-
1
-
-
18144384470
-
An update: spontaneous premature ovarian failure is not an early menopause
-
Nelson LM, Covington SN, Rebar RW, (2005) An update: spontaneous premature ovarian failure is not an early menopause. Fertil Steril 83: 1327-1332.
-
(2005)
Fertil Steril
, vol.83
, pp. 1327-1332
-
-
Nelson, L.M.1
Covington, S.N.2
Rebar, R.W.3
-
4
-
-
33845962386
-
Premature ovarian failure
-
Christin-Maitre S, Pasquier M, Donadille B, Bouchard P, (2006) [Premature ovarian failure]. Ann Endocrinol (Paris) 67: 557-566.
-
(2006)
Ann Endocrinol (Paris)
, vol.67
, pp. 557-566
-
-
Christin-Maitre, S.1
Pasquier, M.2
Donadille, B.3
Bouchard, P.4
-
5
-
-
59749096464
-
Clinical practice. Primary ovarian insufficiency
-
Nelson LM, (2009) Clinical practice. Primary ovarian insufficiency. N Engl J Med 360: 606-614.
-
(2009)
N Engl J Med
, vol.360
, pp. 606-614
-
-
Nelson, L.M.1
-
6
-
-
33745285019
-
Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure
-
Lacombe A, Lee H, Zahed L, Choucair M, Muller JM, et al. (2006) Disruption of POF1B binding to nonmuscle actin filaments is associated with premature ovarian failure. Am J Hum Genet 79: 113-119.
-
(2006)
Am J Hum Genet
, vol.79
, pp. 113-119
-
-
Lacombe, A.1
Lee, H.2
Zahed, L.3
Choucair, M.4
Muller, J.M.5
-
7
-
-
56749095557
-
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus
-
Oldenburg RA, van Dooren MF, de Graaf B, Simons E, Govaerts L, et al. (2008) A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locus. Hum Reprod 23: 2835-2841.
-
(2008)
Hum Reprod
, vol.23
, pp. 2835-2841
-
-
Oldenburg, R.A.1
van Dooren, M.F.2
de Graaf, B.3
Simons, E.4
Govaerts, L.5
-
8
-
-
0032715145
-
Premature ovarian failure: a systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy
-
van Kasteren YM, Schoemaker J, (1999) Premature ovarian failure: a systematic review on therapeutic interventions to restore ovarian function and achieve pregnancy. Hum Reprod Update 5: 483-492.
-
(1999)
Hum Reprod Update
, vol.5
, pp. 483-492
-
-
van Kasteren, Y.M.1
Schoemaker, J.2
-
9
-
-
0034732352
-
Premature ovarian failure
-
Vegetti W, Marozzi A, Manfredini E, Testa G, Alagna F, et al. (2000) Premature ovarian failure. Mol Cell Endocrinol 161: 53-57.
-
(2000)
Mol Cell Endocrinol
, vol.161
, pp. 53-57
-
-
Vegetti, W.1
Marozzi, A.2
Manfredini, E.3
Testa, G.4
Alagna, F.5
-
11
-
-
3042601976
-
Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene
-
Di Pasquale E, Beck-Peccoz P, Persani L, (2004) Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene. Am J Hum Genet 75: 106-111.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 106-111
-
-
Di Pasquale, E.1
Beck-Peccoz, P.2
Persani, L.3
-
12
-
-
33645750342
-
Missense mutations in the BMP15 gene are associated with ovarian failure
-
Dixit H, Rao LK, Padmalatha VV, Kanakavalli M, Deenadayal M, et al. (2006) Missense mutations in the BMP15 gene are associated with ovarian failure. Hum Genet 119: 408-415.
-
(2006)
Hum Genet
, vol.119
, pp. 408-415
-
-
Dixit, H.1
Rao, L.K.2
Padmalatha, V.V.3
Kanakavalli, M.4
Deenadayal, M.5
-
13
-
-
33744519199
-
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure
-
Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, et al. (2006) Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure. Eur J Endocrinol 154: 739-744.
-
(2006)
Eur J Endocrinol
, vol.154
, pp. 739-744
-
-
Laissue, P.1
Christin-Maitre, S.2
Touraine, P.3
Kuttenn, F.4
Ritvos, O.5
-
14
-
-
15844426692
-
Atm-deficient mice: a paradigm of ataxia telangiectasia
-
Barlow C, Hirotsune S, Paylor R, Liyanage M, Eckhaus M, et al. (1996) Atm-deficient mice: a paradigm of ataxia telangiectasia. Cell 86: 159-171.
-
(1996)
Cell
, vol.86
, pp. 159-171
-
-
Barlow, C.1
Hirotsune, S.2
Paylor, R.3
Liyanage, M.4
Eckhaus, M.5
-
16
-
-
0029118115
-
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
-
Aittomaki K, Lucena JL, Pakarinen P, Sistonen P, Tapanainen J, et al. (1995) Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 82: 959-968.
-
(1995)
Cell
, vol.82
, pp. 959-968
-
-
Aittomaki, K.1
Lucena, J.L.2
Pakarinen, P.3
Sistonen, P.4
Tapanainen, J.5
-
17
-
-
12344283011
-
Molecular cloning of porcine growth differentiation factor 9 (GDF-9) cDNA and its role in early folliculogenesis: direct ovarian injection of GDF-9 gene fragments promotes early folliculogenesis
-
Shimizu T, Miyahayashi Y, Yokoo M, Hoshino Y, Sasada H, et al. (2004) Molecular cloning of porcine growth differentiation factor 9 (GDF-9) cDNA and its role in early folliculogenesis: direct ovarian injection of GDF-9 gene fragments promotes early folliculogenesis. Reproduction 128: 537-543.
-
(2004)
Reproduction
, vol.128
, pp. 537-543
-
-
Shimizu, T.1
Miyahayashi, Y.2
Yokoo, M.3
Hoshino, Y.4
Sasada, H.5
-
18
-
-
34548288054
-
NOBOX homeobox mutation causes premature ovarian failure
-
Qin Y, Choi Y, Zhao H, Simpson JL, Chen ZJ, et al. (2007) NOBOX homeobox mutation causes premature ovarian failure. Am J Hum Genet 81: 576-581.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 576-581
-
-
Qin, Y.1
Choi, Y.2
Zhao, H.3
Simpson, J.L.4
Chen, Z.J.5
-
19
-
-
63249095263
-
Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure
-
Qin Y, Shi Y, Zhao Y, Carson SA, Simpson JL, et al. (2009) Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure. Fertil Steril 91: 1507-1509.
-
(2009)
Fertil Steril
, vol.91
, pp. 1507-1509
-
-
Qin, Y.1
Shi, Y.2
Zhao, Y.3
Carson, S.A.4
Simpson, J.L.5
-
20
-
-
0032566960
-
Genes and premature ovarian failure
-
Christin-Maitre S, Vasseur C, Portnoi MF, Bouchard P, (1998) Genes and premature ovarian failure. Mol Cell Endocrinol 145: 75-80.
-
(1998)
Mol Cell Endocrinol
, vol.145
, pp. 75-80
-
-
Christin-Maitre, S.1
Vasseur, C.2
Portnoi, M.F.3
Bouchard, P.4
-
21
-
-
58549106975
-
Ovarian histological findings in an adult patient with the steroidogenic acute regulatory protein (StAR) deficiency reveal the impairment of steroidogenesis by lipoid deposition
-
Kaku U, Kameyama K, Izawa M, Yamada M, Miyamoto J, et al. (2008) Ovarian histological findings in an adult patient with the steroidogenic acute regulatory protein (StAR) deficiency reveal the impairment of steroidogenesis by lipoid deposition. Endocr J 55: 1043-1049.
-
(2008)
Endocr J
, vol.55
, pp. 1043-1049
-
-
Kaku, U.1
Kameyama, K.2
Izawa, M.3
Yamada, M.4
Miyamoto, J.5
-
22
-
-
0035131812
-
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
-
Crisponi L, Deiana M, Loi A, Chiappe F, Uda M, et al. (2001) The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet 27: 159-166.
-
(2001)
Nat Genet
, vol.27
, pp. 159-166
-
-
Crisponi, L.1
Deiana, M.2
Loi, A.3
Chiappe, F.4
Uda, M.5
-
23
-
-
0036061053
-
Identification of novel mutations in FOXL2 associated with premature ovarian failure
-
Harris SE, Chand AL, Winship IM, Gersak K, Aittomaki K, et al. (2002) Identification of novel mutations in FOXL2 associated with premature ovarian failure. Mol Hum Reprod 8: 729-733.
-
(2002)
Mol Hum Reprod
, vol.8
, pp. 729-733
-
-
Harris, S.E.1
Chand, A.L.2
Winship, I.M.3
Gersak, K.4
Aittomaki, K.5
-
24
-
-
67650508076
-
Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
-
Laissue P, Lakhal B, Benayoun BA, Dipietromaria A, Braham R, et al. (2009) Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2. J Med Genet 46: 455-457.
-
(2009)
J Med Genet
, vol.46
, pp. 455-457
-
-
Laissue, P.1
Lakhal, B.2
Benayoun, B.A.3
Dipietromaria, A.4
Braham, R.5
-
25
-
-
11144311186
-
A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report
-
Gersak K, Harris SE, Smale WJ, Shelling AN, (2004) A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report. Hum Reprod 19: 2767-2770.
-
(2004)
Hum Reprod
, vol.19
, pp. 2767-2770
-
-
Gersak, K.1
Harris, S.E.2
Smale, W.J.3
Shelling, A.N.4
-
26
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR, (2002) Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30: 97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
27
-
-
17444390125
-
HaploPainter: a tool for drawing pedigrees with complex haplotypes
-
Thiele H, Nurnberg P, (2005) HaploPainter: a tool for drawing pedigrees with complex haplotypes. Bioinformatics 21: 1730-1732.
-
(2005)
Bioinformatics
, vol.21
, pp. 1730-1732
-
-
Thiele, H.1
Nurnberg, P.2
-
28
-
-
85027941242
-
KinSNP software for homozygosity mapping of disease genes using SNP microarrays
-
Amir el AD, Bartal O, Morad E, Nagar T, Sheynin J, et al. (2010) KinSNP software for homozygosity mapping of disease genes using SNP microarrays. Hum Genomics 4: 394-401.
-
(2010)
Hum Genomics
, vol.4
, pp. 394-401
-
-
Amir el, A.D.1
Bartal, O.2
Morad, E.3
Nagar, T.4
Sheynin, J.5
-
29
-
-
42449103536
-
Positive regulation of steroidogenic acute regulatory protein gene expression through the interaction between Dlx and GATA-4 for testicular steroidogenesis
-
Nishida H, Miyagawa S, Vieux-Rochas M, Morini M, Ogino Y, et al. (2008) Positive regulation of steroidogenic acute regulatory protein gene expression through the interaction between Dlx and GATA-4 for testicular steroidogenesis. Endocrinology 149: 2090-2097.
-
(2008)
Endocrinology
, vol.149
, pp. 2090-2097
-
-
Nishida, H.1
Miyagawa, S.2
Vieux-Rochas, M.3
Morini, M.4
Ogino, Y.5
-
30
-
-
84859631522
-
The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology
-
Caburet S, Georges A, L'Hôte D, Todeschini AL, Benayoun BA, et al. (2011) The transcription factor FOXL2: at the crossroads of ovarian physiology and pathology. Molecular and Cellular Endocrinology.
-
(2011)
Molecular and Cellular Endocrinology
-
-
Caburet, S.1
Georges, A.2
L'Hôte, D.3
Todeschini, A.L.4
Benayoun, B.A.5
-
31
-
-
53349129583
-
Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs
-
Jeong J, Li X, McEvilly RJ, Rosenfeld MG, Lufkin T, et al. (2008) Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs. Development 135: 2905-2916.
-
(2008)
Development
, vol.135
, pp. 2905-2916
-
-
Jeong, J.1
Li, X.2
McEvilly, R.J.3
Rosenfeld, M.G.4
Lufkin, T.5
-
32
-
-
79958706951
-
Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency
-
Bouhali K, Dipietromaria A, Fontaine A, Caburet S, Barbieri O, et al. (2011) Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency. Hum Mol Genet 20: 2642-2650.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 2642-2650
-
-
Bouhali, K.1
Dipietromaria, A.2
Fontaine, A.3
Caburet, S.4
Barbieri, O.5
-
33
-
-
44849125102
-
C. elegans dss-1 is functionally conserved and required for oogenesis and larval growth
-
Pispa J, Palmen S, Holmberg CI, Jantti J, (2008) C. elegans dss-1 is functionally conserved and required for oogenesis and larval growth. BMC Dev Biol 8: 51.
-
(2008)
BMC Dev Biol
, vol.8
, pp. 51
-
-
Pispa, J.1
Palmen, S.2
Holmberg, C.I.3
Jantti, J.4
-
34
-
-
9244248158
-
Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
-
Crackower MA, Scherer SW, Rommens JM, Hui CC, Poorkaj P, et al. (1996) Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development. Hum Mol Genet 5: 571-579.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 571-579
-
-
Crackower, M.A.1
Scherer, S.W.2
Rommens, J.M.3
Hui, C.C.4
Poorkaj, P.5
-
35
-
-
0028110965
-
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly
-
Scherer SW, Poorkaj P, Massa H, Soder S, Allen T, et al. (1994) Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly. Hum Mol Genet 3: 1345-1354.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1345-1354
-
-
Scherer, S.W.1
Poorkaj, P.2
Massa, H.3
Soder, S.4
Allen, T.5
-
36
-
-
70449116133
-
Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure
-
Aboura A, Dupas C, Tachdjian G, Portnoi MF, Bourcigaux N, et al. (2009) Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure. J Clin Endocrinol Metab 94: 4540-4546.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 4540-4546
-
-
Aboura, A.1
Dupas, C.2
Tachdjian, G.3
Portnoi, M.F.4
Bourcigaux, N.5
-
37
-
-
77449137856
-
Roles of E3 ubiquitin ligases in cell adhesion and migration
-
Huang C, (2010) Roles of E3 ubiquitin ligases in cell adhesion and migration. Cell Adh Migr 4: 10-8.
-
(2010)
Cell Adh Migr
, vol.4
, pp. 10-18
-
-
Huang, C.1
-
38
-
-
79952849578
-
Steroid regulation of drug-metabolizing cytochromes P450
-
Monostory K, Dvorak Z, (2011) Steroid regulation of drug-metabolizing cytochromes P450. Curr Drug Metab 12: 154-72.
-
(2011)
Curr Drug Metab
, vol.12
, pp. 154-172
-
-
Monostory, K.1
Dvorak, Z.2
-
39
-
-
0001398513
-
Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance
-
Hahm S, Mizuno TM, Wu TJ, Wisor JP, Priest CA, et al. (1999) Targeted deletion of the Vgf gene indicates that the encoded secretory peptide precursor plays a novel role in the regulation of energy balance. Neuron 23: 537-48.
-
(1999)
Neuron
, vol.23
, pp. 537-548
-
-
Hahm, S.1
Mizuno, T.M.2
Wu, T.J.3
Wisor, J.P.4
Priest, C.A.5
|