A trans-species missense SNP in Amhr2 is associated with sex determination in the tiger pufferfish, Takifugu rubripes (fugu) von Kamiya, Takashi, Kai, Wataru, Tasumi, Satoshi, Oka, Ayumi, Matsunaga, Takayoshi, Mizuno, Naoki, Fujita, Masashi, Suetake, Hiroaki, Suzuki, Shigenori, Hosoya, Sho, Tohari, Sumanty, Brenner, Sydney, Miyadai, Toshiaki, Venkatesh, Byrappa, Suzuki, Yuzuru, Kikuchi, Kiyoshi

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Evidence for at least six Hox clusters in the Japanese lamprey (Lethenteron japonicum) von Mehta, Tarang K., Ravi, Vydianathan, Yamasaki, Shinichi, Lee, Alison P., Lian, Michelle M., Tay, Boon-Hui, Tohari, Sumanty, Yanai, Seiji, Tay, Alice, Brenner, Sydney, Venkatesh, Byrappa

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Lampreys, the jawless vertebrates, contain only two ParaHox gene clusters von Zhang, Huixian, Ravi, Vydianathan, Tay, Boon-Hui, Tohari, Sumanty, Pillai, Nisha E., Prasad, Aravind, Lin, Qiang, Brenner, Sydney, Venkatesh, Byrappa

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Voltage-gated sodium channel gene repertoire of lampreys: gene duplications, tissue-specific expression and discovery of a long-lost gene von Zakon, Harold H., Li, Weiming, Pillai, Nisha E., Tohari, Sumanty, Shingate, Prashant, Ren, Jianfeng, Venkatesh, Byrappa

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Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma von Kuick, Chik Hong, Tan, Jia Ying, Jasmine, Deborah, Sumanty, Tohari, Ng, Alvin Y. J, Venkatesh, Byrrappa, Chen, Huiyi, Loh, Eva, Jain, Sudhanshi, Seow, Wan Yi, Ng, Eileen H. Q, Lian, Derrick W. Q, Soh, Shui Yen, Chang, Kenneth T. E, Chen, Zhi Xiong, Loh, Amos H. P

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Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita von Xue, Shifeng, Maluenda, Jérôme, Marguet, Florent, Shboul, Mohammad, Quevarec, Loïc, Bonnard, Carine, Ng, Alvin Yu Jin, Tohari, Sumanty, Tan, Thong Teck, Kong, Mung Kei, Monaghan, Kristin G., Cho, Megan T., Siskind, Carly E., Sampson, Jacinda B., Rocha, Carolina Tesi, Alkazaleh, Fawaz, Gonzales, Marie, Rigonnot, Luc, Whalen, Sandra, Gut, Marta, Gut, Ivo, Bucourt, Martine, Venkatesh, Byrappa, Laquerrière, Annie, Reversade, Bruno, Melki, Judith

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Cenani-Lenz syndactyly syndrome - a case report of a family with isolated syndactyly von Hettiaracchchi, Dineshani, Bonnard, Carine, Jayawardana, S M A, Ng, Alvin Yu Jin, Tohari, Sumanty, Venkatesh, Byrappa, Reversade, Bruno, Singaraja, Roshni, Dissanayake, V H W

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Erythropoietin gene from a teleost fish,Fugu rubripes von Chou, Chih-Fong, Tohari, Sumanty, Brenner, Sydney, Venkatesh, Byrappa

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A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome von Oud, Machteld M, Bonnard, Carine, Mans, Dorus A, Altunoglu, Umut, Tohari, Sumanty, Ng, Alvin Yu Jin, Eskin, Ascia, Lee, Hane, Rupar, C Anthony, de Wagenaar, Nathalie P, Wu, Ka Man, Lahiry, Piya, Pazour, Gregory J, Nelson, Stanley F, Hegele, Robert A, Roepman, Ronald, Kayserili, Hülya, Venkatesh, Byrappa, Siu, Victoria M, Reversade, Bruno, Arts, Heleen H

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A novel nonsense ATP2C1 mutation causes Hailey-Hailey disease in a Tunisian family von Chourabi, Marwa, H’mida-Ben Brahim, Dorra, Bonnard, Carine, Aounallah, Amina, Yu Ng, Alvin, Tohari, Sumanty, Venkatesh, Byrappa, Saad, Ali, Boussofara, Lobna, Reversade, Bruno, Denguezli, Mohamed

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Elephant shark genome provides unique insights into gnathostome evolution von Venkatesh, Byrappa, Lee, Alison P., Ravi, Vydianathan, Maurya, Ashish K., Lian, Michelle M., Swann, Jeremy B., Ohta, Yuko, Flajnik, Martin F., Sutoh, Yoichi, Kasahara, Masanori, Hoon, Shawn, Gangu, Vamshidhar, Roy, Scott W., Irimia, Manuel, Korzh, Vladimir, Kondrychyn, Igor, Lim, Zhi Wei, Tay, Boon-Hui, Tohari, Sumanty, Kong, Kiat Whye, Ho, Shufen, Lorente-Galdos, Belen, Quilez, Javier, Marques-Bonet, Tomas, Raney, Brian J., Ingham, Philip W., Tay, Alice, Hillier, LaDeana W., Minx, Patrick, Boehm, Thomas, Wilson, Richard K., Brenner, Sydney, Warren, Wesley C.

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A loss-of-function NUAK2 mutation in humans causes anencephaly due to impaired Hippo-YAP signaling von Bonnard, Carine, Navaratnam, Naveenan, Ghosh, Kakaly, Chan, Puck Wee, Tan, Thong Teck, Pomp, Oz, Ng, Alvin Yu Jin, Tohari, Sumanty, Changede, Rishita, Carling, David, Venkatesh, Byrappa, Altunoglu, Umut, Kayserili, Hulya, Reversade, Bruno

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Characterization of a hypoxia-response element in the Epo locus of the pufferfish, Takifugu rubripes von Kulkarni, Rashmi P., Tohari, Sumanty, Ho, Adrian, Brenner, Sydney, Venkatesh, Byrappa

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Voltage-gated sodium channel gene repertoire of lampreys: gene duplications, tissue-specific expression and discovery of a long-lost gene von Zakon, Harold H., Li, Weiming, Pillai, Nisha E., Tohari, Sumanty, Shingate, Prashant, Ren, Jianfeng, Venkatesh, Byrappa

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Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates von Szenker-Ravi, Emmanuelle, Ott, Tim, Khatoo, Muznah, Moreau de Bellaing, Anne, Goh, Wei Xuan, Chong, Yan Ling, Beckers, Anja, Kannesan, Darshini, Louvel, Guillaume, Anujan, Priyanka, Ravi, Vydianathan, Bonnard, Carine, Moutton, Sébastien, Schoen, Patric, Fradin, Mélanie, Colin, Estelle, Megarbane, André, Daou, Linda, Chehab, Ghassan, Di Filippo, Sylvie, Rooryck, Caroline, Deleuze, Jean-François, Boland, Anne, Arribard, Nicolas, Eker, Rukiye, Tohari, Sumanty, Ng, Alvin Yu-Jin, Rio, Marlène, Lim, Chun Teck, Eisenhaber, Birgit, Eisenhaber, Frank, Venkatesh, Byrappa, Amiel, Jeanne, Crollius, Hugues Roest, Gordon, Christopher T., Gossler, Achim, Roy, Sudipto, Attie-Bitach, Tania, Blum, Martin, Bouvagnet, Patrice, Reversade, Bruno

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Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy von Hengel, Holger, Bosso-Lefèvre, Célia, Grady, George, Szenker-Ravi, Emmanuelle, Li, Hankun, Pierce, Sarah, Lebigot, Élise, Tan, Thong-Teck, Eio, Michelle Y., Narayanan, Gunaseelan, Utami, Kagistia Hana, Yau, Monica, Handal, Nader, Deigendesch, Werner, Keimer, Reinhard, Marzouqa, Hiyam M., Gunay-Aygun, Meral, Muriello, Michael J., Verhelst, Helene, Weckhuysen, Sarah, Mahida, Sonal, Naidu, Sakkubai, Thomas, Terrence G., Lim, Jiin Ying, Tan, Ee Shien, Haye, Damien, Willemsen, Michèl A. A. P., Oegema, Renske, Mitchell, Wendy G., Pierson, Tyler Mark, Andrews, Marisa V., Willing, Marcia C., Rodan, Lance H., Barakat, Tahsin Stefan, van Slegtenhorst, Marjon, Gavrilova, Ralitza H., Martinelli, Diego, Gilboa, Tal, Tamim, Abdullah M., Hashem, Mais O., AlSayed, Moeenaldeen D., Abdulrahim, Maha M., Al-Owain, Mohammed, Awaji, Ali, Mahmoud, Adel A. H., Faqeih, Eissa A., Asmari, Ali Al, Algain, Sulwan M., Jad, Lamyaa A., Aldhalaan, Hesham M., Helbig, Ingo, Koolen, David A., Riess, Angelika, Kraegeloh-Mann, Ingeborg, Bauer, Peter, Gulsuner, Suleyman, Stamberger, Hannah, Ng, Alvin Yu Jin, Tang, Sha, Tohari, Sumanty, Keren, Boris, Schultz-Rogers, Laura E., Klee, Eric W., Barresi, Sabina, Tartaglia, Marco, Mor-Shaked, Hagar, Maddirevula, Sateesh, Begtrup, Amber, Telegrafi, Aida, Pfundt, Rolph, Schüle, Rebecca, Ciruna, Brian, Bonnard, Carine, Pouladi, Mahmoud A., Stewart, James C., Claridge-Chang, Adam, Lefeber, Dirk J., Alkuraya, Fowzan S., Mathuru, Ajay S., Venkatesh, Byrappa, Barycki, Joseph J., Simpson, Melanie A., Jamuar, Saumya S., Schöls, Ludger, Reversade, Bruno

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Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult von Ziaei, Amin, Garcia‐Miralles, Marta, Radulescu, Carola I., Sidik, Harwin, Silvin, Aymeric, Bae, Han‐Gyu, Bonnard, Carine, Yusof, Nur Amirah Binte Mohammad, Ferrari Bardile, Costanza, Tan, Liang Juin, Ng, Alvin Yu Jin, Tohari, Sumanty, Dehghani, Leila, Henry, Lily, Yeo, Xin Yi, Lee, Sejin, Venkatesh, Byrappa, Langley, Sarah R., Shaygannejad, Vahid, Reversade, Bruno, Jung, Sangyong, Ginhoux, Florent, Pouladi, Mahmoud A.

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Integration of the genetic map and genome assembly of fugu facilitates insights into distinct features of genome evolution in teleosts and mammals von Kai, Wataru, Kikuchi, Kiyoshi, Tohari, Sumanty, Chew, Ah Keng, Tay, Alice, Fujiwara, Atushi, Hosoya, Sho, Suetake, Hiroaki, Naruse, Kiyoshi, Brenner, Sydney, Suzuki, Yuzuru, Venkatesh, Byrappa

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Bone matrix hypermineralization associated with low bone turnover in a case of Nasu-Hakola disease von Shboul, Mohammad, Roschger, Paul, Ganger, Rudolf, Paschalis, Lefteris, Rokidi, Stamatia, Zandieh, Shahin, Behunova, Jana, Muschitz, Christian, Fahrleitner-Pammer, Astrid, Ng, Alvin Yu Jin, Tohari, Sumanty, Venkatesh, Byrappa, Bonnard, Carine, Reversade, Bruno, Klaushofer, Klaus, Al Kaissi, Ali

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Publisher Correction: Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates von Szenker-Ravi, Emmanuelle, Ott, Tim, Khatoo, Muznah, Moreau de Bellaing, Anne, Goh, Wei Xuan, Chong, Yan Ling, Beckers, Anja, Kannesan, Darshini, Louvel, Guillaume, Anujan, Priyanka, Ravi, Vydianathan, Bonnard, Carine, Moutton, Sébastien, Schoen, Patric, Fradin, Mélanie, Colin, Estelle, Megarbane, André, Daou, Linda, Chehab, Ghassan, Di Filippo, Sylvie, Rooryck, Caroline, Deleuze, Jean-François, Boland, Anne, Arribard, Nicolas, Eker, Rukiye, Tohari, Sumanty, Ng, Alvin Yu-Jin, Rio, Marlène, Lim, Chun Teck, Eisenhaber, Birgit, Eisenhaber, Frank, Venkatesh, Byrappa, Amiel, Jeanne, Crollius, Hugues Roest, Gordon, Christopher T., Gossler, Achim, Roy, Sudipto, Attie-Bitach, Tania, Blum, Martin, Bouvagnet, Patrice, Reversade, Bruno

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