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  1. 1.   Allosteric modulation of NF1 GAP: Differential distributions of catalytically competent populations in loss-of-function and gain-of-function mutants
  2. Xu,Liang; Jang,Hyunbum; Nussinov,Ruth
  3. Protein Science : a publication of the Protein Society. 2025, Feb; 34(2): e70042.
  1. 2.   Development and pilot validation of a novel disfigurement severity scale for plexiform neurofibromas in children with neurofibromatosis type 1
  2. John, Liny; Singh, Gurbani; Dombi, Eva; Wolters, Pamela L; Martin, Staci; Baldwin, Andrea; Steinberg, Seth M; Bernstein, Jessica; Whitcomb, Patricia; Pichard, Dominique C; Dufek, Anne; Gillespie, Andy; Heisey, Kara; Bornhorst, Miriam; Fisher, Michael J; Weiss, Brian D; Kim, AeRang; Widemann, Brigitte C; Gross, Andrea M
  3. Clinical Trials (London, England). 2023, Oct 25; 17407745231206402.
  1. 3.   Long-Term Safety and Efficacy of Selumetinib in Children with Neurofibromatosis Type 1 on a Phase 1/2 Trial for Inoperable Plexiform Neurofibromas
  2. Gross, Andrea M; Dombi, Eva; Wolters, Pamela L; Baldwin, Andrea; Dufek, Anne; Herrera, Kailey; Martin, Staci; Derdak, Joanne; Heisey,Kara; Whitcomb, Patricia M; Steinberg, Seth M; Venzon, David J; Fisher, Michael J; Kim, Ae Rang; Bornhorst, Miriam; Weiss, Brian D; Blakeley, Jaishri O; Smith, Malcolm A; Widemann, Brigitte C
  3. Neuro-Oncology. 2023, Apr 28;
  1. 4.   Demographic and Disease-Related Predictors of Socioemotional Development in Children with Neurofibromatosis Type 1 and Plexiform Neurofibromas: An Exploratory Study
  2. Hou, Yang; Wu, Xian; Liu, Dan; Martin, Staci; Tamula,Mary Anne; Allen, Taryn; Baldwin,Andrea; Gillespie, Andy; Goodwin, Anne; Widemann, Brigitte C; Wolters, Pamela L
  3. Cancers. 2022, Dec 01; 14(23):
  1. 5.   Single-cell sequencing reveals activation of core transcription factors in PRC2-deficient malignant peripheral nerve sheath tumor
  2. Zhang, Xiyuan; Lou, Hannah E; Gopalan, Vishaka; Liu, Zhihui; Jafarah, Hilda M; Lei, Haiyan; Jones, Paige; Sayers, Carly M; Yohe, Marielle E; Chittiboina, Prashant; Widemann, Brigitte C; Thiele, Carol J; Kelly,Michael; Hannenhalli, Sridhar; Shern, Jack F
  3. Cell Reports. 2022, Sep 20; 40(12): 111363.
  1. 6.   Verbal learning and memory in youth with neurofibromatosis type 1 and plexiform neurofibromas: Relationships with disease severity
  2. Loucas, Caitlyn; Wolters, Pamela; Tamula,Mary Anne; Rhodes, Amanda; Baldwin,Andrea; Goodwin, Anne; Widemann, Brigitte; Martin, Staci
  3. European Journal of Paediatric Neurology : EJPN : official journal of the European Paediatric Neurology Society. 2022, Mar 13; 38: 7-12.
  1. 7.   Acceptance and commitment therapy for adolescents and adults with neurofibromatosis type 1, plexiform neurofibromas, and chronic pain: Results of a randomized controlled trial
  2. Martin, Staci; Allen,Taryn; Toledo-Tamula, Mary Anne; Struemph,Kari; Reda, Stephanie; Wolters, Pamela L.; Baldwin,Andrea; Quinn, Mary; Widemann, Brigitte C.
  3. Journal of Contextual Behavioral Science. 2021, Oct; 22: 93-101.
  1. 8.   Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1
  2. Sung, Heejong; Hyland, Paula L; Pemov, Alexander; Sabourin, Jeremy A; Baldwin, Andrea M; Bass,Sara; Teshome,Kedest; Luo,Wen; Widemann, Brigitte C; Stewart, Douglas R; Wilson, Alexander F
  3. Molecular genetics & genomic medicine. 2020, Aug 31; e1400.
  1. 9.   Structural Insights into the SPRED1-Neurofibromin-KRAS Complex and Disruption of SPRED1-Neurofibromin Interaction by Oncogenic EGFR
  2. Yan,Wupeng; Markegard, Evan; Dharmaiah, Srisathiyanarayanan; Urisman, Anatoly; Drew, Matthew; Esposito,Dom; Scheffzek, Klaus; Nissley,Dwight; McCormick, Frank; Simanshu,Dhirendra
  3. Cell reports. 2020, Jul 21; 32(3): 107909.
  1. 10.   Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define pre-malignant neurofibromatosis type 1-associated atypical neurofibromas
  2. Pemov, Alexander; Hansen, Nancy F; Sindiri, Sivasish; Patidar, Rajesh; Higham, Christine S; Dombi, Eva; Miettinen, Markku M; Fetsch, Patricia; Brems, Hilde; Chandrasekharappa, Settara; Jones, Kristine; Zhu, Bin; Wei, Jun S; Mullikin, James C; Wallace, Margaret R; Khan, Javed; Legius, Eric; Widemann, Brigitte C; Stewart, Douglas R
  3. Neuro-oncology. 2019, AUG; 21(8): 981-992.
  1. 11.   Proceedings of the fifth international RASopathies symposium: When development and cancer intersect
  2. Rauen, Katherine A.; Schoyer, Lisa; Schill, Lisa; Stronach, Beth; Albeck, John; Andresen, Brage S.; Cave, Helene; Ellis, Michelle; Fruchtman, Steven M.; Gelb, Bruce D.; Gibson, Christopher C.; Gripp, Karen; Hefner, Erin; Huang, William Y. C.; Itkin, Maxim; Kerr, Bronwyn; Linardic, Corinne M.; McMahon, Martin; Oberlander, Beverly; Perlstein, Ethan; Ratner, Nancy; Rogers, Leslie; Schenck, Annette; Shankar, Suma; Shvartsman, Stanislav; Stevenson, David A.; Stites, Edward C.; Stork, Philip J. S.; Sun, Cheng; Therrien, Marc; Ullian, Erik M.; Widemann, Brigitte C.; Yeh, Erika; Zampino, Giuseppe; Zenker, Martin; Timmer, William; McCormick, Frank
  3. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2018, Dec; 176(12): 2924-2929.
  1. 12.   The Relationship between Heart Rate Variability, Psychological Flexibility, and Pain in Neurofibromatosis Type 1
  2. Allen, Taryn; Struemph, Kari L; Tamula, Mary Anne; Wolters, Pamela L; Baldwin, Andrea; Widemann, Brigitte; Martin, Staci
  3. Pain practice : the official journal of World Institute of Pain. 2018, Nov; 18(8): 969-978.
  1. 13.   An Internet support group for parents of children with neurofibromatosis type 1: a qualitative analysis
  2. Martin, Staci; Struemph, Kari L; Poblete, Alyssa; Tamula, Mary Anne; Lockridge, Robin; Roderick, Marie Claire; Wolters, Pamela
  3. Journal of community genetics. 2018, Jul; 9(3): 327-334.
  1. 14.   Feasibility and Preliminary Efficacy of an Internet Support Group for Parents of a Child with Neurofibromatosis Type 1: a Pilot Study
  2. Martin, S.; Roderick, M. C.; Lockridge, R.; Toledo-Tamula, M. A.; Baldwin, A.; Knight, P.; Wolters, P.
  3. Journal of Genetic Counseling. 2017, Jun; 26(3): 576-585.
  1. 15.   Real-time PCR analysis of candidate imprinted genes on mouse chromosome 11 shows balanced expression from the maternal and paternal chromosomes and strain-specific variation in expression levels
  2. Tuskan, R. G.; Tsang, S.; Sun, Z. H.; Baer, J.; Rozenblum, E.; Wu, X. L.; Munroe, D. J.; Reilly, K. M.
  3. Epigenetics. 2008 3(1): 43-50.
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