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The Evolutionary Fates of a Large Segmental Duplication in Mouse
Morgan, Andrew P, Holt, J Matthew, McMullan, Rachel C, Bell, Timothy A, Clayshulte, Amelia M-F, Didion, John P, Yadgary, Liran, Thybert, David, Odom, Duncan T, Flicek, Paul, McMillan, Leonard, de Villena, Fernando Pardo-Manuel
Published in Genetics (Austin) (01.09.2016)
Published in Genetics (Austin) (01.09.2016)
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Segmental duplication as one of the driving forces underlying the diversity of the human immunoglobulin heavy chain variable gene region
Pramanik, Sreemanta, Cui, Xiangfeng, Wang, Hui-Yun, Chimge, Nyam-Osor, Hu, Guohong, Shen, Li, Gao, Richeng, Li, Honghua
Published in BMC genomics (27.01.2011)
Published in BMC genomics (27.01.2011)
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Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects
Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald‐McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, Amelsvoort, Thérèse A., Bree, Marianne, Owen, Michael, Niarchou, Maria, Bearden, Carrie E., Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C., Murphy, Clodagh, Garcia‐Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey‐Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine‐Suner, Damian, Shprintzen, Robert J., Gur, Raquel E., Zackai, Elaine, Emanuel, Beverly S., Wang, Tao, Kates, Wendy R., Bassett, Anne S., Vorstman, Jacob A. S., Morrow, Bernice E.
Published in American journal of medical genetics. Part A (01.10.2018)
Published in American journal of medical genetics. Part A (01.10.2018)
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Fatal Perinatal Mitochondrial Cardiac Failure Caused by Recurrent De Novo Duplications in the ATAD3 Locus
Frazier, Ann E., Compton, Alison G., Kishita, Yoshihito, Hock, Daniella H., Welch, AnneMarie E., Amarasekera, Sumudu S.C., Rius, Rocio, Formosa, Luke E., Imai-Okazaki, Atsuko, Francis, David, Wang, Min, Lake, Nicole J., Tregoning, Simone, Jabbari, Jafar S., Lucattini, Alexis, Nitta, Kazuhiro R., Ohtake, Akira, Murayama, Kei, Amor, David J., McGillivray, George, Wong, Flora Y., van der Knaap, Marjo S., Vermeulen, R. Jeroen, Wiltshire, Esko J., Fletcher, Janice M., Lewis, Barry, Baynam, Gareth, Ellaway, Carolyn, Balasubramaniam, Shanti, Bhattacharya, Kaustuv, Freckmann, Mary-Louise, Arbuckle, Susan, Rodriguez, Michael, Taft, Ryan J., Sadedin, Simon, Cowley, Mark J., Minoche, André E., Calvo, Sarah E., Mootha, Vamsi K., Ryan, Michael T., Okazaki, Yasushi, Stroud, David A., Simons, Cas, Christodoulou, John, Thorburn, David R.
Published in Med (New York, N.Y. : Online) (15.01.2021)
Published in Med (New York, N.Y. : Online) (15.01.2021)
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Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan
Lin, Yi-Wen, Chia-Ling Hsu, Lea, Kuo, Pao-Lin, Huang, William J., Chiang, Han-Sun, Yeh, Shauh-Der, Hsu, Tuan-Yi, Yu, Yueh-Hsiang, Hsiao, Kuang-Nan, Cantor, Rita M., Yen, Pauline H.
Published in Human mutation (01.05.2007)
Published in Human mutation (01.05.2007)
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Genome‐wide and molecular evolution analysis of the Poplar KT/HAK/KUP potassium transporter gene family
He, Caiyun, Cui, Kai, Duan, Aiguo, Zeng, Yanfei, Zhang, Jianguo
Published in Ecology and evolution (01.08.2012)
Published in Ecology and evolution (01.08.2012)
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The divergence and positive selection of the plant‐specific BURP‐containing protein family
Wang, Lihui, Wu, Ningning, Zhu, Yan, Song, Wanlu, Zhao, Xin, Li, Yaxuan, Hu, Yingkao
Published in Ecology and evolution (01.11.2015)
Published in Ecology and evolution (01.11.2015)
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The evolutionary fates of a large segmental duplication in mouse
Andrew Parker Morgan, Holt, James Matthew, Mcmullan, Rachel Clara, Bell, Timothy A, Clayshulte, Amelia Mary-Frances, Didion, John Paul, Yadgary, Liran, Thybert, David, Odom, Duncan T, Flicek, Paul, Mcmillan, Leonard, Fernando Pardo-Manuel De Villena
Published in bioRxiv (29.04.2016)
Published in bioRxiv (29.04.2016)
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Fenestration of the posterior communicating artery
Tripathi, M, Goel, V, Padma, M V, Jain, S, Maheshwari, M C, Gaikwad, S, Gupta, V, Chandra, P S, Mehta, V S
Published in Neurology India (01.03.2003)
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Published in Neurology India (01.03.2003)
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Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR
Tai, Derek J C, Ragavendran, Ashok, Manavalan, Poornima, Stortchevoi, Alexei, Seabra, Catarina M, Erdin, Serkan, Collins, Ryan L, Blumenthal, Ian, Chen, Xiaoli, Shen, Yiping, Sahin, Mustafa, Zhang, Chengsheng, Lee, Charles, Gusella, James F, Talkowski, Michael E
Published in Nature neuroscience (01.03.2016)
Published in Nature neuroscience (01.03.2016)
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CCL3L1 gene-containing segmental duplications and polymorphisms in CCR5 affect risk of systemic lupus erythaematosus
Mamtani, M, Rovin, B, Brey, R, Camargo, J F, Kulkarni, H, Herrera, M, Correa, P, Holliday, S, Anaya, J-M, Ahuja, S K
Published in Annals of the rheumatic diseases (01.08.2008)
Published in Annals of the rheumatic diseases (01.08.2008)
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Evolution and expression analysis of the soybean glutamate decarboxylase gene family
Hyun, Tae Kyung, Eom, Seung Hee, Han, Xiao, Kim, Ju-Sung
Published in Journal of biosciences (01.12.2014)
Published in Journal of biosciences (01.12.2014)
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
Zhao, Yingjie, Diacou, Alexander, Johnston, H. Richard, Musfee, Fadi I., McDonald-McGinn, Donna M., McGinn, Daniel, Crowley, T. Blaine, Repetto, Gabriela M., Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris R., Kates, Wendy R., Digilio, M. Cristina, Unolt, Marta, Marino, Bruno, Pontillo, Maria, Armando, Marco, Di Fabio, Fabio, Vicari, Stefano, van den Bree, Marianne, Moss, Hayley, Owen, Michael J., Murphy, Kieran C., Murphy, Clodagh M., Murphy, Declan, Schoch, Kelly, Shashi, Vandana, Tassone, Flora, Simon, Tony J., Shprintzen, Robert J., Campbell, Linda, Philip, Nicole, Heine-Suñer, Damian, García-Miñaúr, Sixto, Fernández, Luis, Antonarakis, Stylianos E., Biondi, Massimo, Boot, Erik, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Buzzanca, Antonino, Carmel, Miri, Cleynen, Isabelle, Cutler, David, Dallapiccola, Bruno, de la Fuente Sanches, María Angeles, Epstein, Michael P., Evers, Rens, Fernandez, Luis, Fritsch, Rosemarie, Algas, Fernando García, Guo, Tingwei, Gur, Raquel, Hestand, Matthew S., Heung, Tracy, Hooper, Stephen, Jin, Andrea, Kushan-Wells, Leila, Laorden-Nieto, Alejandra Teresa, Lattanzi, Guido, Marshall, Christian, McCabe, Kathryn, Michaelovsky, Elena, Ornstein, Claudia, Silversides, Candice, Tran, Oanh, van Duin, Esther D.A., Vergaelen, Elfi, Warren, Steve T., Weinberger, Ronnie, Weizman, Abraham, Zhang, Zhengdong, Zwick, Michael, Bearden, Carrie E., Vingerhoets, Claudia, van Amelsvoort, Therese, Eliez, Stephan, Schneider, Maude, Vorstman, Jacob A.S., Gothelf, Doron, Zackai, Elaine, Agopian, A.J., Gur, Raquel E., Bassett, Anne S., Emanuel, Beverly S., Goldmuntz, Elizabeth, Mitchell, Laura E., Wang, Tao, Morrow, Bernice E.
Published in American journal of human genetics (02.01.2020)
Published in American journal of human genetics (02.01.2020)
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Rapid detection of Down's syndrome using quantitative real-time PCR (qPCR) targeting segmental duplications on chromosomes 21 and 11
Sun, Lei, Fan, Zuqian, Weng, Xunjin, Ye, Xuehe, Long, Ju, Fu, Kepeng, Yan, Shanhuo, Wang, Bo, Zhuo, Yongguang, Liu, Xinxing, Lao, Kegan
Published in Gene (01.12.2014)
Published in Gene (01.12.2014)
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