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1. Full Text Blimp-1 controls plasma cell function through the regulation of immunoglobulin secretion and the unfolded protein response
by Tellier, Julie and Shi, Wei and Minnich, Martina and Liao, Yang and Crawford, Simon and Smyth, Gordon K and Kallies, Axel and Busslinger, Meinrad and Nutt, Stephen L
Nature Immunology, ISSN 1529-2908, 02/2016, Volume 17, Issue 3, pp. 323 - 330
Plasma cell differentiation requires silencing of B cell transcription, while it establishes antibody-secretory function and long-term survival. The... 
B-CELLS | MULTIPLE-MYELOMA | SURVIVAL | MESSENGER-RNA | IRF4 | BONE-MARROW | DIFFERENTIATION | IMMUNOLOGY | TRANSCRIPTION FACTOR | EXPRESSION | XBP-1 | Immunoglobulins - immunology | Activating Transcription Factor 6 - immunology | Gene Expression Profiling | Activating Transcription Factor 6 - genetics | X-Box Binding Protein 1 | Immunoglobulins - metabolism | Flow Cytometry | TOR Serine-Threonine Kinases - genetics | Chromatin Immunoprecipitation | Plasma Cells - metabolism | Transcription Factors - immunology | Microscopy, Electron, Transmission | DNA-Binding Proteins - immunology | Enzyme-Linked Immunosorbent Assay | Unfolded Protein Response - genetics | Gene Expression Regulation | Interferon Regulatory Factors - genetics | Cell Size | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Regulatory Factor X Transcription Factors | Sequence Analysis, DNA | Mice, Knockout | Cell Differentiation - immunology | TOR Serine-Threonine Kinases - immunology | Unfolded Protein Response - immunology | Interferon Regulatory Factors - immunology | Animals | High-Throughput Nucleotide Sequencing | Mice | Plasma Cells - immunology | Positive Regulatory Domain I-Binding Factor 1 | Transcription factors | Immune response | Plasma cells | Genetic aspects | Regulation | Genetic transcription | Properties | Health aspects | Index Medicus | mTOR | unfolded protein response | transcription factor | immunoglobulin | plasma cell
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2. Full Text Mfn2 modulates the UPR and mitochondrial function via repression of PERK
by Muñoz, Juan Pablo and Ivanova, Saška and Sánchez‐Wandelmer, Jana and Martínez‐Cristóbal, Paula and Noguera, Eduard and Sancho, Ana and Díaz‐Ramos, Angels and Hernández‐Alvarez, María Isabel and Sebastián, David and Mauvezin, Caroline and Palacín, Manuel and Zorzano, Antonio
The EMBO Journal, ISSN 0261-4189, 08/2013, Volume 32, Issue 17, pp. 2348 - 2361
Mitofusin 2 (Mfn2) is a key protein in mitochondrial fusion and it participates in the bridging of mitochondria to the endoplasmic reticulum (ER). Recent data... 
cell death and autophagy | mitochondria | cell metabolism | CANCER-CELLS | OXIDATIVE STRESS | FUSION | MITOFUSIN 2 | CA2+ PUMP | ER STRESS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MUSCLE-CELL APOPTOSIS | ENDOPLASMIC-RETICULUM STRESS | CELL BIOLOGY | UNFOLDED PROTEIN RESPONSE | GENE-EXPRESSION | Reactive Oxygen Species - metabolism | eIF-2 Kinase - metabolism | Humans | Apoptosis - genetics | Activating Transcription Factor 6 - genetics | X-Box Binding Protein 1 | DNA-Binding Proteins - metabolism | Mitochondria - genetics | Membrane Proteins - metabolism | Autophagy - genetics | Protein-Serine-Threonine Kinases - metabolism | Fibroblasts - metabolism | eIF-2 Kinase - genetics | Membrane Proteins - genetics | Cells, Cultured | Protein-Serine-Threonine Kinases - genetics | Mitochondria - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Fibroblasts - pathology | Gene Knockout Techniques | Regulatory Factor X Transcription Factors | Transcription Factors - metabolism | Activating Transcription Factor 6 - metabolism | Animals | GTP Phosphohydrolases - metabolism | GTP Phosphohydrolases - genetics | Endoplasmic Reticulum Stress | Fibroblasts - drug effects | Mice | Unfolded Protein Response - physiology | Proteins | Signal transduction | Mitochondria | Cellular biology | Gene expression | Stress response | Index Medicus
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3. Full Text Epithelial Endoplasmic Reticulum Stress and Apoptosis in Sporadic Idiopathic Pulmonary Fibrosis
by Korfei, Martina and Ruppert, Clemens and Mahavadi, Poornima and Henneke, Ingrid and Markart, Philipp and Koch, Miriam and Lang, Gyoergy and Fink, Ludger and Bohle, Rainer-Maria and Seeger, Werner and Weaver, Timothy E and Guenther, Andreas
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 10/2008, Volume 178, Issue 8, pp. 838 - 846
Rationale The molecular pathomechanisms underlying idiopathic pulmonary fibrosis (IPF) are elusive, but chronic epithelial injury has recently been suggested... 
C/EBP-homologous protein | X-box binding protein-1 | Type II alveolar epithelial cell | Interstitial lung disease | Lung fibrosis | LUNG | OXIDATIVE STRESS | ACTIVATION | INTERSTITIAL PNEUMONIA | lung fibrosis | CELL-DEATH | PATHOGENESIS | UNFOLDED PROTEIN RESPONSE | interstitial lung disease | RESPIRATORY SYSTEM | CHOP | MYOFIBROBLASTS | MUTATIONS | type II alveolar epithelial cell | CRITICAL CARE MEDICINE | Immunohistochemistry | Humans | Middle Aged | Oxidative Stress - physiology | Endoplasmic Reticulum - metabolism | Male | Pulmonary Fibrosis - genetics | Pulmonary Disease, Chronic Obstructive - pathology | Activating Transcription Factor 6 - genetics | X-Box Binding Protein 1 | RNA - genetics | Activating Transcription Factor 6 - biosynthesis | Endoplasmic Reticulum - pathology | Pulmonary Alveoli - metabolism | Female | Pulmonary Fibrosis - metabolism | Pulmonary Disease, Chronic Obstructive - metabolism | Pulmonary Disease, Chronic Obstructive - genetics | In Situ Nick-End Labeling | Severity of Illness Index | Gene Expression | Pulmonary Alveoli - pathology | Activating Transcription Factor 4 - genetics | Transcription Factors - biosynthesis | Pulmonary Fibrosis - pathology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Regulatory Factor X Transcription Factors | Blotting, Western | Activating Transcription Factor 4 - biosynthesis | Apoptosis - physiology | DNA-Binding Proteins - biosynthesis | Index Medicus | Abridged Index Medicus | EBP-homologous protein | E. Interstitial Lung Disease
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4. Full Text Defective podocyte insulin signalling through p85-XBP1 promotes ATF6-dependent maladaptive ER-stress response in diabetic nephropathy
by Madhusudhan, Thati and Wang, Hongjie and Dong, Wei and Ghosh, Sanchita and Bock, Fabian and Thangapandi, Veera Raghavan and Ranjan, Satish and Wolter, Juliane and Kohli, Shrey and Shahzad, Khurrum and Heidel, Florian and Krueger, Martin and Schwenger, Vedat and Moeller, Marcus J and Kalinski, Thomas and Reiser, Jochen and Chavakis, Triantafyllos and Isermann, Berend
Nature Communications, ISSN 2041-1723, 03/2015, Volume 6, Issue 1, pp. 6496 - 6496
Endoplasmic reticulum (ER) stress is associated with diabetic nephropathy (DN), but its pathophysiological relevance and the mechanisms that compromise... 
KIDNEY-DISEASE | GLUCOSE-HOMEOSTASIS | XBP1 | UNFOLDED PROTEIN RESPONSE | GLOMERULAR PODOCYTE | ENDOPLASMIC-RETICULUM-STRESS | BOX-BINDING PROTEIN-1 | REGULATORY SUBUNITS | MULTIDISCIPLINARY SCIENCES | MICE | METABOLIC-DISORDERS | Index Medicus
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5. Full Text Activating Transcription Factor 6 Is Necessary and Sufficient for Alcoholic Fatty Liver Disease in Zebrafish
by Howarth, Deanna L and Lindtner, Claudia and Vacaru, Ana M and Sachidanandam, Ravi and Tsedensodnom, Orkhontuya and Vasilkova, Taisa and Buettner, Christoph and Sadler, Kirsten C
PLoS Genetics, ISSN 1553-7390, 2014, Volume 10, Issue 5, pp. e1004335 - e1004335
Fatty liver disease (FLD) is characterized by lipid accumulation in hepatocytes and is accompanied by secretory pathway dysfunction, resulting in induction of... 
ELEMENT-BINDING PROTEIN-2 | UNFOLDED PROTEIN RESPONSE | ER STRESS | GENETICS & HEREDITY | GENE-EXPRESSION | FED MICE | ENDOPLASMIC-RETICULUM STRESS | CHOLESTEROL-SYNTHESIS | SREBP-1C ACTIVATION | HEPATIC STEATOSIS | ADIPOSE-TISSUE | Liver - pathology | Transcriptional Activation - genetics | Ethanol - toxicity | Liver Neoplasms - genetics | Animals, Genetically Modified | Fatty Liver, Alcoholic - etiology | Humans | Liver - metabolism | Hepatocytes - pathology | Zebrafish | Hepatocytes - metabolism | Fatty Liver, Alcoholic - metabolism | Activating Transcription Factor 6 - genetics | Activating Transcription Factor 6 - toxicity | Activating Transcription Factor 6 - metabolism | Fatty Liver, Alcoholic - genetics | Animals | Carcinoma, Hepatocellular - genetics | Carcinoma, Hepatocellular - pathology | Lipid Metabolism - genetics | Liver Neoplasms - pathology | Disease Models, Animal | Protein research | Transcription factors | Fatty liver | Zoological research | Protein folding | Zebra fish | Physiological aspects | Genetic aspects | Research | Health aspects | Index Medicus | Library collections | Enzymes | Liver diseases | Ethanol | Alcoholism | Lipids | Metabolism | Fatty acids | Proteins | Rodents | Liver cirrhosis | Metabolic disorders
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6. Full Text Activating transcription factor 6 derepression mediates neuroprotection in Huntington disease
by Naranjo, José R and Zhang, Hongyu and Villar, Diego and González, Paz and Dopazo, Xose M and Morón-Oset, Javier and Higueras, Elena and Oliveros, Juan C and Arrabal, María D and Prieto, Angela and Cercós, Pilar and González, Teresa and De La Cruz, Alicia and Casado-Vela, Juan and Rábano, Alberto and Valenzuela, Carmen and Gutierrez-Rodriguez, Marta and Li, Jia-Yi and Mellström, Britt
Journal of Clinical Investigation, ISSN 0021-9738, 02/2016, Volume 126, Issue 2, pp. 627 - 638
Deregulated protein and Ca2+ homeostasis underlie synaptic dysfunction and neurodegeneration in Huntington disease (HD); however, the factors that disrupt... 
MEDICINE, RESEARCH & EXPERIMENTAL | DNA-BINDING | RETICULUM STRESS-RESPONSE | PROTEIN | ER STRESS | MOUSE MODEL | DREAM | GENE-EXPRESSION | EIF2-ALPHA | REPRESSOR | ATF6 | Neurons - pathology | Cricetulus | Signal Transduction | Humans | Huntington Disease - pathology | Repressor Proteins - genetics | Activating Transcription Factor 6 - genetics | Corpus Striatum - metabolism | Huntington Disease - metabolism | Kv Channel-Interacting Proteins - genetics | Kv Channel-Interacting Proteins - metabolism | Activating Transcription Factor 6 - metabolism | Animals | Piperidines - pharmacology | HEK293 Cells | Huntington Disease - genetics | Mice | Neurons - metabolism | HeLa Cells | Corpus Striatum - pathology | Repressor Proteins - metabolism | CHO Cells | Carbamates - pharmacology | Disease Models, Animal | Index Medicus | Abridged Index Medicus
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7. Full Text BMP2 protein regulates osteocalcin expression via Runx2-mediated Atf6 gene transcription
by Jang, Won-Gu and Kim, Eun-Jung and Kim, Don-Kyu and Ryoo, Hyun-Mo and Lee, Keun-Bae and Kim, Sun-Hun and Choi, Hueng-Sik and Koh, Jeong-Tae
Journal of Biological Chemistry, ISSN 0021-9258, 01/2012, Volume 287, Issue 2, pp. 905 - 915
Bone morphogenetic protein 2 (BMP2) activates unfolded protein response (UPR) transducers, such as PERK and OASIS, in osteoblast cells. ATF6, a bZIP... 
CELLS | DOMAIN | OSTEOBLAST DIFFERENTIATION | OASIS | PATHWAY | BIOCHEMISTRY & MOLECULAR BIOLOGY | IN-VIVO | BONE MORPHOGENETIC PROTEINS | RECEPTOR | ENDOPLASMIC-RETICULUM STRESS | BINDING | Bone Morphogenetic Protein 2 - genetics | Cell Line | Cyclic AMP Response Element-Binding Protein - biosynthesis | Osteocalcin - biosynthesis | Alkaline Phosphatase - genetics | Humans | Osteocalcin - genetics | Gene Expression Regulation - physiology | Activating Transcription Factor 6 - genetics | Core Binding Factor Alpha 1 Subunit - metabolism | Nerve Tissue Proteins - genetics | Mice, Knockout | Cyclic AMP Response Element-Binding Protein - genetics | Activating Transcription Factor 6 - metabolism | Transcription, Genetic - physiology | Animals | Alkaline Phosphatase - biosynthesis | Bone Morphogenetic Protein 2 - metabolism | Nerve Tissue Proteins - biosynthesis | Mice | Osteoblasts - cytology | Osteoblasts - metabolism | Response Elements - physiology | Core Binding Factor Alpha 1 Subunit - genetics | Index Medicus | Gene Regulation | Gene Transcription | Bone Morphogenetic Protein (BMP) | ER Stress | Extracellular Matrix | Cell Differentiation | Transcription Factors
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8. Full Text VEGF Signals through ATF6 and PERK to Promote Endothelial Cell Survival and Angiogenesis in the Absence of ER Stress
by Karali, Evdoxia and Bellou, Sofia and Stellas, Dimitris and Klinakis, Apostolos and Murphy, Carol and Fotsis, Theodore
Molecular Cell, ISSN 1097-2765, 05/2014, Volume 54, Issue 4, pp. 559 - 572
Accumulation of unfolded proteins in the endoplasmic reticulum (ER) initiates IRE1α, ATF6, and PERK cascades, leading to a transcriptional/translational... 
APOPTOSIS | RICTOR-MTOR COMPLEX | ACTIVATION | UNFOLDED-PROTEIN RESPONSE | PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | KINASE | GENE-EXPRESSION | ENDOPLASMIC-RETICULUM STRESS | TRANSCRIPTION FACTOR | SECRETORY PATHWAY | CELL BIOLOGY | Human Umbilical Vein Endothelial Cells | Phosphorylation | TOR Serine-Threonine Kinases - metabolism | Protein Unfolding | eIF-2 Kinase - metabolism | Humans | Male | Multiprotein Complexes - genetics | Vascular Endothelial Growth Factor A - metabolism | Endoplasmic Reticulum Stress - genetics | Vascular Endothelial Growth Factor A - genetics | Activating Transcription Factor 6 - genetics | Mechanistic Target of Rapamycin Complex 1 | Multiprotein Complexes - metabolism | TOR Serine-Threonine Kinases - genetics | Endothelial Cells - physiology | eIF-2 Kinase - genetics | Phospholipase C gamma - metabolism | Unfolded Protein Response - genetics | Cell Survival | Mice, Inbred C57BL | Gene Expression Regulation | Signal Transduction - genetics | Activating Transcription Factor 6 - metabolism | Animals | Neovascularization, Pathologic - genetics | Mice | Neovascularization, Pathologic - metabolism | HeLa Cells | Proteins | Stress (Physiology) | Vascular endothelial growth factor | Endothelium | Index Medicus
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9. Full Text The Unfolded Protein Response Mediates Adaptation to Exercise in Skeletal Muscle through a PGC-1α/ATF6α Complex
by Wu, Jun and Ruas, Jorge L and Estall, Jennifer L and Rasbach, Kyle A and Choi, Jang Hyun and Ye, Li and Boström, Pontus and Tyra, Heather M and Crawford, Robert W and Campbell, Kevin P and Rutkowski, D. Thomas and Kaufman, Randal J and Spiegelman, Bruce M
Cell Metabolism, ISSN 1550-4131, 2011, Volume 13, Issue 2, pp. 160 - 169
Exercise has been shown to be effective for treating obesity and type 2 diabetes. However, the molecular mechanisms for adaptation to exercise training are not... 
PATHWAYS | CELL FUNCTION | ER STRESS | TRANSCRIPTION | DISEASE | ENDOCRINOLOGY & METABOLISM | PGC-1 | INCREASES | ENDOPLASMIC-RETICULUM STRESS | EXPRESSION | COACTIVATORS | CELL BIOLOGY | Adaptation, Physiological | Mice, Inbred C57BL | Cells, Cultured | Gene Expression Regulation | Male | Muscle, Skeletal - metabolism | Unfolded Protein Response | Activating Transcription Factor 6 - genetics | Mice, Knockout | Activating Transcription Factor 6 - metabolism | Animals | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Trans-Activators - genetics | Trans-Activators - metabolism | Transcription, Genetic | Mice | Transcription Factors | Transcription Factor CHOP - metabolism | Physical Conditioning, Animal | Index Medicus
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10. Full Text Activation of the unfolded protein response is required for defenses against bacterial pore-forming toxin in vivo
by Bischof, Larry J and Kao, Cheng-Yuan and Los, Ferdinand C. O and Gonzalez, Manuel R and Shen, Zhouxin and Briggs, Steven P and Van Der Goot, F. Gisou and Aroian, Raffi V
PLoS Pathogens, ISSN 1553-7366, 10/2008, Volume 4, Issue 10, pp. e1000176 - e1000176
Pore-forming toxins (PFTs) constitute the single largest class of proteinaceous bacterial virulence factors and are made by many of the most important... 
PATHWAYS | CAENORHABDITIS-ELEGANS | MESSENGER-RNA | ER STRESS | KINASE | RESISTANCE | MICROBIOLOGY | C-ELEGANS | ENDOPLASMIC-RETICULUM STRESS | CELL-SURVIVAL | UP-REGULATION | PARASITOLOGY | Endoribonucleases - genetics | Activating Transcription Factor 6 - immunology | Escherichia coli | Humans | Immunity, Innate - genetics | Endoplasmic Reticulum - metabolism | Activating Transcription Factor 6 - genetics | X-Box Binding Protein 1 | DNA-Binding Proteins - metabolism | Bacterial Infections - genetics | Bacterial Proteins - toxicity | Bacterial Infections - immunology | Hemolysin Proteins - toxicity | Membrane Proteins - metabolism | p38 Mitogen-Activated Protein Kinases - metabolism | Transcription Factors - immunology | Protein-Serine-Threonine Kinases - metabolism | Caenorhabditis elegans - metabolism | DNA-Binding Proteins - immunology | Endoplasmic Reticulum - genetics | Endoribonucleases - metabolism | Caenorhabditis elegans - genetics | Membrane Proteins - genetics | Protein-Serine-Threonine Kinases - genetics | p38 Mitogen-Activated Protein Kinases - genetics | Membrane Proteins - immunology | p38 Mitogen-Activated Protein Kinases - immunology | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Caenorhabditis elegans - immunology | Regulatory Factor X Transcription Factors | Protein Folding | Transcription Factors - metabolism | Activating Transcription Factor 6 - metabolism | Animals | Endoplasmic Reticulum - immunology | Protein-Serine-Threonine Kinases - immunology | HeLa Cells | Endotoxins - toxicity | Bacterial Infections - metabolism | Endoribonucleases - immunology | Index Medicus | Proteins | Enzymes | Signal transduction | Statistical analysis | E coli | Toxins | Kinases | Stress response | Experiments
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11. Full Text Gene regulatory network of unfolded protein response genes in endoplasmic reticulum stress
by Sayuri Takayanagi and Riga Fukuda and Yuuki Takeuchi and Sakiko Tsukada and Kenichi Yoshida
Cell Stress & Chaperones, ISSN 1355-8145, 1/2013, Volume 18, Issue 1, pp. 11 - 23
In the endoplasmic reticulum (ER), secretory and membrane proteins are properly folded and modified, and the failure of these processes leads to ER stress. At... 
Polymerase chain reaction | Messenger RNA | Plasmids | Genes | HeLa cells | Gene expression regulation | Stress response | Endoplasmic reticulum | Apoptosis | Unfolded protein response | Biochemistry, general | Neurosciences | Gene regulation | ER stress | BiP | UPRE | Biomedicine general | Cell Biology | Biomedicine | Immunology | Cancer Research | ERSE | NF-Y | SITE | ACTIVATION | CELL BIOLOGY | ELEMENT | GRP78/BIP | CHOP | PROMOTER | TRANSCRIPTION FACTOR | ATF6 | Transcription Factor CHOP - genetics | Up-Regulation | Humans | Endoplasmic Reticulum - metabolism | Endoplasmic Reticulum Stress - genetics | Gene Regulatory Networks | Activating Transcription Factor 6 - genetics | X-Box Binding Protein 1 | DNA-Binding Proteins - metabolism | Heat-Shock Proteins - genetics | Antineoplastic Agents - pharmacology | DNA Damage - drug effects | Promoter Regions, Genetic | Unfolded Protein Response - genetics | Stress, Physiological - genetics | Heat-Shock Proteins - metabolism | Activating Transcription Factor 4 - genetics | Etoposide - pharmacology | Proteasome Endopeptidase Complex - chemistry | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Regulatory Factor X Transcription Factors | Transcription Factors - metabolism | Activating Transcription Factor 6 - metabolism | Activating Transcription Factor 4 - metabolism | HeLa Cells | Proteasome Endopeptidase Complex - metabolism | Transcription Factor CHOP - metabolism | Doxorubicin - pharmacology | Index Medicus | Immunoglobulins | Transcription | Activating transcription factor 6 | DNA damage | Etoposide | Homeostasis | Regulatory sequences | CCAAT/enhancer-binding protein | Chaperones | Doxorubicin | Promoters | Stress | Membrane proteins | Protein folding | Activating transcription factor 1 | Post-translation | BiP protein | Original Paper
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12. Full Text Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
by Kohl, S and Zobor, D and Chiang, W.C and Weisschuh, N and Staller, J and Menendez, I.G and Chang, S and Beck, S.C and Garrido, M. Garcia and Sothilingam, V and Seeliger, M.W and Stanzial, F and Benedicenti, F and Inzana, F and Heon, E and Vincent, A and Beis, J and Strom, T.M and Rudolph, G and Roosing, S and Hollander, A.I. den and Cremers, F.P.M and Lopez, I and Ren, H and Moore, A.T and Webster, A.R and Michaelides, M and Koenekoop, R.K and Zrenner, E and Kaufman, R.J and Tsang, S.H and Wissinger, B and Lin, J.H
Nature Genetics, ISSN 1061-4036, 2015, Volume 47, Issue 7, pp. 757 - 765
Achromatopsia (ACHM) is an autosomal recessive disorder characterized by color blindness, photophobia, nystagmus and severely reduced visual acuity. Using... 
LONG-TERM | RETINAL STRUCTURE | ALPHA-SUBUNIT | CONGENITAL ACHROMATOPSIA | OPTICAL COHERENCE TOMOGRAPHY | MOUSE MODEL | GENETICS & HEREDITY | GENE-THERAPY | ENDOPLASMIC-RETICULUM STRESS | TRANSCRIPTION FACTOR | TOTAL COLOURBLINDNESS | Genetic Association Studies | Humans | Mice, Inbred C57BL | Middle Aged | Male | Mutation, Missense | Unfolded Protein Response | Activating Transcription Factor 6 - genetics | Color Vision Defects - genetics | Mice, Knockout | Young Adult | Animals | Pedigree | Retinal Cone Photoreceptor Cells - pathology | Adolescent | HEK293 Cells | Aged, 80 and over | Adult | Female | Transcription, Genetic | Child | Gene mutations | Genetic susceptibility | Genetic research | Genetic aspects | Research | Color blindness | Health aspects | Risk factors | Haplotypes | Medical research | Biomedical research | Laboratories | Genes | Grants | Patients | Proteins | Hospitals | Photoreceptors | Software | Mutation | Chromosomes | Index Medicus
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