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401.
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Homozygous DNA ligase IV R278H mutation in mice leads to leaky SCID and represents a model for human LIG4 syndrome. [electronic resource] by
- Rucci, Francesca
- Notarangelo, Luigi D
- Fazeli, Alex
- Patrizi, Laura
- Hickernell, Thomas
- Paganini, Tiziana
- Coakley, Kristen M
- Detre, Cynthia
- Keszei, Marton
- Walter, Jolan E
- Feldman, Lauren
- Cheng, Hwei-Ling
- Poliani, Pietro Luigi
- Wang, Jing H
- Balter, Barbara B
- Recher, Mike
- Andersson, Emma-Maria
- Zha, Shan
- Giliani, Silvia
- Terhorst, Cox
- Alt, Frederick W
- Yan, Catherine T
Producer: 20100510
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 107
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404.
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405.
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Differential micronucleus frequency in isogenic human cells deficient in DNA repair pathways is a valuable indicator for evaluating genotoxic agents and their genotoxic mechanisms. [electronic resource] by
- Saha, Liton Kumar
- Kim, Sujin
- Kang, Habyeong
- Akter, Salma
- Choi, Kyungho
- Sakuma, Tetsushi
- Yamamoto, Takashi
- Sasanuma, Hiroyuki
- Hirota, Kouji
- Nakamura, Jun
- Honma, Masamitsu
- Takeda, Shunichi
- Dertinger, S
Producer: 20190102
In:
Environmental and molecular mutagenesis vol. 59
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406.
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415.
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416.
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Two hits in one: whole genome sequencing unveils LIG4 syndrome and urofacial syndrome in a case report of a child with complex phenotype. [electronic resource] by
- Fadda, Abeer
- Butt, Fiza
- Tomei, Sara
- Deola, Sara
- Lo, Bernice
- Robay, Amal
- Al-Shakaki, Alya
- Al-Hajri, Noor
- Crystal, Ronald
- Kambouris, Marios
- Wang, Ena
- Marincola, Francesco M
- Fakhro, Khalid A
- Cugno, Chiara
Producer: 20170502
In:
BMC medical genetics vol. 17
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417.
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Organization and dynamics of the nonhomologous end-joining machinery during DNA double-strand break repair. [electronic resource] by
- Reid, Dylan A
- Keegan, Sarah
- Leo-Macias, Alejandra
- Watanabe, Go
- Strande, Natasha T
- Chang, Howard H
- Oksuz, Betul Akgol
- Fenyo, David
- Lieber, Michael R
- Ramsden, Dale A
- Rothenberg, Eli
Producer: 20160428
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 112
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418.
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419.
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Polymorphisms of LIG4 and XRCC4 involved in the NHEJ pathway interact to modify risk of glioma. [electronic resource] by
- Liu, Yanhong
- Zhou, Keke
- Zhang, Haishi
- Shugart, Yin Yao
- Chen, Lina
- Xu, Zhonghui
- Zhong, Yu
- Liu, Hongliang
- Jin, Li
- Wei, Qingyi
- Huang, Fengping
- Lu, Daru
- Zhou, Liangfu
Producer: 20080402
In:
Human mutation vol. 29
Availability: No items available.
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420.
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