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1. Little stories of married life
by Cutting, Mary Stewart (Doubleday) 1851-1924
1971, Short story index reprint series, ISBN 0836937961, 260
Married people | Domestic fiction, American | United States Social life and customs
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2. Full Text Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene
by Sosnay, Patrick R and Siklosi, Karen R and Van Goor, Fredrick and Kaniecki, Kyle and Yu, Haihui and Sharma, Neeraj and Ramalho, Anabela S and Amaral, Margarida D and Dorfman, Ruslan and Zielenski, Julian and Masica, David L and Karchin, Rachel and Millen, Linda and Thomas, Philip J and Patrinos, George P and Corey, Mary and Lewis, Michelle H and Rommens, Johanna M and Castellani, Carlo and Penland, Christopher M and Cutting, Garry R
Nature genetics, ISSN 1061-4036, 10/2013, Volume 45, Issue 10, pp. 1160 - 1167
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Phenotype | Cystic Fibrosis - genetics | Gene Frequency | Humans | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Genotype | Male | Usage | Cystic fibrosis | Genetic aspects | Research | Diagnosis | Genetic translation | Genetic screening | Methods | Genotype & phenotype | Liability | Algorithms | Databases | Laboratories | Colleges & universities | Experiments | Index Medicus
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3. Perfunctory estimates of allowable harvests of Atlantic salmon in 18 rivers of Scotia-Fundy Region
by Marshall, T.L and Amiro, P.G and Ritter, J.A and Jessop, B.M and Cutting, R.E and O'Neil, S.F and Canadian Atlantic Fisheries Scientific Advisory Committee
1992, 92/16, Volume 92/16., 28
Mersey R | Gold R | salmon fisheries | Baddeck R | Sheet Harbour R | LaHave R | Musquodoboit R | Medway R | freshwater | North R | Nashwaak R | Mactaquac R | sport fishing statistics | Salmo salar (anadromous/anadrome) | Middle R | Shubenacadie R | Canada | Grand R | Nova Scotia | Tusket R | Stewiacke R | Saint John R | spawning populations | escapement | St. Mary's R | Liscomb R | stock assessment
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4. Full Text Circulating Plasma Biomarkers of Progressive Interstitial Lung Disease
by Alqalyoobi, Shehabaldin and Adegunsoye, Ayodeji and Linderholm, Angela and Hrusch, Cara and Cutting, Claire and Ma, Shwu-Fan and Sperling, Anne and Noth, Imre and Strek, Mary E and Oldham, Justin M
American journal of respiratory and critical care medicine, ISSN 1073-449X, 01/2020, Volume 201, Issue 2, pp. 250 - 253
Respiratory System | Life Sciences & Biomedicine | Critical Care Medicine | General & Internal Medicine | Science & Technology | Lung Diseases, Interstitial - surgery | Prognosis | Humans | Middle Aged | Male | Alveolitis, Extrinsic Allergic - physiopathology | Lung Diseases, Interstitial - mortality | Lung Transplantation | Lung Diseases, Interstitial - blood | Alveolitis, Extrinsic Allergic - surgery | Chitinase-3-Like Protein 1 - blood | Female | Lung Diseases, Interstitial - physiopathology | Matrix Metalloproteinase 7 - blood | CA-125 Antigen - blood | Proportional Hazards Models | Pulmonary Surfactant-Associated Protein D - blood | Biomarkers - blood | Chemokine CXCL13 - blood | Alveolitis, Extrinsic Allergic - mortality | Disease Progression | Vascular Cell Adhesion Molecule-1 - blood | Vital Capacity | Alveolitis, Extrinsic Allergic - blood | Progression-Free Survival | Aged | Connective Tissue Diseases - blood | Biomarkers | Inflammation | Pulmonary fibrosis | Lung diseases | Index Medicus | Abridged Index Medicus
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5. Full Text Correlating Cystic Fibrosis Transmembrane Conductance Regulator Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis
by McCague, Allison F and Raraigh, Karen S and Pellicore, Matthew J and Davis-Marcisak, Emily F and Evans, Taylor A and Han, Sangwoo T and Lu, Zhongzhou and Joynt, Anya T and Sharma, Neeraj and Castellani, Carlo and Collaco, Joseph M and Corey, Mary and Lewis, Michelle H and Penland, Chris M and Rommens, Johanna M and Stephenson, Anne L and Sosnay, Patrick R and Cutting, Garry R
American journal of respiratory and critical care medicine, ISSN 1073-449X, 05/2019, Volume 199, Issue 9, pp. 1116 - 1126
Respiratory System | Life Sciences & Biomedicine | Critical Care Medicine | General & Internal Medicine | Science & Technology | Genetic Association Studies | Cystic Fibrosis - physiopathology | Humans | Middle Aged | Cystic Fibrosis Transmembrane Conductance Regulator - physiology | Male | Forced Expiratory Volume | Young Adult | Cystic Fibrosis - genetics | Adolescent | Adult | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Female | Child | Precision Medicine - methods | Genotype & phenotype | Chloride | Statistical analysis | Clinical trials | Cystic fibrosis | Regression analysis | Age | Clinical outcomes | Index Medicus | Abridged Index Medicus | genotype–phenotype | cystic fibrosis transmembrane conductance regulator modulator | sweat chloride | lung function | Original
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6. Full Text Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2
by Wright, Fred A and Strug, Lisa J and Doshi, Vishal K and Commander, Clayton W and Blackman, Scott M and Sun, Lei and Berthiaume, Yves and Cutler, David and Cojocaru, Andreea and Collaco, J Michael and Corey, Mary and Dorfman, Ruslan and Goddard, Katrina and Green, Deanna and Kent Jr, Jack W and Lange, Ethan M and Lee, Seunggeun and Li, Weili and Luo, Jingchun and Mayhew, Gregory M and Naughton, Kathleen M and Pace, Rhonda G and Paré, Peter and Rommens, Johanna M and Sandford, Andrew and Stonebraker, Jaclyn R and Sun, Wei and Taylor, Chelsea and Vanscoy, Lori L and Zou, Fei and Blangero, John and Zielenski, Julian and O'Neal, Wanda K and Drumm, Mitchell L and Durie, Peter R and Knowles, Michael R and Cutting, Garry R
Nature genetics, ISSN 1061-4036, 06/2011, Volume 43, Issue 6, pp. 539 - 546
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Errors of metabolism | Biological and medical sciences | Metabolic diseases | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Miscellaneous hereditary metabolic disorders | Methods, theories and miscellaneous | Genome-Wide Association Study | Humans | Male | Lung Diseases - genetics | Phenotype | Cystic Fibrosis - genetics | Adolescent | Adult | Female | Chromosomes, Human, Pair 11 | Chromosomes, Human, Pair 20 | Quantitative Trait Loci | Child | Genetic Linkage | Cystic fibrosis | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Design | Health sciences | Hospitals | Lungs | Mortality | Lung diseases | Genomes | Children & youth | Index Medicus
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7. Full Text The Human Microbiome Project strategy for comprehensive sampling of the human microbiome and why it matters
by Aagaard, Kjersti and Petrosino, Joseph and Keitel, Wendy and Watson, Mark and Katancik, James and Garcia, Nathalia and Patel, Shital and Cutting, Mary and Madden, Tessa and Hamilton, Holli and Harris, Emily and Gevers, Dirk and Simone, Gina and McInnes, Pamela and Versalovic, James
The FASEB journal, ISSN 0892-6638, 03/2013, Volume 27, Issue 3, pp. 1012 - 1022
clinical metadata | clinical research studies | HMP clinical data | metagenomic medicine | metagenomics | Metagenomics | Clinical research studies | Clinical metadata | Metagenomic medicine | Biochemistry & Molecular Biology | Biology | Life Sciences & Biomedicine - Other Topics | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Body Mass Index | Skin - microbiology | Mouth - microbiology | Humans | Adolescent | Specimen Handling - methods | Gastrointestinal Tract - microbiology | Adult | Female | Male | Vagina - microbiology | Metagenome | Index Medicus | Research Communications
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8. Full Text Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis
by Sun, Lei and Rommens, Johanna M and Corvol, Harriet and Li, Weili and Li, Xin and Chiang, Theodore A and Lin, Fan and Dorfman, Ruslan and Busson, Pierre-François and Parekh, Rashmi V and Zelenika, Diana and Blackman, Scott M and Corey, Mary and Doshi, Vishal K and Henderson, Lindsay and Naughton, Kathleen M and O'neal, Wanda K and Pace, Rhonda G and Stonebraker, Jaclyn R and Wood, Sally D and Wright, Fred A and Zielenski, Julian and Clement, Annick and Drumm, Mitchell L and Boëlle, Pierre-Yves and Cutting, Garry R and Knowles, Michael R and Durie, Peter R and Strug, Lisa J
Nature genetics, ISSN 1061-4036, 05/2012, Volume 44, Issue 5, pp. 562 - 569
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gastroenterology. Liver. Pancreas. Abdomen | Stomach. Duodenum. Small intestine. Colon. Rectum. Anus | Errors of metabolism | Biological and medical sciences | Metabolic diseases | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Other diseases. Semiology | Miscellaneous hereditary metabolic disorders | Intestinal Obstruction - etiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Ileus - genetics | Humans | Genotype | Amino Acid Transport Systems, Neutral - genetics | Cystic Fibrosis - genetics | Antiporters - genetics | Meconium | Polymorphism, Single Nucleotide - genetics | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Sodium-Hydrogen Exchangers - genetics | Cell Membrane - metabolism | Sodium-Hydrogen Exchanger 3 | Plasma | Cystic fibrosis | Genetics | Genomes | Genes | Rodents | Index Medicus
Journal Article
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9. Full Text More stories of married life
by Cutting, Mary Stewart, 1851-1924
1906
eBook
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10. Full Text Cystic fibrosis-related diabetes onset can be predicted using biomarkers measured at birth
by Lin, Yu-Chung and Keenan, Katherine and Gong, Jiafen and Panjwani, Naim and Avolio, Julie and Lin, Fan and Adam, Damien and Barrett, Paula and Bégin, Stéphanie and Berthiaume, Yves and Bilodeau, Lara and Bjornson, Candice and Brusky, Janna and Burgess, Caroline and Chilvers, Mark and Consunji-Araneta, Raquel and Côté-Maurais, Guillaume and Dale, Andrea and Donnelly, Christine and Fairservice, Lori and Griffin, Katie and Henderson, Natalie and Hillaby, Angela and Hughes, Daniel and Iqbal, Shaikh and Itterman, Jennifer and Jackson, Mary and Karlsen, Emma and Kosteniuk, Lorna and Lazosky, Lynda and Leung, Winnie and Levesque, Valerie and Maille, Émilie and Mateos-Corral, Dimas and McMahon, Vanessa and Merjaneh, Mays and Morrison, Nancy and Parkins, Michael and Pike, Jennifer and Price, April and Quon, Bradley S and Reisman, Joe and Smith, Clare and Smith, Mary Jane and Vadeboncoeur, Nathalie and Veniott, Danny and Viczko, Terry and Wilcox, Pearce and van Wylick, Richard and Cutting, Garry and Tullis, Elizabeth and Ratjen, Felix and Rommens, Johanna M and Sun, Lei and Solomon, Melinda and Stephenson, Anne L and Brochiero, Emmanuelle and Blackman, Scott and Corvol, Harriet and Strug, Lisa J
Genetics in medicine, ISSN 1098-3600, 01/2021
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Index Medicus
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11. Full Text Systematic Computational Identification of Variants That Activate Exonic and Intronic Cryptic Splice Sites
by Lee, Melissa and Roos, Patrick and Sharma, Neeraj and Atalar, Melis and Evans, Taylor A and Pellicore, Matthew J and Davis, Emily and Lam, Anh-Thu N and Stanley, Susan E and Khalil, Sara E and Solomon, George M and Walker, Doug and Raraigh, Karen S and Vecchio-Pagan, Briana and Armanios, Mary and Cutting, Garry R
American journal of human genetics, ISSN 0002-9297, 05/2017, Volume 100, Issue 5, pp. 751 - 765
splice donor | cystic fibrosis | minigene | cryptic splicing | splicing | machine learning | splice acceptor | splice variant | pseudoexon | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | RNA Splice Sites | Exons | Introns | Genomics | Humans | Cell Cycle Proteins - metabolism | Computational Biology | Gene Expression Regulation | Nuclear Proteins - metabolism | Cystic Fibrosis Transmembrane Conductance Regulator - metabolism | Genetic Loci | Mutation, Missense | Support Vector Machine | Dyskeratosis Congenita - genetics | Sequence Analysis, DNA | Genetic Variation | RNA Splicing | Algorithms | Cystic Fibrosis - genetics | HEK293 Cells | Cell Cycle Proteins - genetics | Cystic Fibrosis Transmembrane Conductance Regulator - genetics | Nuclear Proteins - genetics | Nucleotide sequencing | Observations | Genetic variation | Methods | DNA sequencing | Index Medicus
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12. Full Text Clinical Sensitivity of Cystic Fibrosis Mutation Panels in a Diverse Population
by Hughes, Erin E and Stevens, Colleen F and Saavedra‐Matiz, Carlos A and Tavakoli, Norma P and Krein, Lea M and Parker, April and Zhang, Zhen and Maloney, Breanne and Vogel, Beth and DeCelie‐Germana, Joan and Kier, Catherine and Anbar, Ran D and Berdella, Maria N and Comber, Paul G and Dozor, Allen J and Goetz, Danielle M and Guida, Louis and Kattan, Meyer and Ting, Andrew and Voter, Karen Z and Roey, Patrick and Caggana, Michele and Kay, Denise M and New York State Cystic Fibrosis New and New York State Cystic Fibrosis Newborn Screening Consortium
Human mutation, ISSN 1059-7794, 02/2016, Volume 37, Issue 2, pp. 201 - 208
clinical sensitivity | cystic fibrosis | NGS | newborn screening | CFTR | mutation panel | next‐generation sequencing | Next-generation sequencing | Clinical sensitivity | Mutation panel | Newborn screening | Cystic fibrosis | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Testing | Dried Blood Spot Testing | Humans | Cystic Fibrosis - pathology | Hispanic Americans | European Continental Ancestry Group | Infant | Male | Genotyping Techniques | Neonatal Screening