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Debra Crumrine

US Department of Veterans Affairs

60H指数
144论文数
1.0W被引数
收录论文 85
发表时间
Mitochondrial Activity Is Upregulated in Nonlesional Atopic Dermatitis and Amenable to Therapeutic Intervention
err2022-10-01
err19
PREAI
errLeman, Geraldine; Pavel, Petra; Hermann, Martin; Crumrine, Debra; Elias, Peter M.; Minzaghi, Deborah; Goudouneche, Dominique; Prieto, Natalia M. Roshardt; Cavinato, Maria; Wanner, Andrea; Blunder, Stefan; Gruber, Robert; Jansen-Duerr, Pidder; Dubrac, Sandrine
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Unique skin abnormality in patients with peanut allergy but no atopic dermatitis花生过敏但无特应性皮炎患者的独特皮肤异常
err2021-01-01
err13
errOAAI
errBerdyshev, Evgeny; Goleva, Elena; Bronova, Irina; Bronoff, Anna-Sofia; Hoffman, Bryce C.; Ramirez-Gama, Marco A.; Garcia, Shannon L.; Crumrine, Debra; Elias, Peter M.; Cho, Christine B.; Leung, Donald Y. M.
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Exosomes from Human Adipose Tissue-Derived Mesenchymal Stem Cells Promote Epidermal Barrier Repair by Inducing de Novo Synthesis of Ceramides in Atopic Dermatitis
errCELLS
IF5.2
err2020-03-10
err131
errOAAI
errShin, Kyong-Oh; Ha, Dae Hyun; Kim, Jin Ock; Crumrine, Debra A.; Meyer, Jason M.; Wakefield, Joan S.; Lee, Yerin; Kim, Bogyeong; Kim, Sungeun; Kim, Hyun-keun; Lee, Joon; Kwon, Hyuck Hoon; Park, Gyeong-Hun; Lee, Jun Ho; Lim, Jihye; Park, Sejeong; Elias, Peter M.; Park, Kyungho; Yi, Yong Weon; Cho, Byong Seung
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Conditional Alox12b Knockout: Degradation of the Corneocyte Lipid Envelope in a Mouse Model of Autosomal Recessive Congenital Ichthyoses
err2020-01-01
err9
errOAAI
errKrieg, Peter; Dick, Angela; Latzko, Susanne; Rosenberger, Sabine; Meyer, Jason; Crumrine, Debra; Hielscher, Thomas; Elias, Peter M.; Rauh, Manfred; Schneider, Holm
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Fatty acid transport protein 4 is required for incorporation of saturated ultralong-chain fatty acids into epidermal ceramides and monoacylglycerols
err2019-09-13
err31
errOAAI
errLin, Meei-Hua; Hsu, Fong-Fu; Crumrine, Debra; Meyer, Jason; Elias, Peter M.; Miner, Jeffrey H.
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Synthetic adiponectin-derived peptide enhances skin barrier function
err2019-09-01
err0
errOAAI
errHong, S.; Seo, H.; Lee, C.; Crumrine, D.; Man, M.; Elias, P.; Hahn, J.
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Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope
err2019-04-01
err41
errOAAI
errCrumrine, Debra; Khnykin, Denis; Krieg, Peter; Man, Mao-Qiang; Celli, Anna; Mauro, Theodora M.; Wakefield, Joan S.; Menon, Gopinathan; Mauldin, Elizabeth; Miner, Jeffrey H.; Lin, Meei-Hua; Brash, Alan R.; Sprecher, Eli; Radner, Franz P. W.; Choate, Keith; Roop, Dennis; Uchida, Yoshikazu; Gruber, Robert; Schmuth, Matthias; Elias, Peter M.
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The nonlesional skin surface distinguishes atopic dermatitis with food allergy as a unique endotype
err2019-02-20
err170
errOAAI
errLeung, Donald Y. M.; Calatroni, Agustin; Zaramela, Livia S.; LeBeau, Petra K.; Dyjack, Nathan; Brar, Kanwaljit; David, Gloria; Johnson, Keli; Leung, Susan; Ramirez-Gama, Marco; Liang, Bo; Rios, Cydney; Montgomery, Michael T.; Richers, Brittany N.; Hall, Clifton F.; Norquest, Kathryn A.; Jung, John; Bronova, Irina; Kreimer, Simion; Talbot, C. Conover, Jr.; Crumrine, Debra; Cole, Robert N.; Elias, Peter; Zengler, Karsten; Seibold, Max A.; Berdyshev, Evgeny; Goleva, Elena
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Origin and functions of the corneocyte lipid envelope
err2018-05-01
err0
errOAAI
errCrumrine, D.; Khnykin, D.; Krieg, P.; Man, M.; Celli, A.; Mauro, T.; Menon, G.; Mauldin, E.; Miner, J.; Brash, A.; Sprecher, E.; Radner, F.; Choate, K.; Roop, D. R.; Uchida, Y.; Gruber, R.; Schmuth, M.; Elias, P.
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Embryonic AP1 Transcription Factor Deficiency Causes a Collodion Baby-Like Phenotype
err2017-09-01
err6
errOAAI
errYoung, Christina A.; Eckert, Richard L.; Adhikary, Gautam; Crumrine, Debra; Elias, Peter M.; Blumenberg, Miroslav; Rorke, Ellen A.
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Ichthyotic-like skin abnormality occurs in neonatal SMS2-deficient mice
err2017-05-01
err0
errOAAI
errSakai, S.; Makino, A.; Nishi, A.; Ichikawa, T.; Yamashita, T.; Tokudome, Y.; Crumrine, D.; Uchida, Y.; Elias, P. M.; Tsuchida, T.; Hamanaka, S.
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Autosomal Recessive Keratoderma-Ichthyosis- Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification常染色体隐性角化病-鱼鳞病-耳聋 (ARKID) 综合征是由影响Rab蛋白相互作用和胶原蛋白修饰的VPS33B突变引起的
err2017-04-01
err32
errOAAI
errGruber, Robert; Rogerson, Clare; Windpassinger, Christian; Banushi, Blerida; Straatman-Iwanowska, Anna; Hanley, Joanna; Forneris, Federico; Strohal, Robert; Ulz, Peter; Crumrine, Debra; Menon, Gopinathan K.; Blunder, Stefan; Schmuth, Matthias; Mueller, Thomas; Smith, Holly; Mills, Kevin; Kroisel, Peter; Janecke, Andreas R.; Gissen, Paul
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Alterations in Epidermal Eicosanoid Metabolism Contribute to Inflammation and Impaired Late Differentiation in FLG-Mutated Atopic Dermatitis
err2017-03-01
err43
errOAAI
errBlunder, Stefan; Ruehl, Ralph; Moosbrugger-Martinz, Verena; Krimmel, Christine; Geisler, Anita; Zhu, Huiting; Crumrine, Debra; Elias, Peter M.; Gruber, Robert; Schmuth, Matthias; Dubrac, Sandrine
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PNPLA1 Deficiency in Mice and Humans Leads to a Defect in the Synthesis of Omega-O-Acylceramides
err2017-02-01
err78
errOAAI
errGrond, Susanne; Eichmann, Thomas O.; Dubrac, Sandrine; Kolb, Dagmar; Schmuth, Matthias; Fischer, Judith; Crumrine, Debra; Elias, Peter M.; Haemmerle, Guenter; Zechner, Rudolf; Lass, Achim; Radner, Franz P. W.
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Endoplasmic Reticulum Calcium Regulates Epidermal Barrier Response and Desmosomal Structure
err2016-09-01
err25
errOAAI
errCelli, Anna; Crumrine, Debra; Meyer, Jason M.; Mauro, Theodora M.
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Epidermal fragility in Keratin 10 ichthyosis with confetti mutation results from loss of keratin 1-desmoplakin interaction
err2016-05-01
err0
errOAAI
errLu, Y.; Mirza, H.; Hu, R.; Zhou, J.; Crumrine, D. A.; Elias, P. M.; Lifton, R.; Choate, K.
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Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome
err2015-11-24
err31
errOAAI
errBoyden, Lynn M.; Kam, Chen Y.; Hernandez-Martin, Angela; Zhou, Jing; Craiglow, Brittany G.; Sidbury, Robert; Mathes, Erin F.; Maguiness, Sheilagh M.; Crumrine, Debra A.; Williams, Mary L.; Hu, Ronghua; Lifton, Richard P.; Elias, Peter M.; Green, Kathleen J.; Choate, Keith A.
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Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin
err2015-11-01
err99
errOAAI
errMcAleer, Maeve A.; Pohler, Elizabeth; Smith, Frances J. D.; Wilson, Neil J.; Cole, Christian; MacGowan, Stuart; Koetsier, Jennifer L.; Godsel, Lisa M.; Harmon, Robert M.; Gruber, Robert; Crumrine, Debra; Elias, Peter M.; McDermott, Michael; Butler, Karina; Broderick, Annemarie; Sarig, Ofer; Sprecher, Eli; Green, Kathleen J.; McLean, W. H. Irwin; Irvine, Alan D.
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