATA box by Fei, Y J, Stoming, T A, Efremov, G D, Efremov, D G, Battacharia, R, Gonzalez-Redondo, J M, Altay, C, Gurgey, A, Huisman, T H

“…Sequence analyses of amplified DNA from a Yugoslavian patient with Hb Lepore-beta-thalassemia and from his father with a simple beta-thalassemia trait have…”
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Hemoglobin F levels in end-stage renal disease patients after correction of anemia with erythropoietin by Sikole, A, Efremov, D G, Dimovski, A, Efremov, G D, Polenakovic, M

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A C → T Substitution at nt – 101 in a Conserved DNA Sequence of the Promotor Region of the β-GIobin Gene Is Associated With “Silent” β-Thalassemia by Gonzalez-Redondo, J.M., Stoming, T.A., Kutlar, A., Kutlar, F., Lanclos, K.D., Howard, E.F., Fei, Y.J., Aksoy, M., Altay, Ç., Gurgey, A., Başak, A.N., Efremov, G.D., Petkov, G., Huisman, T.H.J.

“…Sequence analyses and dot-blot analyses with synthetic oligonucleotide probes have identified eight individuals in three Turkish families and one Bulgarian…”
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Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya by LANCLOS, K. D, PATTERSON, J, EFREMOV, G. D, WONG, S. C, VILLEGAS, A, OJWANG, P. J, WILSON, J. B, KUTLAR, F, HUISMAN, T. H. J

“…This study concerns the characterization of chromosomes with hybrid genes for Hb Lepore-Washington (44 chromosomes), for Hb Lepore-Baltimore (5 chromosomes),…”
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Mutant oligonucleotide extension amplification: a nonlabeling polymerase-chain-reaction-based assay for the detection of point mutations by Efremov, D G, Dimovski, A J, Janković, L, Efremov, G D

“…We have developed a new nonradioactive method for the identification of mutations causing beta-thalassemia and cystic fibrosis. The method is based on the…”
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