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Published in Nature cell biology (01.04.2019)
Published in Nature cell biology (01.04.2019)
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Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina
Eblimit, Aiden, Nguyen, Thanh-Minh T, Chen, Yiyun, Esteve-Rudd, Julian, Zhong, Hua, Letteboer, Stef, Van Reeuwijk, Jeroen, Simons, David L, Ding, Qian, Wu, Ka Man, Li, Yumei, Van Beersum, Sylvia, Moayedi, Yalda, Xu, Huidan, Pickard, Patrick, Wang, Keqing, Gan, Lin, Wu, Samuel M, Williams, David S, Mardon, Graeme, Roepman, Ronald, Chen, Rui
Published in Human molecular genetics (15.03.2015)
Published in Human molecular genetics (15.03.2015)
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Mastermind-like transcriptional co-activator-mediated Notch signaling is indispensable for maintaining conjunctival epithelial identity
Zhang, Yujin, Lam, Oliver, Nguyen, Minh-Thanh T, Ng, Gracia, Pear, Warren S, Ai, Walden, Wang, I-Jong, Kao, Winston W-Y, Liu, Chia-Yang
Published in Development (Cambridge) (01.02.2013)
Published in Development (Cambridge) (01.02.2013)
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Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the cranio-cervical joints of the axial skeleton
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Published in Developmental biology (15.08.2009)
Published in Developmental biology (15.08.2009)
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CiliaCarta: An integrated and validated compendium of ciliary genes
van Dam, Teunis J P, Kennedy, Julie, van der Lee, Robin, de Vrieze, Erik, Wunderlich, Kirsten A, Rix, Suzanne, Dougherty, Gerard W, Lambacher, Nils J, Li, Chunmei, Jensen, Victor L, Leroux, Michel R, Hjeij, Rim, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, van Reeuwijk, Jeroen, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F, Franco, Brunella, Mans, Dorus A, van Wijk, Erwin, Képès, François, Slaats, Gisela G, Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T, Letteboer, Stef J F, Oud, Machteld M, van Beersum, Sylvia E C, Schmidts, Miriam, Beales, Philip L, Lu, Qianhao, Giles, Rachel H, Szklarczyk, Radek, Russell, Robert B, Gibson, Toby J, Johnson, Colin A, Blacque, Oliver E, Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A
Published in PloS one (16.05.2019)
Published in PloS one (16.05.2019)
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SPATA7 maintains a novel photoreceptor-specific zone in the distal connecting cilium
Dharmat, Rachayata, Eblimit, Aiden, Robichaux, Michael A, Zhang, Zhixian, Nguyen, Thanh-Minh T, Jung, Sung Yun, He, Feng, Jain, Antrix, Li, Yumei, Qin, Jun, Overbeek, Paul, Roepman, Ronald, Mardon, Graeme, Wensel, Theodore G, Chen, Rui
Published in The Journal of cell biology (06.08.2018)
Published in The Journal of cell biology (06.08.2018)
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ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
Hoff, Sylvia, Halbritter, Jan, Epting, Daniel, Frank, Valeska, Nguyen, Thanh-Minh T, van Reeuwijk, Jeroen, Boehlke, Christopher, Schell, Christoph, Yasunaga, Takayuki, Helmstädter, Martin, Mergen, Miriam, Filhol, Emilie, Boldt, Karsten, Horn, Nicola, Ueffing, Marius, Otto, Edgar A, Eisenberger, Tobias, Elting, Mariet W, van Wijk, Joanna A E, Bockenhauer, Detlef, Sebire, Neil J, Rittig, Søren, Vyberg, Mogens, Ring, Troels, Pohl, Martin, Pape, Lars, Neuhaus, Thomas J, Elshakhs, Neveen A Soliman, Koon, Sarah J, Harris, Peter C, Grahammer, Florian, Huber, Tobias B, Kuehn, E Wolfgang, Kramer-Zucker, Albrecht, Bolz, Hanno J, Roepman, Ronald, Saunier, Sophie, Walz, Gerd, Hildebrandt, Friedhelm, Bergmann, Carsten, Lienkamp, Soeren S
Published in Nature genetics (01.08.2013)
Published in Nature genetics (01.08.2013)
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Missense mutations in the WD40 domain of AHI1 cause non-syndromic retinitis pigmentosa
Nguyen, Thanh-Minh T, Hull, Sarah, Roepman, Ronald, van den Born, L Ingeborgh, Oud, Machteld M, de Vrieze, Erik, Hetterschijt, Lisette, Letteboer, Stef J F, van Beersum, Sylvia E C, Blokland, Ellen A, Yntema, Helger G, Cremers, Frans P M, van der Zwaag, Paul A, Arno, Gavin, van Wijk, Erwin, Webster, Andrew R, Haer-Wigman, Lonneke
Published in Journal of medical genetics (01.09.2017)
Published in Journal of medical genetics (01.09.2017)
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Melanocyte development in vivo and in neural crest cell cultures: crucial dependence on the Mitf basic-helix-loop-helix-zipper transcription factor
Opdecamp, K, Nakayama, A, Nguyen, M T, Hodgkinson, C A, Pavan, W J, Arnheiter, H
Published in Development (Cambridge) (01.06.1997)
Published in Development (Cambridge) (01.06.1997)
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Mutations in microphthalmia, the mouse homolog of the human deafness gene MITF, affect neuroepithelial and neural crest-derived melanocytes differently
Nakayama, Atsuo, Nguyen, Minh-Thanh T, Chen, Catherine C, Opdecamp, Karin, Hodgkinson, Colin A, Arnheiter, Heinz
Published in Mechanisms of development (1998)
Published in Mechanisms of development (1998)
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Riedhammer, Korbinian M., Nguyen, Thanh-Minh T., Koşukcu, Can, Calzada-Wack, Julia, Li, Yong, Assia Batzir, Nurit, Saygılı, Seha, Wimmers, Vera, Kim, Gwang-Jin, Chrysanthou, Marialena, Bakey, Zeineb, Sofrin-Drucker, Efrat, Kraiger, Markus, Sanz-Moreno, Adrián, Amarie, Oana V., Rathkolb, Birgit, Klein-Rodewald, Tanja, Garrett, Lillian, Hölter, Sabine M., Seisenberger, Claudia, Haug, Stefan, Schlosser, Pascal, Marschall, Susan, Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Wuttke, Matthias, Hrabe de Angelis, Martin, Ćomić, Jasmina, Akgün Doğan, Özlem, Özlük, Yasemin, Taşdemir, Mehmet, Ağbaş, Ayşe, Canpolat, Nur, Orenstein, Naama, Çalışkan, Salim, Weber, Ruthild G., Bergmann, Carsten, Jeanpierre, Cecile, Saunier, Sophie, Lim, Tze Y., Hildebrandt, Friedhelm, Alhaddad, Bader, Basel-Salmon, Lina, Borovitz, Yael, Wu, Kaman, Antony, Dinu, Matschkal, Julia, Schaaf, Christian W., Renders, Lutz, Schmaderer, Christoph, Rogg, Manuel, Schell, Christoph, Meitinger, Thomas, Heemann, Uwe, Köttgen, Anna, Arnold, Sebastian J., Ozaltin, Fatih, Schmidts, Miriam, Hoefele, Julia
Published in Kidney international (01.04.2024)
Published in Kidney international (01.04.2024)
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CiliaCarta: An integrated and validated compendium of ciliary genes
Dam, Teunis J. P. Van, Kennedy, Julie, Lee, Robin van Der, Vrieze, Erik De, Wunderlich, Kirsten A., Rix, Suzanne, Dougherty, Gerard W., Lambacher, Nils J., Li, Chunmei M., Jensen, Victor L., Leroux, Michel R., Hjeij, Rim, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, Reeuwijk, Jeroen Van, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F., Franco, Brunella, Mans, Dorus A., Wijk, Erwin Van, Kepes, François, Slaats, Gisela G., Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T., Letteboer, Stef J. F., Oud, Machteld M., Beersum, Sylvia E. C. Van, Schmidts, Miriam, Beales, Philip L., Lu, Qianhao H., Giles, Rachel H., Szklarczyk, Radek, Russell, Robert B., Gibson, Toby J., Johnson, Colin A., Blacque, Olivier E., Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A.
Published in PloS one (2019)
Published in PloS one (2019)
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Lack of the mesodermal homeodomain protein MEOX1 disrupts sclerotome polarity and leads to a remodeling of the craniocervical joints of the axial skeleton
Skuntz, Susan, Mankoo, Baljinder, Nguyen, Minh-Thanh T., Hustert, Elisabeth, Nakayama, Atsuo, Tournier-Lasserve, Elisabeth, Wright, Christopher V.E., Pachnis, Vassilis, Bharti, Kapil, Arnheiter, Heinz
Published in Developmental biology (09.06.2009)
Published in Developmental biology (09.06.2009)
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Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Riedhammer, Korbinian M, Nguyen, Thanh-Minh T, Koşukcu, Can, Calzada-Wack, Julia, Li, Yong, Saygılı, Seha, Wimmers, Vera, Kim, Gwang-Jin, Chrysanthou, Marialena, Bakey, Zeineb, Kraiger, Markus, Sanz-Moreno, Adrián, Amarie, Oana V, Rathkolb, Birgit, Klein-Rodewald, Tanja, Garrett, Lillian, Hölter, Sabine M, Seisenberger, Claudia, Haug, Stefan, Marschall, Susan, Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Wuttke, Matthias, de Angelis, Martin Hrabe, Ćomić, Jasmina, Doğan, Özlem Akgün, Özlük, Yasemin, Taşdemir, Mehmet, Ağbaş, Ayşe, Canpolat, Nur, Ćalışkan, Salim, Weber, Ruthild, Bergmann, Carsten, Jeanpierre, Cecile, Saunier, Sophie, Lim, Tze Y, Hildebrandt, Friedhelm, Alhaddad, Bader, Wu, Kaman, Antony, Dinu, Matschkal, Julia, Schaaf, Christian, Renders, Lutz, Schmaderer, Christoph, Meitinger, Thomas, Heemann, Uwe, Köttgen, Anna, Arnold, Sebastian, Ozaltin, Fatih, Schmidts, Miriam, Hoefele, Julia
Published in medRxiv : the preprint server for health sciences (22.03.2023)
Published in medRxiv : the preprint server for health sciences (22.03.2023)
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Journal Article
CiliaCarta: An Integrated And Validated Compendium Of Ciliary Genes
Teunis J P Van Dam, Kennedy, Julie, Van Der Lee, Robin, De Vrieze, Erik, Wunderlich, Kirsten A, Rix, Suzanne, Dougherty, Gerard W, Lambacher, Nils J, Li, Chunmei, Jensen, Victor L, Leroux, Michael R, Rim Hjeij, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, Jeroen Van Reeuwijk, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F, Franco, Brunella, Mans, Dorus A, Erwin Van Wijk, Fran ois K p s, Slaats, Gisela G, Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T, Letteboer, Stef J F, Oud, Machteld M, Sylvia E C Van Beersum, Schmidts, Miriam, Beales, Philip L, Lu, Qianhao, Giles, Rachel H, Szklarczyk, Radek, Russell, Robert B, Gibson, Toby J, Johnson, Colin A, Blacque, Oliver E, Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A
Published in bioRxiv (03.04.2017)
Published in bioRxiv (03.04.2017)
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Paper
Ubiquitin-directed antibodies inhibit neuronal transporters in rat brain synaptosomes
Meyer, E M, West, C M, Stevens, B R, Chau, V, Nguyen, M T, Judkins, J H
Published in Journal of neurochemistry (01.12.1987)
Published in Journal of neurochemistry (01.12.1987)
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