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Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding. [electronic resource] by
- Collin, Rob W J
- Chellappa, Ramesh
- Pauw, Robert-Jan
- Vriend, Gert
- Oostrik, Jaap
- van Drunen, Wendy
- Huygen, Patrick L
- Admiraal, Ronald
- Hoefsloot, Lies H
- Cremers, Frans P M
- Xiang, Mengqing
- Cremers, Cor W R J
- Kremer, Hannie
Producer: 20080416
In:
Human mutation vol. 29
Availability: No items available.
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110.
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111.
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Performance of a new HPV and biomarker assay in the management of hrHPV positive women: Subanalysis of the ongoing multicenter TRACE clinical trial (n > 6,000) to evaluate POU4F3 methylation as a potential biomarker of cervical precancer and cancer. [electronic resource] by
- Kocsis, Adrienn
- Takács, Tibor
- Jeney, Csaba
- Schaff, Zsuzsa
- Koiss, Róbert
- Járay, Balázs
- Sobel, Gábor
- Pap, Károly
- Székely, István
- Ferenci, Tamás
- Lai, Hung-Cheng
- Nyíri, Miklós
- Benczik, Márta
Producer: 20170515
In:
International journal of cancer vol. 140
Availability: No items available.
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Characterization of a transformed rat retinal ganglion cell line. [electronic resource] by
- Krishnamoorthy, R R
- Agarwal, P
- Prasanna, G
- Vopat, K
- Lambert, W
- Sheedlo, H J
- Pang, I H
- Shade, D
- Wordinger, R J
- Yorio, T
- Clark, A F
- Agarwal, N
Producer: 20010510
In:
Brain research. Molecular brain research vol. 86
Availability: No items available.
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