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The Alia Camel of Jordan: a genetically distinct dromedary breed 约旦的Alia Camel：一个基因独特的单峰骆驼品种 Haddad, Nizar J.; Al-Araishi, Mohamad A.; Awabdeh, Sami; Patidar, Rajesh; Bell, Ryan; Jawasreh, Khaleel; Alhurani, Heba; Alharbed, Leqaa J.; Sweidan, Rawad; Al-Anaswah, Eman N.; Brake, Mohammad; Sadder, Monther T.; Blanco, Omar A.; Sbeih, Loai; Uduman, Mohamed; Lakhani, Saquib A.; Khokha, Mustafa K.; Weir, Ahmed 分享 收藏
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia Diarra, Salimata; Ghosh, Saikat; Ciss, Lassana; Coulibaly, Thomas; Yalcouy, Abdoulaye; Harmison, George; Diallo, Salimata; Diallo, Seybou H.; Coulibaly, Oumar; Schindler, Alice; Ciss, Cheick A. K.; Maiga, Alassane B.; Bamba, Salia; Samassekou, Oumar; Khokha, Mustafa K.; Mis, Emily K.; Lakhani, Saquib A.; Donovan, Frank X.; Jacobson, Steve; Blackstone, Craig; Guinto, Cheick O.; Landour, Guida; Bonifacino, Juan S.; Fischbeck, Kenneth H.; Grunseich, Christopher 分享 收藏
Conserved chromatin and repetitive patterns reveal slow genome evolution in frogs Bredeson, Jessen V.; Mudd, Austin B.; Medina-Ruiz, Sofia; Mitros, Therese; Smith, Owen Kabnick; Miller, Kelly E.; Lyons, Jessica B.; Batra, Sanjit S.; Park, Joseph; Berkoff, Kodiak C.; Plott, Christopher; Grimwood, Jane; Schmutz, Jeremy; Aguirre-Figueroa, Guadalupe; Khokha, Mustafa K.; Lane, Maura; Philipp, Isabelle; Laslo, Mara; Hanken, James; Kerdivel, Gwenneg; Buisine, Nicolas; Sachs, Laurent M.; Buchholz, Daniel R.; Kwon, Taejoon; Smith-Parker, Heidi; Gridi-Papp, Marcos; Ryan, Michael J.; Denton, Robert D.; Malone, John H.; Wallingford, John B.; Straight, Aaron F.; Heald, Rebecca; Hockemeyer, Dirk; Harland, Richard M.; Rokhsar, Daniel S. 分享 收藏
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Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR (vol 13. 6681, 2022) Sempou, Emily; Kostiuk, Valentyna; Zhu, Jie; Guerra, M. Cecilia; Tyan, Leonid; Hwang, Woong; Camacho-Aguilar, Elena; Caplan, Michael J.; Zenisek, David; Warmflash, Aryeh; Owens, Nick D. L.; Khokha, Mustafa K. 分享 收藏
Membrane potential drives the exit from pluripotency and cell fate commitment via calcium and mTOR Sempou, Emily; Kostiuk, Valentyna; Zhu, Jie; Guerra, M. Cecilia; Tyan, Leonid; Hwang, Woong; Camacho-Aguilar, Elena; Caplan, Michael J.; Zenisek, David; Warmflash, Aryeh; Owens, Nick D. L.; Khokha, Mustafa K. 分享 收藏
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PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans Barak, Tanyeri; Ristori, Emma; Ercan-Sencicek, A. Gulhan; Miyagishima, Danielle F.; Nelson-Williams, Carol; Dong, Weilai; Jin, Sheng Chih; Prendergast, Andrew; Armero, William; Henegariu, Octavian; Erson-Omay, E. Zeynep; Harmanal, Akdes Serin; Guy, Mikhael; Gultekin, Batur; Kilic, Deniz; Rai, Devendra K.; Goc, Nukte; Aguilera, Stephanie Marie; Gulez, Burcu; Altinok, Selin; Ozcan, Kent; Yarman, Yanki; Coskun, Suleyman; Sempou, Emily; Deniz, Engin; Hintzen, Jared; Cox, Andrew; Fomchenko, Elena; Jung, Su Woong; Ozturk, Ali Kemal; Louvi, Angeliki; Bilguvar, Kaya; Connolly, E. Sander, Jr.; Khokha, Mustafa K.; Kahle, Kristopher T.; Yasuno, Katsuhito; Lifton, Richard P.; Mishra-Gorur, Ketu; Nicoli, Stefania; Gunel, Murat 分享 收藏
A convergent molecular network underlying autism and congenital heart disease 自闭症和先天性心脏病的融合分子网络 Rosenthal, Sara Brin; Willsey, Helen Rankin; Xu, Yuxiao; Mei, Yuan; Dea, Jeanselle; Wang, Sheng; Curtis, Charlotte; Sempou, Emily; Khokha, Mustafa K.; Chi, Neil C.; Willsey, Arthur Jeremy; Fisch, Kathleen M.; Ideker, Trey 分享 收藏
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Recessive Mutations in SYNPO2 as a Candidate of Monogenic Nephrotic Syndrome Mao, Youying; Schneider, Ronen; van der Ven, Peter F. M.; Assent, Marvin; Lohanadan, Keerthika; Klambt, Verena; Buerger, Florian; Kitzler, Thomas M.; Deutsch, Konstantin; Nakayama, Makiko; Majmundar, Amar J.; Mann, Nina; Hermle, Tobias; Onuchic-Whitford, Ana C.; Zhou, Wei; Margam, Nandini Nagarajan; Duncan, Roy; Marquez, Jonathan; Khokha, Mustafa; Fathy, Hanan M.; Kari, Jameela A.; El Desoky, Sherif; Eid, Loai A.; Awad, Hazem Subhi; Al-Saffar, Muna; Mane, Shrikant; Lifton, Richard P.; Fuerst, Dieter O.; Shril, Shirlee; Hildebrandt, Friedhelm 分享 收藏
DAAM2 Variants Cause Nephrotic Syndrome via Actin Dysregulation Schneider, Ronen; Deutsch, Konstantin; Hoeprich, Gregory J.; Marquez, Jonathan; Hermle, Tobias; Braun, Daniela A.; Seltzsam, Steve; Kitzler, Thomas M.; Mao, Youying; Buerger, Florian; Majmundar, Amar J.; Onuchic-Whitford, Ana C.; Kolvenbach, Caroline M.; Schierbaum, Luca; Schneider, Sophia; Halawi, Abdul A.; Nakayama, Makiko; Mann, Nina; Connaughton, Dervla M.; Klambt, Verena; Wagner, Matias; Riedhammer, Korbinian M.; Renders, Lutz; Katsura, Yoshichika; Thumkeo, Dean; Soliman, Neveen A.; Mane, Shrikant; Lifton, Richard P.; Shril, Shirlee; Khokha, Mustafa K.; Hoefele, Julia; Goode, Bruce L.; Hildebrandt, Friedhelm 分享 收藏
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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations Connaughton, Dervla M.; Dai, Rufeng; Owen, Danielle J.; Marquez, Jonathan; Mann, Nina; Graham-Paquin, Adda L.; Nakayama, Makiko; Coyaud, Etienne; Laurent, Estelle Mn; St-Germain, Jonathan R.; Blok, Lot Snijders; Vino, Arianna; Klambt, Verena; Deutsch, Konstantin; Wu, Chen-Han Wilfred; Kolvenbach, Caroline M.; Kause, Franziska; Ottlewski, Isabel; Schneider, Ronen; Kitzler, Thomas M.; Majmundar, Amar J.; Buerger, Florian; Onuchic-Whitford, Ana C.; Mao Youying; Kolb, Amy; Salmanullah, Daanya; Chen, Evan; van der Ven, Amelie T.; Rao, Jia; Ityel, Hadas; Seltzsam, Steve; Rieke, Johanna M.; Chen, Jing; Vivante, Asaf; Hwang, Daw-Yang; Kohl, Stefan; Dworschak, Gabriel C.; Hermle, Tobias; Alders, Marielle; Bartolomaeus, Tobias; Bauer, Stuart B.; Baum, Michelle A.; Brilstra, Eva H.; Challman, Thomas D.; Zyskind, Jacob; Costin, Carrie E.; Dipple, Katrina M.; Duijkers, Floor A.; Ferguson, Marcia; Fitzpatrick, David R.; Fick, Roger; Glass, Ian A.; Hulick, Peter J.; Kline, Antonie D.; Krey, Ilona; Kumar, Selvin; Lu, Weining; Marco, Elysa J.; Wentzensen, Ingrid M.; Mefford, Heather C.; Platzer, Konrad; Povolotskaya, Inna S.; Savatt, Juliann M.; Shcherbakova, Natalia, V; Senguttuvan, Prabha; Squire, Audrey E.; Stein, Deborah R.; Thiffault, Isabelle; Voinova, Victoria Y.; Somers, Michael J. G.; Ferguson, Michael A.; Traum, Avram Z.; Daouk, Ghaleb H.; Daga, Ankana; Rodig, Nancy M.; Terhal, Paulien A.; van Binsbergen, Ellen; Eid, Loai A.; Tasic, Velibor; Rasouly, Hila Milo; Lim, Tze Y.; Ahram, Dina F.; Gharavi, Ali G.; Reutter, Heiko M.; Rehm, Heidi L.; MacArthur, Daniel G.; Lek, Monkol; Laricchia, Kristen M.; Lifton, Richard P.; Xu, Hong; Mane, Shrikant M.; Sanna-Cherchi, Simone; Sharrocks, Andrew D.; Raught, Brian; Fisher, Simon E.; Bouchard, Maxime; Khokha, Mustafa K.; Shril, Shirlee; Hildebrandt, Friedhelm 分享 收藏
A nonsense variant in Rap Guanine Nucleotide Exchange Factor 5 (RAPGEF5) is associated with equine familial isolated hypoparathyroidism in Thoroughbred Foals Rivas, Victor N.; Magdesian, K. Gary; Fagan, Sophia; Slovis, Nathan M.; Luethy, Daniela; Javsicas, Laura H.; Caserto, Brian G.; Miller, Andrew D.; Dahlgren, Anna R.; Peterson, Janel; Hales, Erin N.; Peng, Sichong; Watson, Katherine D.; Khokha, Mustafa K.; Finno, Carrie J. 分享 收藏
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