PubMed for id: 22522

Year	Number of Results
1998	1
2004	1
2006	2
2008	1
2009	2
2011	1
2012	1
2013	1
2024	0

1

Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?

Javaher P, Stuhrmann M, Wilke C, Frenzel E, Manukjan G, Grosshenig A, Dechend F, Schwaab E, Schmidtke J, Schubert S. Javaher P, et al. Fertil Steril. 2012 Feb;97(2):402-6. doi: 10.1016/j.fertnstert.2011.11.002. Epub 2011 Dec 2. Fertil Steril. 2012. PMID: 22137496 Free article.

2

Mutations in the TSPYL1 gene associated with 46,XY disorder of sex development and male infertility.

Vinci G, Brauner R, Tar A, Rouba H, Sheth J, Sheth F, Ravel C, McElreavey K, Bashamboo A. Vinci G, et al. Fertil Steril. 2009 Oct;92(4):1347-1350. doi: 10.1016/j.fertnstert.2009.04.009. Epub 2009 May 21. Fertil Steril. 2009. PMID: 19463995 Free article.

3

Genetic investigation of the TSPYL1 gene in sudden infant death syndrome.

Hering R, Frade-Martinez R, Bajanowski T, Poets CF, Tschentscher F, Riess O. Hering R, et al. Genet Med. 2006 Jan;8(1):55-8. doi: 10.1097/01.gim.0000195898.15290.03. Genet Med. 2006. PMID: 16418600 Free article.

4

TSPY expression is variably altered in transgenic mice with testicular feminization.

Schubert S, Kamino K, Böhm D, Adham I, Engel W, von Wasielewski R, Moharregh-Khiabani D, Mauceri G, Vaske B, Meinhardt A, Schöner A, Gonzalez-Fassrainer D, Schmidtke J. Schubert S, et al. Biol Reprod. 2008 Jul;79(1):125-33. doi: 10.1095/biolreprod.107.067025. Epub 2008 Apr 9. Biol Reprod. 2008. PMID: 18401008

5

Identification of novel candidate genes for globin regulation in erythroid cells containing large deletions of the human beta-globin gene cluster.

de Andrade TG, Peterson KR, Cunha AF, Moreira LS, Fattori A, Saad ST, Costa FF. de Andrade TG, et al. Blood Cells Mol Dis. 2006 Sep-Oct;37(2):82-90. doi: 10.1016/j.bcmd.2006.07.003. Epub 2006 Sep 6. Blood Cells Mol Dis. 2006. PMID: 16952470

6

Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function.

Puffenberger EG, Hu-Lince D, Parod JM, Craig DW, Dobrin SE, Conway AR, Donarum EA, Strauss KA, Dunckley T, Cardenas JF, Melmed KR, Wright CA, Liang W, Stafford P, Flynn CR, Morton DH, Stephan DA. Puffenberger EG, et al. Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11689-94. doi: 10.1073/pnas.0401194101. Epub 2004 Jul 23. Proc Natl Acad Sci U S A. 2004. PMID: 15273283 Free PMC article.

7

Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family.

Vogel T, Dittrich O, Mehraein Y, Dechend F, Schnieders F, Schmidtke J. Vogel T, et al. Cytogenet Cell Genet. 1998;81(3-4):265-70. doi: 10.1159/000015042. Cytogenet Cell Genet. 1998. PMID: 9730615

8

A high-confidence interaction map identifies SIRT1 as a mediator of acetylation of USP22 and the SAGA coactivator complex.

Armour SM, Bennett EJ, Braun CR, Zhang XY, McMahon SB, Gygi SP, Harper JW, Sinclair DA. Armour SM, et al. Mol Cell Biol. 2013 Apr;33(8):1487-502. doi: 10.1128/MCB.00971-12. Epub 2013 Feb 4. Mol Cell Biol. 2013. PMID: 23382074 Free PMC article.

9

Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair.

Svendsen JM, Smogorzewska A, Sowa ME, O'Connell BC, Gygi SP, Elledge SJ, Harper JW. Svendsen JM, et al. Cell. 2009 Jul 10;138(1):63-77. doi: 10.1016/j.cell.2009.06.030. Cell. 2009. PMID: 19596235 Free PMC article.

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