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PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0125515 - e0125515
Journal Article
by Du, N and Bao, WG and Zhang, KY and Lu, XL and Crew, R and Wang, XF and Liu, GM and Wang, F
BMC CANCER, ISSN 1471-2407, 05/2019, Volume 19, Issue 1, p. 412
BackgroundThe SK-PN-DW cell line was established in 1979 and is commercially available. Despite the use of this cell line as an in vitro model for functional... 
MYC GENE | EWINGS-SARCOMA | Ewing sarcoma | PROTEIN | Primitive neuroectodermal tumor | DCC | SK-PN-DW | PNET | CHROMOSOMES | REGION | P53 | DMBT1 | ONCOLOGY | MEDULLOBLASTOMA | EXPRESSION | Usage | Sarcoma | Fluorescence | Cytogenetics | Comparative analysis | Chromosomes | Health aspects | Cell lines | Genetic research | Youth | Teenagers | Research | Mycoplasma
Journal Article
Journal Article
by Liu, Ke and Kurien, Biji T and Zimmerman, Sarah L and Kaufman, Kenneth M and Taft, Diana H and Kottyan, Leah C and Lazaro, Sara and Weaver, Carrie A and Ice, John A and Adler, Adam J and Chodosh, James and Radfar, Lida and Rasmussen, Astrid and Stone, Donald U and Lewis, David M and Li, Shibo and Koelsch, Kristi A and Igoe, Ann and Talsania, Mitali and Kumar, Jay and Maier‐Moore, Jacen S and Harris, Valerie M and Gopalakrishnan, Rajaram and Jonsson, Roland and Lessard, James A and Lu, Xianglan and Gottenberg, Jacques‐Eric and Anaya, Juan‐Manuel and Cunninghame‐Graham, Deborah S and Huang, Andrew J. W and Brennan, Michael T and Hughes, Pamela and Illei, Gabor G and Miceli‐Richard, Corinne and Keystone, Edward C and Bykerk, Vivian P and Hirschfield, Gideon and Xie, Gang and Ng, Wan‐Fai and Nordmark, Gunnel and Eriksson, Per and Omdal, Roald and Rhodus, Nelson L and Rischmueller, Maureen and Rohrer, Michael and Segal, Barbara M and Vyse, Timothy J and Wahren‐Herlenius, Marie and Witte, Torsten and Pons‐Estel, Bernardo and Alarcón‐Riquelme, Marta E and Guthridge, Joel M and James, Judith A and Lessard, Christopher J and Kelly, Jennifer A and Thompson, Susan D and Gaffney, Patrick M and Montgomery, Courtney G and Edberg, Jeffrey C and Kimberly, Robert P and Alarcón, Graciela S and Langefeld, Carl L and Gilkeson, Gary S and Kamen, Diane L and Tsao, Betty P and Joseph McCune, W and Salmon, Jane E and Merrill, Joan T and Weisman, Michael H and Wallace, Daniel J and Utset, Tammy O and Bottinger, Erwin P and Amos, Christopher I and Siminovitch, Katherine A and Mariette, Xavier and Sivils, Kathy L and Harley, John B and Hal Scofield, R
Arthritis & Rheumatology, ISSN 2326-5191, 05/2016, Volume 68, Issue 5, pp. 1290 - 1300
Journal Article
Science of the Total Environment, ISSN 0048-9697, 04/2018, Volume 619-620, Issue C, pp. 649 - 653
Estimating gross primary production (GPP) regionally and globally remains challenging despite its primary role in driving ecosystem productivity and carbon... 
High-spatial-resolution | Orbiting Carbon Observatory-2 | Eddy covariance | Remote sensing | Sun-induced fluorescence | Gross primary productivity | CANOPY | MODEL | RETRIEVAL | ENVIRONMENTAL SCIENCES | PRODUCTIVITY | INDUCED CHLOROPHYLL FLUORESCENCE | PHOTOSYNTHESIS | CYCLE | Biomes | Fluorescence | Ecosystems
Journal Article
Molecular Cytogenetics, ISSN 1755-8166, 12/2015, Volume 8, Issue 1, p. 102
Central nervous system features have been rarely described to be associated with the small deletion or duplication of chromosome 22q11.21. We report two... 
Central nervous system abnormalities | Duplication | Array CGH | Deletion | Chiari I malformation | Microarray | Chromosome 22q11 | Semilobar holoprosencephaly | Usage | Nervous system diseases | Analysis | Cytogenetics | Causes of | Chromosome deletion | Research | Health aspects
Journal Article
Arthritis & Rheumatology, ISSN 2326-5191, 11/2017, Volume 69, Issue 11, pp. 2187 - 2192
Objective Sjögren's syndrome (SS) and systemic lupus erythematosus (SLE) are related by clinical and serologic manifestations as well as genetic risks. Both... 
Lupus | Women | Sex chromosomes | Sjogren's syndrome | Abnormalities | Health risks | Single-nucleotide polymorphism | Patients | Chronic conditions | Systemic lupus erythematosus | X Chromosomes | Autoimmune diseases | Chromosome aberrations | Polymorphism
Journal Article
Clinical Case Reports, ISSN 2050-0904, 10/2016, Volume 4, Issue 10, pp. 913 - 918
Key Clinical Message We report a half‐sibling cohort with deletion of 4p16.1, astigmatism, gross and fine motor delay, variable intellectual disability, and... 
chromosome 4 | 4p16.1 | microarray | deletion | WFS1 | Attention deficit disorder | Food allergies | Pediatrics | Auditory processing disorder | Laboratories | Intellectual disabilities | Cloning | Hybridization | Hearing impairment | Sensory perception | Asthma | Atrophy | Genotype & phenotype | Genetic counseling | Genetics | Diabetes | Mutation | Chromosomes | Siblings | Astigmatism
Journal Article
Journal Article
Fetal and Pediatric Pathology, ISSN 1551-3815, 2019, pp. 1 - 11
Epithelioid sarcoma is a malignant mesenchymal tumor exhibiting epithelioid cytomorphology and epithelial phenotype. Its histogenesis is unknown, but its... 
YAP1 | heel tumor | Epithelioid sarcoma | infant | SMARCB1/INI1 | BIRC3
Journal Article