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1. Full Text Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmaña, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Blok, Marinus J and Bodelon, Clara and Bogdanova, Natalia and Bojesen, Anders and Bonanni, Bernardo and Borg, Åke and Bradbury, Angela R and Brenton, James D and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Bruinsma, Fiona and Brunet, Joan and Buecher, Bruno and Butzow, Ralf and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Cannioto, Rikki and Carney, Michael E and Cescon, Terence and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen and Chen, Xiao Qing and Chiew, Yoke-Eng and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Conner, Thomas and Cook, Linda S and Cook, Jackie and Cramer, Daniel W and Cunningham, Julie M and D'Aloisio, Aimee A and Daly, Mary B and Damiola, Francesca and Damirovna, Sakaeva Dina and Dansonka-Mieszkowska, Agnieszka and Dao, Fanny and Davidson, Rosemarie and Defazio, Anna and Delnatte, Capucine and Doheny, Kimberly F and Diez, Orland and Ding, Yuan Chun and Doherty, Jennifer Anne and Domchek, Susan M and Dorfling, Cecilia M and Dörk, Thilo and ... and KConFab Investigators and EMEMBRACE Study and GEMO Study Collaborators and OPAL Study Grp and AOCS Study Grp and HEBON Study and AOCS study group and EMBRACE Study and OPAL study group and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 5, pp. 680 - 691
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping... 
BREAST-CANCER | COMMON VARIANTS | METAANALYSIS | CLEAR-CELL | ALGORITHM | GENETICS & HEREDITY | RISK | ASSOCIATION | CARCINOMA | ENDOMETRIOSIS | TELOMERE LENGTH | Neoplasms, Glandular and Epithelial - pathology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Risk Factors | Genetic Loci - genetics | Ovarian Neoplasms - pathology | Genotype | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Neoplasms, Glandular and Epithelial - genetics | Telomere-Binding Proteins - genetics | Alleles | Carcinoma, Ovarian Epithelial | Female | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Genetic susceptibility | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Health aspects | Risk factors | Ovarian cancer | Carriers | Medical research | Ovarian carcinoma | Genes | Gene regulation | Genomes | Breast cancer | Loci | Cancer | Life Sciences | Human health and pathology | Genetics | Medical and Health Sciences | Medicin och hälsovetenskap
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2. Full Text Coping strategies as a mediator of internet-delivered psychosocial treatment: Secondary analysis from a NIDA CTN multisite effectiveness trial
by Lévesque, Annie, MD and Campbell, Aimee N.C., PhD and Pavlicova, Martina, PhD and Hu, Mei-Chen, PhD and Walker, Robrina, PhD and McClure, Erin A., PhD and Ghitza, Udi E., PhD and Bailey, Genie, MD and Stitzer, Maxine, PhD and Nunes, Edward V., MD
Addictive Behaviors, ISSN 0306-4603, 2016, Volume 65, pp. 74 - 80
Abstract Objective. Coping strategies are a predictor of abstinence among patients with substance use disorders. However, little is known regarding the role of... 
Psychiatry | Community reinforcement approach | Substance use disorders | Coping strategies | Internet-delivered treatment | Behavioral therapies | SKILLS | ACQUISITION | SUBSTANCE ABUSE | RANDOMIZED CONTROLLED-TRIAL | PSYCHOLOGY, CLINICAL | ADDICTION | PRIMARY-CARE | ALCOHOL | COGNITIVE-BEHAVIORAL THERAPY | COCAINE DEPENDENCE | COMMUNITY-REINFORCEMENT APPROACH | Follow-Up Studies | Humans | Reinforcement (Psychology) | Male | Treatment Outcome | Substance-Related Disorders - therapy | Therapy, Computer-Assisted - methods | Substance-Related Disorders - psychology | Adult | Female | Internet | Behavior Therapy - methods | Adaptation, Psychological | Psychological aspects | Clinical trials | Analysis | Drug abuse | Drug addiction | Substance abuse treatment | Effectiveness | Coping | Index Medicus | community reinforcement approach | computer-assisted treatment | behavioral therapies | substance use disorders
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3. Full Text Whole-exome sequencing identifies a recurrent NAB2-STAT6 fusion in solitary fibrous tumors
by Chmielecki, Juliann and Crago, Aimee M and Rosenberg, Mara and O'Connor, Rachael and Walker, Sarah R and Ambrogio, Lauren and Auclair, Daniel and McKenna, Aaron and Heinrich, Michael C and Frank, David A and Meyerson, Matthew
Nature Genetics, ISSN 1061-4036, 02/2013, Volume 45, Issue 2, pp. 131 - 132
Solitary fibrous tumors (SFTs) are rare mesenchymal tumors. Here, we describe the identification of a NAB2-STAT6 fusion from whole-exome sequencing of 17 SFTs.... 
ACTIVATION | COREPRESSOR | NAB2 | GROWTH | GENETICS & HEREDITY | STAT6 | MUTATIONS | EXPRESSION | CANCER | Usage | Identification and classification | Health aspects | Gene fusion | Exome sequencing | Medical research | Genomics | Genomes | Mutation | Gene expression | Deoxyribonucleic acid--DNA | Tumors
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4. Full Text Association of peripartum synthetic oxytocin administration and depressive and anxiety disorders within the first postpartum year
by Kroll‐Desrosiers, Aimee R and Nephew, Benjamin C and Babb, Jessica A and Guilarte‐Walker, Yurima and Moore Simas, Tiffany A and Deligiannidis, Kristina M
Depression and Anxiety, ISSN 1091-4269, 02/2017, Volume 34, Issue 2, pp. 137 - 146
Background: Due to its potent effects on social behavior, including maternal behavior, oxytocin has been identified as a potential mediator of postpartum... 
biological markers | pregnancy and postpartum | anxiety/anxiety disorders | maternal‐child | depression | maternal-child | DSM-IV | HUMAN AFFILIATION | PSYCHIATRY | CLINICALLY ANXIOUS YOUTH | INTRANASAL OXYTOCIN | SOCIAL ANXIETY | PSYCHOLOGY, CLINICAL | CHILD | PSYCHOLOGY | INTERVIEW SCHEDULE | SEPARATION ANXIETY | PARENT | FAMILY ACCOMMODATION | Humans | Middle Aged | Treatment Outcome | Peripartum Period | Pregnancy | Young Adult | Adolescent | Adult | Female | Anxiety Disorders - drug therapy | Depression, Postpartum - drug therapy | Oxytocics - therapeutic use | Oxytocin - therapeutic use | Anxiety | Postpartum depression
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5. Full Text Guidelines for the use and interpretation of assays for monitoring autophagy
by Klionsky, Daniel J and Abdalla, Fabio C and Abeliovich, Hagai and Abraham, Robert T and Acevedo-Arozena, Abraham and Adeli, Khosrow and Agholme, Lotta and Agnello, Maria and Agostinis, Patrizia and Aguirre-Ghiso, Julio A and Ahn, Hyung Jun and Ait-Mohamed, Ouardia and Ait-Si-Ali, Slimane and Akematsu, Takahiko and Akira, Shizuo and Al-Younes, Hesham M and Al-Zeer, Munir A and Albert, Matthew L and Albin, Roger L and Alegre-Abarrategui, Javier and Aleo, Maria Francesca and Alirezaei, Mehrdad and Almasan, Alexandru and Almonte-Becerril, Maylin and Amano, Atsuo and Amaravadi, Ravi K and Amarnath, Shoba and Amer, Amal O and Andrieu-Abadie, Nathalie and Anantharam, Vellareddy and Ann, David K and Anoopkumar-Dukie, Shailendra and Aoki, Hiroshi and Apostolova, Nadezda and Arancia, Giuseppe and Aris, John P and Asanuma, Katsuhiko and Asare, Nana Y.O and Ashida, Hisashi and Askanas, Valerie and Askew, David S and Auberger, Patrick and Baba, Misuzu and Backues, Steven K and Baehrecke, Eric H and Bahr, Ben A and Bai, Xue-Yuan and Bailly, Yannick and Baiocchi, Robert and Baldini, Giulia and Balduini, Walter and Ballabio, Andrea and Bamber, Bruce A and Bampton, Edward T.W and Juhász, Gábor and Bartholomew, Clinton R and Bassham, Diane C and Bast, Robert C and Batoko, Henri and Bay, Boon-Huat and Beau, Isabelle and Béchet, Daniel M and Begley, Thomas J and Behl, Christian and Behrends, Christian and Bekri, Soumeya and Bellaire, Bryan and Bendall, Linda J and Benetti, Luca and Berliocchi, Laura and Bernardi, Henri and Bernassola, Francesca and Besteiro, Sébastien and Bhatia-Kissova, Ingrid and Bi, Xiaoning and Biard-Piechaczyk, Martine and Blum, Janice S and Boise, Lawrence H and Bonaldo, Paolo and Boone, David L and Bornhauser, Beat C and Bortoluci, Karina R and Bossis, Ioannis and Bost, Frédéric and Bourquin, Jean-Pierre and Boya, Patricia and Boyer-Guittaut, Michaël and Bozhkov, Peter V and Brady, Nathan R and Brancolini, Claudio and Brech, Andreas and Brenman, Jay E and Brennand, Ana and Bresnick, Emery H and Brest, Patrick and Bridges, Dave and Bristol, Molly L and Brookes, Paul S and Brown, Eric J and Brumell, John H and ... and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Geriatrik and Institutionen för medicin och hälsa and Farmakologi and Experimentell patologi and Hälsouniversitetet and Cellbiologi
Autophagy, ISSN 1554-8627, 04/2012, Volume 8, Issue 4, pp. 445 - 544
In 2008 we published the first set of guidelines for standardizing research in autophagy. Since then, research on this topic has continued to accelerate, and... 
stress | vacuole | autolysosome | flux | LC3 | autophagosome | lysosome | phagophore | Binding | Proteins | Landes | Calcium | Bioscience | Biology | Cell | Cycle | Cancer | Organogenesis | Phagophore | Lysosome | Autolysosome | Flux | Autophagosome | Vacuole | Stress | ACTIVATED PROTEIN-KINASE | CHAPERONE-MEDIATED AUTOPHAGY | VACUOLE TARGETING PATHWAY | ENDOPLASMIC-RETICULUM STRESS | ISOLATED RAT HEPATOCYTES | STARVATION-INDUCED AUTOPHAGY | GLUCAGON-INDUCED AUTOPHAGY | CELL BIOLOGY | PROGRAMMED CELL-DEATH | BREAST-CANCER CELLS | BETAINE HOMOCYSTEINE METHYLTRANSFERASE | Biological Assay - methods | Animals | Autophagy - genetics | Models, Biological | Humans | Life Sciences | Cellular Biology | Review | Medical and Health Sciences | Medicin och hälsovetenskap
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6. Full Text Protein Interactions in Genome Maintenance as Novel Antibacterial Targets
by Marceau, Aimee H and Bernstein, Douglas A and Walsh, Brian W and Shapiro, Walker and Simmons, Lyle A and Keck, James L
PLoS ONE, ISSN 1932-6203, 03/2013, Volume 8, Issue 3, pp. e58765 - e58765
Antibacterial compounds typically act by directly inhibiting essential bacterial enzyme activities. Although this general mechanism of action has fueled... 
CELL-DIVISION | MESSENGER-RNA | BACILLUS-SUBTILIS | SMALL-MOLECULE | MULTIDISCIPLINARY SCIENCES | ESCHERICHIA-COLI K-12 | DNA-BINDING-PROTEIN | EXONUCLEASE-I | RECR PROTEINS | SINGLE-STRANDED-DNA | NUCLEIC-ACIDS | Bacteria - metabolism | Genome, Bacterial | Rec A Recombinases - metabolism | DNA Replication - drug effects | Bacteria - drug effects | Cell Membrane Permeability | Drug Resistance, Bacterial | Bacteria - genetics | DNA-Binding Proteins - metabolism | Microbial Sensitivity Tests | Carrier Proteins - metabolism | Protein Binding - drug effects | Bacterial Proteins - metabolism | Protein Biosynthesis - drug effects | Anti-Bacterial Agents - pharmacology | Enzymes | DNA replication | Bacterial infections | Cell death | Genomics | Protein biosynthesis | Binding proteins | Drug resistance | Antibacterial agents | Health aspects | Protein-protein interactions | Protein binding | Recombination | Single-stranded DNA | Genomes | Infections | Biochemistry | Antibacterial materials | DNA repair | Proteins | DNA-binding protein | E coli | Enzymatic activity | Single-stranded DNA-binding protein | RecA protein | Bacteria | Antibacterial activity | Inhibition | Public health | Deoxyribonucleic acid--DNA | Developmental biology | Cell division | Cultures | Substrates | Medicine | Studies | DNA biosynthesis | Chemistry | Antibiotics | Protein synthesis | Replication | Protein interaction | Binding sites | Index Medicus | Deoxyribonucleic acid | DNA
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7. Full Text Cell culture model that mimics drusen formation and triggers complement activation associated with age-related macular degeneration
by Lincoln V. Johnson and David L. Forest and Christopher D. Banna and Carolyn M. Radeke and Michelle A. Maloney and Jane Hu and Christine N. Spencer and Aimee M. Walker and Marlene S. Tsie and Dean Bok and Monte J. Radeke and Don H. Anderson
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2011, Volume 108, Issue 45, pp. 18277 - 18282
We introduce a human retinal pigmented epithelial (RPE) cell-culture model that mimics several key aspects of early stage age-related macular degeneration... 
Macular degeneration | Cell culture techniques | Molecules | Complement activation | Drusen | Lipids | Cultured cells | Cell membranes | Cellular immunity | Blood proteins | IN-VITRO | C1Q | DEPOSITS | CHOLESTEROL | RPE | MULTIDISCIPLINARY SCIENCES | BRUCHS MEMBRANE | APOLIPOPROTEIN-B | EXPRESSION | MODULATION | RETINAL-PIGMENT EPITHELIUM | Immunohistochemistry | Macular Degeneration - metabolism | Retinal Pigment Epithelium - metabolism | Retinal Pigment Epithelium - pathology | Complement Activation | Models, Biological | Retinal Drusen - pathology | Humans | Cell Culture Techniques | Apolipoproteins E - metabolism | Macular Degeneration - pathology | Human cytogenetics | Cell culture | Usage | Care and treatment | Genetic aspects | Research | Biological Sciences
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