-
1
-
-
85003166195
-
Syndrome characterized by gynecomastia, aspermatogenesis without a Leydigism and increased excretion of follicle-stimulating hormone
-
H.F. Klinefelter, E.C. Reifenstein and F. Albright (1942) Syndrome characterized by gynecomastia, aspermatogenesis without a Leydigism and increased excretion of follicle-stimulating hormone. J Clin Endocrinol Metab 2 615-627.
-
(1942)
J Clin Endocrinol Metab
, vol.2
, pp. 615-627
-
-
Klinefelter, H.F.1
Reifenstein, E.C.2
Albright, F.3
-
2
-
-
33747686159
-
A case of human intersexuality having a possible XXY sex-determining mechanism
-
P.A. Jacobs and J.A. Strong (1959) A case of human intersexuality having a possible XXY sex-determining mechanism. Nature 183 302-303.
-
(1959)
Nature
, vol.183
, pp. 302-303
-
-
Jacobs, P.A.1
Strong, J.A.2
-
4
-
-
0037326103
-
Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study
-
A. Bojesen, S. Juul and C.H. Gravholt (2003) Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study. J Clin Endocrinol Metab 88 622-626.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 622-626
-
-
Bojesen, A.1
Juul, S.2
Gravholt, C.H.3
-
5
-
-
84856389510
-
Clinical presentation of Klinefelter's syndrome: differences according to age
-
N. Pacenza, T. Pasqualini, S. Gottlieb, P. Knoblovits, P.R. Costanzo, J.S. Usher, et al. (2012) Clinical presentation of Klinefelter's syndrome: differences according to age. Internat J Endocrinol doi: 101155/2012/324835
-
(2012)
Internat J Endocrinol
-
-
Pacenza, N.1
Pasqualini, T.2
Gottlieb, S.3
Knoblovits, P.4
Costanzo, P.R.5
Usher, J.S.6
-
6
-
-
84864478607
-
It's not all about the testes: medical issues in Klinefelter patients
-
online before press
-
R.Z. Sokol (2012) It's not all about the testes: medical issues in Klinefelter patients. Fertil Steril http://dx.doi.org/10.1016/fertnstert.2012.05.026 online before press
-
(2012)
Fertil Steril
-
-
Sokol, R.Z.1
-
7
-
-
77953931323
-
Animal models for Klinefelter’s syndrome and their relevance for the clinic
-
J. Wistuba (2010) Animal models for Klinefelter’s syndrome and their relevance for the clinic. Mol Hum Reprod 16 375-385.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 375-385
-
-
Wistuba, J.1
-
8
-
-
0025918287
-
∗ chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region
-
E.M. Eicher, D.W. Hale, P.A. Hunt, B.K. Lee, P.K. Tucker, T.R. King, et al. (1991) The mouse Y∗ chromosome involves a complex rearrangement, including interstitial positioning of the pseudoautosomal region. Cytogenet Cell Genet 57 221-230.
-
(1991)
Cytogenet Cell Genet
, vol.57
, pp. 221-230
-
-
Eicher, E.M.1
Hale, D.W.2
Hunt, P.A.3
Lee, B.K.4
Tucker, P.K.5
King, T.R.6
-
9
-
-
73949144105
-
Severe XIST hypomethylation clearly distinguishes (SRY+) 46, XX-maleness from Klinefelter syndrome
-
A. Poplinski, P. Wieacker, S. Kliesch and J. Gromoll (2010) Severe XIST hypomethylation clearly distinguishes (SRY+) 46, XX-maleness from Klinefelter syndrome. Eur J Endocrinol 162 169-175.
-
(2010)
Eur J Endocrinol
, vol.162
, pp. 169-175
-
-
Poplinski, A.1
Wieacker, P.2
Kliesch, S.3
Gromoll, J.4
-
10
-
-
79955521239
-
Mouse model for men with Klinefelter syndrome: a multifaceted fit for a complex disorder
-
R.S. Swerdloff, Y. Lue, P.Y. Liu, K. Erkkilä and C. Wang (2011) Mouse model for men with Klinefelter syndrome: a multifaceted fit for a complex disorder. Acta Paediatr 100 892-899.
-
(2011)
Acta Paediatr
, vol.100
, pp. 892-899
-
-
Swerdloff, R.S.1
Lue, Y.2
Liu, P.Y.3
Erkkilä, K.4
Wang, C.5
-
11
-
-
79955489716
-
Y∗ mouse model for Klinefelter’s syndrome
-
S. Werler, A. Poplinski, J. Gromoll and J. Wistuba (2011) Expression of genes escaping from X inactivation in the 41, XXY∗ mouse model for Klinefelter’s syndrome. Acta Paediatr 100 885-891.
-
(2011)
Acta Paediatr
, vol.100
, pp. 885-891
-
-
Werler, S.1
Poplinski, A.2
Gromoll, J.3
Wistuba, J.4
-
12
-
-
77953941607
-
Y∗ mice as a model for Klinefelter syndrome: hyperactivation of Leydig cells
-
J. Wistuba, C.M. Luetjens, M. Dittmann, S. Werler, A. Poplinski, O. Damm, et al. (2010) Male 41, XXY∗ mice as a model for Klinefelter syndrome: hyperactivation of Leydig cells. Endocrinology 151 2898-2910.
-
(2010)
Endocrinology
, vol.151
, pp. 2898-2910
-
-
Wistuba, J.1
Luetjens, C.M.2
Dittmann, M.3
Werler, S.4
Poplinski, A.5
Damm, O.6
-
13
-
-
0032931007
-
Germ cell development in the XXY mouse: evidence that a compromised testicular environment increases the incidence of meiotic errors
-
K. Mroz, L. Carrel and P.A. Hunt (1998) Germ cell development in the XXY mouse: evidence that a compromised testicular environment increases the incidence of meiotic errors. Hum Reprod 14 1151-1156.
-
(1998)
Hum Reprod
, vol.14
, pp. 1151-1156
-
-
Mroz, K.1
Carrel, L.2
Hunt, P.A.3
-
14
-
-
57649237968
-
Impaired recognition memory in male mice with a supernumerary X chromosome
-
L. Lewejohann, O. Damm, C.M. Luetjens, T. Hämäläinen, M. Simoni, E. Nieschlag, et al. (2009) Impaired recognition memory in male mice with a supernumerary X chromosome. Physiol Behav 96 23-29.
-
(2009)
Physiol Behav
, vol.96
, pp. 23-29
-
-
Lewejohann, L.1
Damm, O.2
Luetjens, C.M.3
Hämäläinen, T.4
Simoni, M.5
Nieschlag, E.6
-
15
-
-
67349205061
-
Transgenic Alzheimer mice in a semi-naturalistic environment: more plaques, yet not compromised in daily life
-
L. Lewejohann, N. Reefmann, P. Widmann, O. Ambrée, A. Herring, K. Keyvani, et al. (2009) Transgenic Alzheimer mice in a semi-naturalistic environment: more plaques, yet not compromised in daily life. Behav Brain Res 201 99-102.
-
(2009)
Behav Brain Res
, vol.201
, pp. 99-102
-
-
Lewejohann, L.1
Reefmann, N.2
Widmann, P.3
Ambrée, O.4
Herring, A.5
Keyvani, K.6
-
16
-
-
77956831681
-
Genetic, hormonal and metabolomic influences on social behaviour and gender preference of XXY mice
-
P.Y. Liu, K. Erkkila, Y. Lue, J.D. Jentsch, M.D. Schwarcz, D. Abuyounes, et al. (2010) Genetic, hormonal and metabolomic influences on social behaviour and gender preference of XXY mice. Am J Physiol Endocrinol Metab 299 E446-E455.
-
(2010)
Am J Physiol Endocrinol Metab
, vol.299
, pp. E446-E455
-
-
Liu, P.Y.1
Erkkila, K.2
Lue, Y.3
Jentsch, J.D.4
Schwarcz, M.D.5
Abuyounes, D.6
-
17
-
-
77956722433
-
Genetic and hormonal control of bone volume, architecture and remodelling in XXY mice
-
P.Y. Liu, R. Kalak, Y. Lue, Y. Jia, K. Erkkila, H. Zhou, et al. (2010) Genetic and hormonal control of bone volume, architecture and remodelling in XXY mice. J Bone Miner Res 25 2148-2154.
-
(2010)
J Bone Miner Res
, vol.25
, pp. 2148-2154
-
-
Liu, P.Y.1
Kalak, R.2
Lue, Y.3
Jia, Y.4
Erkkila, K.5
Zhou, H.6
-
18
-
-
79952273535
-
Insights into the pathogenesis of XXY phenotype from comparison of the clinical syndrome with an experimental XXY mouse model
-
Y.H. Lue, C. Wang, P.Y. Liu, K. Erkilla and R.S. Swerdloff (2010) Insights into the pathogenesis of XXY phenotype from comparison of the clinical syndrome with an experimental XXY mouse model. Pediatr Endocrinol Rev 8 140-144.
-
(2010)
Pediatr Endocrinol Rev
, vol.8
, pp. 140-144
-
-
Lue, Y.H.1
Wang, C.2
Liu, P.Y.3
Erkilla, K.4
Swerdloff, R.S.5
-
19
-
-
79961025012
-
In search for significant cognitive features in Klinefelter syndrome through cross-species comparison of a supernumerary X chromosome
-
H. Bruining, H. Swaab, L.M. de Sonneville, S. van Rijn, H. van Engeland and M.J. Kas (2011) In search for significant cognitive features in Klinefelter syndrome through cross-species comparison of a supernumerary X chromosome. Genes Brain Behav 10 658-662.
-
(2011)
Genes Brain Behav
, vol.10
, pp. 658-662
-
-
Bruining, H.1
Swaab, H.2
de Sonneville, L.M.3
van Rijn, S.4
van Engeland, H.5
Kas, M.J.6
-
20
-
-
29544435187
-
Natural history of seminiferous tubule degeneration in Klinefelter syndrome
-
L. Askglaede, A.M. Wikström, E. Rajpert-De Meyts, L. Dunkel, N.E. Skakkebaek and A. Juul (2006) Natural history of seminiferous tubule degeneration in Klinefelter syndrome. Hum Reprod Update 12 39-48.
-
(2006)
Hum Reprod Update
, vol.12
, pp. 39-48
-
-
Askglaede, L.1
Wikström, A.M.2
Rajpert-De Meyts, E.3
Dunkel, L.4
Skakkebaek, N.E.5
Juul, A.6
-
21
-
-
44949190511
-
Testicular function in Klinefelter syndrome
-
A.M. Wikström and L. Dunkel (2008) Testicular function in Klinefelter syndrome. Horm Res 69 317-326.
-
(2008)
Horm Res
, vol.69
, pp. 317-326
-
-
Wikström, A.M.1
Dunkel, L.2
-
23
-
-
84902027099
-
Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies
-
K. Hager, K. Jennings, S. Hososno, S. Howell, J.R. Gruen, A.R. Scott, et al. (2012) Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies. Int J Pediatr Endocrinol 8
-
(2012)
Int J Pediatr Endocrinol
, vol.8
-
-
Hager, K.1
Jennings, K.2
Hososno, S.3
Howell, S.4
Gruen, J.R.5
Scott, A.R.6
-
24
-
-
79955522645
-
Clinical and biological parameters in 166 boys, adolescents and adults with nonmosaic Klinefelter syndrome: a Copenhagen experience
-
L. Aksglaede, N.E. Skakkebaek, K. Almstrup and A. Juul (2011) Clinical and biological parameters in 166 boys, adolescents and adults with nonmosaic Klinefelter syndrome: a Copenhagen experience. Acta Paediatr 100 793-806.
-
(2011)
Acta Paediatr
, vol.100
, pp. 793-806
-
-
Aksglaede, L.1
Skakkebaek, N.E.2
Almstrup, K.3
Juul, A.4
-
25
-
-
33645129598
-
Extragonadal germ cell tumours are often associated with Klinefelter syndrome
-
D. Aguirre, K. Nieto, M. Lazos, Y.R. Pena, I. Palma, S. Kofman-Alfaro, et al. (2006) Extragonadal germ cell tumours are often associated with Klinefelter syndrome. Hum Pathol 37 477-480.
-
(2006)
Hum Pathol
, vol.37
, pp. 477-480
-
-
Aguirre, D.1
Nieto, K.2
Lazos, M.3
Pena, Y.R.4
Palma, I.5
Kofman-Alfaro, S.6
-
26
-
-
0030806569
-
Klinefelter’s syndrome associated with testicular microlithiasis and mediastenal germ cell neoplasm
-
R.I. Aizenstein, J.F. Hibbeln, B. Sagireddy, A.C. Wilbur and H.K. O'Neill (1997) Klinefelter’s syndrome associated with testicular microlithiasis and mediastenal germ cell neoplasm. J Clin Ultrasound 9 508-510.
-
(1997)
J Clin Ultrasound
, vol.9
, pp. 508-510
-
-
Aizenstein, R.I.1
Hibbeln, J.F.2
Sagireddy, B.3
Wilbur, A.C.4
O'Neill, H.K.5
-
27
-
-
23844435408
-
UK Cytogenetics Group. Cancer incidence and mortality in men with Kilnefelter syndrome: a cohort study
-
A.J. Swerdlow, M.J. Schoemaker, C.D. Higgins, A.F. Wright and P.A. Jacobs (2005) UK Cytogenetics Group. Cancer incidence and mortality in men with Kilnefelter syndrome: a cohort study. J Natl Cancer Inst 97 1204-1210.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 1204-1210
-
-
Swerdlow, A.J.1
Schoemaker, M.J.2
Higgins, C.D.3
Wright, A.F.4
Jacobs, P.A.5
-
28
-
-
79955524082
-
Morbidity and mortality in Klinefelter Syndrome
-
A. Bojesen and C.H. Gravholt (2011) Morbidity and mortality in Klinefelter Syndrome. Acta Paediatr 100 807-813.
-
(2011)
Acta Paediatr
, vol.100
, pp. 807-813
-
-
Bojesen, A.1
Gravholt, C.H.2
-
29
-
-
84862777341
-
Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes
-
J.F. Hughes, H. Skaletsky, L.G. Brown, T. Pyntikova, T. Graves, R.S. Fulton, et al. (2012) Strict evolutionary conservation followed rapid gene loss on human and rhesus Y chromosomes. Nature 483 82-86.
-
(2012)
Nature
, vol.483
, pp. 82-86
-
-
Hughes, J.F.1
Skaletsky, H.2
Brown, L.G.3
Pyntikova, T.4
Graves, T.5
Fulton, R.S.6
-
30
-
-
33847020017
-
Global analysis of X-chromosome dosage compensation
-
V. Gupta, M. Parisi, D. Sturgill, R. Nuttall, M. Doctolero, O.K. Dudko, et al. (2006) Global analysis of X-chromosome dosage compensation. J Biol 5 3.
-
(2006)
J Biol
, vol.5
, pp. 3
-
-
Gupta, V.1
Parisi, M.2
Sturgill, D.3
Nuttall, R.4
Doctolero, M.5
Dudko, O.K.6
-
31
-
-
38749117957
-
Dosage compensation in the mouse balances up-regulation and silencing of X-linked genes
-
H. Lin, V. Gupta, M.D. Vermilyea, F. Falciani, J.T. Lee, L.P. O’Neill, et al. (2007) Dosage compensation in the mouse balances up-regulation and silencing of X-linked genes. PLoS Biol 5 e326.
-
(2007)
PLoS Biol
, vol.5
, pp. e326
-
-
Lin, H.1
Gupta, V.2
Vermilyea, M.D.3
Falciani, F.4
Lee, J.T.5
O’Neill, L.P.6
-
32
-
-
78649458548
-
He X RNA sequencing shows no dosage compensation of the active X-chromosome
-
Y. Xiong, X. Chen, Z. Chen, X. Wang, S. Shi, X. Wang, et al. (2010) He X RNA sequencing shows no dosage compensation of the active X-chromosome. Nat Genet 42 1043-1047.
-
(2010)
Nat Genet
, vol.42
, pp. 1043-1047
-
-
Xiong, Y.1
Chen, X.2
Chen, Z.3
Wang, X.4
Shi, S.5
Wang, X.6
-
33
-
-
82255192364
-
Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster
-
X. Deng, J.B. Hiatt, D.K. Nguyen, S. Ercan, D. Sturgill, L.W. Hillier, et al. (2011) Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster. Nat Genet 43 1179-1185.
-
(2011)
Nat Genet
, vol.43
, pp. 1179-1185
-
-
Deng, X.1
Hiatt, J.B.2
Nguyen, D.K.3
Ercan, S.4
Sturgill, D.5
Hillier, L.W.6
-
34
-
-
82255179690
-
Evidence for dosage compensation between the X chromosome and autosomes in mammals
-
P.V. Kharchenko, R. Xi and P.J. Park (2011) Evidence for dosage compensation between the X chromosome and autosomes in mammals. Nat Genet 43 1167-1169.
-
(2011)
Nat Genet
, vol.43
, pp. 1167-1169
-
-
Kharchenko, P.V.1
Xi, R.2
Park, P.J.3
-
35
-
-
78650305154
-
What dosage compensation?
-
T. Casci (2011) What dosage compensation? Nat Rev Genet 12 2.
-
(2011)
Nat Rev Genet
, vol.12
, pp. 2
-
-
Casci, T.1
-
36
-
-
0028212159
-
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation
-
C.J. Brown and H.F. Willard (1994) The human X-inactivation centre is not required for maintenance of X-chromosome inactivation. Nature 368(6467), 154-156.
-
(1994)
Nature
, vol.368
, Issue.6467
, pp. 154-156
-
-
Brown, C.J.1
Willard, H.F.2
-
37
-
-
0032805149
-
Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation
-
G. Csankovszki, B. Panning, B. Bates, J.R. Pehrson and R. Jaenisch (1999) Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation. Nat Genet 22 323-324.
-
(1999)
Nat Genet
, vol.22
, pp. 323-324
-
-
Csankovszki, G.1
Panning, B.2
Bates, B.3
Pehrson, J.R.4
Jaenisch, R.5
-
39
-
-
15244353967
-
X-inactivation profile reveals extensive variability in X-linked gene expression in females
-
L. Carrel and H.F. Willard (2005) X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature 434 400-404.
-
(2005)
Nature
, vol.434
, pp. 400-404
-
-
Carrel, L.1
Willard, H.F.2
-
40
-
-
77951794067
-
Global survey of escape from X inactivation by RNA-sequencing in mouse
-
F. Yang, T. Babak, J. Shendure and C.M. Disteche (2010) Global survey of escape from X inactivation by RNA-sequencing in mouse. Genome Res 20 614-622.
-
(2010)
Genome Res
, vol.20
, pp. 614-622
-
-
Yang, F.1
Babak, T.2
Shendure, J.3
Disteche, C.M.4
-
41
-
-
80054758182
-
Clustered transcripts that escape X inactivation at mouse XqD
-
A.M. Lopes, S.E. Arnold-Croop, A. Amorim and L. Carrel (2011) Clustered transcripts that escape X inactivation at mouse XqD. Mamm Genome 22 572-582.
-
(2011)
Mamm Genome
, vol.22
, pp. 572-582
-
-
Lopes, A.M.1
Arnold-Croop, S.E.2
Amorim, A.3
Carrel, L.4
-
42
-
-
0031820331
-
X-chromosome inactivation: a repeat hypothesis
-
M.F. Lyon (1998) X-chromosome inactivation: a repeat hypothesis. Cytogenet Cell Genet 80 133-137.
-
(1998)
Cytogenet Cell Genet
, vol.80
, pp. 133-137
-
-
Lyon, M.F.1
-
43
-
-
77953703353
-
LINE-1 activity in facultative heterochromatin formation during X chromosome inactivation
-
J.C. Chow, C. Ciaudo, M.J. Fazzari, N. Mise, N. Servant, J.L. Glass, et al. (2010) LINE-1 activity in facultative heterochromatin formation during X chromosome inactivation. Cell 141(6), 956-969.
-
(2010)
Cell
, vol.141
, Issue.6
, pp. 956-969
-
-
Chow, J.C.1
Ciaudo, C.2
Fazzari, M.J.3
Mise, N.4
Servant, N.5
Glass, J.L.6
-
44
-
-
85045923953
-
Genomic environment predicts expression patterns on the human inactive X chromosome
-
L. Carrel, C. Park, S. Tyekucheva, J. Dunn, F. Chiaromonte and K.D. Makova (2006) Genomic environment predicts expression patterns on the human inactive X chromosome. PLoS Genet 29(2), e151.
-
(2006)
PLoS Genet
, vol.29
, Issue.2
, pp. e151
-
-
Carrel, L.1
Park, C.2
Tyekucheva, S.3
Dunn, J.4
Chiaromonte, F.5
Makova, K.D.6
-
45
-
-
75649095637
-
Inactive X chromosome-specific histone H3 modifications and CpG hypomethylation flank a chromatin boundary between an X-inactivated and an escape gene
-
Y. Goto and H. Kimura (2009) Inactive X chromosome-specific histone H3 modifications and CpG hypomethylation flank a chromatin boundary between an X-inactivated and an escape gene. Nucleic Acids Res 37 7416-7428.
-
(2009)
Nucleic Acids Res
, vol.37
, pp. 7416-7428
-
-
Goto, Y.1
Kimura, H.2
-
46
-
-
78649720674
-
Genome-wide distribution of macroH2A1 histone variants in mouse liver chromatin
-
L.N. Changolkar, G. Singh, K. Cui, J.B. Berletch, K. Zhao, C.M. Disteche, et al. (2010) Genome-wide distribution of macroH2A1 histone variants in mouse liver chromatin. Mol Cell Biol 30(23), 5473-5483.
-
(2010)
Mol Cell Biol
, vol.30
, Issue.23
, pp. 5473-5483
-
-
Changolkar, L.N.1
Singh, G.2
Cui, K.3
Berletch, J.B.4
Zhao, K.5
Disteche, C.M.6
-
47
-
-
0027183088
-
The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression
-
P. Jeppesen and B.M. Turner (1993) The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression. Cell 74 281-289.
-
(1993)
Cell
, vol.74
, pp. 281-289
-
-
Jeppesen, P.1
Turner, B.M.2
-
48
-
-
68149144367
-
High-resolution analysis of epigenetic changes associated with X inactivation
-
H. Marks, J.C. Chow, S. Denissov, K.J. Françoijs, N. Brockdorff, E. Heard, et al. (2009) High-resolution analysis of epigenetic changes associated with X inactivation. Genome Res 19 1361-1373.
-
(2009)
Genome Res
, vol.19
, pp. 1361-1373
-
-
Marks, H.1
Chow, J.C.2
Denissov, S.3
Françoijs, K.J.4
Brockdorff, N.5
Heard, E.6
-
49
-
-
38449089882
-
Trimethylation of histone H3 lysine 4 is an epigenetic mark at regions escaping mammalian X inactivation
-
A.M. Khalil and D.J. Driscoll (2007) Trimethylation of histone H3 lysine 4 is an epigenetic mark at regions escaping mammalian X inactivation. Epigenetics 2 114-118.
-
(2007)
Epigenetics
, vol.2
, pp. 114-118
-
-
Khalil, A.M.1
Driscoll, D.J.2
-
50
-
-
35348924169
-
Genetics and Epigenetics of the multifunctional protein CTCF
-
G.N. Filippova (2008) Genetics and Epigenetics of the multifunctional protein CTCF. Curr Top Dev Biol 80 337-360.
-
(2008)
Curr Top Dev Biol
, vol.80
, pp. 337-360
-
-
Filippova, G.N.1
-
51
-
-
0032014618
-
Escape from X inactivation of Smcx is preceded by silencing during mouse development
-
P.A. Lingenfelter, D.A. Adler, D. Poslinski, S. Thomas, R.W. Elliott, V.M. Chapman, et al. (1998) Escape from X inactivation of Smcx is preceded by silencing during mouse development. Nat Genet 18 212-213.
-
(1998)
Nat Genet
, vol.18
, pp. 212-213
-
-
Lingenfelter, P.A.1
Adler, D.A.2
Poslinski, D.3
Thomas, S.4
Elliott, R.W.5
Chapman, V.M.6
-
52
-
-
57649148571
-
Fertility in a i(Xq) Klinefelter patient: importance of XIST expression level determined by qRT-PCR in ruling out Klinefelter cryptic mosaicism as cause of oligozoospermia
-
M. Stabile, T. Angelino, F. Caiazzo, P. Olivieri, N. De Marchi, L. De Petrocellis, et al. (2008) Fertility in a i(Xq) Klinefelter patient: importance of XIST expression level determined by qRT-PCR in ruling out Klinefelter cryptic mosaicism as cause of oligozoospermia. Mol Hum Reprod 14 635-640.
-
(2008)
Mol Hum Reprod
, vol.14
, pp. 635-640
-
-
Stabile, M.1
Angelino, T.2
Caiazzo, F.3
Olivieri, P.4
De Marchi, N.5
De Petrocellis, L.6
-
53
-
-
77953955158
-
Novel genetic aspects of Klinefelter’s syndrome
-
F. Tüttelmann and J. Gromoll (2010) Novel genetic aspects of Klinefelter’s syndrome. Mol Hum Reprod 16 386-395.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 386-395
-
-
Tüttelmann, F.1
Gromoll, J.2
-
54
-
-
33745773870
-
LWPES Consensus group, ESPE Consensus Group. Consensus statement on management of intersex disorders
-
I.A. Hughes, C. Houk, S.F. Ahmed and P.A. Lee (2006) LWPES Consensus group, ESPE Consensus Group. Consensus statement on management of intersex disorders. Arch Dis Child 91 554-563.
-
(2006)
Arch Dis Child
, vol.91
, pp. 554-563
-
-
Hughes, I.A.1
Houk, C.2
Ahmed, S.F.3
Lee, P.A.4
-
55
-
-
33748439007
-
International Consensus Conference on intersex organized by the Lawson Wilkins Pediatric Endocrine Society and the European Society Paediatric Endocrinology. Consensus statement on management of intersex disorders. International Consensus Conference on intersex
-
P.A. Lee, C.P. Houk, S.F. Ahmed and I.A. Hughes (2006) International Consensus Conference on intersex organized by the Lawson Wilkins Pediatric Endocrine Society and the European Society Paediatric Endocrinology. Consensus statement on management of intersex disorders. International Consensus Conference on intersex. Pediatrics 118 e488-e500.
-
(2006)
Pediatrics
, vol.118
, pp. e488-e500
-
-
Lee, P.A.1
Houk, C.P.2
Ahmed, S.F.3
Hughes, I.A.4
-
56
-
-
33745778703
-
Methylation of two Homo sapiens-specific X-Y homologous genes in Klinefelter’s syndrome (XXY)
-
N.L. Ross, R. Wadekar, A. Lopes, A. Dagnall, J. Close, L.E. Delisi, et al. (2006) Methylation of two Homo sapiens-specific X-Y homologous genes in Klinefelter’s syndrome (XXY). Am J Med Genet B Neuropsychiatr Genet 141B 544-548.
-
(2006)
Am J Med Genet B Neuropsychiatr Genet
, vol.141B
, pp. 544-548
-
-
Ross, N.L.1
Wadekar, R.2
Lopes, A.3
Dagnall, A.4
Close, J.5
Delisi, L.E.6
-
57
-
-
0035071815
-
An abundance of X-linked genes expressed in spermatogonia
-
P.J. Wang, J.R. McCarrey, F. Yang and D.C. Page (2001) An abundance of X-linked genes expressed in spermatogonia. Nat Genet 27 422-426.
-
(2001)
Nat Genet
, vol.27
, pp. 422-426
-
-
Wang, P.J.1
McCarrey, J.R.2
Yang, F.3
Page, D.C.4
-
58
-
-
33745201592
-
Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome
-
A.M. Wikström, J.N. Painter, T. Raivio, K. Aittomäki and L. Dunkel (2006) Genetic features of the X chromosome affect pubertal development and testicular degeneration in adolescent boys with Klinefelter syndrome. Clin Endocrinol 65 92-97.
-
(2006)
Clin Endocrinol
, vol.65
, pp. 92-97
-
-
Wikström, A.M.1
Painter, J.N.2
Raivio, T.3
Aittomäki, K.4
Dunkel, L.5
-
59
-
-
76749101885
-
Should non-mosaic Klinefelter syndrome men be labelled as infertile in 2009?
-
G. Fullerton, M. Hamilton and A. Maheshwari (2010) Should non-mosaic Klinefelter syndrome men be labelled as infertile in 2009? Hum Reprod 25 588-597.
-
(2010)
Hum Reprod
, vol.25
, pp. 588-597
-
-
Fullerton, G.1
Hamilton, M.2
Maheshwari, A.3
-
61
-
-
0026764927
-
Fertility in a 47, XXY patient: assessment of biological paternity by deoxyribonucleic acid fingerprinting
-
G. Terzoli, F. Lalatta, A. Lobbiani, G. Simoni and G. Colucci (1992) Fertility in a 47, XXY patient: assessment of biological paternity by deoxyribonucleic acid fingerprinting. Fertil Steril 58 821-822.
-
(1992)
Fertil Steril
, vol.58
, pp. 821-822
-
-
Terzoli, G.1
Lalatta, F.2
Lobbiani, A.3
Simoni, G.4
Colucci, G.5
-
62
-
-
0025922098
-
Cytogenetic studies in male infertility: a review
-
M. De Braekeleer and T.N. Dao (1991) Cytogenetic studies in male infertility: a review. Hum Reprod 6 245-250.
-
(1991)
Hum Reprod
, vol.6
, pp. 245-250
-
-
De Braekeleer, M.1
Dao, T.N.2
-
63
-
-
0242472011
-
Clinical and diagnostic features of patients with suspected Klinefelter syndrome
-
A. Kamischke, A. Baumgardt, J. Horst and E. Nieschlag (2003) Clinical and diagnostic features of patients with suspected Klinefelter syndrome. J Androl 24 41-48.
-
(2003)
J Androl
, vol.24
, pp. 41-48
-
-
Kamischke, A.1
Baumgardt, A.2
Horst, J.3
Nieschlag, E.4
-
64
-
-
0025921769
-
Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark
-
J. Nielsen and M. Wohlert (1991) Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark. Hum Genet 87 81-83.
-
(1991)
Hum Genet
, vol.87
, pp. 81-83
-
-
Nielsen, J.1
Wohlert, M.2
-
65
-
-
0037326355
-
Longitudinal studies of inhibin B levels in boys and young adults with Klinefelter syndrome
-
P. Christiansen, A.M. Andersson and N.E. Skakkebaek (2003) Longitudinal studies of inhibin B levels in boys and young adults with Klinefelter syndrome. J Clin Endocrinol Metab 88 888-891.
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 888-891
-
-
Christiansen, P.1
Andersson, A.M.2
Skakkebaek, N.E.3
-
66
-
-
10744225919
-
Klinefelter syndrome: expanding the phenotype and identifying new research directions
-
J.L. Simpson, F. de la Cruz, R.S. Swerdloff, C. Samango-Sprouse, N.E. Skakkebaek, J.M. Graham Jr., et al. (2003) Klinefelter syndrome: expanding the phenotype and identifying new research directions. Genet Med 5 460-468.
-
(2003)
Genet Med
, vol.5
, pp. 460-468
-
-
Simpson, J.L.1
de la Cruz, F.2
Swerdloff, R.S.3
Samango-Sprouse, C.4
Skakkebaek, N.E.5
Graham, J.M.6
-
68
-
-
33646059921
-
Morbidity in Klinefelter syndrome: a Danish register study based on hospital discharge diagnoses
-
A. Bojesen, S. Juul, N.H. Birkebaek and C.H. Gravholt (2006) Morbidity in Klinefelter syndrome: a Danish register study based on hospital discharge diagnoses. J Clin Endocrinol Metab 91 1254-1260.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1254-1260
-
-
Bojesen, A.1
Juul, S.2
Birkebaek, N.H.3
Gravholt, C.H.4
-
69
-
-
38049187890
-
Normal bone mineral content but unfavourable muscle/fat ratio in Klinefelter syndrome
-
L. Askglaede, C. Moolgard, N.E. Skakkebaek and A. Juul (2008) Normal bone mineral content but unfavourable muscle/fat ratio in Klinefelter syndrome. Arch Dis Child 93 30-34.
-
(2008)
Arch Dis Child
, vol.93
, pp. 30-34
-
-
Askglaede, L.1
Moolgard, C.2
Skakkebaek, N.E.3
Juul, A.4
-
70
-
-
84866165867
-
Reduced artery diameters in Klinefelter syndrome
-
online before press
-
C. Foresta, N. Caretta, P. Palego, A. Ferlin, D. Zuccarello, A. Lenzi, et al. (2012) Reduced artery diameters in Klinefelter syndrome. Int J Androl 10.1111/j.1365-2605.2012.01269.x online before press
-
(2012)
Int J Androl
-
-
Foresta, C.1
Caretta, N.2
Palego, P.3
Ferlin, A.4
Zuccarello, D.5
Lenzi, A.6
-
71
-
-
33646027042
-
The structural brain correlates of cognitive deficits in adults with Klinefelter’s syndrome
-
E. Itti, I.T. Gaw Gonzalo, A. Pawlikowska-Haddal, K.B. Boone, A. Mlikotic, L. Itti, et al. (2006) The structural brain correlates of cognitive deficits in adults with Klinefelter’s syndrome. J Clin Endocrinol Metab 91 1423-1427.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1423-1427
-
-
Itti, E.1
Gaw Gonzalo, I.T.2
Pawlikowska-Haddal, A.3
Boone, K.B.4
Mlikotic, A.5
Itti, L.6
-
72
-
-
0038383708
-
Executive skills in Klinefelter’s syndrome
-
C.M. Temple and P.M. Sanfilippo (2003) Executive skills in Klinefelter’s syndrome. Neuropsychologia 41 1547-1559.
-
(2003)
Neuropsychologia
, vol.41
, pp. 1547-1559
-
-
Temple, C.M.1
Sanfilippo, P.M.2
-
73
-
-
33750589017
-
Klinefelter’s syndrome (karyotype 47, XXY) and schizophrenia-spectrum pathology
-
S. van Rijn, A. Aleman, H. Swaab and R. Kahn (2006) Klinefelter’s syndrome (karyotype 47, XXY) and schizophrenia-spectrum pathology. Br J Psychiatry 189 459-460.
-
(2006)
Br J Psychiatry
, vol.189
, pp. 459-460
-
-
van Rijn, S.1
Aleman, A.2
Swaab, H.3
Kahn, R.4
-
74
-
-
0015265706
-
Analytic review: nature and origin of males with XX sex chromosomes
-
A. de la Chapelle (1972) Analytic review: nature and origin of males with XX sex chromosomes. Am J Hum Genet 24 71-105.
-
(1972)
Am J Hum Genet
, vol.24
, pp. 71-105
-
-
de la Chapelle, A.1
-
75
-
-
77952695103
-
Diagnosis and mortality in 47, XYY persons: a registry study
-
K. Stochholm, S. Juul and C.H. Gravholt (2010) Diagnosis and mortality in 47, XYY persons: a registry study. Orphanet J Rare Dis 5 15.
-
(2010)
Orphanet J Rare Dis
, vol.5
, pp. 15
-
-
Stochholm, K.1
Juul, S.2
Gravholt, C.H.3
-
76
-
-
34548776061
-
Clinical, endocrinological, and epigenetic features of the 46, XX male syndrome, compared with 47, XXY Klinefelter patients
-
E. Vorona, M. Zitzmann, J. Gromoll, A.N. Schüring and E. Nieschlag (2007) Clinical, endocrinological, and epigenetic features of the 46, XX male syndrome, compared with 47, XXY Klinefelter patients. J Clin Endocrinol Metab 92 3458-3465.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 3458-3465
-
-
Vorona, E.1
Zitzmann, M.2
Gromoll, J.3
Schüring, A.N.4
Nieschlag, E.5
-
77
-
-
31144439066
-
46, XX male syndrome: a case report
-
F. Yencilek and C. Baykal (2005) 46, XX male syndrome: a case report. Clin Exp Obst Gyn 32 263-264.
-
(2005)
Clin Exp Obst Gyn
, vol.32
, pp. 263-264
-
-
Yencilek, F.1
Baykal, C.2
-
78
-
-
0016550787
-
An animal model for the XXY Klinefelter’s syndrome in man: tortoiseshell and calico male cats
-
W.R. Centerwall and K. Benirschke (1975) An animal model for the XXY Klinefelter’s syndrome in man: tortoiseshell and calico male cats. Am J Vet Res 36 1275-1280.
-
(1975)
Am J Vet Res
, vol.36
, pp. 1275-1280
-
-
Centerwall, W.R.1
Benirschke, K.2
-
79
-
-
0347539068
-
Theriogenology question of the month. Azoospermia associated with 79, XXY chromosome complement (canine Klinefelter’s syndrome)
-
G.J. Nie, S.D. Johnston, D.W. Hayden, L.C. Buoen and M. Stephens (1998) Theriogenology question of the month. Azoospermia associated with 79, XXY chromosome complement (canine Klinefelter’s syndrome). J Am Vet Med Assoc 212 1545-1547.
-
(1998)
J Am Vet Med Assoc
, vol.212
, pp. 1545-1547
-
-
Nie, G.J.1
Johnston, S.D.2
Hayden, D.W.3
Buoen, L.C.4
Stephens, M.5
-
80
-
-
0014703627
-
An XXY sex-chromosome constitution in a dog with testicular hypoplasia and congenital heart disease
-
E. Clough, R.L. Pyle, W.C. Hare, D.F. Kelly and D.F. Patterson (1970) An XXY sex-chromosome constitution in a dog with testicular hypoplasia and congenital heart disease. Cytogenetics 9 71-77.
-
(1970)
Cytogenetics
, vol.9
, pp. 71-77
-
-
Clough, E.1
Pyle, R.L.2
Hare, W.C.3
Kelly, D.F.4
Patterson, D.F.5
-
81
-
-
43949094375
-
Benevides Filho IM. Cryptorchidism associated with 78, XY/79, XXY mosaicism in dog
-
B. Goldschmidt, K.B. El-Jaick, L.M. Souza, E.C.Q. Carvalho and V.L.S. Moura (2001) Benevides Filho IM. Cryptorchidism associated with 78, XY/79, XXY mosaicism in dog. Isr J Vet Med 56 56-58.
-
(2001)
Isr J Vet Med
, vol.56
, pp. 56-58
-
-
Goldschmidt, B.1
El-Jaick, K.B.2
Souza, L.M.3
Carvalho, E.C.Q.4
Moura, V.L.S.5
-
82
-
-
0027349870
-
Genetics of sexual differentiation and anomalies in dogs and cats
-
V.N. Meyers-Wallen (1993) Genetics of sexual differentiation and anomalies in dogs and cats. J Reprod Fertil Suppl 47 441-452.
-
(1993)
J Reprod Fertil Suppl
, vol.47
, pp. 441-452
-
-
Meyers-Wallen, V.N.1
-
84
-
-
0019499039
-
Testicular hypoplasia in a boar with abnormal sex chromosome constitution (39 XXY)
-
J.L. Hancock and M.G. Daker (1981) Testicular hypoplasia in a boar with abnormal sex chromosome constitution (39 XXY). J Reprod Fertil 61 395-397.
-
(1981)
J Reprod Fertil
, vol.61
, pp. 395-397
-
-
Hancock, J.L.1
Daker, M.G.2
-
85
-
-
0032500776
-
Detection of the X-chromosomes in a Klinefelter boar using a whole human X-chromosome painting probe
-
A. Mäkinen, M. Andersson and S. Nikunen (1998) Detection of the X-chromosomes in a Klinefelter boar using a whole human X-chromosome painting probe. Anim Reprod Sci 52 317-323.
-
(1998)
Anim Reprod Sci
, vol.52
, pp. 317-323
-
-
Mäkinen, A.1
Andersson, M.2
Nikunen, S.3
-
86
-
-
0019003550
-
Testicular hypoplasia in a Hereford bull with 61, XXY karyotype: the bovine counterpart of human Klinefelter’s syndrome
-
H.O. Dunn, D.H. Lein and K. McEntee (1980) Testicular hypoplasia in a Hereford bull with 61, XXY karyotype: the bovine counterpart of human Klinefelter’s syndrome. Cornell Vet 70 137-146.
-
(1980)
Cornell Vet
, vol.70
, pp. 137-146
-
-
Dunn, H.O.1
Lein, D.H.2
McEntee, K.3
-
87
-
-
0033582921
-
New cases of XXY constitution in cattle
-
L. Molteni, A. De Giovanni Macchi, D. Meggiolaro, G. Sironi, F. Enice and P. Popescu (1999) New cases of XXY constitution in cattle. Anim Reprod Sci 55 107-113.
-
(1999)
Anim Reprod Sci
, vol.55
, pp. 107-113
-
-
Molteni, L.1
De Giovanni Macchi, A.2
Meggiolaro, D.3
Sironi, G.4
Enice, F.5
Popescu, P.6
-
88
-
-
0141799810
-
Detection of the XXY trisomy in a bull by using sex chromosome painting probes
-
E. Słota, A. Kozubska-Sobocińska, M. Kościelny, B. Danielak-Czech and B. Rejduch (2003) Detection of the XXY trisomy in a bull by using sex chromosome painting probes. J Appl Genet 44 379-382.
-
(2003)
J Appl Genet
, vol.44
, pp. 379-382
-
-
Słota, E.1
Kozubska-Sobocińska, A.2
Kościelny, M.3
Danielak-Czech, B.4
Rejduch, B.5
-
89
-
-
0344306681
-
Germ cell transplantation in an azoospermic Klinefelter bull
-
H. Joerg, F. Janett, S. Schlatt, S. Mueller, D. Graphodatskaya, D. Suwattana, et al. (2003) Germ cell transplantation in an azoospermic Klinefelter bull. Biol Reprod 69 1940-1944.
-
(2003)
Biol Reprod
, vol.69
, pp. 1940-1944
-
-
Joerg, H.1
Janett, F.2
Schlatt, S.3
Mueller, S.4
Graphodatskaya, D.5
Suwattana, D.6
-
90
-
-
0002178982
-
Cytogenetics and physical gene map. CAB international
-
A.T. Bowling, A. Ruvinsky (Eds)
-
B.P. Chowdhary and T. Rausepp (2000) Cytogenetics and physical gene map. CAB international. A.T. Bowling, A. Ruvinsky (Eds) The genetics of the horse 171-242.
-
(2000)
The genetics of the horse
, pp. 171-242
-
-
Chowdhary, B.P.1
Rausepp, T.2
-
91
-
-
48449102923
-
Clinical, cytogenetic and molecular studies on sterile stallion and mare affected by XXY and sex reversal syndromes, respectively
-
L. Iannuzzi, G.P. Di Meo, A. Perucatti, M. Spadetta, D. Incarnato, P. Parma, et al. (2004) Clinical, cytogenetic and molecular studies on sterile stallion and mare affected by XXY and sex reversal syndromes, respectively. Caryologia 57 400-404.
-
(2004)
Caryologia
, vol.57
, pp. 400-404
-
-
Iannuzzi, L.1
Di Meo, G.P.2
Perucatti, A.3
Spadetta, M.4
Incarnato, D.5
Parma, P.6
-
92
-
-
0027630359
-
Clinical, cytogenetic and endocrine evaluation of a horse with a 65, XXY karyotype
-
E.M. Kubień, M.A. Pozor and M. Tischner (1993) Clinical, cytogenetic and endocrine evaluation of a horse with a 65, XXY karyotype. Equine Vet J 25 333-335.
-
(1993)
Equine Vet J
, vol.25
, pp. 333-335
-
-
Kubień, E.M.1
Pozor, M.A.2
Tischner, M.3
-
94
-
-
0038266579
-
Klinefelter syndrome (39 XXY) in an adult Siberian tiger (Panthera tigris altaica)
-
W.K. Suedmeyer, M.L. Houck and J. Kreeger (2003) Klinefelter syndrome (39 XXY) in an adult Siberian tiger (Panthera tigris altaica). J Zoo Wildl Med 34 96-99.
-
(2003)
J Zoo Wildl Med
, vol.34
, pp. 96-99
-
-
Suedmeyer, W.K.1
Houck, M.L.2
Kreeger, J.3
-
95
-
-
30144444395
-
A male baboon (Papio hamadryas) with a mosaic 43, XXY/42, XY karyotype
-
C.J. Dudley, G.B. Hubbard, C.M. Moore, B.G. Dunn, M. Raveendran, J. Rogers, et al. (2006) A male baboon (Papio hamadryas) with a mosaic 43, XXY/42, XY karyotype. Am J Med Genet A 140 94-97.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 94-97
-
-
Dudley, C.J.1
Hubbard, G.B.2
Moore, C.M.3
Dunn, B.G.4
Raveendran, M.5
Rogers, J.6
-
96
-
-
0014293873
-
A case of XXY sex chromosome constitution in an intersex pig
-
Jun
-
A.J. Breeuwsma (1968 Jun) A case of XXY sex chromosome constitution in an intersex pig. J Reprod Fertil 16(1), 119-120.
-
(1968)
J Reprod Fertil
, vol.16
, Issue.1
, pp. 119-120
-
-
Breeuwsma, A.J.1
-
97
-
-
0018197421
-
A chimaeric calf with XY/XXY mosaicism and intersexuality
-
A.R. Dain and P.S. Bridge (1978) A chimaeric calf with XY/XXY mosaicism and intersexuality. J Reprod Fertil 54(1), 197-201.
-
(1978)
J Reprod Fertil
, vol.54
, Issue.1
, pp. 197-201
-
-
Dain, A.R.1
Bridge, P.S.2
-
98
-
-
79954625493
-
Meiotic studies of a 38, XY/39, XXY mosaic boar
-
A. Pinton, H. Barasc, I. Raymond Letron, M. Bordedebat, N. Mary, K. Massip, et al. (2011) Meiotic studies of a 38, XY/39, XXY mosaic boar. Cytogenet Genome Res 133 202-208.
-
(2011)
Cytogenet Genome Res
, vol.133
, pp. 202-208
-
-
Pinton, A.1
Barasc, H.2
Raymond Letron, I.3
Bordedebat, M.4
Mary, N.5
Massip, K.6
-
99
-
-
44949271847
-
True hermaphroditism in a wild sheep: a clinical report
-
T.D. Bunch, R.J. Callan, A. Maciulis, J.C. Dalton, M.R. Figueroa, R. Kunzler, et al. (1991) True hermaphroditism in a wild sheep: a clinical report. Theriogenology 36 185-190.
-
(1991)
Theriogenology
, vol.36
, pp. 185-190
-
-
Bunch, T.D.1
Callan, R.J.2
Maciulis, A.3
Dalton, J.C.4
Figueroa, M.R.5
Kunzler, R.6
-
100
-
-
0020360927
-
Intersexuality associated with XX/XY mosaicism in a horned goat
-
T.A. Bongso, M. Thavalingam and T.K. Mukherjee (1982) Intersexuality associated with XX/XY mosaicism in a horned goat. Cytogenet Cell Genet 34 315-319.
-
(1982)
Cytogenet Cell Genet
, vol.34
, pp. 315-319
-
-
Bongso, T.A.1
Thavalingam, M.2
Mukherjee, T.K.3
-
101
-
-
0036044226
-
Sex chromosome aneuploidy in wild small mammals
-
J.B. Searle and R.M. Jones (2002) Sex chromosome aneuploidy in wild small mammals. Cytogenet Genome Res 96 239-243.
-
(2002)
Cytogenet Genome Res
, vol.96
, pp. 239-243
-
-
Searle, J.B.1
Jones, R.M.2
-
102
-
-
0021350626
-
A wild common shrew (Sorex araneus) with an XXY sex chromosome constitution
-
J.B. Searle (1984) A wild common shrew (Sorex araneus) with an XXY sex chromosome constitution. J Reprod Fertil 70 353-356.
-
(1984)
J Reprod Fertil
, vol.70
, pp. 353-356
-
-
Searle, J.B.1
-
103
-
-
0031854578
-
An XXY sex chromosome constitution in a house musk shrew (Suncus murinus L.) with testicular hypoplasia
-
M.B. Rogatcheva, S.I. Oda, A.I. Zhelezova and P.M. Borodin (1998) An XXY sex chromosome constitution in a house musk shrew (Suncus murinus L.) with testicular hypoplasia. J Reprod Fertil 113 91-93.
-
(1998)
J Reprod Fertil
, vol.113
, pp. 91-93
-
-
Rogatcheva, M.B.1
Oda, S.I.2
Zhelezova, A.I.3
Borodin, P.M.4
-
105
-
-
0035046095
-
XXY male mice: an experimental model for Klinefelter syndrome
-
Y. Lue, P.N. Rao, A.P. Sinha Hikim, M. Im, W.A. Salameh, P.H. Yen, et al. (2001) XXY male mice: an experimental model for Klinefelter syndrome. Endocrinology 142 1461-1470.
-
(2001)
Endocrinology
, vol.142
, pp. 1461-1470
-
-
Lue, Y.1
Rao, P.N.2
Sinha Hikim, A.P.3
Im, M.4
Salameh, W.A.5
Yen, P.H.6
-
106
-
-
0025756519
-
Fertile male mice with three sex chromosomes: evidence that infertility in XYY mice is an effect of two Y chromosomes
-
P. Hunt and E. Eicher (1991) Fertile male mice with three sex chromosomes: evidence that infertility in XYY mice is an effect of two Y chromosomes. Chromosoma 100 293.
-
(1991)
Chromosoma
, vol.100
, pp. 293
-
-
Hunt, P.1
Eicher, E.2
-
107
-
-
23844444214
-
XXY mice exhibit gonadal similar to Klinefelter syndrome
-
Y. Lue, J.D. Jentsch, C. Wang, P.N. Rao, A.P. Sinha Hikim, W. Salameh and R.S. Swerdloff (2005) XXY mice exhibit gonadal similar to Klinefelter syndrome. Endocrinology 146 4148-4154.
-
(2005)
Endocrinology
, vol.146
, pp. 4148-4154
-
-
Lue, Y.1
Jentsch, J.D.2
Wang, C.3
Rao, P.N.4
Sinha Hikim, A.P.5
Salameh, W.6
Swerdloff, R.S.7
-
108
-
-
0031973664
-
Germ cell loss in the XXY male mouse: altered X-chromosome dosage affects prenatal development
-
P.A. Hunt, C. Worthman, H. Levinson, J. Stallings, R. LeMaire, K. Mroz, et al. (1998) Germ cell loss in the XXY male mouse: altered X-chromosome dosage affects prenatal development. Mol Reprod Dev 49 101-111.
-
(1998)
Mol Reprod Dev
, vol.49
, pp. 101-111
-
-
Hunt, P.A.1
Worthman, C.2
Levinson, H.3
Stallings, J.4
LeMaire, R.5
Mroz, K.6
-
109
-
-
0033104435
-
Meiotic aneuploidy in the XXY mouse: evidence that X chomosome reactivation is independent of sexual differentiation
-
K. Mroz, T.J. Hassold and P.A. Hunt (1999) Meiotic aneuploidy in the XXY mouse: evidence that X chomosome reactivation is independent of sexual differentiation. DevBiol 207 229-238.
-
(1999)
DevBiol
, vol.207
, pp. 229-238
-
-
Mroz, K.1
Hassold, T.J.2
Hunt, P.A.3
-
111
-
-
78649823499
-
Sry: the master switch in mammalian sex determination
-
K. Kashimada and P. Koopman (2010) Sry: the master switch in mammalian sex determination. Development 137 3921-3930.
-
(2010)
Development
, vol.137
, pp. 3921-3930
-
-
Kashimada, K.1
Koopman, P.2
-
112
-
-
36749082438
-
Identification of JmjC domain-containing UTX and JMJD3 as histone H3 lysine 27 demethylases
-
S. Hong, Y.W. Cho, L.R. Yu, H. Yu, T.D. Veenstra and K. Ge (2007) Identification of JmjC domain-containing UTX and JMJD3 as histone H3 lysine 27 demethylases. Pro Natl Acad Sci USA 104 18439-18444.
-
(2007)
Pro Natl Acad Sci USA
, vol.104
, pp. 18439-18444
-
-
Hong, S.1
Cho, Y.W.2
Yu, L.R.3
Yu, H.4
Veenstra, T.D.5
Ge, K.6
-
113
-
-
77954662295
-
Crosstalk between histone modifications maintains the developmental pattern of gene expression on a tissue-specific locus
-
A.M. Hosey, C.P. Chaturvedi and M. Brand (2010) Crosstalk between histone modifications maintains the developmental pattern of gene expression on a tissue-specific locus. Epigenetics 5 273-281.
-
(2010)
Epigenetics
, vol.5
, pp. 273-281
-
-
Hosey, A.M.1
Chaturvedi, C.P.2
Brand, M.3
-
114
-
-
33749466728
-
Structural characterization and expression studies of Dby and its homologs in the mouse
-
Q.P. Vong, Y. Li, Y.F. Lau, M. Dym, O.M. Rennert and W.Y. Chan (2006) Structural characterization and expression studies of Dby and its homologs in the mouse. J Androl 27 653-661.
-
(2006)
J Androl
, vol.27
, pp. 653-661
-
-
Vong, Q.P.1
Li, Y.2
Lau, Y.F.3
Dym, M.4
Rennert, O.M.5
Chan, W.Y.6
-
115
-
-
85017411131
-
A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis
-
S. Mazeyrat, N. Saut, V. Grigoriev, S.K. Mahadevaiah, O.A. Ojarikre, A. Rattigan, et al. (2001) A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis. Nat Genet 29 49-53.
-
(2001)
Nat Genet
, vol.29
, pp. 49-53
-
-
Mazeyrat, S.1
Saut, N.2
Grigoriev, V.3
Mahadevaiah, S.K.4
Ojarikre, O.A.5
Rattigan, A.6
-
116
-
-
30444447780
-
Sexually dimorphic expression of the X-linked gene Eif2s3x mRNA but not protein in mouse brain
-
J. Xu, R. Watkins and A.P. Arnold (2006) Sexually dimorphic expression of the X-linked gene Eif2s3x mRNA but not protein in mouse brain. Gene Expr Patterns 6 146-155.
-
(2006)
Gene Expr Patterns
, vol.6
, pp. 146-155
-
-
Xu, J.1
Watkins, R.2
Arnold, A.P.3
-
117
-
-
33947302685
-
The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases
-
S. Iwase, F. Lan, P. Bayliss, L. de la Torre-Ubieta, M. Huarte, H.H. Qi, et al. (2007) The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases. Cell 128 1077-1088.
-
(2007)
Cell
, vol.128
, pp. 1077-1088
-
-
Iwase, S.1
Lan, F.2
Bayliss, P.3
de la Torre-Ubieta, L.4
Huarte, M.5
Qi, H.H.6
-
118
-
-
84863702634
-
The number of x chromosomes causes sex differences in adiposity in mice
-
X. Chen, R. McClusky, J. Chen, S.W. Beaven, P. Tontonoz, A.P. Arnold, et al. (2012) The number of x chromosomes causes sex differences in adiposity in mice. PLoS Genet 8 e1002709.
-
(2012)
PLoS Genet
, vol.8
, pp. e1002709
-
-
Chen, X.1
McClusky, R.2
Chen, J.3
Beaven, S.W.4
Tontonoz, P.5
Arnold, A.P.6
-
119
-
-
0032854670
-
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle
-
S. Cainarca, S. Messali, A. Ballabio and G. Meroni (1999) Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle. Hum Molec Genet 8 1387-1396.
-
(1999)
Hum Molec Genet
, vol.8
, pp. 1387-1396
-
-
Cainarca, S.1
Messali, S.2
Ballabio, A.3
Meroni, G.4
-
120
-
-
6844261193
-
The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region
-
L. Dal Zotto, N.A. Quaderi, R. Elliott, P.A. Lingerfelter, L. Carrel, V. Valsecchi, et al. (1998) The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Molec Genet 7 489-499.
-
(1998)
Hum Molec Genet
, vol.7
, pp. 489-499
-
-
Dal Zotto, L.1
Quaderi, N.A.2
Elliott, R.3
Lingerfelter, P.A.4
Carrel, L.5
Valsecchi, V.6
-
121
-
-
13044280808
-
The Opitz syndrome gene product, MID1, associates with microtubules
-
S. Schweiger, J. Foerster, T. Lehmann, V. Suckow, Y.A. Muller, G. Walter, et al. (1999) The Opitz syndrome gene product, MID1, associates with microtubules. Proc Natl Acad Sci USA 96 2794-2799.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2794-2799
-
-
Schweiger, S.1
Foerster, J.2
Lehmann, T.3
Suckow, V.4
Muller, Y.A.5
Walter, G.6
-
122
-
-
29244431667
-
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
-
O. Hagens, A. Dubos, F. Abidi, G. Barbi, L. Van Zutven, M. Hoeltzenbein, et al. (2006) Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation. Hum Genet 118 578-590.
-
(2006)
Hum Genet
, vol.118
, pp. 578-590
-
-
Hagens, O.1
Dubos, A.2
Abidi, F.3
Barbi, G.4
Van Zutven, L.5
Hoeltzenbein, M.6
-
123
-
-
33845547600
-
Shroom4 (Kiaa1202) is an actin-associated protein implicated in cytoskeletal organization
-
M. Yoder and J.D. Hildebrand (2007) Shroom4 (Kiaa1202) is an actin-associated protein implicated in cytoskeletal organization. Cell Motil Cytoskeleton 64 49-63.
-
(2007)
Cell Motil Cytoskeleton
, vol.64
, pp. 49-63
-
-
Yoder, M.1
Hildebrand, J.D.2
-
126
-
-
0022367026
-
Quantitative histology of human fetal testes in chromosomal disease
-
W. Coerdt, H. Rehder, I. Gausmann, R. Johannisson and A. Gropp (1985) Quantitative histology of human fetal testes in chromosomal disease. Pediatr Pathol 3 245-259.
-
(1985)
Pediatr Pathol
, vol.3
, pp. 245-259
-
-
Coerdt, W.1
Rehder, H.2
Gausmann, I.3
Johannisson, R.4
Gropp, A.5
-
127
-
-
0016398376
-
Letter: Klinefelter’s syndrome in a fetus
-
J.D. Murken, S. Stengel-Rutkowski, J.U. Walther, S.R. Westenfelder, K.H. Remberger and F. Zimmer (1974) Letter: Klinefelter’s syndrome in a fetus. Lancet 2 171.
-
(1974)
Lancet
, vol.2
, pp. 171
-
-
Murken, J.D.1
Stengel-Rutkowski, S.2
Walther, J.U.3
Westenfelder, S.R.4
Remberger, K.H.5
Zimmer, F.6
-
128
-
-
0033305420
-
Analysis of meiosis in intratesticular germ cells from subjects affected by classic Klinefelter’s syndrome
-
C. Foresta, C. Galeazzi, A. Bettella, P. Marin, M. Rossato, A. Garolla, et al. (1999) Analysis of meiosis in intratesticular germ cells from subjects affected by classic Klinefelter’s syndrome. J Clin Endocrinol Metab 84 3807-3810.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 3807-3810
-
-
Foresta, C.1
Galeazzi, C.2
Bettella, A.3
Marin, P.4
Rossato, M.5
Garolla, A.6
-
129
-
-
27744462460
-
Success of testicular sperm injection and intracytoplasmic sperm injection in men with Klinefelter syndrome
-
J.D. Schiff, G.D. Palermo, L.L. Veeck, M. Goldstein, Z. Rosenwaks and P.N. Schlegel (2005) Success of testicular sperm injection and intracytoplasmic sperm injection in men with Klinefelter syndrome. J Clin Endocrinol Metab 90 6263-6267.
-
(2005)
J Clin Endocrinol Metab
, vol.90
, pp. 6263-6267
-
-
Schiff, J.D.1
Palermo, G.D.2
Veeck, L.L.3
Goldstein, M.4
Rosenwaks, Z.5
Schlegel, P.N.6
-
130
-
-
5144219565
-
Assisted reproductive techniques in patients with Klinefelter syndrome: a critical review
-
D. Denschlag, C. Tempfer, M. Kunze, G. Wolff and C. Keck (2004) Assisted reproductive techniques in patients with Klinefelter syndrome: a critical review. Fertil Steril 82 775-779.
-
(2004)
Fertil Steril
, vol.82
, pp. 775-779
-
-
Denschlag, D.1
Tempfer, C.2
Kunze, M.3
Wolff, G.4
Keck, C.5
-
131
-
-
33846838882
-
Seven pregnancies and deliveries from non-mosaic Klinefelter syndrome patients using fresh and frozen testicular sperm
-
K. Kyono, H. Uto, Y. Nakajo, S. Kumagai, Y. Araki and S. Kanto (2007) Seven pregnancies and deliveries from non-mosaic Klinefelter syndrome patients using fresh and frozen testicular sperm. J Assist Reprod Genet 24 47-51.
-
(2007)
J Assist Reprod Genet
, vol.24
, pp. 47-51
-
-
Kyono, K.1
Uto, H.2
Nakajo, Y.3
Kumagai, S.4
Araki, Y.5
Kanto, S.6
-
132
-
-
68949202936
-
Focal spermatogenesis originates in euploid germ cells in classical Klinefelter patients
-
R.B. Sciurano, C.V. Luna Hisano, M.I. Rahn, S. Brugo Olmedo, G. Rey Valzacchi, R. Coco, et al. (2009) Focal spermatogenesis originates in euploid germ cells in classical Klinefelter patients. Hum Reprod 24 2353-2360.
-
(2009)
Hum Reprod
, vol.24
, pp. 2353-2360
-
-
Sciurano, R.B.1
Luna Hisano, C.V.2
Rahn, M.I.3
Brugo Olmedo, S.4
Rey Valzacchi, G.5
Coco, R.6
-
133
-
-
34247470199
-
Male germline stem cells: from mice to men
-
R.L. Brinster (2007) Male germline stem cells: from mice to men. Science 316 404-405.
-
(2007)
Science
, vol.316
, pp. 404-405
-
-
Brinster, R.L.1
-
134
-
-
77953953977
-
Transplanted XY germ cells produce spermatozoa in testes of XXY mice
-
Y. Lue, P.Y. Liu, K. Erkkila, K. Ma, M. Schwarcz, C. Wang, et al. (2010) Transplanted XY germ cells produce spermatozoa in testes of XXY mice. Int J Androl 33 581-587.
-
(2010)
Int J Androl
, vol.33
, pp. 581-587
-
-
Lue, Y.1
Liu, P.Y.2
Erkkila, K.3
Ma, K.4
Schwarcz, M.5
Wang, C.6
-
135
-
-
48749122495
-
Olfactory cues are sufficient to elicit social approach behaviors but not social transmission of food preference in C57BL/6J mice
-
B.C. Ryan, N.B. Young, S.S. Moy and J.N. Crawley (2008) Olfactory cues are sufficient to elicit social approach behaviors but not social transmission of food preference in C57BL/6J mice. Behav Brain Res 193 235-242.
-
(2008)
Behav Brain Res
, vol.193
, pp. 235-242
-
-
Ryan, B.C.1
Young, N.B.2
Moy, S.S.3
Crawley, J.N.4
-
136
-
-
43249096157
-
Effects of environmental enrichment on exploration, anxiety, and memory in female TgCRND8 alzheimer mice
-
N. Görtz, L. Lewejohann, M. Tomm, O. Ambrée, K. Keyvani, W. Paulus, et al. (2008) Effects of environmental enrichment on exploration, anxiety, and memory in female TgCRND8 alzheimer mice. Behav Brain Res 191 43-48.
-
(2008)
Behav Brain Res
, vol.191
, pp. 43-48
-
-
Görtz, N.1
Lewejohann, L.2
Tomm, M.3
Ambrée, O.4
Keyvani, K.5
Paulus, W.6
-
137
-
-
48049118700
-
Reduced size of the amygdala in individuals with 47, XXY and 47, XXX karyotypes
-
A.J. Patwardhan, W.E. Brown, B.G. Bender, M.G. Linden, S. Eliez and A.L. Reiss (2002) Reduced size of the amygdala in individuals with 47, XXY and 47, XXX karyotypes. Am J Med Genet 114 93-98.
-
(2002)
Am J Med Genet
, vol.114
, pp. 93-98
-
-
Patwardhan, A.J.1
Brown, W.E.2
Bender, B.G.3
Linden, M.G.4
Eliez, S.5
Reiss, A.L.6
-
138
-
-
5744220126
-
Automated morphometric study of brain variation in XXY males
-
D. Shen, D. Liu, H. Liu, L. Clasen, J. Giedd and C. Davatzikos (2004) Automated morphometric study of brain variation in XXY males. NeuroImage 23 648-653.
-
(2004)
NeuroImage
, vol.23
, pp. 648-653
-
-
Shen, D.1
Liu, D.2
Liu, H.3
Clasen, L.4
Giedd, J.5
Davatzikos, C.6
-
139
-
-
0023255981
-
The use of a plus-maze to measure anxiety in the mouse
-
R.G. Lister (1987) The use of a plus-maze to measure anxiety in the mouse. Psychopharmacology 92 180-185.
-
(1987)
Psychopharmacology
, vol.92
, pp. 180-185
-
-
Lister, R.G.1
-
140
-
-
17744392634
-
Klinefelter’s syndrome (XXY) as a genetic model for psychotic disorders
-
L.E. DeLisi, A.M. Maurizio, C. Svetina, B. Ardekani, K. Szulc, J. Nierenberg, et al. (2005) Klinefelter’s syndrome (XXY) as a genetic model for psychotic disorders. Am J Med Genet B Neuropsychiatr Genet 135B 15-23.
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.135B
, pp. 15-23
-
-
DeLisi, L.E.1
Maurizio, A.M.2
Svetina, C.3
Ardekani, B.4
Szulc, K.5
Nierenberg, J.6
-
141
-
-
77952420169
-
Social status and day-to-day behaviour of male serotonin transporter knockout mice
-
L. Lewejohann, V. Kloke, R.S. Heiming, F. Jansen, S. Kaiser, A. Schmitt, et al. (2010) Social status and day-to-day behaviour of male serotonin transporter knockout mice. Behav Brain Res 211 220-228.
-
(2010)
Behav Brain Res
, vol.211
, pp. 220-228
-
-
Lewejohann, L.1
Kloke, V.2
Heiming, R.S.3
Jansen, F.4
Kaiser, S.5
Schmitt, A.6
-
142
-
-
33746899690
-
Novel approach to the behavioural characterization of inbred mice: automated home cage observations
-
L. de Visser, R. van den Bos, W.W. Kuurman, M.J. Kas and B.M. Spruijt (2006) Novel approach to the behavioural characterization of inbred mice: automated home cage observations. Genes Brain Behav 5 458-466.
-
(2006)
Genes Brain Behav
, vol.5
, pp. 458-466
-
-
de Visser, L.1
van den Bos, R.2
Kuurman, W.W.3
Kas, M.J.4
Spruijt, B.M.5
-
143
-
-
80051874045
-
“Personality” in laboratory mice used for biomedical research: a way of understanding variability?
-
L. Lewejohann, B. Zipser and N. Sachser (2011) “Personality” in laboratory mice used for biomedical research: a way of understanding variability? Dev Psychobiology 53 631-640.
-
(2011)
Dev Psychobiology
, vol.53
, pp. 631-640
-
-
Lewejohann, L.1
Zipser, B.2
Sachser, N.3
-
144
-
-
77953952014
-
Klinefelter’s syndrome, type 2 diabetes and the metabolic syndrome: the impact of body composition
-
A. Bojesen, C. Høst and C.H. Gravholt (2010) Klinefelter’s syndrome, type 2 diabetes and the metabolic syndrome: the impact of body composition. Mol Hum Reprod 16 396-401.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 396-401
-
-
Bojesen, A.1
Høst, C.2
Gravholt, C.H.3
-
145
-
-
79955489888
-
Body composition, metabolic syndrome and type 2 diabetes in Klinefelter syndrome
-
C.H. Gravholt, A.S. Jensen, C. Høst and A. Bojesen (2011) Body composition, metabolic syndrome and type 2 diabetes in Klinefelter syndrome. Acta Paediatr 100 871-877.
-
(2011)
Acta Paediatr
, vol.100
, pp. 871-877
-
-
Gravholt, C.H.1
Jensen, A.S.2
Høst, C.3
Bojesen, A.4
-
146
-
-
79952264894
-
Considerations for androgen therapy in children and adolescents with Klinefelter syndrome (47, XXY)
-
A.D. Rogol and N. Tartaglia (2010) Considerations for androgen therapy in children and adolescents with Klinefelter syndrome (47, XXY). Pediatr Endocrinol Rev 8 145-150.
-
(2010)
Pediatr Endocrinol Rev
, vol.8
, pp. 145-150
-
-
Rogol, A.D.1
Tartaglia, N.2
-
147
-
-
0016215654
-
1974 the effect of short and long term human chorionic gonadotrophin (HCG) administration on plasma testosterone levels in Klinefelter’s syndrome
-
A.G. Smals, P.W. Kloppenborg and T.J. Benraad (1974) 1974 the effect of short and long term human chorionic gonadotrophin (HCG) administration on plasma testosterone levels in Klinefelter’s syndrome. Acta Endocrinol 77 753-764.
-
(1974)
Acta Endocrinol
, vol.77
, pp. 753-764
-
-
Smals, A.G.1
Kloppenborg, P.W.2
Benraad, T.J.3
-
148
-
-
84858017936
-
Differentiation of murine male germ cells to spermatozoa in a soft agar culture system
-
M. Abu Elhija, E. Lunenfeld, S. Schlatt and M. Huleihel (2012) Differentiation of murine male germ cells to spermatozoa in a soft agar culture system. Asian J Androl 14 285-293.
-
(2012)
Asian J Androl
, vol.14
, pp. 285-293
-
-
Abu Elhija, M.1
Lunenfeld, E.2
Schlatt, S.3
Huleihel, M.4
-
149
-
-
69049109915
-
New horizons for in vitro spermatogenesis? An update on novel three-dimensional culture systems as tools for meiotic and post-meiotic differentiation of testicular germ cells
-
J.B. Stukenborg, S. Schlatt, M. Simoni, C.H. Yeung, M.A. Elhija, C.M. Luetjens, et al. (2009) New horizons for in vitro spermatogenesis? An update on novel three-dimensional culture systems as tools for meiotic and post-meiotic differentiation of testicular germ cells. Mol Hum Reprod 15 521-529.
-
(2009)
Mol Hum Reprod
, vol.15
, pp. 521-529
-
-
Stukenborg, J.B.1
Schlatt, S.2
Simoni, M.3
Yeung, C.H.4
Elhija, M.A.5
Luetjens, C.M.6
-
150
-
-
43449103963
-
Coculture of spermatogonia with somatic cells in a novel three-dimensional soft-agar-culture-system
-
J.B. Stukenborg, J. Wistuba, C.M. Luetjens, M.A. Elhija, M. Huleihel, E. Lunenfeld, et al. (2008) Coculture of spermatogonia with somatic cells in a novel three-dimensional soft-agar-culture-system. J Androl 29 312-329.
-
(2008)
J Androl
, vol.29
, pp. 312-329
-
-
Stukenborg, J.B.1
Wistuba, J.2
Luetjens, C.M.3
Elhija, M.A.4
Huleihel, M.5
Lunenfeld, E.6
-
152
-
-
33947529497
-
Male pubertal development and the role of androgen therapy
-
E.J. Richmond and A.D. Rogol (2007) Male pubertal development and the role of androgen therapy. Nat Clin Pract Endocrinol Metab 3 338-344.
-
(2007)
Nat Clin Pract Endocrinol Metab
, vol.3
, pp. 338-344
-
-
Richmond, E.J.1
Rogol, A.D.2
-
153
-
-
0036398035
-
Transgenic mouse models and germ cell transplantation: two excellent tools for the analysis of genes regulating male fertility
-
J. Wistuba and S. Schlatt (2002) Transgenic mouse models and germ cell transplantation: two excellent tools for the analysis of genes regulating male fertility. Mol Genet Metab 77 61-67.
-
(2002)
Mol Genet Metab
, vol.77
, pp. 61-67
-
-
Wistuba, J.1
Schlatt, S.2
-
154
-
-
0030880012
-
Sexual function and clinical features of patients with Klinefelter’s syndrome with the chief complaint of male infertility
-
A. Yoshida, K. Miura, K. Nagao, H. Hara, N. Ishii and M. Shirai (1997) Sexual function and clinical features of patients with Klinefelter’s syndrome with the chief complaint of male infertility. Int J Androl 20 80-85.
-
(1997)
Int J Androl
, vol.20
, pp. 80-85
-
-
Yoshida, A.1
Miura, K.2
Nagao, K.3
Hara, H.4
Ishii, N.5
Shirai, M.6
-
155
-
-
7144223296
-
Gene action in the X-chromosome of the mouse (Mus musculus L.)
-
M.F. Lyon (1961) Gene action in the X-chromosome of the mouse (Mus musculus L.). Nature 190 372-373.
-
(1961)
Nature
, vol.190
, pp. 372-373
-
-
Lyon, M.F.1
-
156
-
-
84859033235
-
Sex matters during adolescence: testosterone-related cortical thickness maturation differs between boys and girls
-
J.E. Bramen, J.A. Hranilovich, R.E. Dahl, J. Chen, C. Rosso, E.E. Forbes, et al. (2012) Sex matters during adolescence: testosterone-related cortical thickness maturation differs between boys and girls. PLoS One 7 e33850.
-
(2012)
PLoS One
, vol.7
, pp. e33850
-
-
Bramen, J.E.1
Hranilovich, J.A.2
Dahl, R.E.3
Chen, J.4
Rosso, C.5
Forbes, E.E.6
-
157
-
-
0019422956
-
The etiology of maleness in XX men
-
A. de la Chapelle (1981) The etiology of maleness in XX men. Hum Genet 58 105-116.
-
(1981)
Hum Genet
, vol.58
, pp. 105-116
-
-
de la Chapelle, A.1
-
158
-
-
0029026641
-
The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene
-
C. Geerkens, U. Vetter, W. Just, N.S. Fedarko, L.W. Fisher, M.F. Young, et al. (1995) The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous gene. Hum Genet 96 44-52.
-
(1995)
Hum Genet
, vol.96
, pp. 44-52
-
-
Geerkens, C.1
Vetter, U.2
Just, W.3
Fedarko, N.S.4
Fisher, L.W.5
Young, M.F.6
-
159
-
-
0036195674
-
Changes in Leydig cell gene expression during development in the mouse
-
P.J. O'Shaugnessy, L. Willerton and P.J. Baker (2002) Changes in Leydig cell gene expression during development in the mouse. Biol Reprod 66 966-975.
-
(2002)
Biol Reprod
, vol.66
, pp. 966-975
-
-
O'Shaugnessy, P.J.1
Willerton, L.2
Baker, P.J.3
-
160
-
-
0010231936
-
The scientific investigation of the psychical faculties or process in the higher animals
-
I.P. Pavlov (1906) The scientific investigation of the psychical faculties or process in the higher animals. Science 24 613-619.
-
(1906)
Science
, vol.24
, pp. 613-619
-
-
Pavlov, I.P.1
-
161
-
-
15244363491
-
The DNA sequence of the human X chromosome
-
M.T. Ross, D.V. Grafham, A.J. Coffey, S. Scherer, K. McLay, D. Muzny, et al. (2005) The DNA sequence of the human X chromosome. Nature 434 325-337.
-
(2005)
Nature
, vol.434
, pp. 325-337
-
-
Ross, M.T.1
Grafham, D.V.2
Coffey, A.J.3
Scherer, S.4
McLay, K.5
Muzny, D.6
-
162
-
-
3042799936
-
Adolescent brain development and animal models
-
L.P. Spear (2004) Adolescent brain development and animal models. Ann NY Acad Sci 1021 23-26.
-
(2004)
Ann NY Acad Sci
, vol.1021
, pp. 23-26
-
-
Spear, L.P.1
-
163
-
-
84866511899
-
Socio-economic factors affect mortality in 47, XYY syndrome—A comparison with the background population and Klinefelter syndrome
-
K. Stockholm, S. Juul and C.H. Gravholt (2012) Socio-economic factors affect mortality in 47, XYY syndrome—A comparison with the background population and Klinefelter syndrome. Am J Med Genet A 158A 2421-2429.
-
(2012)
Am J Med Genet A
, vol.158A
, pp. 2421-2429
-
-
Stockholm, K.1
Juul, S.2
Gravholt, C.H.3
|