Expression of the P2X2 Receptor Subunit of the ATP-Gated Ion Channel in the Cochlea: Implications for Sound Transduction and Auditory Neurotransmission von Housley, Gary D, Kanjhan, Refik, Raybould, Nicholas P, Greenwood, Denise, Salih, Salam G, Jarlebark, Leif, Burton, Lucille D, Setz, Vera C. M, Cannell, Mark B, Soeller, Christian, Christie, David L, Usami, Shin-ichi, Matsubara, Atsushi, Yoshie, Haruhide, Ryan, Allen F, Thorne, Peter R

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ATP-gated ion channel expression in primary auditory neurones von Salih, Salam G, Housley, Gary D, Raybould, Nicholas P, Thorne, Peter R

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Expression of ATP-gated ion channels by Reissnerʼs membrane epithelial cells von King, Maria, Housley, Gary D, Raybould, Nicholas P, Greenwood, Denise, Salih, Salam G

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P2X2 receptor subunit expression in a subpopulation of cochlear type I spiral ganglion neurones von Salih, Salam G, Housley, Gary D, Burton, Lucille D, Greenwood, Denise

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P2X2 receptor expression by interstitial cells of Cajal in vas deferens implicated in semen emission von BURTON, Lucille D, HOUSLEY, Gary D, SALIH, Salam G, JÄRLEBARK, Leif, CHRISTIE, David L, GREENWOOD, Denise

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Expression of the P2X 2 Receptor Subunit of the ATP-Gated Ion Channel in the Cochlea: Implications for Sound Transduction and Auditory Neurotransmission von Housley, Gary D., Kanjhan, Refik, Raybould, Nicholas P., Greenwood, Denise, Salih, Salam G., Järlebark, Leif, Burton, Lucille D., Setz, Vera C. M., Cannell, Mark B., Soeller, Christian, Christie, David L., Usami, Shin-ichi, Matsubara, Atsushi, Yoshie, Haruhide, Ryan, Allen F., Thorne, Peter R.

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Genetic investigation of 93 families with microphthalmia or posterior microphthalmos von Patel, N., Khan, A.O., Alsahli, S., Abdel‐Salam, G., Nowilaty, S.R., Mansour, A.M., Nabil, A., Al‐Owain, M., Sogati, S., Salih, M.A., Kamal, A.M., Alsharif, H., Alsaif, H.S., Alzahrani, S.S., Abdulwahab, F., Ibrahim, N., Hashem, M., Faquih, T., Shah, Z.A., Abouelhoda, M., Monies, D., Dasouki, M., Shaheen, R., Wakil, S.M., Aldahmesh, M.A., Alkuraya, F.S.

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Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities von Cali, E., Suri, M., Scala, M., Ferla, M.P., Alavi, S., Faqeih, E.A., Bijlsma, E.K., Wigby, K.M., Baralle, D., Mehrjardi, M.Y.V., Schwab, J., Platzer, K., Steindl, K., Hashem, M., Jones, M., Niyazov, D.M., Jacober, J., Littlejohn, R.O., Weis, D., Zadeh, N., Rodan, L., Goldenberg, A., Lecoquierre, F., Dutra-Clarke, M., Horvath, G., Young, D., Orenstein, N., Bawazeer, S., Vulto-van Silfhout, A.T., Herenger, Y., Dehghani, M., Seyedhassani, S.M., Bahreini, A., Nasab, M.E., Ercan-Sencicek, A.G., Firoozfar, Z., Movahedinia, M., Efthymiou, S., Striano, P., Karimiani, E.G., Salpietro, V., Taylor, J.C., Redman, M., Stegmann, A.P.A., Laner, A., Abdel-Salam, G., Li, M.G., Bengala, M., Müller, A.J., Digilio, M.C., Rauch, A., Gunel, M., Titheradge, H., Schweitzer, D.N., Kraus, A., Valenzuela, I., McLean, S.D., Phornphutkul, C., Salih, M., Begtrup, A., Schnur, R.E., Torti, E., Haack, T.B., Prada, C.E., Alkuraya, F.S., Houlden, H., Maroofian, R.

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