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Journal of Biological Chemistry, ISSN 0021-9258, 01/2010, Volume 285, Issue 4, pp. 2580 - 2590
Collagen triple helices are stabilized by 4-hydroxyproline residues. No function is known for the much less common 3-hydroxyproline (3Hyp), although genetic... 
PROLYL 3-HYDROXYLATION | AMINO-ACID-SEQUENCE | ARTICULAR-CARTILAGE | BIOCHEMISTRY & MOLECULAR BIOLOGY | CYANOGEN-BROMIDE PEPTIDES | RECESSIVE OSTEOGENESIS IMPERFECTA | TRIPLE-HELIX | BASEMENT-MEMBRANE COLLAGEN | CARTILAGE COLLAGEN | HIGHER-ORDER STRUCTURES | COVALENT STRUCTURE | Collagen Type V - genetics | Humans | Collagen Type I - chemistry | Collagen Type III - metabolism | Molecular Sequence Data | Collagen - chemistry | Collagen Type XI - chemistry | Collagen Type XI - metabolism | Collagen Type II - metabolism | Young Adult | Tandem Mass Spectrometry | Collagen Type I - genetics | Collagen Type XI - genetics | Cattle | Bone and Bones - metabolism | Adult | Collagen - genetics | Collagen Type V - metabolism | Hydroxyproline - chemistry | Extracellular Matrix Proteins - metabolism | Amino Acid Sequence | Extracellular Matrix Proteins - chemistry | Collagen Type I - metabolism | Collagen Type V - chemistry | Bone and Bones - chemistry | Extracellular Matrix Proteins - genetics | Hydroxyproline - metabolism | Collagen Type III - chemistry | Collagen Type III - genetics | Cartilage - metabolism | Collagen Type II - genetics | Collagen - metabolism | Hydroxyproline - genetics | Animals | Chickens | Cartilage - chemistry | Collagen Type II - chemistry | Protein Processing, Post-Translational | Index Medicus | Mammal | Protein Structure and Folding | Cartilage | Extracellular Matrix | Post-translational Modification | Collagen | Hydroxyproline | Organisms | 3-hydroxyproline | Bone | Protein
Journal Article
Journal Article
by Vithana, Eranga N and Khor, Chiea-Chuen and Qiao, Chunyan and Nongpiur, Monisha E and George, Ronnie and Chen, Li-Jia and Do, Tan and Abu-Amero, Khaled and Huang, Chor Kai and Low, Sancy and Tajudin, Liza-Sharmini A and Perera, Shamira A and Cheng, Ching-Yu and Xu, Liang and Jia, Hongyan and Ho, Ching-Lin and Sim, Kar Seng and Wu, Ren-Yi and Tham, Clement C. Y and Chew, Paul T. K and Su, Daniel H and Oen, Francis T and Sarangapani, Sripriya and Soumittra, Nagaswamy and Osman, Essam A and Wong, Hon-Tym and Tang, Guangxian and Fan, Sujie and Meng, Hailin and Huong, Dao T. L and Wang, Hua and Feng, Bo and Baskaran, Mani and Shantha, Balekudaru and Ramprasad, Vedam L and Kumaramanickavel, Govindasamy and Iyengar, Sudha K and How, Alicia C and Lee, Kelvin Y and Sivakumaran, Theru A and Yong, Victor H. K and Ting, Serena M. L and Li, Yang and Wang, Ya-Xing and Tay, Wan-Ting and Sim, Xueling and Lavanya, Raghavan and Cornes, Belinda K and Zheng, Ying-Feng and Wong, Tina T and Loon, Seng-Chee and Yong, Vernon K. Y and Waseem, Naushin and Yaakub, Azhany and Chia, Kee-Seng and Rand Allingham, R and Hauser, Michael A and Lam, Dennis S. C and Hibberd, Martin L and Bhattacharya, Shomi S and Zhang, Mingzhi and Teo, Yik Ying and Tan, Donald T and Jonas, Jost B and Tai, E-Shyong and Saw, Seang-Mei and Hon, Do Nhu and Al-Obeidan, Saleh A and Liu, Jianjun and Chau, Tran Nguyen Bich and Simmons, Cameron P and Bei, Jin-Xin and Zeng, Yi-Xin and Foster, Paul J and Vijaya, Lingam and Wong, Tien-Yin and Pang, Chi-Pui and Wang, Ningli and Aung, Tin
Nature Genetics, ISSN 1061-4036, 10/2012, Volume 44, Issue 10, pp. 1142 - 1146
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 01/2014, Volume 66, Issue 4, pp. 940 - 949
Journal Article
British Journal of Cancer, ISSN 0007-0920, 12/2013, Volume 109, Issue 12, pp. 3049 - 3056
Journal Article
Breast Cancer Research and Treatment, ISSN 0167-6806, 8/2012, Volume 135, Issue 1, pp. 153 - 165
The progression of ductal carcinoma in situ (DCIS) to invasive ductal carcinoma (IDC) marks a critical step in the evolution of breast cancer. There is some... 
Tumour progression | Ductal carcinoma in situ | Tumour stroma | Medicine & Public Health | Oncology | Invasive ductal carcinoma | Formalin fixed paraffin embedded tissue | Whole-genome DASL | METHYLATION | COL11A1 | MICROARRAY ANALYSIS | INVASIVE CARCINOMAS | SFRP1 | CARCINOGENESIS | PARAFFIN-EMBEDDED TISSUE | ONCOLOGY | IN-SITU | DUCTAL CARCINOMA | MICRODISSECTION | Carcinoma, Ductal, Breast - genetics | Collagen Type V - genetics | Epithelial Cells - metabolism | Humans | Carcinoma, Intraductal, Noninfiltrating - metabolism | Gene Expression Regulation, Neoplastic | Tumor Microenvironment | Intercellular Signaling Peptides and Proteins - biosynthesis | Carcinoma, Intraductal, Noninfiltrating - genetics | Gene Expression Profiling | Matrix Metalloproteinase 13 - biosynthesis | Breast Neoplasms - metabolism | Extracellular Matrix - genetics | Collagen Type XI - genetics | Collagen Type XI - biosynthesis | Carcinoma, Ductal, Breast - pathology | Female | Carcinoma, Ductal, Breast - metabolism | Membrane Proteins - genetics | Matrix Metalloproteinase 13 - genetics | Stromal Cells - metabolism | Collagen Type V - biosynthesis | Intercellular Signaling Peptides and Proteins - genetics | Disease Progression | Membrane Proteins - biosynthesis | Breast Neoplasms - genetics | Carcinoma, Intraductal, Noninfiltrating - pathology | Breast Neoplasms - pathology | Index Medicus
Journal Article
Oncogene, ISSN 0950-9232, 06/2014, Volume 33, Issue 26, pp. 3432 - 3440
Biomarkers that predict disease progression might assist the development of better therapeutic strategies for aggressive cancers, such as ovarian cancer. Here,... 
ovarian carcinoma | COL11A1 | tumor progression | TGF-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENE-EXPRESSION PROFILES | ETS-1 TRANSCRIPTION FACTOR | MICROARRAY ANALYSIS | CELL BIOLOGY | MATRIX METALLOPROTEINASES | HEPATOCELLULAR-CARCINOMA | CLEAR-CELL | ONCOLOGY | GENETICS & HEREDITY | SQUAMOUS-CELL CARCINOMA | EXTRACELLULAR-MATRIX | IN-SITU | Neoplasm Transplantation | Oligonucleotide Array Sequence Analysis | Humans | Middle Aged | Transforming Growth Factor beta1 - metabolism | Transplantation, Heterologous | Gene Expression Profiling | Ovarian Neoplasms - mortality | Promoter Regions, Genetic - genetics | Ovarian Neoplasms - genetics | RNA, Messenger - biosynthesis | Smad2 Protein - biosynthesis | Collagen Type XI - genetics | RNA Interference | Female | Transforming Growth Factor beta1 - pharmacology | Neoplasm Invasiveness | Smad2 Protein - metabolism | Matrix Metalloproteinase 3 - metabolism | Survival Rate | Treatment Outcome | Signal Transduction - genetics | Mice, SCID | Disease Progression | Matrix Metalloproteinase 3 - biosynthesis | Animals | Cell Line, Tumor | Proto-Oncogene Protein c-ets-1 - genetics | Neoplasm Recurrence, Local - genetics | Biomarkers, Tumor - genetics | Mice | RNA, Small Interfering | Development and progression | Genetic aspects | Cellular signal transduction | Properties | Collagen | Ovarian cancer | Tumorigenesis | Clinical outcomes | Index Medicus
Journal Article
Genome Research, ISSN 1088-9051, 11/2015, Volume 25, Issue 11, pp. 1646 - 1655
Journal Article
ONCOTARGET, ISSN 1949-2553, 09/2015, Volume 6, Issue 27, pp. 23748 - 23763
Chemoresistance to anticancer drugs substantially reduces survival in epithelial ovarian carcinoma (EOC). Here, microarray analysis showed that collagen type... 
PROFILES | METASTASIS | PHOSPHORYLATION | PROTEIN-KINASE | CISPLATIN RESISTANCE | Akt | epithelial ovarian carcinoma | CHEMOTHERAPY | P53 | CELL BIOLOGY | chemoresistance | INHIBITION | EXPRESSION | collagen type XI alpha 1 | PDK1 | Index Medicus
Journal Article