-
1
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
Stankiewicz P., Lupski J.R. Structural variation in the human genome and its role in disease. Annu Rev Med. 2010; 61:437-455.
-
(2010)
Annu Rev Med.
, vol.61
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
2
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
Zhang E, Gu W., Hurles M.E., Lupski J.R. Copy number variation in human health, disease, and evolution. Annu Rev Genomics Hum Genet2009;10:451-481.
-
(2009)
Annu Rev Genomics Hum Genet
, vol.10
, pp. 451-481
-
-
Zhang, E.1
Gu, W.2
Hurles, M.E.3
Lupski, J.R.4
-
3
-
-
84857192718
-
Causes and consequences of aneuploidy in cancer
-
Gordon D.J., Resio B., Pellman D. Causes and consequences of aneuploidy in cancer. Nat Rev Genet 2012; 13 (3): 189-203.
-
(2012)
Nat Rev Genet
, vol.13
, Issue.3
, pp. 189-203
-
-
Gordon, D.J.1
Resio, B.2
Pellman, D.3
-
4
-
-
33845646696
-
Intercellular genomic (chromosomal) variations resulting in somatic mosaicism: Mechanisms and consequences
-
DOI 10.2174/138920206779116756
-
Iourov I.Y., Vorsanova S.G., Yurov Y.B. Intercellular gnomic (chromosomal) variations resulting in somatic mosaicism: mechanisms and consequences. Curr Genomics. 2006; 7:435-446. (Pubitemid 44942065)
-
(2006)
Current Genomics
, vol.7
, Issue.7
, pp. 435-446
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
5
-
-
78650033928
-
Somatic genome variations in health and disease
-
URL
-
Iourov I.Y., Vorsanova S.G., Yurov Y.B. Somatic genome variations in health and disease. Cwr Genomics 2010; 11 (6): 420-425. URL: http://www.els.net
-
(2010)
Cwr Genomics
, vol.11
, Issue.6
, pp. 420-425
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
6
-
-
14844328676
-
The variation of aneuploidy frequency in the developing and adult human brain revealed by an interphase FISH study
-
DOI 10.1369/jhc.4A6430.2005
-
YurovYB.,IourovI.Y.,Monakhov VV,Soloviev I.V, Vostrikov VM., Vorsanova S.G. The variation of aneuploidy frequency in the developing and adult human brain revealed by an interphase FISH study. J Histochem Cytochem. 2005; 53: 385-390. (Pubitemid 40344081)
-
(2005)
Journal of Histochemistry and Cytochemistry
, vol.53
, Issue.3
, pp. 385-390
-
-
Yurov, Y.B.1
Iourov, I.Y.2
Monakhov, V.V.3
Soloviev, I.V.4
Vostrikov, V.M.5
Versanova, S.G.6
-
7
-
-
37049012350
-
Aneuploidy and confined chromosomal mosaicism in the developing human brain
-
Yurov Y.B., Iourov I.Y., Vorsanova S.G., Lieh, T., Kolotii A.D., Kutsev S.I., Pellestor F., Beresheva A.K., Demidova I.A., Kravets VS., Monakhov V.V., Soloviev I.V. Aneuploidy and confined chromosomal mosaicism in the developing human brain. PLoS ONE 2007; 2: e558.
-
(2007)
PLoS ONE
, vol.2
-
-
Yurov, Y.B.1
Iourov, I.Y.2
Vorsanova, S.G.3
Lieh, T.4
Kolotii, A.D.5
Kutsev, S.I.6
Pellestor, F.7
Beresheva, A.K.8
Demidova, I.A.9
Kravets, V.S.10
Monakhov, V.V.11
Soloviev, I.V.12
-
8
-
-
66749169417
-
Chromosome instability is common in human cleavage-stage embryos
-
Vanneste E., Voet T., Le Caignec C, Ampe M., Konings P., Melotte C, Debrock S., Amyere M., Vikkula M., Schuit E, Fryns J.P., Verbeke G., D'Hooghe T., Moreau Y, Vermeesch J.R. Chromosome instability is common in human cleavage-stage embryos. Nat Med. 2009; 15: 577-583.
-
(2009)
Nat Med.
, vol.15
, pp. 577-583
-
-
Vanneste, E.1
Voet, T.2
Le Caignec, C.3
Ampe, M.4
Konings, P.5
Melotte, C.6
Debrock, S.7
Amyere, M.8
Vikkula, M.9
Schuit, E.10
Fryns, J.P.11
Verbeke, G.12
D'Hooghe, T.13
Moreau, Y.14
Vermeesch, J.R.15
-
9
-
-
33646486987
-
Chromosomal variation in mammalian neuronal cells: Known facts and attractive hypotheses
-
Iourov I.Y., Vorsanova S.G., Yurov YB. Chromosomal variation in mammalian neuronal cells: known facts and attractive hypotheses. Int Rev Cytol 2006; 249: 143-191.
-
(2006)
Int Rev Cytol
, vol.249
, pp. 143-191
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
11
-
-
33646062895
-
Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB)
-
Iourov LY, Liehr T., Vorsanova S.G., Kolotii A.D., Yurov YB. Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB). Chromosome Res. 2006; 14: 223-229.
-
(2006)
Chromosome Res.
, vol.14
, pp. 223-229
-
-
Iourov, L.Y.1
Liehr, T.2
Vorsanova, S.G.3
Kolotii, A.D.4
Yurov, Y.B.5
-
12
-
-
0035200633
-
Multicolor fluorescent in situ hybridization on postmortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatrie diseases
-
Yurov YB., Vostrikov V.M., Vorsanova S.G., Monakhov VV, Iourov LY Multicolor fluorescent in situ hybridization on postmortem brain in schizophrenia as an approach for identification of low-level chromosomal aneuploidy in neuropsychiatrie diseases Brain Dev2001;23:186-190.
-
(2001)
Brain Dev
, vol.23
, pp. 186-190
-
-
Yurov, Y.B.1
Vostrikov, V.M.2
Vorsanova, S.G.3
Monakhov, V.V.4
Iourov, L.Y.5
-
13
-
-
34548225995
-
Unexplained autism is frequently associated with low-level mosaic aneuploidy
-
DOI 10.1136/jmg.2007.049312
-
Yurov YB., Vorsanova S.G., Iourov LY, Demidova IA, Beresheva A.K., Kravetz VS., Monakhov VV, Kolotii AD., Voinova-Ulas VY, Gorbachevskaya N.L. Unexplained autism is frequently associated with low-level mosaic aneuploidy. J Med Genet. 2007; 44:521-525. (Pubitemid 47325739)
-
(2007)
Journal of Medical Genetics
, vol.44
, Issue.8
, pp. 521-525
-
-
Yurov, Y.B.1
Vorsanova, S.G.2
Iourov, I.Y.3
Demidova, I.A.4
Beresheva, A.K.5
Kravetz, V.S.6
Monakhov, V.V.7
Kolotii, A.D.8
Voinova-Ulas, V.Y.9
Gorbachevskaya, N.L.10
-
14
-
-
60849088633
-
Molecular cytogenetics and cytogenomics of brain diseases
-
Iourov LY, Vorsanova S.G., Yurov YB. Molecular cytogenetics and cytogenomics of brain diseases. Curr Genomics 2008; 9:452-465.
-
(2008)
Curr Genomics
, vol.9
, pp. 452-465
-
-
Iourov, L.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
15
-
-
37049032150
-
The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1
-
DOI 10.1016/j.schres.2007.07.035, PII S0920996407003295
-
Yurov YB.,Iourov LY, Vorsanova S.G.,Demidova I.A.,Kravets VS., Beresheva A.K., Kolotii A.D., Monakhov VV, Uranová NA., Vostrikov V.M., Soloviev I.V., Liehr T. The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1. Schizophr Res. 2008; 98: 139-147. (Pubitemid 350245588)
-
(2008)
Schizophrenia Research
, vol.98
, Issue.1-3
, pp. 139-147
-
-
Yurov, Y.B.1
Iourov, I.Y.2
Vorsanova, S.G.3
Demidova, I.A.4
Kravetz, V.S.5
Beresheva, A.K.6
Kolotii, A.D.7
Monakchov, V.V.8
Uranova, N.A.9
Vostrikov, V.M.10
Soloviev, I.V.11
Liehr, T.12
-
16
-
-
67651036860
-
Aneuploidy: From a physiological mechanism of variance to Down syndrome
-
Dierssen M., Hérault Y, Estivill X. Aneuploidy: from a physiological mechanism of variance to Down syndrome. Physiol Rev. 2009; 89: 887-920.
-
(2009)
Physiol Rev.
, vol.89
, pp. 887-920
-
-
Dierssen, M.1
Hérault, Y.2
Estivill, X.3
-
17
-
-
64449088956
-
Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: Differential expression and pathological meaning
-
Iourov LY, Vorsanova S.G., Liehr T., Yurov YB. Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiol Dis. 2009; 34: 212-220.
-
(2009)
Neurobiol Dis.
, vol.34
, pp. 212-220
-
-
Iourov, L.Y.1
Vorsanova, S.G.2
Liehr, T.3
Yurov, Y.B.4
-
18
-
-
0034737456
-
Mitotic misregulation and human aging
-
DOI 10.1126/science.287.5462.2486
-
Ly D.H., Lockhar D.J., Lerne RA., Schultz P.G. Mitotic misregulation and human aging. Science. 2000; 287: 2486-2492. (Pubitemid 30185444)
-
(2000)
Science
, vol.287
, Issue.5462
, pp. 2486-2492
-
-
Ly, D.H.1
Lockhart, D.J.2
Lerner, R.A.3
Schultz, P.G.4
-
19
-
-
4344680935
-
Human chromosomes with shorter telomeres and large heterochromatin regions have a higher frequency of acquired somatic cell aneuploidy
-
DOI 10.1016/j.mad.2004.06.006, PII S0047637404001198
-
Leach N.T., Rehder D., Jensen K., Holt S., Jackson-Cook C. Human chromosomes with shorter telomeres and large heterochromatin regions have a higher frequency of acquired somatic cell aneuploidy. Mech Ageing Dev. 2004; 125: 563-573. (Pubitemid 39150000)
-
(2004)
Mechanisms of Ageing and Development
, vol.125
, Issue.8
, pp. 563-573
-
-
Leach, N.T.1
Rehder, C.2
Jensen, K.3
Holt, S.4
Jackson-Cook, C.5
-
20
-
-
34547941973
-
The common biology of cancer and ageing
-
DOI 10.1038/nature05985, PII NATURE05985
-
Finkel T, Serrano M., Blasco MA. The common biology of cancer and ageing. Nature. 2007; 448: 767-774. (Pubitemid 47266334)
-
(2007)
Nature
, vol.448
, Issue.7155
, pp. 767-774
-
-
Finkel, T.1
Serrano, M.2
Blasco, M.A.3
-
21
-
-
72849129177
-
GIN'n'CIN hypothesis of brain aging: Deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny
-
Yuro YB., Vorsanova S.G., Iourov LY GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny. MoI Cytogenet 2009; 2:23.
-
(2009)
MoI Cytogenet
, vol.2
, pp. 23
-
-
Yuro, Y.B.1
Vorsanova, S.G.2
Iourov, L.Y.3
-
23
-
-
78650033928
-
Somatic genome variations in health and disease
-
Iourov I.Y., Vorsanova S.G., Yurov Yu.B. Somatic genome variations in health and disease. Current Genomics2010; 11 (6): 387-396.
-
(2010)
Current Genomics
, vol.11
, Issue.6
, pp. 387-396
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Yurov, Yu.B.3
-
24
-
-
78650031746
-
Molecular cytogenetic diagnosis and somatic genome variations
-
Vorsanova S.G., Yurov YB., Soloviev I.V., Iourov I.Y. Molecular cytogenetic diagnosis and somatic genome variations. Current Genomics 2010; 11 (6): 440-446.
-
(2010)
Current Genomics
, vol.11
, Issue.6
, pp. 440-446
-
-
Vorsanova, S.G.1
Yurov, Y.B.2
Soloviev, I.V.3
Iourov, I.Y.4
-
25
-
-
38949204058
-
Alzheimer's presenilin 1 causes chromosome missegregation and aneuploidy
-
DOI 10.1016/j.neurobiolaging.2006.10.027, PII S0197458006003988
-
Boeras D.I.,Granic A.,Padmanabhan J.,Crespo N.C.,Rojiani A.M., Potter H. Alzheimer's presenilin 1 causes chromosome missegregation and aneuploidy. Neurobiol Aging. 2008; 29: 319-328. (Pubitemid 351215587)
-
(2008)
Neurobiology of Aging
, vol.29
, Issue.3
, pp. 319-328
-
-
Boeras, D.I.1
Granic, A.2
Padmanabhan, J.3
Crespo, N.C.4
Rojiani, A.M.5
Potter, H.6
-
26
-
-
76649129325
-
Alzheimer Abeta peptide induces chromosome mis-segregation and aneuploidy, including trisomy 21: Requirement for tau and APP
-
Granic A., Padmanabhan J., Norden M., Potte H. Alzheimer Abeta peptide induces chromosome mis-segregation and aneuploidy, including trisomy 21 : requirement for tau and APP. MoI Biol Cell 2010; 21: 511-520.
-
(2010)
MoI Biol Cell
, vol.21
, pp. 511-520
-
-
Granic, A.1
Padmanabhan, J.2
Norden, M.3
Potte, H.4
-
27
-
-
1342327391
-
The development of cytogenetically normal, abnormal and mosaic embryos: A theoretical model
-
DOI 10.1093/humupd/dmh005
-
Los F.J., van Opstal D., van den Berg C. The development of cytogenetically normal, abnormal and mosaic embryos: a theoretical model. Hum Reprod Update. 2004; 10: 79-94. (Pubitemid 38263165)
-
(2004)
Human Reproduction Update
, vol.10
, Issue.1
, pp. 79-94
-
-
Los, F.J.1
Van Opstal, D.2
Van Den, B.C.3
-
28
-
-
77649331363
-
On the paternal origin of trisomy 21 Down syndrome
-
Hulten M.A., Patel S.D., Westgren M., Papadogiannaki N., Jonsso A.M., Jonasson J., Iwarsson E. On the paternal origin of trisomy 21 Down syndrome. MoI Cytogenet 2010; 3: 4.
-
(2010)
MoI Cytogenet
, vol.3
, pp. 4
-
-
Hulten, M.A.1
Patel, S.D.2
Westgren, M.3
Papadogiannaki, N.4
Jonsso, A.M.5
Jonasson, J.6
Iwarsson, E.7
-
29
-
-
38449087657
-
The origin of human aneuploidy: Where we have been, where we are going
-
Hassold T., Hall H., Hunt P. The origin of human aneuploidy: Where we have been, where we are going. Hum MoI Genet 2007; 16: 203-208.
-
(2007)
Hum MoI Genet
, vol.16
, pp. 203-208
-
-
Hassold, T.1
Hall, H.2
Hunt, P.3
-
30
-
-
33748464364
-
Molecular cytogenetic studies towards the full karyotype analysis of human blastocysts and cytotrophoblasts
-
DOI 10.1159/000094218
-
Weier J.F., Ferlatte C, Baumgartner A., Jung CJ., Nguyen H.N., Chu L.W., Pedersen R.A., Fisher S.J., Weier H.U. Molecular cytogenetic studies towards the full karyotype analysis of human blastocysts and cytotrophoblasts. Cytogenet Genome Res. 2006; 114:302-311. (Pubitemid 44352690)
-
(2006)
Cytogenetic and Genome Research
, vol.114
, Issue.3-4
, pp. 302-311
-
-
Weier, J.F.1
Ferlatte, C.2
Baumgartner, A.3
Jung, C.J.4
Nguyen, H.-N.5
Chu, L.W.6
Pedersen, R.A.7
Fisher, S.J.8
Weier, H.-U.G.9
-
31
-
-
14844304699
-
Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis
-
DOI 10.1369/jhc.4A6424.2005
-
Vorsanova S.G., Kolotii A.D., Iourov I.Y, Monakhov V.V., Kirillova E.A., Soloviev I.V., Yurov YB. Evidence for high frequency of chromosomal mosaicism in spontaneous abortions revealed by interphase FISH analysis. J Histochem Cytochem. 2005; 53: 375-380. (Pubitemid 40344079)
-
(2005)
Journal of Histochemistry and Cytochemistry
, vol.53
, Issue.3
, pp. 375-380
-
-
Vorsanova, S.G.1
Kolotii, A.D.2
Iourov, I.Y.3
Monakhov, V.V.4
Kirillova, E.A.5
Soloviev, I.V.6
Yurov, Y.B.7
-
32
-
-
34548246019
-
Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: Identification of genetic markers of autistic spectrum disorders
-
DOI 10.1007/s11055-007-0052-1
-
Vorsanova S.G., Yurov I.Y, Demidova I.A., Voinova-Ulas VY, Kravets VS., Soloviev I.V., Gorbachevskaya N.L., Yurov YB. Variability in the heterochromatin regions of the chromosomes and chromosomal anomalies in children with autism: identification of genetic markers of autistic spectrum disorders. Neurosci Behav Physiol. 2007; 37: 553-558. (Pubitemid 47322125)
-
(2007)
Neuroscience and Behavioral Physiology
, vol.37
, Issue.6
, pp. 553-558
-
-
Vorsanova, S.G.1
Yurov, I.Y.2
Demidova, I.A.3
Voinova-Ulas, V.Y.4
Kravets, V.S.5
Solov'Ev, I.V.6
Gorbachevskaya, N.L.7
Yurov, Y.B.8
-
34
-
-
34547768278
-
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1 - Evidence for high variability in mosaicism in different tissues of sSMC carriers
-
DOI 10.1002/pd.1776
-
Fickelscher I., Starke H., Schulze E., Ernst G., Kosyakova N., Mkrtchyan H., MacDermont K., Sebire N., LiehrT. A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1 - evidence for high variability in mosaicism in different tissues of sSMC carriers. Prenat Diagn. 2007; 27: 783-785. (Pubitemid 47242411)
-
(2007)
Prenatal Diagnosis
, vol.27
, Issue.8
, pp. 783-785
-
-
Fickelscher, I.1
Starke, H.2
Schulze, E.3
Ernst, G.4
Kosyakova, N.5
Mkrtchyan, H.6
MacDermont, K.7
Sebire, N.8
Liehr, T.9
-
35
-
-
14544300125
-
Human cytotrophoblasts acquire aneuploidies as they differentiate to an invasive phenotype
-
DOI 10.1016/j.ydbio.2004.12.035
-
Weier J.F., Weier H.U., Jung C.J., Gormley M., Zhou Y, Chu L.W., Genbacev O., Wright A.A., Fisher S.J. Human cytotrophoblasts acquire aneuploidies as they differentiate to an invasive phenotype. Dev Biol. 2005; 279: 420-432. (Pubitemid 40298749)
-
(2005)
Developmental Biology
, vol.279
, Issue.2
, pp. 420-432
-
-
Weier, J.F.1
Weier, H.-U.G.2
Jung, C.J.3
Gormley, M.4
Zhou, Y.5
Chu, L.W.6
Genbacev, O.7
Wright, A.A.8
Fisher, S.J.9
-
36
-
-
67649859655
-
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain
-
Iourov I.Y, Vorsanova S.G., Liehr T, Kolotii A.D., Yurov YB. Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain. Hum MoI Genet 2009; 18: 2656-2669.
-
(2009)
Hum MoI Genet
, vol.18
, pp. 2656-2669
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Liehr, T.3
Kolotii, A.D.4
Yurov, Y.B.5
-
37
-
-
33845809989
-
Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome
-
Vorsanova S.G., Iourov I.Y, Beresheva A.K., Demidova I.A., Monakhov VV, KravetsV.S., BartsevaO.B., Goyko EA, Soloviev I.V, Yurov YB. Non-disjunction of chromosome 21, alphoid DNA variation, and sociogenetic features of Down syndrome. Tsitol Genet. 2005; 39 (6): 30-36. (Pubitemid 46003920)
-
(2005)
Cytology and Genetics
, vol.39
, Issue.6
, pp. 30-36
-
-
Vorsanova, S.G.1
Iourov, I.Y.2
Beresheva, A.K.3
Demidova, I.A.4
Monakhov, V.V.5
Kravets, V.S.6
Bartseva, O.B.7
Goyko, E.A.8
Soloviev, I.V.9
Yurov, Y.B.10
-
38
-
-
77649292704
-
Human interphase chromosomes: A review of available molecular cytogenetic technologies
-
Vorsanova S.G., Yurov Y.B., lourov LY. Human interphase chromosomes: A review of available molecular cytogenetic technologies. MoI Cytogenet 2010; 3: 1.
-
(2010)
MoI Cytogenet
, vol.3
, pp. 1
-
-
Vorsanova, S.G.1
Yurov, Y.B.2
Lourov, L.Y.3
-
39
-
-
77956161900
-
Somatic gene mutation and human disease other than cancer: An update
-
Erickson R. P. Somatic gene mutation and human disease other than cancer: An update. Mutat Res. 2010; 705 (2): 96-106.
-
(2010)
Mutat Res.
, vol.705
, Issue.2
, pp. 96-106
-
-
Erickson, R.P.1
-
40
-
-
0025306672
-
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history
-
Nowinski G.P.,vanDyke D.L.,Tilley B.C.,Jacobsen G., Babu V.R., Worsham M.J., Wilson G.N., Weiss L. The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history. Am J Hum Genet1990; 46: 1101-1111.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 1101-1111
-
-
Nowinski, G.P.1
VanDyke, D.L.2
Tilley, B.C.3
Jacobsen, G.4
Babu, V.R.5
Worsham, M.J.6
Wilson, G.N.7
Weiss, L.8
-
41
-
-
0028815566
-
Sex chromosomes loss and aging: In situ hybridization studies on human interphase nuclei
-
Guttenbach M., Koschorz B., Bernthaler U., Grimm T., Schmid M. Sex chromosomes loss and aging: In situ hybridization studies on human interphase nuclei. Am J Hum Genet 1995; 57:1143-1150.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1143-1150
-
-
Guttenbach, M.1
Koschorz, B.2
Bernthaler, U.3
Grimm, T.4
Schmid, M.5
-
42
-
-
9244240317
-
Analysis of gene expression patterns and chromosomal changes associated with aging
-
Geigl J.B., Langer S., Barwisch S., Pfleghaar K., Lederer G., Speicher M.R. Analysis of gene expression patterns and chromosomal changes associated with aging. Cancer Res. 2004; 64: 8850-8557.
-
(2004)
Cancer Res.
, vol.64
, pp. 8850-18557
-
-
Geigl, J.B.1
Langer, S.2
Barwisch, S.3
Pfleghaar, K.4
Lederer, G.5
Speicher, M.R.6
-
44
-
-
4444281968
-
What1 can progeroid syndromes tell us about human aging?
-
DOI 10.1126/science.1102587
-
Kipling D., Davis T., Ostler E.L., Faragher R.G. What can progeroid syndromes tell us about human aging? Science. 2004; 305: 1426-1431. (Pubitemid 39167654)
-
(2004)
Science
, vol.305
, Issue.5689
, pp. 1426-1431
-
-
Kipling, D.1
Davis, T.2
Ostler, E.L.3
Faragher, R.G.A.4
-
45
-
-
35548974875
-
Genetic instability syndromes with progeroid features
-
Neveling K., Bechtold A., Hoehn H. Genetic instability syndromes with progeroid features. Z Gerontol Geriatr 2007; 40: 339-348.
-
(2007)
Z Gerontol Geriatr
, vol.40
, pp. 339-348
-
-
Neveling, K.1
Bechtold, A.2
Hoehn, H.3
-
46
-
-
0017403242
-
Changes in human abnormal cells under prolonged cultivation in stationary phase. Investigation of cells with trisomia 7
-
Vorsanova S.G. Dynamics of changes in anomalous human cells during prolonged cultivation in the stationary phase. Trisomy 7 cells. Biull Eksp Biol Med. 1977; 3: 742-744. (Pubitemid 8118683)
-
(1977)
Byulleten Eksperimentalnoi Biologii I Meditsiny
, vol.83
, Issue.6
, pp. 742-744
-
-
Vorsanova, S.G.1
-
47
-
-
77950944313
-
Cytogenetic contribution to uniparental disomy (UPD)
-
Liehr T. Cytogenetic contribution to uniparental disomy (UPD). MoI Cytogenet 2010; 3: 8.
-
(2010)
MoI Cytogenet
, vol.3
, pp. 8
-
-
Liehr, T.1
-
48
-
-
0028917209
-
Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of postreplicated cells with sitespecific cosmid and cosmid contig probes
-
Soloviev I. V.,YurwY.B., Vorsanova S.G.,Fayet F, Roizes G., Malet P. Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of postreplicated cells with sitespecific cosmid and cosmid contig probes. Prenat Diagn1995; 15: 237-248.
-
(1995)
Prenat Diagn
, vol.15
, pp. 237-248
-
-
Soloviev, I.V.1
Yurw, Y.B.2
Vorsanova, S.G.3
Fayet, F.4
Roizes, G.5
Malet, P.6
-
49
-
-
0035202921
-
FISH analysis of replication and transcription of chromosome X loci: New approach for genetic analysis of Rett syndrome
-
Vorsanova S.G., Yurov YB., Koloti A.D., Soloviev LV. FISH analysis of replication and transcription of chromosome X loci: New approach for genetic analysis of Rett syndrome. Brain Dev. 2001; 23: 191-195.
-
(2001)
Brain Dev.
, vol.23
, pp. 191-195
-
-
Vorsanova, S.G.1
Yurov, Y.B.2
Koloti, A.D.3
Soloviev, L.V.4
-
50
-
-
63149168931
-
Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA
-
Yeshaya J., Amir L, Rimon A., Freedman J., Shohat M., Avivi L. Microdeletion syndromes disclose replication timing alterations of genes unrelated to the missing DNA. Mol Cytogenet2009; 2:11.
-
(2009)
Mol Cytogenet
, vol.2
, pp. 11
-
-
Yeshaya, J.1
Amir, L.2
Rimon, A.3
Freedman, J.4
Shohat, M.5
Avivi, L.6
-
51
-
-
33947289969
-
Cell division in the CNS: Protective response or lethal event in post-mitotic neurons?
-
Yang Y, Herrup K. Cell division in the CNS: protective response or lethal event in post-mitotic neurons? Biochim Biophys Acta 2007; 1772: 457-466.
-
(2007)
Biochim Biophys Acta
, vol.1772
, pp. 457-466
-
-
Yang, Y.1
Herrup, K.2
-
52
-
-
78650011643
-
Genomic landscape of the Alzheimer's disease brain: Chromosome instability - Aneuploidy, but not tetraploidy - Mediates neurodegeneration
-
lourov LY, Vorsanova S.G., Yurov YB. Genomic landscape of the Alzheimer's disease brain: Chromosome instability - aneuploidy, but not tetraploidy - Mediates neurodegeneration. Neurodegener Dis. 2010; 8: 35-37.
-
(2010)
Neurodegener Dis.
, vol.8
, pp. 35-37
-
-
Lourov, L.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
54
-
-
77949874335
-
Somatic genome variations interact with environment, genome and epigenome in the determination of the phenotype: A paradigm shift in genomics?
-
Sgaramella V., Astolfi P.A. Somatic genome variations interact with environment, genome and epigenome in the determination of the phenotype: a paradigm shift in genomics? DNA Repair 2010; 9:470-473.
-
(2010)
DNA Repair
, vol.9
, pp. 470-473
-
-
Sgaramella, V.1
Astolfi, P.A.2
-
55
-
-
47549106466
-
An integrative view of dynamic genomic elements influencing human brain evolution and individual neurodevelopment
-
Gericke G.S. An integrative view of dynamic genomic elements influencing human brain evolution and individual neurodevelopment. Med Hypotheses 2008; 71: 360-373.
-
(2008)
Med Hypotheses
, vol.71
, pp. 360-373
-
-
Gericke, G.S.1
-
56
-
-
60849121066
-
Developmental neural chromosome instability as a possible cause of childhood brain cancers
-
lourov I.Y., Vorsanova S.G., Yurov Y.B. Developmental neural chromosome instability as a possible cause of childhood brain cancers. Med Hypotheses2009; 72: 615-616.
-
(2009)
Med Hypotheses
, vol.72
, pp. 615-616
-
-
Lourov, I.Y.1
Vorsanova, S.G.2
Yurov, Y.B.3
-
57
-
-
77950947945
-
Cancer models, genomic instability and somatic cellular Darwinian evolution
-
Little M.P. Cancer models, genomic instability and somatic cellular Darwinian evolution. Biol Direct2010; 5:19.
-
(2010)
Biol Direct
, vol.5
, pp. 19
-
-
Little, M.P.1
-
58
-
-
84866707888
-
Single cell genomics of the brain: Focus on neuronal diversity and neuropsychiatrie diseases
-
lourov I.Y., Vbrsanova S.G., Yurov Y.B. Single cell genomics of the brain: Focus on neuronal diversity and neuropsychiatrie diseases. Current Genomics 2012; 13 (6): 477-488.
-
(2012)
Current Genomics
, vol.13
, Issue.6
, pp. 477-488
-
-
Lourov, I.Y.1
Vbrsanova, S.G.2
Yurov, Y.B.3
-
59
-
-
78650016138
-
Editorial: Somatic genome variations
-
Yurov YB., lourov I.Y. Editorial: Somatic genome variations. Current Genomics 2010; 11: 377-378.
-
(2010)
Current Genomics
, vol.11
, pp. 377-378
-
-
Yurov, Y.B.1
Lourov, I.Y.2
-
60
-
-
0030937663
-
Cytogenetic and molecular-cytogenetic investigation of Rett syndrome: Analysis of 31 cases
-
Vorsanova S.G., Demidova I.A., Ulas VY. et al. Cytogenetic and molecular-cytogenetic investigation of Rett syndrome. Analysis of 31 cases. NeuroReport. 1996; 7: 187-189. (Pubitemid 126785556)
-
(1996)
NeuroReport
, vol.8
, Issue.1
, pp. 187-189
-
-
Vorsanova, S.G.1
Demidova, I.A.2
Ulas, V.Y.3
Soloviev, I.V.4
Kazantzeva, L.Z.5
Yurov, Y.B.6
-
61
-
-
0035204270
-
Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): A retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys)
-
Vbrsanova S.G., Yurov YB., Ulas VY. et al. Cytogenetic and molecular-cytogenetic studies of Rett syndrome (RTT): A retrospective analysis of a Russian cohort of RTT patients (the investigation of 57 girls and three boys). Brain Dev. 2001; 23:196-201.
-
(2001)
Brain Dev.
, vol.23
, pp. 196-201
-
-
Vbrsanova, S.G.1
Yurov, Y.B.2
Ulas, V.Y.3
-
62
-
-
77955550211
-
Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: A search for familial genetic markers for autistic disorders
-
Vorsanova S.G., Vbinova V.Yu., Yurov I.Yu., Kurinnaya O.S., Demidova I.A., Yurov Yu.B. Cytogenetic, molecular-cytogenetic, and clinical-genealogical studies of the mothers of children with autism: A search for familial genetic markers for autistic disorders. Neurosciense and Behavioral Physiology 2010; 40: 745-756.
-
(2010)
Neurosciense and Behavioral Physiology
, vol.40
, pp. 745-756
-
-
Vorsanova, S.G.1
Vbinova, V.Y.2
Yurov, I.Y.3
Kurinnaya, O.S.4
Demidova, I.A.5
Yurov, Yu.B.6
-
63
-
-
84872287476
-
Aneuploidy in the autistic brain: The first molecular cytogenetic study
-
Yurov YB., Vorsanova S.G., Kolotii A.D., Liehr T, lourov I.Y. Aneuploidy in the autistic brain: the first molecular cytogenetic study. Balkan Journal of Medical Genetics2011; 14: 73.
-
(2011)
Balkan Journal of Medical Genetics
, vol.14
, pp. 73
-
-
Yurov, Y.B.1
Vorsanova, S.G.2
Kolotii, A.D.3
Liehr, T.4
Lourov, I.Y.5
|