Hybrid Condition Monitoring System for Power Transformer Fault Diagnosis von Baker, Engin, Nese, Secil Varbak, Dursun, Erkan

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Xeroderma Pigmentosum-Variant Patients from America, Europe, and Asia von Inui, Hiroki, Oh, Kyu-Seon, Nadem, Carine, Ueda, Takahiro, Khan, Sikandar G., Metin, Ahmet, Gozukara, Engin, Emmert, Steffen, Slor, Hanoch, Busch, David B., Baker, Carl C., DiGiovanna, John J., Tamura, Deborah, Seitz, Cornelia S., Gratchev, Alexei, Wu, Wen Hao, Chung, Kee Yang, Chung, Hye Jin, Azizi, Esther, Woodgate, Roger, Schneider, Thomas D., Kraemer, Kenneth H.

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XPC branch-point sequence mutations disrupt U2 snRNP binding, resulting in abnormal pre-mRNA splicing in xeroderma pigmentosum patients von Khan, Sikandar G, Yamanegi, Koji, Zheng, Zhi-Ming, Boyle, Jennifer, Imoto, Kyoko, Oh, Kyu-Seon, Baker, Carl C, Gozukara, Engin, Metin, Ahmet, Kraemer, Kenneth H

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Two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced XPC mRNA levels that correlate with cancer r... von Khan, Sikandar G., Metin, Ahmet, Gozukara, Engin, Inui, Hiroki, Shahlavi, Tala, Muniz-Medina, Vanessa, Baker, Carl C., Ueda, Takahiro, Aiken, Juliet R., Schneider, Thomas D., Kraemer, Kenneth H.

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Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients von Khan, Sikandar G., Oh, Kyu-Seon, Shahlavi, Tala, Ueda, Takahiro, Busch, David B., Inui, Hiroki, Emmert, Steffen, Imoto, Kyoko, Muniz-Medina, Vanessa, Baker, Carl C., DiGiovanna, John J., Schmidt, Deborah, Khadavi, Arash, Metin, Ahmet, Gozukara, Engin, Slor, Hanoch, Sarasin, Alain, Kraemer, Kenneth H.

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Advance access published on december o, 2003 two essential splice lariat branchpoint sequences in one intron in a xeroderma pigmentosum DNA repair gene: mutations result in reduced... von KHAN, Sikandar G, METIN, Ahmet, KRAEMER, Kenneth H, GOZUKARA, Engin, INUI, Hiroki, SHAHLAVI, Tala, MUNIZ-MEDINA, Vanessa, BAKER, Carl C, UEDA, Takahiro, AIKEN, Juliet R, SCHNEIDER, Thomas D

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