244 related articles for article (PubMed ID: 30779420)
1. The mouse as a model of fundamental concepts related to Turner syndrome.
Arnold AP
Am J Med Genet C Semin Med Genet; 2019 Mar; 181(1):76-85. PubMed ID: 30779420
[TBL] [Abstract][Full Text] [Related]
2. High resolution whole brain imaging of anatomical variation in XO, XX, and XY mice.
Raznahan A; Probst F; Palmert MR; Giedd JN; Lerch JP
Neuroimage; 2013 Dec; 83():962-8. PubMed ID: 23891883
[TBL] [Abstract][Full Text] [Related]
3. Transcriptional changes in response to X chromosome dosage in the mouse: implications for X inactivation and the molecular basis of Turner Syndrome.
Lopes AM; Burgoyne PS; Ojarikre A; Bauer J; Sargent CA; Amorim A; Affara NA
BMC Genomics; 2010 Feb; 11():82. PubMed ID: 20122165
[TBL] [Abstract][Full Text] [Related]
4. Studying early lethality of 45,XO (Turner's syndrome) embryos using human embryonic stem cells.
Urbach A; Benvenisty N
PLoS One; 2009; 4(1):e4175. PubMed ID: 19137066
[TBL] [Abstract][Full Text] [Related]
5. Epigenetics in Turner syndrome.
Álvarez-Nava F; Lanes R
Clin Epigenetics; 2018; 10():45. PubMed ID: 29636833
[TBL] [Abstract][Full Text] [Related]
6. The 39,XO mouse as a model for the neurobiology of Turner syndrome and sex-biased neuropsychiatric disorders.
Lynn PM; Davies W
Behav Brain Res; 2007 May; 179(2):173-82. PubMed ID: 17367875
[TBL] [Abstract][Full Text] [Related]
7. X-monosomy effects on visuospatial attention in mice: a candidate gene and implications for Turner syndrome and attention deficit hyperactivity disorder.
Davies W; Humby T; Isles AR; Burgoyne PS; Wilkinson LS
Biol Psychiatry; 2007 Jun; 61(12):1351-60. PubMed ID: 17161381
[TBL] [Abstract][Full Text] [Related]
8. The phenotype of a pig with monosomy X resembling Turner syndrome symptoms: a case report.
Umeyama K; Nakano K; Matsunari H; Yamada T; Hasegawa K; Tang K; Tokuyama Y; Watanabe M; Nagaya M; Nagashima H
J Reprod Dev; 2019 Jun; 65(3):231-237. PubMed ID: 30773506
[TBL] [Abstract][Full Text] [Related]
9. A strategic research alliance: Turner syndrome and sex differences.
San Roman AK; Page DC
Am J Med Genet C Semin Med Genet; 2019 Mar; 181(1):59-67. PubMed ID: 30790449
[TBL] [Abstract][Full Text] [Related]
10. Effects on fear reactivity in XO mice are due to haploinsufficiency of a non-PAR X gene: implications for emotional function in Turner's syndrome.
Isles AR; Davies W; Burrmann D; Burgoyne PS; Wilkinson LS
Hum Mol Genet; 2004 Sep; 13(17):1849-55. PubMed ID: 15238507
[TBL] [Abstract][Full Text] [Related]
11. Premature ovarian insufficiency in the XO female mouse on the C57BL/6J genetic background.
Vaz B; El Mansouri F; Liu X; Taketo T
Mol Hum Reprod; 2020 Sep; 26(9):678-688. PubMed ID: 32634219
[TBL] [Abstract][Full Text] [Related]
12. Analysis of genetic variability in Turner syndrome linked to long-term clinical features.
Suntharalingham JP; Ishida M; Cameron-Pimblett A; McGlacken-Byrne SM; Buonocore F; Del Valle I; Madhan GK; Brooks T; Conway GS; Achermann JC
Front Endocrinol (Lausanne); 2023; 14():1227164. PubMed ID: 37800145
[TBL] [Abstract][Full Text] [Related]
13. Expression level of Rps4 mRNA in 39,X mice and 40,XX mice.
Omoe K; Endo A
Cytogenet Cell Genet; 1994; 67(1):52-4. PubMed ID: 8187552
[TBL] [Abstract][Full Text] [Related]
14. Genomic imprinting and Turner syndrome.
Bondy CA; Hougen HY; Zhou J; Cheng CM
Pediatr Endocrinol Rev; 2012 May; 9 Suppl 2():728-32. PubMed ID: 22946286
[TBL] [Abstract][Full Text] [Related]
15. Bioinformatic Analysis Identifies Potential Key Genes in the Pathogenesis of Turner Syndrome.
Wang H; Zhu H; Zhu W; Xu Y; Wang N; Han B; Song H; Qiao J
Front Endocrinol (Lausanne); 2020; 11():104. PubMed ID: 32210915
[No Abstract] [Full Text] [Related]
16. Bioinformatic analysis identifies the immunological profile of turner syndrome with different X chromosome origins.
Qi X; Wang Q; Yu M; Kong Y; Shi F; Wang S
Front Endocrinol (Lausanne); 2023; 14():1024244. PubMed ID: 36733527
[TBL] [Abstract][Full Text] [Related]
17. Turner syndrome: the case of the missing sex chromosome.
Zinn AR; Page DC; Fisher EM
Trends Genet; 1993 Mar; 9(3):90-3. PubMed ID: 8488568
[TBL] [Abstract][Full Text] [Related]
18. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.
Daggag H; Srour W; El-Khateeb M; Ajlouni K
Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405
[TBL] [Abstract][Full Text] [Related]
19. Epigenetics and genomics in Turner syndrome.
Viuff M; Skakkebaek A; Nielsen MM; Chang S; Gravholt CH
Am J Med Genet C Semin Med Genet; 2019 Mar; 181(1):68-75. PubMed ID: 30811826
[TBL] [Abstract][Full Text] [Related]
20. X-chromosome gene dosage and the risk of diabetes in Turner syndrome.
Bakalov VK; Cheng C; Zhou J; Bondy CA
J Clin Endocrinol Metab; 2009 Sep; 94(9):3289-96. PubMed ID: 19567529
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]