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Items: 1 to 20 of 226

1.

A conserved RNA-protein complex component involved in physiological germline apoptosis regulation in C. elegans.

Boag PR, Nakamura A, Blackwell TK.

Development. 2005 Nov;132(22):4975-86. Epub 2005 Oct 12.

2.

Requirement for P granules and meiosis for accumulation of the germline RNA helicase CGH-1.

Navarro RE, Blackwell TK.

Genesis. 2005 Jul;42(3):172-80.

PMID:
15986473
3.
4.

NANOS-3 and FBF proteins physically interact to control the sperm-oocyte switch in Caenorhabditis elegans.

Kraemer B, Crittenden S, Gallegos M, Moulder G, Barstead R, Kimble J, Wickens M.

Curr Biol. 1999 Sep 23;9(18):1009-18.

5.
6.

A conserved RNA-binding protein that regulates sexual fates in the C. elegans hermaphrodite germ line.

Zhang B, Gallegos M, Puoti A, Durkin E, Fields S, Kimble J, Wickens MP.

Nature. 1997 Dec 4;390(6659):477-84.

PMID:
9393998
7.

C. elegans CPB-3 interacts with DAZ-1 and functions in multiple steps of germline development.

Hasegawa E, Karashima T, Sumiyoshi E, Yamamoto M.

Dev Biol. 2006 Jul 15;295(2):689-99. Epub 2006 Apr 7.

8.

Caenorhabditis elegans inhibitor of apoptosis protein (IAP) homologue BIR-1 plays a conserved role in cytokinesis.

Fraser AG, James C, Evan GI, Hengartner MO.

Curr Biol. 1999 Mar 25;9(6):292-301.

9.

C. elegans dss-1 is functionally conserved and required for oogenesis and larval growth.

Pispa J, Palmén S, Holmberg CI, Jäntti J.

BMC Dev Biol. 2008 May 9;8:51. doi: 10.1186/1471-213X-8-51.

10.

Depletion of the cap-associated isoform of translation factor eIF4G induces germline apoptosis in C. elegans.

Contreras V, Richardson MA, Hao E, Keiper BD.

Cell Death Differ. 2008 Aug;15(8):1232-42. doi: 10.1038/cdd.2008.46. Epub 2008 May 2.

11.

Germ cell survival in C. elegans and C. remanei is affected when the DEAD box RNA helicases VBH-1 or Cre-VBH-1 are silenced.

Salinas LS, Franco-Cea A, Láscarez-Lagunas LI, Villanueva-Chimal E, Maldonado E, Navarro RE.

Genesis. 2012 Nov;50(11):801-18. doi: 10.1002/dvg.22043. Epub 2012 Jul 11.

PMID:
22674898
12.

ATX-2, the C. elegans ortholog of ataxin 2, functions in translational regulation in the germline.

Ciosk R, DePalma M, Priess JR.

Development. 2004 Oct;131(19):4831-41. Epub 2004 Sep 1.

13.

Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis.

Boag PR, Atalay A, Robida S, Reinke V, Blackwell TK.

J Cell Biol. 2008 Aug 11;182(3):543-57. doi: 10.1083/jcb.200801183.

14.

The DEAD box RNA helicase VBH-1 is required for germ cell function in C. elegans.

Salinas LS, Maldonado E, Macías-Silva M, Blackwell TK, Navarro RE.

Genesis. 2007 Sep;45(9):533-46.

PMID:
17868112
16.

HRP-2, a heterogeneous nuclear ribonucleoprotein, is essential for embryogenesis and oogenesis in Caenorhabditis elegans.

Kinnaird JH, Maitland K, Walker GA, Wheatley I, Thompson FJ, Devaney E.

Exp Cell Res. 2004 Aug 15;298(2):418-30.

PMID:
15265690
17.

Distinct roles for two C. elegans anillins in the gonad and early embryo.

Maddox AS, Habermann B, Desai A, Oegema K.

Development. 2005 Jun;132(12):2837-48.

18.

The Caenorhabditis elegans homologue of deleted in azoospermia is involved in the sperm/oocyte switch.

Otori M, Karashima T, Yamamoto M.

Mol Biol Cell. 2006 Jul;17(7):3147-55. Epub 2006 Apr 26.

19.

cdc-25.2, a C. elegans ortholog of cdc25, is required to promote oocyte maturation.

Kim J, Kawasaki I, Shim YH.

J Cell Sci. 2010 Mar 15;123(Pt 6):993-1000. doi: 10.1242/jcs.060442.

20.

Large P body-like RNPs form in C. elegans oocytes in response to arrested ovulation, heat shock, osmotic stress, and anoxia and are regulated by the major sperm protein pathway.

Jud MC, Czerwinski MJ, Wood MP, Young RA, Gallo CM, Bickel JS, Petty EL, Mason JM, Little BA, Padilla PA, Schisa JA.

Dev Biol. 2008 Jun 1;318(1):38-51. doi: 10.1016/j.ydbio.2008.02.059. Epub 2008 Mar 14.

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