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1Academic Journal
المؤلفون: Jan C-C Hu, Yuanyuan Hu, Yuhe Lu, Charles E Smith, Rangsiyakorn Lertlam, John Timothy Wright, Cynthia Suggs, Marc D McKee, Elia Beniash, M Enamul Kabir, James P Simmer
المصدر: PLoS ONE, Vol 9, Iss 3, p e89303 (2014)
وصف الملف: electronic resource
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2Academic Journal
المؤلفون: Shih-Kai Wang, Parissa Aref, Yuanyuan Hu, Rachel N Milkovich, James P Simmer, Mohammad El-Khateeb, Hinda Daggag, Zaid H Baqain, Jan C-C Hu
المصدر: PLoS Genetics, Vol 9, Iss 2, p e1003302 (2013)
وصف الملف: electronic resource
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3Academic Journal
المؤلفون: Shih-Kai Wang, Hui-Chen Chan, Igor Makovey, James P Simmer, Jan C-C Hu
المصدر: PLoS ONE, Vol 7, Iss 12, p e51533 (2012)
وصف الملف: electronic resource
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4Academic Journal
المؤلفون: Jan C-C Hu, Hui-Chen Chan, Stephen G Simmer, Figen Seymen, Amelia S Richardson, Yuanyuan Hu, Rachel N Milkovich, Ninna M R P Estrella, Mine Yildirim, Merve Bayram, Chiung-Fen Chen, James P Simmer
المصدر: PLoS ONE, Vol 7, Iss 12, p e52052 (2012)
وصف الملف: electronic resource
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5Academic Journal
المؤلفون: Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
المصدر: Journal of Personalized Medicine; Volume 13; Issue 2; Pages: 326
مصطلحات موضوعية: hereditary, mutation, WDR72, exon deletion, enamel defects
وصف الملف: application/pdf
Relation: Mechanisms of Diseases; https://dx.doi.org/10.3390/jpm13020326
الاتاحة: https://doi.org/10.3390/jpm13020326
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6Academic Journal
المؤلفون: Tian Liang, Charles E. Smith, Yuanyuan Hu, Hong Zhang, Chuhua Zhang, Qian Xu, Yongbo Lu, Ling Qi, Jan C.-C. Hu, James P. Simmer
المصدر: Scientific Reports, Vol 13, Iss 1, Pp 1-18 (2023)
Relation: https://doi.org/10.1038/s41598-023-33362-1; https://doaj.org/toc/2045-2322; https://doaj.org/article/55ab9e745bdb4551b1c1f56ebfdaf75c
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7Academic Journal
المؤلفون: Tian Liang, Yuanyuan Hu, Hong Zhang, Qian Xu, Charles E. Smith, Chuhua Zhang, Jung-Wook Kim, Shih-Kai Wang, Thomas L. Saunders, Yongbo Lu, Jan C.-C. Hu, James P. Simmer
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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8Academic Journal
المؤلفون: Mengqi Zhou, Hong Zhang, Heather Camhi, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Hera Kim-Berman, Ninna M. R. Yuson, Paul J. Benke, Yiqun Wu, Feng Wang, Yaqin Zhu, James P. Simmer, Jan C-C. Hu
المصدر: International Journal of Oral Science, Vol 13, Iss 1, Pp 1-11 (2021)
وصف الملف: electronic resource
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9Academic Journal
المؤلفون: Tian Liang, Yuanyuan Hu, Kazuhiko Kawasaki, Hong Zhang, Chuhua Zhang, Thomas L. Saunders, James P. Simmer, Jan C.-C. Hu
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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10Academic Journal
المؤلفون: James P. Simmer, Hong Zhang, Sophie J. H. Moon, Lori A-J. Donnelly, Yuan-Ling Lee, Figen Seymen, Mine Koruyucu, Hui-Chen Chan, Kevin Y. Lee, Suwei Wu, Chia-Lan Hsiang, Anthony T. P. Tsai, Rebecca L. Slayton, Melissa Morrow, Shih-Kai Wang, Edward D. Shields, Jan C.-C. Hu
المصدر: Genes; Volume 13; Issue 5; Pages: 858
مصطلحات موضوعية: dentinogenesis imperfecta, Shields Classification, DSPP mutations, dentin dysplasia, enamel malformations, whole-exome sequencing (WES), Single Molecule Real-Time (SMRT) DNA sequencing
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Human Genomics and Genetic Diseases; https://dx.doi.org/10.3390/genes13050858
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11Academic Journal
المؤلفون: Youn Jung Kim, Yejin Lee, Hong Zhang, Figen Seymen, Mine Koruyucu, Sule Bayrak, Nuray Tuloglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
المصدر: Journal of Personalized Medicine; Volume 12; Issue 6; Pages: 1002
مصطلحات موضوعية: hereditary, splicing mutation, dentinogenesis imperfecta, dentin sialophosphoprotein, DSPP, silent mutation, genotype−phenotype relationship
وصف الملف: application/pdf
Relation: Mechanisms of Diseases; https://dx.doi.org/10.3390/jpm12061002
الاتاحة: https://doi.org/10.3390/jpm12061002
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12Academic Journal
المؤلفون: Yejin Lee, Hong Zhang, Figen Seymen, Youn Jung Kim, Yelda Kasimoglu, Mine Koruyucu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
المصدر: Journal of Personalized Medicine; Volume 12; Issue 2; Pages: 150
مصطلحات موضوعية: whole exome sequencing, kallikrein 4, amelogenesis imperfecta, genetic diseases, hypomaturation, zymography
وصف الملف: application/pdf
Relation: Mechanisms of Diseases; https://dx.doi.org/10.3390/jpm12020150
الاتاحة: https://doi.org/10.3390/jpm12020150
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13Academic Journal
المؤلفون: Tian Liang, Shih-Kai Wang, Charles Smith, Hong Zhang, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Chuhua Zhang, Thomas L. Saunders, James P. Simmer, Jan C.-C. Hu
المصدر: Scientific Reports, Vol 12, Iss 1, Pp 1-20 (2022)
Relation: https://doi.org/10.1038/s41598-022-20684-9; https://doaj.org/toc/2045-2322; https://doaj.org/article/b1ed9c32d099421cbc3e834f910de5b2
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14Academic Journal
المؤلفون: Kuan-Yu Chu, Yin-Lin Wang, Yu-Ren Chou, Jung-Tsu Chen, Yi-Ping Wang, James P. Simmer, Jan C.-C. Hu, Shih-Kai Wang
المصدر: Journal of Personalized Medicine; Volume 11; Issue 11; Pages: 1217
مصطلحات موضوعية: hypodontia, oligodontia, tooth development, WNT signaling, genetic mutation, exome sequencing, digenic inheritance, incomplete penetrance, variable expressivity, precision medicine
وصف الملف: application/pdf
Relation: https://dx.doi.org/10.3390/jpm11111217
الاتاحة: https://doi.org/10.3390/jpm11111217
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15Academic Journal
المؤلفون: Youn Jung Kim, Yejin Lee, Hong Zhang, John Timothy Wright, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
المصدر: Biomedicines; Volume 9; Issue 5; Pages: 456
مصطلحات موضوعية: whole exome sequencing, ENAM, amelogenesis imperfecta, hereditary enamel defects, intron retention, splicing donor site mutation
وصف الملف: application/pdf
Relation: Endocrinology and Metabolism Research; https://dx.doi.org/10.3390/biomedicines9050456
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16Academic Journal
المؤلفون: Youn Jung Kim, Yejin Lee, Hong Zhang, Ji-Soo Song, Jan C.-C. Hu, James P. Simmer, Jung-Wook Kim
المصدر: Genes; Volume 12; Issue 3; Pages: 346
مصطلحات موضوعية: whole exome sequencing, SP6, amelogenesis imperfecta, hereditary enamel defects, de novo mutation
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Human Genomics and Genetic Diseases; https://dx.doi.org/10.3390/genes12030346
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17Academic Journal
المؤلفون: Figen Seymen, Hong Zhang, Yelda Kasimoglu, Mine Koruyucu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
المصدر: Journal of Personalized Medicine, Vol 12, Iss 13, p 13 (2021)
مصطلحات موضوعية: whole exome sequencing, pH sensing, ion transportation, hereditary enamel defects, hypomaturation, Medicine
Relation: https://www.mdpi.com/2075-4426/12/1/13; https://doaj.org/toc/2075-4426; https://doaj.org/article/80206d2d500e486d9de1ae80887afb12
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18Academic Journal
المؤلفون: Mengqi Zhou, Hong Zhang, Heather Camhi, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Hera Kim-Berman, Ninna M. R. Yuson, Paul J. Benke, Yiqun Wu, Feng Wang, Yaqin Zhu, James P. Simmer, Jan C-C. Hu
المصدر: International Journal of Oral Science, Vol 13, Iss 1, Pp 1-1 (2021)
Relation: https://doi.org/10.1038/s41368-021-00141-5; https://doaj.org/toc/1674-2818; https://doaj.org/toc/2049-3169; https://doaj.org/article/69aca93b9fdf4733af20c92ca8e7c19f
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19Academic Journal
المؤلفون: John D. Bartlett, Charles E. Smith, Yuanyuan Hu, Atsushi Ikeda, Mike Strauss, Tian Liang, Ya-Hsiang Hsu, Amanda H. Trout, David W. McComb, Rebecca C. Freeman, James P. Simmer, Jan C.-C. Hu
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Relation: https://doi.org/10.1038/s41598-021-90005-z; https://doaj.org/toc/2045-2322; https://doaj.org/article/373d5cee0dcd4f0582e0f4f3a8212285
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20Academic Journal
المؤلفون: Shih‐Kai Wang, Hong Zhang, Michael B. Chavez, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Connor D. Colvin, Tamara N. Kolli, Michelle H. Tan, Yin‐Lin Wang, Pei‐Ying Lu, Jung‐Wook Kim, Brian L. Foster, John D. Bartlett, James P. Simmer, Jan C.‐C. Hu
المصدر: Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
مصطلحات موضوعية: amelogenesis imperfecta, enamel hardness, dentin defects, hypomineralization, MMP20 mutations, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2324-9269