-
1
-
-
70449245071
-
Etude des chromosomes somatiqaues de neuf enfants mongoliens.
-
Lejeune, J., Gautier, M., and Turpin, R. (1959) Etude des chromosomes somatiqaues de neuf enfants mongoliens. C. R. Acad. Sci. 248, 1721-1722.
-
(1959)
C. R. Acad. Sci
, vol.248
, pp. 1721-1722
-
-
Lejeune, J.1
Gautier, M.2
Turpin, R.3
-
2
-
-
0000521855
-
Down syndrome (trisomy 21)
-
7th ed. Stansbury, J.B, Wyngarden, J.B, and Fredrickson, D.S, Eds. McGraw-Hill, New York. pp
-
Epstein, C.J. (1995) Down syndrome (trisomy 21). In The Metabolic and Molecular Bases of Inherited Disease. 7th ed. Stansbury, J.B., Wyngarden, J.B., and Fredrickson, D.S., Eds. McGraw-Hill, New York. pp 749-795.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, pp. 749-795
-
-
Epstein, C.J.1
-
3
-
-
4243116886
-
Down syndrome
-
Jameson, J.L, Ed. Humana Press, Totowa, N.J. pp
-
Antonarakis, S.E. (1998) Down syndrome. In Principles of Molecular Medicine. Jameson, J.L., Ed. Humana Press, Totowa, N.J. pp. 1069-1078.
-
(1998)
Principles of Molecular Medicine
, pp. 1069-1078
-
-
Antonarakis, S.E.1
-
4
-
-
0037320553
-
Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction
-
Berend, S.A., Page, S.L., Atkinson, W., McCaskill, C., Lamb, N.E., Sherman, S.L., and Shaffer, L.G. (2003) Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction. Am. J. Hum. Genet. 72, 488-495.
-
(2003)
Am. J. Hum. Genet
, vol.72
, pp. 488-495
-
-
Berend, S.A.1
Page, S.L.2
Atkinson, W.3
McCaskill, C.4
Lamb, N.E.5
Sherman, S.L.6
Shaffer, L.G.7
-
5
-
-
0036908675
-
Parental origin and timing of de novo Robertsonian translocation formation
-
Bandyopadhyay, R., Heller, A., Knox-DuBois, C., McCaskill, C., Berend, S.A., Page, S.L., and Shaffer, L.G. (2002) Parental origin and timing of de novo Robertsonian translocation formation. Am. J. Hum. Genet. 71, 1456-1462.
-
(2002)
Am. J. Hum. Genet
, vol.71
, pp. 1456-1462
-
-
Bandyopadhyay, R.1
Heller, A.2
Knox-DuBois, C.3
McCaskill, C.4
Berend, S.A.5
Page, S.L.6
Shaffer, L.G.7
-
6
-
-
63749094761
-
The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues
-
Papavassiliou, P., York, T.P., Gursoy, N., Hill, G., Nicely, L.V., Sundaram, U., McClain, A., Aggen, S.H., Eaves, L., Riley, B., and Jackson-Cook, C. (2009) The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues. Am. J. Med. Genet. A 149, 573-583.
-
(2009)
Am. J. Med. Genet. A
, vol.149
, pp. 573-583
-
-
Papavassiliou, P.1
York, T.P.2
Gursoy, N.3
Hill, G.4
Nicely, L.V.5
Sundaram, U.6
McClain, A.7
Aggen, S.H.8
Eaves, L.9
Riley, B.10
Jackson-Cook, C.11
-
7
-
-
58849085419
-
Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: A report from the Atlanta and National Down Syndrome Projects
-
Allen, E.G., Freeman, S.B., Druschel, C., Hobbs, C.A., O'Leary, L.A., Romitti, P.A., Royle, M.H., Torfs, C.P., and Sherman, S.L. (2009) Maternal age and risk for trisomy 21 assessed by the origin of chromosome nondisjunction: a report from the Atlanta and National Down Syndrome Projects. Hum. Genet. 125, 41-52.
-
(2009)
Hum. Genet
, vol.125
, pp. 41-52
-
-
Allen, E.G.1
Freeman, S.B.2
Druschel, C.3
Hobbs, C.A.4
O'Leary, L.A.5
Romitti, P.A.6
Royle, M.H.7
Torfs, C.P.8
Sherman, S.L.9
-
8
-
-
0028095222
-
Increased risk of Alzheimer's disease in mothers of adults with Down's syndrome
-
Schupf, N., Kapell, D., Lee, J.H., Ottman, R., and Mayeux, R. (1994) Increased risk of Alzheimer's disease in mothers of adults with Down's syndrome. Lancet 344, 353-356.
-
(1994)
Lancet
, vol.344
, pp. 353-356
-
-
Schupf, N.1
Kapell, D.2
Lee, J.H.3
Ottman, R.4
Mayeux, R.5
-
9
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II
-
Lamb, N.E., Freeman, S.B., Savage-Austin, A., Pettay, D., Taft, L., Hersey, J., Gu, Y., Shen, J., Saker, D., May, K.M., Avramopoulos, D., Petersen, M.B., Hallberg, A., Mikkelsen, M., Hassold, T.J., and Sherman., S.L. (1996) Susceptible chiasmate configurations of chromosome 21 predispose to non-disjunction in both maternal meiosis I and meiosis II. Nat. Genet. 14, 400-405.
-
(1996)
Nat. Genet
, vol.14
, pp. 400-405
-
-
Lamb, N.E.1
Freeman, S.B.2
Savage-Austin, A.3
Pettay, D.4
Taft, L.5
Hersey, J.6
Gu, Y.7
Shen, J.8
Saker, D.9
May, K.M.10
Avramopoulos, D.11
Petersen, M.B.12
Hallberg, A.13
Mikkelsen, M.14
Hassold, T.J.15
Sherman, S.L.16
-
10
-
-
0030747338
-
Estimating meiotic exchange patterns from recombination data: An application to humans
-
Lamb, N.E., Feingold, E., and Sherman, S.L. (1997) Estimating meiotic exchange patterns from recombination data: an application to humans. Genetics 146, 1011-1017.
-
(1997)
Genetics
, vol.146
, pp. 1011-1017
-
-
Lamb, N.E.1
Feingold, E.2
Sherman, S.L.3
-
11
-
-
11144261739
-
Association between maternal age and meiotic recombination for trisomy 21
-
Lamb, N.E., Yu, K., Shaffer, J., Feingold, E., and Sherman, S.L. (2005) Association between maternal age and meiotic recombination for trisomy 21. Am. J. Hum. Genet. 76, 91-99.
-
(2005)
Am. J. Hum. Genet
, vol.76
, pp. 91-99
-
-
Lamb, N.E.1
Yu, K.2
Shaffer, J.3
Feingold, E.4
Sherman, S.L.5
-
12
-
-
41949097237
-
-
Oliver, T.R., Feingold, E., Yu, K., Cheung, V., Tinker, S., Yadav-Shah, M., Masse, N., and Sherman, S.L. (2008) New insights into human nondisjunction of chromosome 21 in oocytes. PLoS Genet. 4e1000033.
-
Oliver, T.R., Feingold, E., Yu, K., Cheung, V., Tinker, S., Yadav-Shah, M., Masse, N., and Sherman, S.L. (2008) New insights into human nondisjunction of chromosome 21 in oocytes. PLoS Genet. 4e1000033.
-
-
-
-
13
-
-
68049085066
-
On the origin of trisomy 21 Down syndrome
-
Hultén, M.A., Patel, S.D., Tankimanova, M., Westgren, M., Papadogiannakis, N., Jonsson, A.M., and Iwarsson, E. (2008) On the origin of trisomy 21 Down syndrome. Mol. Cytogenet. 1, 21.
-
(2008)
Mol. Cytogenet
, vol.1
, pp. 21
-
-
Hultén, M.A.1
Patel, S.D.2
Tankimanova, M.3
Westgren, M.4
Papadogiannakis, N.5
Jonsson, A.M.6
Iwarsson, E.7
-
14
-
-
0043093697
-
Transposable elements: Targets for early nutritional effects on epigenetic gene regulation
-
Waterland, R.A. and Jirtle, R.L. (2003) Transposable elements: targets for early nutritional effects on epigenetic gene regulation. Mol. Cell. Biol. 23, 5293-5300.
-
(2003)
Mol. Cell. Biol
, vol.23
, pp. 5293-5300
-
-
Waterland, R.A.1
Jirtle, R.L.2
-
15
-
-
0032845227
-
Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome
-
James, S.J., Pogribna, M., Pogribny, I.P., Melnyk, S., Hine, R.J., Gibson, J.B., Yi, P., Tafoya, D.L., Swenson, D.H., Wilson, V.L., and Gaylor, D.W. (1999) Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome. Am. J. Clin. Nutr. 70, 495-501.
-
(1999)
Am. J. Clin. Nutr
, vol.70
, pp. 495-501
-
-
James, S.J.1
Pogribna, M.2
Pogribny, I.P.3
Melnyk, S.4
Hine, R.J.5
Gibson, J.B.6
Yi, P.7
Tafoya, D.L.8
Swenson, D.H.9
Wilson, V.L.10
Gaylor, D.W.11
-
16
-
-
34248631955
-
Playing hide and seek with mammalian meiotic crossover hotspots
-
Buard, J. and de Massy, B. (2007) Playing hide and seek with mammalian meiotic crossover hotspots. Trends Genet. 23, 301-309.
-
(2007)
Trends Genet
, vol.23
, pp. 301-309
-
-
Buard, J.1
de Massy, B.2
-
17
-
-
42149101071
-
DNA methylation reprogramming in the germ line
-
Lees-Murdock, D.J. and Walsh, C.P. (2008) DNA methylation reprogramming in the germ line. Epigenetics 3, 5-13.
-
(2008)
Epigenetics
, vol.3
, pp. 5-13
-
-
Lees-Murdock, D.J.1
Walsh, C.P.2
-
18
-
-
44449111154
-
The association of folate, zinc and antioxidant intake with sperm aneuploidy in healthy non-smoking men
-
Young, S.S., Eskenazi, B., Marchetti, F.M., Block, G., and Wyrobek, A.J. (2008) The association of folate, zinc and antioxidant intake with sperm aneuploidy in healthy non-smoking men. Hum. Reprod. 23, 1014-1022.
-
(2008)
Hum. Reprod
, vol.23
, pp. 1014-1022
-
-
Young, S.S.1
Eskenazi, B.2
Marchetti, F.M.3
Block, G.4
Wyrobek, A.J.5
-
19
-
-
35748973239
-
Abnormal meiotic recombination in infertile men and its association with sperm aneuploidy
-
Ferguson, K.A., Wong, E.C., Chow, V., Nigro, M., and Ma, S. (2007) Abnormal meiotic recombination in infertile men and its association with sperm aneuploidy. Hum. Mol. Genet. 16, 2870-2879.
-
(2007)
Hum. Mol. Genet
, vol.16
, pp. 2870-2879
-
-
Ferguson, K.A.1
Wong, E.C.2
Chow, V.3
Nigro, M.4
Ma, S.5
-
20
-
-
33751380396
-
Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility
-
Lee, H.C., Jeong, Y.M., Lee, S.H., Cha, K.Y., Song, S.H., Kim, N.K., Lee, K.W., and Lee, S. (2006) Association study of four polymorphisms in three folate-related enzyme genes with non-obstructive male infertility. Hum. Reprod. 21, 3162-3170.
-
(2006)
Hum. Reprod
, vol.21
, pp. 3162-3170
-
-
Lee, H.C.1
Jeong, Y.M.2
Lee, S.H.3
Cha, K.Y.4
Song, S.H.5
Kim, N.K.6
Lee, K.W.7
Lee, S.8
-
21
-
-
3042591660
-
Folate deficiency induces aneuploidy in human lymphocytes in vitro-evidence using cytokinesis-blocked cells and probes specific for chromosomes 17 and 21
-
Wang, X., Thomas, P., Xue, J., and Fenech, M. (2004) Folate deficiency induces aneuploidy in human lymphocytes in vitro-evidence using cytokinesis-blocked cells and probes specific for chromosomes 17 and 21. Mutat. Res. 551, 167-180.
-
(2004)
Mutat. Res
, vol.551
, pp. 167-180
-
-
Wang, X.1
Thomas, P.2
Xue, J.3
Fenech, M.4
-
22
-
-
0033846999
-
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
-
Hobbs, C.A., Sherman, S.L., Yi, P., Hopkins, S.E., Torfs, C.P., Hine, R.J., Pogribna, M., Rozen, R., and James, S.J. (2000) Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome. Am. J. Hum. Genet. 67, 623-630.
-
(2000)
Am. J. Hum. Genet
, vol.67
, pp. 623-630
-
-
Hobbs, C.A.1
Sherman, S.L.2
Yi, P.3
Hopkins, S.E.4
Torfs, C.P.5
Hine, R.J.6
Pogribna, M.7
Rozen, R.8
James, S.J.9
-
23
-
-
0042194787
-
Methionine synthase (MTR) 2756 (A>G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome
-
Bosco, P., Gueant-Rodriguez, R.M., Anello, G., Barone, C., Namour, F., Caraci, F., Roman, A., Romano, C., and Gueant, J.L. (2003) Methionine synthase (MTR) 2756 (A>G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome. Am. J. Med. Genet. A 121, 219-224.
-
(2003)
Am. J. Med. Genet. A
, vol.121
, pp. 219-224
-
-
Bosco, P.1
Gueant-Rodriguez, R.M.2
Anello, G.3
Barone, C.4
Namour, F.5
Caraci, F.6
Roman, A.7
Romano, C.8
Gueant, J.L.9
-
24
-
-
33646240576
-
Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women
-
Coppedè, F., Marini, G., Bargagna, S., Stuppia, L., Minichilli, F., Fontana, I., Colognato, R., Astrea, G., Palka, G., and Migliore, L. (2006) Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women. Am. J. Med. Genet. A 140, 1083-1091.
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 1083-1091
-
-
Coppedè, F.1
Marini, G.2
Bargagna, S.3
Stuppia, L.4
Minichilli, F.5
Fontana, I.6
Colognato, R.7
Astrea, G.8
Palka, G.9
Migliore, L.10
-
25
-
-
33747873426
-
Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring
-
Scala, I., Granese, B., Sellitto, M., Salomè, S., Sammartino, A., Pepe, A., Mastroiacovo, P., Sebastio, G., and Andria, G. (2006) Analysis of seven maternal polymorphisms of genes involved in homocysteine/folate metabolism and risk of Down syndrome offspring. Genet. Med. 8, 409-416.
-
(2006)
Genet. Med
, vol.8
, pp. 409-416
-
-
Scala, I.1
Granese, B.2
Sellitto, M.3
Salomè, S.4
Sammartino, A.5
Pepe, A.6
Mastroiacovo, P.7
Sebastio, G.8
Andria, G.9
-
26
-
-
40749124471
-
Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: Maternal risk factors for Down syndrome in Brazil
-
Biselli, J.M., Goloni-Bertollo, E.M., Zampieri, B.L., Haddad, R., Eberlin, M.N., and Pavarino-Bertelli, E.C. (2008) Genetic polymorphisms involved in folate metabolism and elevated plasma concentrations of homocysteine: maternal risk factors for Down syndrome in Brazil. Genet. Mol. Res. 7, 33-42.
-
(2008)
Genet. Mol. Res
, vol.7
, pp. 33-42
-
-
Biselli, J.M.1
Goloni-Bertollo, E.M.2
Zampieri, B.L.3
Haddad, R.4
Eberlin, M.N.5
Pavarino-Bertelli, E.C.6
-
27
-
-
56749097937
-
Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring
-
Coppedè, F., Migheli, F., Bargagna, S., Siciliano, G., Antonucci, I., Stuppia, L., Palka, G., and Migliore, L. (2009) Association of maternal polymorphisms in folate metabolizing genes with chromosome damage and risk of Down syndrome offspring. Neurosci. Lett. 449, 15-19.
-
(2009)
Neurosci. Lett
, vol.449
, pp. 15-19
-
-
Coppedè, F.1
Migheli, F.2
Bargagna, S.3
Siciliano, G.4
Antonucci, I.5
Stuppia, L.6
Palka, G.7
Migliore, L.8
-
28
-
-
33646119427
-
-
Martínez-Frías, M.L., Pérez, B., Desviat, L.R., Castro, M., Leal, F., Rodríguez, L., Mansilla, E., Martínez- Fernández, M.L., Bermejo, E., Rodríguez-Pinilla, E., Prieto, D., Ugarte, M.; ECEMC Working Group (2006) Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome? Am. J. Med. Genet. A 140, 987-997.
-
Martínez-Frías, M.L., Pérez, B., Desviat, L.R., Castro, M., Leal, F., Rodríguez, L., Mansilla, E., Martínez- Fernández, M.L., Bermejo, E., Rodríguez-Pinilla, E., Prieto, D., Ugarte, M.; ECEMC Working Group (2006) Maternal polymorphisms 677C-T and 1298A-C of MTHFR, and 66A-G MTRR genes: is there any relationship between polymorphisms of the folate pathway, maternal homocysteine levels, and the risk for having a child with Down syndrome? Am. J. Med. Genet. A 140, 987-997.
-
-
-
-
29
-
-
58149345081
-
Folate metabolism and the risk of Down syndrome
-
Patterson, D. (2008) Folate metabolism and the risk of Down syndrome. Downs Syndr. Res. Pract. 12, 93-97.
-
(2008)
Downs Syndr. Res. Pract
, vol.12
, pp. 93-97
-
-
Patterson, D.1
-
30
-
-
34247869695
-
-
Scala, I., Granese, B., Lisi, A., Mastroiacovo, P., and Andria, G. (2007) Response to folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women by F. Coppedè et al. (2006). Am. J. Med. Genet. A 143, 1015-1017.
-
Scala, I., Granese, B., Lisi, A., Mastroiacovo, P., and Andria, G. (2007) Response to "folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women" by F. Coppedè et al. (2006). Am. J. Med. Genet. A 143, 1015-1017.
-
-
-
-
31
-
-
58849137063
-
Prevalence of the polymorphism MTHFR A1298C and not MTHFR C677T is related to chromosomal aneuploidy in Brazilian Turner Syndrome patients
-
Oliveira, K.C., Bianco, B.B., Verreschi, I.T., Guedes, A.D., Galera, B.B., Galera, M.F., Barbosa, C.P., and Lipay, M.V. (2008) Prevalence of the polymorphism MTHFR A1298C and not MTHFR C677T is related to chromosomal aneuploidy in Brazilian Turner Syndrome patients. Arq. Bras. Endocrinol. Metabol. 52, 1374-1381.
-
(2008)
Arq. Bras. Endocrinol. Metabol
, vol.52
, pp. 1374-1381
-
-
Oliveira, K.C.1
Bianco, B.B.2
Verreschi, I.T.3
Guedes, A.D.4
Galera, B.B.5
Galera, M.F.6
Barbosa, C.P.7
Lipay, M.V.8
-
32
-
-
0034920304
-
Maternal folate polymorphisms and the etiology of human nondisjunction
-
Hassold, T.J., Burrage, L.C., Chan, E.R., Judis, L.M., Schwartz, S., James, S.J., Jacobs, P.A., and Thomas, N.S. (2001) Maternal folate polymorphisms and the etiology of human nondisjunction. Am. J. Hum. Genet. 69, 434-439.
-
(2001)
Am. J. Hum. Genet
, vol.69
, pp. 434-439
-
-
Hassold, T.J.1
Burrage, L.C.2
Chan, E.R.3
Judis, L.M.4
Schwartz, S.5
James, S.J.6
Jacobs, P.A.7
Thomas, N.S.8
-
33
-
-
33645993587
-
Susceptibility to chromosome malsegregation in lymphocytes of women who had a Down syndrome child in young age
-
Migliore, L., Boni, G., Bernardini, R., Trippi, F., Colognato, R., Fontana, I., Coppedè, F., and Sbrana, I. (2006) Susceptibility to chromosome malsegregation in lymphocytes of women who had a Down syndrome child in young age. Neurobiol. Aging 27, 710-716.
-
(2006)
Neurobiol. Aging
, vol.27
, pp. 710-716
-
-
Migliore, L.1
Boni, G.2
Bernardini, R.3
Trippi, F.4
Colognato, R.5
Fontana, I.6
Coppedè, F.7
Sbrana, I.8
-
34
-
-
34548312384
-
Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children
-
Coppedè, F., Colognato, R., Bonelli, A., Astrea, G., Bargagna, S., Siciliano, G., and Migliore, L. (2007) Polymorphisms in folate and homocysteine metabolizing genes and chromosome damage in mothers of Down syndrome children. Am. J. Med. Genet. A 143, 2006-2015.
-
(2007)
Am. J. Med. Genet. A
, vol.143
, pp. 2006-2015
-
-
Coppedè, F.1
Colognato, R.2
Bonelli, A.3
Astrea, G.4
Bargagna, S.5
Siciliano, G.6
Migliore, L.7
-
35
-
-
0032816455
-
Alzheimer's disease and Down syndrome: From meiosis to dementia
-
Petronis, A. (1999) Alzheimer's disease and Down syndrome: from meiosis to dementia. Exp. Neurol. 58, 403-413.
-
(1999)
Exp. Neurol
, vol.58
, pp. 403-413
-
-
Petronis, A.1
-
36
-
-
0035949802
-
Specificity of the fivefold increase in AD in mothers of adults with Down syndrome
-
Schupf, N., Kapell, D., Nightingale, B., Lee, J.H., Mohlenhoff, J., Bewley, S., Ottman, R., and Mayeux, R. (2001) Specificity of the fivefold increase in AD in mothers of adults with Down syndrome. Neurology 57, 979-984.
-
(2001)
Neurology
, vol.57
, pp. 979-984
-
-
Schupf, N.1
Kapell, D.2
Nightingale, B.3
Lee, J.H.4
Mohlenhoff, J.5
Bewley, S.6
Ottman, R.7
Mayeux, R.8
-
37
-
-
0025801967
-
Alzheimer disease and Down syndrome-chromosome 21 non-disjunction may underlie both disorders
-
Potter, H. (1991) Alzheimer disease and Down syndrome-chromosome 21 non-disjunction may underlie both disorders. Am. J. Hum. Genet. 48, 1192-1200.
-
(1991)
Am. J. Hum. Genet
, vol.48
, pp. 1192-1200
-
-
Potter, H.1
-
38
-
-
33751279395
-
Aneuploidy in the normal and diseased brain
-
Kingsbury, M.A., Yung, Y.C., Peterson, S.E., Westra, J.W., and Chun, J. (2006) Aneuploidy in the normal and diseased brain. Cell. Mol. Life Sci. 63, 2626-2641.
-
(2006)
Cell. Mol. Life Sci
, vol.63
, pp. 2626-2641
-
-
Kingsbury, M.A.1
Yung, Y.C.2
Peterson, S.E.3
Westra, J.W.4
Chun, J.5
-
39
-
-
64449088956
-
Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: Differential expression and pathological meaning
-
Iourov, I.Y., Vorsanova, S.G., Liehr, T., and Yurov, Y.B. (2009) Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning. Neurobiol. Dis. 34, 212-220.
-
(2009)
Neurobiol. Dis
, vol.34
, pp. 212-220
-
-
Iourov, I.Y.1
Vorsanova, S.G.2
Liehr, T.3
Yurov, Y.B.4
-
40
-
-
40849113052
-
Mosaicism for trisomy 21 in a patient with youngonset dementia: A case report and brief literature review
-
Ringman, J.M., Rao, P.N., Lu, P.H., and Cederbaum, S. (2008) Mosaicism for trisomy 21 in a patient with youngonset dementia: a case report and brief literature review. Arch. Neurol. 65, 412-415.
-
(2008)
Arch. Neurol
, vol.65
, pp. 412-415
-
-
Ringman, J.M.1
Rao, P.N.2
Lu, P.H.3
Cederbaum, S.4
-
41
-
-
3042856300
-
-
Beck, J.A., Poulter, M., Campbell, T.A., Uphill, J.B., Adamson, G., Geddes, J.F., Revesz, T., Davis, M.B., Wood, N.W., Collinge, J., and Tabrizi, S.J. (2004) Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Hum. Mol. Genet. 13, 1219-1224.
-
Beck, J.A., Poulter, M., Campbell, T.A., Uphill, J.B., Adamson, G., Geddes, J.F., Revesz, T., Davis, M.B., Wood, N.W., Collinge, J., and Tabrizi, S.J. (2004) Somatic and germline mosaicism in sporadic early-onset Alzheimer's disease. Hum. Mol. Genet. 13, 1219-1224.
-
-
-
-
42
-
-
0030761059
-
Alzheimer presenilins in the nuclear membrane, interphase kinetochores, and centrosomes suggest role in chromosome segregation
-
Li, J., Xu, M., Zhou, H., Ma, J., and Potter, H. (1997) Alzheimer presenilins in the nuclear membrane, interphase kinetochores, and centrosomes suggest role in chromosome segregation. Cell 90, 917-927.
-
(1997)
Cell
, vol.90
, pp. 917-927
-
-
Li, J.1
Xu, M.2
Zhou, H.3
Ma, J.4
Potter, H.5
-
43
-
-
0033033062
-
Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease
-
Geller, L.N. and Potter, H. (1999) Chromosome missegregation and trisomy 21 mosaicism in Alzheimer's disease. Neurobiol. Dis. 6, 67-79.
-
(1999)
Neurobiol. Dis
, vol.6
, pp. 67-79
-
-
Geller, L.N.1
Potter, H.2
-
44
-
-
0033399922
-
Preferential occurrence of chromosome 21 malsegregation in peripheral blood lymphocytes of Alzheimer disease patients
-
Migliore, L., Botto, N., Scarpato, R., Petrozzi, L., Cipriani, G., and Bonuccelli, U. (1999) Preferential occurrence of chromosome 21 malsegregation in peripheral blood lymphocytes of Alzheimer disease patients. Cytogenet. Cell Genet. 87, 41-46.
-
(1999)
Cytogenet. Cell Genet
, vol.87
, pp. 41-46
-
-
Migliore, L.1
Botto, N.2
Scarpato, R.3
Petrozzi, L.4
Cipriani, G.5
Bonuccelli, U.6
-
45
-
-
38549181768
-
Chromosome 17 and 21 aneuploidy in buccal cells is increased with ageing and in Alzheimer's disease
-
Thomas, P. and Fenech, M. (2008) Chromosome 17 and 21 aneuploidy in buccal cells is increased with ageing and in Alzheimer's disease. Mutagenesis 23, 57-65.
-
(2008)
Mutagenesis
, vol.23
, pp. 57-65
-
-
Thomas, P.1
Fenech, M.2
-
46
-
-
49549083587
-
Neuronal binucleation in Alzheimer disease hippocampus
-
Zhu, X., Siedlak, S.L., Wang, Y., Perry, G., Castellani, R.J., Cohen, M.L., and Smith, M.A. (2008) Neuronal binucleation in Alzheimer disease hippocampus. Neuropathol. Appl. Neurobiol. 34, 457-465.
-
(2008)
Neuropathol. Appl. Neurobiol
, vol.34
, pp. 457-465
-
-
Zhu, X.1
Siedlak, S.L.2
Wang, Y.3
Perry, G.4
Castellani, R.J.5
Cohen, M.L.6
Smith, M.A.7
-
47
-
-
50449095363
-
Is the time dimension of the cell cycle re-entry in AD regulated by centromere cohesion dynamics?
-
Bajic, V.P., Spremo-Potparevic, B., Zivkovic, L, Djelic, N., and Smith, M.A. (2008) Is the time dimension of the cell cycle re-entry in AD regulated by centromere cohesion dynamics? Biosci. Hypotheses 1, 156-161.
-
(2008)
Biosci. Hypotheses
, vol.1
, pp. 156-161
-
-
Bajic, V.P.1
Spremo-Potparevic, B.2
Zivkovic, L.3
Djelic, N.4
Smith, M.A.5
-
48
-
-
33750968801
-
Analysis of premature centromere division (PCD) of the chromosome 18 in peripheral blood lymphocytes in Alzheimer disease patients
-
Zivkovic, L., Spremo-Potparevic, B., Djelic, N., and Bajic, V. (2006) Analysis of premature centromere division (PCD) of the chromosome 18 in peripheral blood lymphocytes in Alzheimer disease patients. Mech. Ageing Dev. 127, 892-896.
-
(2006)
Mech. Ageing Dev
, vol.127
, pp. 892-896
-
-
Zivkovic, L.1
Spremo-Potparevic, B.2
Djelic, N.3
Bajic, V.4
-
49
-
-
49549098397
-
Premature centromere division of the X chromosome in neurons in Alzheimer's disease
-
Spremo-Potparevic, B., Zivkovic, L., Djelic, N., Plecas-Solarovic, B., Smith, M.A., and Bajic, V.J. (2008) Premature centromere division of the X chromosome in neurons in Alzheimer's disease. Neurochemistry 106, 2218-2223.
-
(2008)
Neurochemistry
, vol.106
, pp. 2218-2223
-
-
Spremo-Potparevic, B.1
Zivkovic, L.2
Djelic, N.3
Plecas-Solarovic, B.4
Smith, M.A.5
Bajic, V.J.6
-
50
-
-
43549095229
-
Alzheimer's disease, aneuploidy and neurogenesis
-
Taupin, P. (2008) Alzheimer's disease, aneuploidy and neurogenesis. Med. Sci. Monit. 14, LE6-6.
-
(2008)
Med. Sci. Monit
, vol.14
-
-
Taupin, P.1
-
51
-
-
62149107892
-
DNA damage and repair in Alzheimer's disease
-
Coppedè, F. and Migliore, L. (2009) DNA damage and repair in Alzheimer's disease. Curr. Alzheimer Res. 6, 36-47.
-
(2009)
Curr. Alzheimer Res
, vol.6
, pp. 36-47
-
-
Coppedè, F.1
Migliore, L.2
-
52
-
-
0034068273
-
Serum folate and the severity of atrophy of the neocortex in Alzheimer disease: Findings from the Nun study
-
Snowdon, D.A., Tully, C.L., Smith, C.D., Riley, K.P., and Markesbery, W.R. (2000) Serum folate and the severity of atrophy of the neocortex in Alzheimer disease: findings from the Nun study. Am. J. Clin. Nutr. 71, 993-998.
-
(2000)
Am. J. Clin. Nutr
, vol.71
, pp. 993-998
-
-
Snowdon, D.A.1
Tully, C.L.2
Smith, C.D.3
Riley, K.P.4
Markesbery, W.R.5
-
53
-
-
29144432126
-
Folate, but not homocysteine, predicts the risk of fracture in elderly persons
-
Ravaglia, G., Forti, P., Maioli, F., Servadei, L., Martelli, M., Brunetti, N., Bastagli, L., Cucinotta, D., and Mariani, E. (2005) Folate, but not homocysteine, predicts the risk of fracture in elderly persons. J. Gerontol. A Biol. Sci. Med. Sci. 60, 1458-1462.
-
(2005)
J. Gerontol. A Biol. Sci. Med. Sci
, vol.60
, pp. 1458-1462
-
-
Ravaglia, G.1
Forti, P.2
Maioli, F.3
Servadei, L.4
Martelli, M.5
Brunetti, N.6
Bastagli, L.7
Cucinotta, D.8
Mariani, E.9
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