Results
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8541.
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Structural Alterations Driving Castration-Resistant Prostate Cancer Revealed by Linked-Read Genome Sequencing. [electronic resource] by
- Viswanathan, Srinivas R
- Ha, Gavin
- Hoff, Andreas M
- Wala, Jeremiah A
- Carrot-Zhang, Jian
- Whelan, Christopher W
- Haradhvala, Nicholas J
- Freeman, Samuel S
- Reed, Sarah C
- Rhoades, Justin
- Polak, Paz
- Cipicchio, Michelle
- Wankowicz, Stephanie A
- Wong, Alicia
- Kamath, Tushar
- Zhang, Zhenwei
- Gydush, Gregory J
- Rotem, Denisse
- Love, J Christopher
- Getz, Gad
- Gabriel, Stacey
- Zhang, Cheng-Zhong
- Dehm, Scott M
- Nelson, Peter S
- Van Allen, Eliezer M
- Choudhury, Atish D
- Adalsteinsson, Viktor A
- Beroukhim, Rameen
- Taplin, Mary-Ellen
- Meyerson, Matthew
Producer: 20190403
In:
Cell vol. 174
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8542.
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8543.
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8544.
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8545.
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8546.
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8547.
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8548.
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8549.
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Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. [electronic resource] by
- Bucan, Maja
- Abrahams, Brett S
- Wang, Kai
- Glessner, Joseph T
- Herman, Edward I
- Sonnenblick, Lisa I
- Alvarez Retuerto, Ana I
- Imielinski, Marcin
- Hadley, Dexter
- Bradfield, Jonathan P
- Kim, Cecilia
- Gidaya, Nicole B
- Lindquist, Ingrid
- Hutman, Ted
- Sigman, Marian
- Kustanovich, Vlad
- Lajonchere, Clara M
- Singleton, Andrew
- Kim, Junhyong
- Wassink, Thomas H
- McMahon, William M
- Owley, Thomas
- Sweeney, John A
- Coon, Hilary
- Nurnberger, John I
- Li, Mingyao
- Cantor, Rita M
- Minshew, Nancy J
- Sutcliffe, James S
- Cook, Edwin H
- Dawson, Geraldine
- Buxbaum, Joseph D
- Grant, Struan F A
- Schellenberg, Gerard D
- Geschwind, Daniel H
- Hakonarson, Hakon
Producer: 20090930
In:
PLoS genetics vol. 5
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8550.
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8551.
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8552.
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Mutation frequency for Charcot-Marie-Tooth disease type 1 in the Chinese population is similar to that in the global ethnic patients. [electronic resource] by
- Song, Shujuan
- Zhang, Yuanzhi
- Chen, Biao
- Zhang, Yuanjin
- Wang, Manjie
- Wang, Yueying
- Yan, Ming
- Zou, Junhua
- Huang, Yu
- Zhong, Nanbert
Producer: 20060928
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 8
Availability: No items available.
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8553.
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8554.
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An ancient duplication of apple MYB transcription factors is responsible for novel red fruit-flesh phenotypes. [electronic resource] by
- Chagné, David
- Lin-Wang, Kui
- Espley, Richard V
- Volz, Richard K
- How, Natalie M
- Rouse, Simon
- Brendolise, Cyril
- Carlisle, Charmaine M
- Kumar, Satish
- De Silva, Nihal
- Micheletti, Diego
- McGhie, Tony
- Crowhurst, Ross N
- Storey, Roy D
- Velasco, Riccardo
- Hellens, Roger P
- Gardiner, Susan E
- Allan, Andrew C
Producer: 20130618
In:
Plant physiology vol. 161
Availability: No items available.
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8555.
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Copy number gain of hsa-miR-569 at 3q26.2 leads to loss of TP53INP1 and aggressiveness of epithelial cancers. [electronic resource] by
- Chaluvally-Raghavan, Pradeep
- Zhang, Fan
- Pradeep, Sunila
- Hamilton, Mark P
- Zhao, Xi
- Rupaimoole, Rajesha
- Moss, Tyler
- Lu, Yiling
- Yu, Shuangxing
- Pecot, Chad V
- Aure, Miriam R
- Peuget, Sylvain
- Rodriguez-Aguayo, Cristian
- Han, Hee-Dong
- Zhang, Dong
- Venkatanarayan, Avinashnarayan
- Krohn, Marit
- Kristensen, Vessela N
- Gagea, Mihai
- Ram, Prahlad
- Liu, Wenbin
- Lopez-Berestein, Gabriel
- Lorenzi, Philip L
- Børresen-Dale, Anne-Lise
- Chin, Koei
- Gray, Joe
- Dusetti, Nelson J
- McGuire, Sean E
- Flores, Elsa R
- Sood, Anil K
- Mills, Gordon B
Producer: 20150213
In:
Cancer cell vol. 26
Availability: No items available.
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8556.
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8557.
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Odontogenic keratocysts in the Basal Cell Nevus (Gorlin-Goltz) Syndrome associated with paresthesia of the lower jaw: Case report, retrospective analysis of a representative Czech cohort and recommendations for the early diagnosis. [electronic resource] by
- Hubacek, Milan
- Kripnerova, Tereza
- Nemcikova, Michaela
- Krepelová, Anna
- Puchmajerova, Alena
- Malikova, Marcela
- Havlovicová, Markéta
- Cadova, Jana
- Kodet, Roman
- Macek, Milan
- Dostalova, Tatjana
Producer: 20170221
In:
Neuro endocrinology letters vol. 37
Availability: No items available.
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8558.
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8559.
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Clinical features of SMARCA2 duplication overlap with Coffin-Siris syndrome. [electronic resource] by
- Miyake, Noriko
- Abdel-Salam, Ghada
- Yamagata, Takanori
- Eid, Maha M
- Osaka, Hitoshi
- Okamoto, Nobuhiko
- Mohamed, Amal M
- Ikeda, Takahiro
- Afifi, Hanan H
- Piard, Juliette
- van Maldergem, Lionel
- Mizuguchi, Takeshi
- Miyatake, Satoko
- Tsurusaki, Yoshinori
- Matsumoto, Naomichi
Producer: 20171019
In:
American journal of medical genetics. Part A vol. 170
Availability: No items available.
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8560.
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