-
1
-
-
20944441422
-
Recombinant human LH supplementation versus recombinant human FSH (rFSH) step-up protocol during controlled ovarian stimulation in normogonadotrophic women with initial inadequate ovarian response to rFSH. A multicentre, prospective, randomized controlled trial[J]
-
De Placido G. Alviggi C, Perino A, et al. Recombinant human LH supplementation versus recombinant human FSH (rFSH) step-up protocol during controlled ovarian stimulation in normogonadotrophic women with initial inadequate ovarian response to rFSH. A multicentre, prospective, randomized controlled trial[J]. Hum Reprod, 2005, 20(2):390-396.
-
(2005)
Hum Reprod
, vol.20
, Issue.2
, pp. 390-396
-
-
De Placido, G.1
Alviggi, C.2
Perino, A.3
-
2
-
-
58649124341
-
Suboptimal response to GnRH - A long protocol is associated with a common LH polymorphism[J]
-
Alviggi C, Clarizia R, Pettersson K, et al. Suboptimal response to GnRH-a long protocol is associated with a common LH polymorphism[J]. Reprod Biomed Online, 2009, 18(1):9-14.
-
(2009)
Reprod Biomed Online
, vol.18
, Issue.1
, pp. 9-14
-
-
Alviggi, C.1
Clarizia, R.2
Pettersson, K.3
-
3
-
-
84863837427
-
Polymorphisms of the bovine luteinizing hormone/choriogonadotropin receptor(LHCGR) gene and its association with superovulation traits[J]
-
Yang WC, Tang KQ, Li SJ, et al. Polymorphisms of the bovine luteinizing hormone/choriogonadotropin receptor(LHCGR) gene and its association with superovulation traits[J]. Mol Biol Rep, 2012, 39(3): 2481-2487.
-
(2012)
Mol Biol Rep
, vol.39
, Issue.3
, pp. 2481-2487
-
-
Yang, W.C.1
Tang, K.Q.2
Li, S.J.3
-
4
-
-
78651256136
-
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3[J]
-
Chen ZJ, Zhao H, He L, et al. Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3[J]. Nat Genet, 2011, 43 (1): 55-59.
-
(2011)
Nat Genet
, vol.43
, Issue.1
, pp. 55-59
-
-
Chen, Z.J.1
Zhao, H.2
He, L.3
-
5
-
-
80054851736
-
Susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in acohort of Caucasian women [J]
-
Lerchbaum E, Trummer O, Giuliani A, et al. Susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21, and 9q33.3 in acohort of Caucasian women [J]. Horm Metab Res, 2011, 43(11):743-747.
-
(2011)
Horm Metab Res
, vol.43
, Issue.11
, pp. 743-747
-
-
Lerchbaum, E.1
Trummer, O.2
Giuliani, A.3
-
6
-
-
33646793005
-
Is there a need for recombinant human luteinizing hormone (lutropin alfa) supplementation inovarian stimulation for assisted reproduction? [J]
-
Nawroth F, Ludwig M. Is there a need for recombinant human luteinizing Hormone (lutropin alfa) supplementation inovarian stimulation for assisted reproduction? [J]. Womens Health (Lond Engl), 2006, 2(3): 375-384.
-
(2006)
Womens Health (Lond Engl)
, vol.2
, Issue.3
, pp. 375-384
-
-
Nawroth, F.1
Ludwig, M.2
-
7
-
-
84867404664
-
Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma [J]
-
Wang Z, Li T, Zhang W, et al. Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma [J]. Gynecol Oncol, 2012, 127(2): 403-405.
-
(2012)
Gynecol Oncol
, vol.127
, Issue.2
, pp. 403-405
-
-
Wang, Z.1
Li, T.2
Zhang, W.3
-
8
-
-
0242363235
-
A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig[J]
-
Van Laere AS, Nguyen M, Braunschweig M, et al. A regulatory mutation in IGF2 causes a major QTL effect on muscle growth in the pig[J]. Nature, 2003, 425 (6960): 832-836.
-
(2003)
Nature
, vol.425
, Issue.6960
, pp. 832-836
-
-
Van Laere, A.S.1
Nguyen, M.2
Braunschweig, M.3
-
9
-
-
79951577452
-
The polymorphisms of bovine VEGF gene and their associations with growth traits in Chinese cattle[J]
-
Pang Y, Wang J, Zhang C, et al. The polymorphisms of bovine VEGF gene and their associations with growth traits in Chinese cattle[J]. Mol Biol Rep, 2011, 38(2):755-759.
-
(2011)
Mol Biol Rep
, vol.38
, Issue.2
, pp. 755-759
-
-
Pang, Y.1
Wang, J.2
Zhang, C.3
-
10
-
-
83755185526
-
Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3[J]
-
Zhao H, Xu X, Xing X, et al. Family-based analysis of susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3[J]. Hum Reprod, 2012, 27(1): 294-298.
-
(2012)
Hum Reprod
, vol.27
, Issue.1
, pp. 294-298
-
-
Zhao, H.1
Xu, X.2
Xing, X.3
-
11
-
-
33845249747
-
Evidence for a 3p25 breakpoint hot spot region in thyroid tumors of follicular origin [J]
-
Drieschner N, Belge G, Rippe V, et al. Evidence for a 3p25 breakpoint hot spot region in thyroid tumors of follicular origin [J]. Thyroid, 2006, 16(11): 1091-1096.
-
(2006)
Thyroid
, vol.16
, Issue.11
, pp. 1091-1096
-
-
Drieschner, N.1
Belge, G.2
Rippe, V.3
-
12
-
-
44349083202
-
A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele[J]
-
Haasl RJ, Ahmadi MR, Meethal SV, et al. A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele[J]. BMC Med Genet, 2008, 9: 37.
-
(2008)
BMC Med Genet
, vol.9
, pp. 37
-
-
Haasl, R.J.1
Ahmadi, M.R.2
Meethal, S.V.3
-
13
-
-
33846934728
-
Single base-pair substitutions in exon-intron junctions of human genes: Nature, distribution, and consequences for mRNA splicing [J]
-
Krawczak M, Thomas NS, Hundrieser B, et al. Single base-pair substitutions in exon-intron junctions of human genes: nature, distribution, and consequences for mRNA splicing [J]. Hum Mutat, 2007, 28(2):150-158.
-
(2007)
Hum Mutat
, vol.28
, Issue.2
, pp. 150-158
-
-
Krawczak, M.1
Thomas, N.S.2
Hundrieser, B.3
-
15
-
-
0035667849
-
Single nucleotide polymorphisms (SNPs) and SNP databases[J]
-
(in Chinese)
-
Gu F. Single nucleotide polymorphisms (SNPs) and SNP databases[J]. Chin J Med Genet, 2001, 18 (6): 479-481. (in Chinese)
-
(2001)
Chin J Med Genet
, vol.18
, Issue.6
, pp. 479-481
-
-
Gu, F.1
-
17
-
-
22544475352
-
Significance of a common single nucleotide polymorphism in exon 10 of the follicle-stimulating hormone(FSH) receptor gene for the ovarian response to FSH: A pharmacogenetic approach to controlled ovarian hyperstimulation[J]
-
Behre HM, Greb RR, Mempel A, et al. Significance of a common single nucleotide polymorphism in exon 10 of the follicle-stimulating hormone(FSH) receptor gene for the ovarian response to FSH: a pharmacogenetic approach to controlled ovarian hyperstimulation[J]. Pharmacogenet Genomics, 2005, 15(7):451-456.
-
(2005)
Pharmacogenet Genomics
, vol.15
, Issue.7
, pp. 451-456
-
-
Behre, H.M.1
Greb, R.R.2
Mempel, A.3
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