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Select item 103802381.

Hydration and Structural Adaptations of the Human CYP1A1, CYP1A2, and CYP1B1 Active Sites by Molecular Dynamics Simulations

Zbigniew Dutkiewicz, Renata Mikstacka

Int J Mol Sci. 2023 Jul; 24(14): 11481. Published online 2023 Jul 14. doi: 10.3390/ijms241411481

PMCID:: PMC10380238

Article PDF–5.3M

Select item 100019412.

Accelerating the Discovery of Anticancer Peptides through Deep Forest Architecture with Deep Graphical Representation

Lantian Yao, Wenshuo Li, Yuntian Zhang, Junyang Deng, Yuxuan Pang, Yixian Huang, Chia-Ru Chung, Jinhan Yu, Ying-Chih Chiang, Tzong-Yi Lee

Int J Mol Sci. 2023 Mar; 24(5): 4328. Published online 2023 Feb 21. doi: 10.3390/ijms24054328

PMCID:: PMC10001941

Article PDF–2.1M

Select item 94249593.

Single mutations toggle the substrate selectivity of multifunctional Camptotheca secologanic acid synthases

Justin C. Miller, Mary A. Schuler

J Biol Chem. 2022 Sep; 298(9): 102237. Published online 2022 Jul 6. doi: 10.1016/j.jbc.2022.102237

PMCID:: PMC9424959

Article PDF–2.5M

Select item 90034714.

gRDF: An Efficient Compressor with Reduced Structural Regularities That Utilizes gRePair

Tangina Sultana, Young-Koo Lee

Sensors (Basel) 2022 Apr; 22(7): 2545. Published online 2022 Mar 26. doi: 10.3390/s22072545

PMCID:: PMC9003471

Article PDF–1.3M

Select item 62947515.

Fine mapping and discovery of candidate genes for seed size in watermelon by genome survey sequencing

Na Li, Jianli Shang, Jiming Wang, Dan Zhou, Nannan Li, Shuangwu Ma

Sci Rep. 2018; 8: 17843. Published online 2018 Dec 14. doi: 10.1038/s41598-018-36104-w

PMCID:: PMC6294751

Article PDF–1.8M

Select item 61412596.

Data maps and method for evaluating the indicator of the risk of propagation of invasive exotic plant species on work zones

Samira Mobaied, Elvia Marcellan, Nathalie Machon

Data Brief. 2018 Aug; 19: 1779–1784. Published online 2018 Jun 26. doi: 10.1016/j.dib.2018.06.038

PMCID:: PMC6141259

Article PDF–193K

Select item 48606817.

Whole-Genome Identification, Phylogeny, and Evolution of the Cytochrome P450 Family 2 (CYP2) Subfamilies in Birds

Daniela Almeida, Emanuel Maldonado, Imran Khan, Liliana Silva, M. Thomas P. Gilbert, Guojie Zhang, Erich D. Jarvis, Stephen J. O’Brien, Warren E. Johnson, Agostinho Antunes

Genome Biol Evol. 2016 Apr; 8(4): 1115–1131. Published online 2016 Mar 14. doi: 10.1093/gbe/evw041

PMCID:: PMC4860681

Article PDF–2.2M

Select item 38835828.

Development and characterization of a gastroretentive dosage form composed of chitosan and hydroxyethyl cellulose for alendronate

Ying-Chen Chen, Hsiu-O Ho, Chiao-Chi Chiu, Ming-Thau Sheu

Drug Des Devel Ther. 2014; 8: 67–78. Published online 2013 Dec 27. doi: 10.2147/DDDT.S52791

PMCID:: PMC3883582

Article PDF–754K

Select item 32836429.

Antagonistic Actions of HLH/bHLH Proteins Are Involved in Grain Length and Weight in Rice

Dany Heang, Hidenori Sassa

PLoS One. 2012; 7(2): e31325. Published online 2012 Feb 21. doi: 10.1371/journal.pone.0031325

PMCID:: PMC3283642

Article PDF–1.2M

Select item 10818710.

The Surface of Toxoplasma Tachyzoites Is Dominated by a Family of Glycosylphosphatidylinositol-Anchored Antigens Related to SAG1

Ian D. Manger, Adrian B. Hehl, John C. Boothroyd

Infect Immun. 1998 May; 66(5): 2237–2244. doi: 10.1128/iai.66.5.2237-2244.1998

PMCID:: PMC108187

Article PDF–851K

Select item 1075032911.

Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell Syndrome

Hsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, Ya-Hui Chang, Dau-Ming Niu, Chia-Ying Chang, Pao Chin Chiu, Yen-Yin Chou, Hui-Pin Hsiao, Meng-Che Tsai, Mei-Chyn Chao, Li-Ping Tsai, Chia-Feng Yang, Pen-Hua Su, Yu-Wen Pan, Chen-Hao Lee, Tzu-Hung Chu, Chih-Kuang Chuang, Shuan-Pei Lin

Int J Med Sci. 2024; 21(1): 8–18. Published online 2024 Jan 1. doi: 10.7150/ijms.84154

PMCID:: PMC10750329

Article PDF–2.5M

Select item 975662112.

Efficient generation of epigenetic disease model mice by epigenome editing using the piggyBac transposon system

Takuro Horii, Sumiyo Morita, Mika Kimura, Izuho Hatada

Epigenetics Chromatin. 2022; 15: 40. Published online 2022 Dec 16. doi: 10.1186/s13072-022-00474-3

PMCID:: PMC9756621

Article PDF–3.6M

Select item 943387413.

Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome

Jenifer P. Suntharalingham, Miho Ishida, Ignacio Del Valle, Susanne E. Stalman, Nita Solanky, Emma Wakeling, Gudrun E. Moore, John C. Achermann, Federica Buonocore

Front Endocrinol (Lausanne) 2022; 13: 953707. Published online 2022 Aug 18. doi: 10.3389/fendo.2022.953707

PMCID:: PMC9433874

Article PDF–4.2M

Select item 853071514.

Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes

Afiya Andrews, Avinaash Maharaj, Emily Cottrell, Sumana Chatterjee, Pratik Shah, Louise Denvir, Katja Dumic, Artur Bossowski, Talat Mushtaq, Rade Vukovic, Mohamed Didi, Nick Shaw, Louise A Metherell, Martin O Savage, Helen L Storr

J Clin Endocrinol Metab. 2021 Nov; 106(11): e4716–e4733. Published online 2021 Jun 16. doi: 10.1210/clinem/dgab437

PMCID:: PMC8530715

Article

Select item 814245715.

Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome

Kazuki Yamazawa, Takanobu Inoue, Yoshihiro Sakemi, Toshinori Nakashima, Hironori Yamashita, Kaduki Khono, Hideki Fujita, Keisuke Enomoto, Kazuhiko Nakabayashi, Kenichiro Hata, Moeko Nakashima, Tatsuo Matsunaga, Akie Nakamura, Keiko Matsubara, Tsutomu Ogata, Masayo Kagami

J Med Genet. 2021 Jun; 58(6): 427–432. Published online 2020 Jun 23. doi: 10.1136/jmedgenet-2020-107019

PMCID:: PMC8142457

Article PDF–1.4M

Select item 807355216.

Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases

Pierpaola Tannorella, Daniele Minervino, Sara Guzzetti, Alessandro Vimercati, Luciano Calzari, Giuseppa Patti, Mohamad Maghnie, Anna Elsa Maria Allegri, Donatella Milani, Giulietta Scuvera, Milena Mariani, Piergiorgio Modena, Angelo Selicorni, Lidia Larizza, Silvia Russo

Genes (Basel) 2021 Apr; 12(4): 588. Published online 2021 Apr 17. doi: 10.3390/genes12040588

PMCID:: PMC8073552

Article PDF–1.5M

Select item 802870517.

Parthenogenetic mosaicism: generation via second polar body retention and unmasking of a likely causative PER2 variant for hypersomnia

Yohei Masunaga, Masayo Kagami, Fumiko Kato, Takeshi Usui, Takako Yonemoto, Kazuo Mishima, Maki Fukami, Kazushi Aoto, Hirotomo Saitsu, Tsutomu Ogata

Clin Epigenetics. 2021; 13: 73. Published online 2021 Apr 7. doi: 10.1186/s13148-021-01062-0

PMCID:: PMC8028705

Article PDF–5.5M

Select item 794775318.

Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum

Tomoko Fuke, Akie Nakamura, Takanobu Inoue, Sayaka Kawashima, Kaori Isono Hara, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami

J Clin Endocrinol Metab. 2021 Mar; 106(3): 802–813. Published online 2020 Nov 24. doi: 10.1210/clinem/dgaa856

PMCID:: PMC7947753

Article

Select item 794062819.

A paternally inherited 1.4 kb deletion of the 11p15.5 imprinting center 2 is associated with a mild familial Silver–Russell syndrome phenotype

Catia Mio, Lorenzo Allegri, Nadia Passon, Elisa Bregant, Eliana Demori, Alessandra Franzoni, Daniela Driul, Andrea Riccio, Giuseppe Damante, Federica Baldan

Eur J Hum Genet. 2021 Mar; 29(3): 447–454. Published online 2020 Nov 11. doi: 10.1038/s41431-020-00753-1