Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Nikolai Rubtsov"'
Autor:
Anna Torgasheva, Lyubov Malinovskaya, Kira Zadesenets, Elena Shnaider, Nikolai Rubtsov, Pavel Borodin
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
All songbirds studied so far have a germline-restricted chromosome (GRC), which is present in the germ cells and absent in the somatic cells. It shows a wide variation in size, morphology, and genetic content between the songbird species. In this pap
Externí odkaz:
https://doaj.org/article/d5c470c3813748b4aea3f791d1cf4009
Autor:
Martin Voigt, Anja Weise, Sona Pekova, Thomas Liehr, Nadine Aust, Tereza Jancuskova, Kathleen Wilhelm, Vladimir A. Trifonov, Xiaobo Fan, Nikolai Rubtsov, Sharon Löhmer, Nadezda Kosyakova, Tatyana V. Karamysheva, David Hardekopf, Kristin Mrasek
Publikováno v:
Cytogenetic and Genome Research. 145:42-49
Gibbon species (Hylobatidae) impress with an unusually high number of numerical and structural chromosomal changes within the family itself as well as compared to other Hominoidea including humans. In former studies applying molecular cytogenetic met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b093269702389d60f0484738338c6cc
https://doi.org/10.1159/000381764
https://doi.org/10.1159/000381764
Autor:
Alexei Akifyev, Nikolai Rubtsov, Grigory Makarevich, Sergei Degtyarev, Igor F. Zhimulev, Tatiana Boykova, Tatiana Karamysheva, Stepan N. Belyakin, Andrei Grishanin
Publikováno v:
Genome Research. 14:2287-2294
Presumptive somatic cells of the copepod Cyclops kolensis specifically eliminate a large fraction of their genome by the process of chromatin diminution. The eliminated DNA (eDNA) remains only in the germline cells. Very little is known about the nat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::017292deae4697df73701449793f3a34
https://doi.org/10.1101/gr.2794604
https://doi.org/10.1101/gr.2794604
Autor:
Thomas Liehr, Susanne Michel, Ulrich-Walter Grummt, Martin Westermann, Ilse Chudoba, Jan Claussen, Karl Sperling, Peter Ullmann, Peter Mühlig, Nikolai Rubtsov, Johannes R. Lemke, Uwe Claussen, Katrin Kromeyer-Hauschild
Publikováno v:
The American Journal of Human Genetics. 71:1051-1059
In contrast to those of metaphase chromosomes, the shape, length, and architecture of human interphase chromosomes are not well understood. This is mainly due to technical problems in the visualization of interphase chromosomes in total and of their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::302810e08ce32eed928dcc0ae8a3a185
https://doi.org/10.1086/344286
https://doi.org/10.1086/344286
Autor:
Dorothea Rau, Heike Starke, Uwe Claussen, Thomas Liehr, Nikolai Rubtsov, Anita Heller, Hanne Tittelbach, Gabriele Senger, Vladimir A. Trifonov, Isabell Hartmann, Maria Kossakiewicz
Publikováno v:
Prenatal Diagnosis. 21:1049-1052
Objectives Different aberrations in one chromosome 18 were prenatally detected during each of three different pregnancies of a healthy woman. Routine cytogenetic analysis revealed a morphologically altered maternal chromosome 18 as well. The purpose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77ef638670ddf00a1602f1c7d7028aeb
https://doi.org/10.1002/pd.192
https://doi.org/10.1002/pd.192
Autor:
Thomas Liehr, Beate Mitulla, Monika Ziegler, Volkmar Beensen, Heike Starke, Vladimir A. Trifonov, Uwe Claussen, Annett Neumann, Anita Heller, Nikolai Rubtsov
Publikováno v:
Prenatal Diagnosis. 23:765-767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9e23c071c8969d9f985e4c4d9fa59b3
https://doi.org/10.1002/pd.666
https://doi.org/10.1002/pd.666
Autor:
Nikolai Rubtsov, Martina Merkas, Ahmed B. Hamid, Thomas Liehr, Alma Küchler, Isolde Schreyer, Ferdinand von Eggeling, Raimund Fahsold, Jasen Anderson, Nadezda Kosyakova, Kristin Mrasek, Julia Hentschel, Elisabeth Ewers, Heike Nelle, Anikó Ujfalusi, Anja Weise
Mental retardation is correlated in approximately 0.4% of cases with the presence of a small supernumerary marker chromosome (sSMC). However, here we report a case of a carrier of a heterochromatic harmless sSMC with fragile X syndrome (Fra X). In ap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1c92d1ba50c42acbfef3d532589cb18
Autor:
Heike Starke, Winfried Hindermann, Nikolai Rubtsov, Jimsgene Sanjmyatav, Joerg Schubert, Kerstin Junker
Publikováno v:
The Journal of urology. 174(2)
We developed a rapid interphase fluorescence in situ hybridization (FISH) test to differentiate renal cell carcinoma (RCC) based on known genetic alterations and verified the suitability of this test for practical use.We composed 2 FISH test sets usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cadb21a537b1d626f9df922ae42c3e6
https://pubmed.ncbi.nlm.nih.gov/16006966
https://pubmed.ncbi.nlm.nih.gov/16006966
Autor:
Ivan F. Loncarevic, Vladimir A. Trifonov, Axel Sauerbrey, Nikolai Rubtsov, Heike Starke, Uwe Claussen, Anita Heller, Thomas Liehr
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
We report on the cytogenetic findings from a patient with a de novo TNF-receptor-associated periodic syndrome (TRAPS), who showed first symptoms at the age of four months. Thus, he obtained a long-term therapy with cortisone, chlorambucile, methotrex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15480f4cd7473e0e5a945b45a29da882
https://doi.org/10.3892/or.10.6.1789
https://doi.org/10.3892/or.10.6.1789
Autor:
Vladimir A. Trifonov, Anita Heller, Nikolai Rubtsov, Thomas Liehr, Heike Starke, Gabriele Kittner, Matthias Schmidt, Monika Ziegler, Uwe Claussen
Publikováno v:
Fetal diagnosis and therapy. 17(3)
Objectives: In a case with severe sonographic abnormalities followed by missed abortion in week 14 + 5 days, cytogenetic analysis was performed on placental tissue. A mosaic karyotype 47,XY,+13,add(1)(q44)[3]/47,XY, +13[9]/46,XY[36] was detected. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::207025ade9666e9deb28ad10df3c6209
https://pubmed.ncbi.nlm.nih.gov/11914563
https://pubmed.ncbi.nlm.nih.gov/11914563