| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Paula Pennanen, Sirkku Peltonen, Roope A Kallionpää, Juha Peltone. The effect of estradiol, testosterone, and human chorionic gonadotropin on the proliferation of Schwann cells with NF1 Molecular and cellular biochemistry. vol 444. issue 1-2. 2018-07-25. PMID:29185159. |
the effect of estradiol, testosterone, and human chorionic gonadotropin on the proliferation of schwann cells with nf1 dermal neurofibromas are the hallmarks of neurofibromatosis type 1 (nf1). |
2018-07-25 |
2023-08-13 |
human |
| Paula Pennanen, Sirkku Peltonen, Roope A Kallionpää, Juha Peltone. The effect of estradiol, testosterone, and human chorionic gonadotropin on the proliferation of Schwann cells with NF1 Molecular and cellular biochemistry. vol 444. issue 1-2. 2018-07-25. PMID:29185159. |
neurofibromas harbor schwann cells with two different genotypes: schwann cells which carry the germline mutation and a healthy nf1 allele (nf1 |
2018-07-25 |
2023-08-13 |
human |
| Arianna Tucci, Veronica Saletti, Francesca Menni, Claudia Cesaretti, Giulietta Scuvera, Silvia Esposito, Giulia Melloni, Susanna Esposito, Donatella Milani, Cristina Cereda, Mario Cigada, Laura Tresoldi, Francesco Viola, Federica Natacc. The absence that makes the difference: choroidal abnormalities in Legius syndrome. Journal of human genetics. vol 62. issue 11. 2018-06-19. PMID:28747691. |
neurofibromatosis type 1 (nf1) is an hereditary disorder characterized by abnormal proliferation of multiple tissues of neural crest origin, and presents mainly with multiple café-au-lait macules, axillary freckling and neurofibromas. |
2018-06-19 |
2023-08-13 |
Not clear |
| Santasree Banerjee, Dongzhu Lei, Shengran Liang, Li Yang, Saijun Liu, Zhu Wei, Jian Ping Tan. Novel phenotypes of NF1 patients from unrelated Chinese families with tibial pseudarthrosis and anemia. Oncotarget. vol 8. issue 24. 2018-05-24. PMID:27980226. |
neurofibromatosis type 1 (nf1) is an autosomal dominant, multi-system, neurocutaneous disorder, manifested with neurofibromas and cafe´-au-lait spots. |
2018-05-24 |
2023-08-13 |
Not clear |
| Charlotte Philpott, Hannah Tovell, Ian M Frayling, David N Cooper, Meena Upadhyay. The NF1 somatic mutational landscape in sporadic human cancers. Human genomics. vol 11. issue 1. 2018-05-23. PMID:28637487. |
nf1 exhibits variable clinical expression and is characterized by benign cutaneous lesions including neurofibromas and café-au-lait macules, as well as a predisposition to various types of malignancy, such as breast cancer and leukaemia. |
2018-05-23 |
2023-08-13 |
human |
| Sirkku Peltonen, Roope A Kallionpää, Juha Peltone. Neurofibromatosis type 1 (NF1) gene: Beyond café au lait spots and dermal neurofibromas. Experimental dermatology. vol 26. issue 7. 2018-05-18. PMID:27622733. |
neurofibromatosis type 1 (nf1) gene: beyond café au lait spots and dermal neurofibromas. |
2018-05-18 |
2023-08-13 |
Not clear |
| Teresa Esposito, Carla Schettino, Paola Polverino, Salvatore Allocca, Laura Adelfi, Alessandra D'Amico, Guglielmo Capaldo, Bruno Varriale, Anna Di Salle, Gianfranco Peluso, Giuseppe Sorrentino, Giacomo Lus, Simone Sampaolo, Giuseppe Di Iorio, Mariarosa Anna Beatrice Melon. Synergistic Interplay between Curcumin and Polyphenol-Rich Foods in the Mediterranean Diet: Therapeutic Prospects for Neurofibromatosis 1 Patients. Nutrients. vol 9. issue 7. 2018-05-18. PMID:28754004. |
neurofibromas are the hallmark lesions in neurofibromatosis 1 (nf1); these tumors are classified as cutaneous, subcutaneous and plexiform. |
2018-05-18 |
2023-08-13 |
Not clear |
| Yuhei Hakozaki, Shinichi Sameshima, Teppei Tatsuoka, Takashi Okuyama, Yukinori Yamagata, Tamaki Noie, Masatoshi Oya, Akiko Fujii, Yoshihiko Ueda, Chieko Shimura, Kazumoto Katagir. Rectal carcinoma and multiple gastrointestinal stromal tumors (GIST) of the small intestine in a patient with neurofibromatosis type 1: a case report. World journal of surgical oncology. vol 15. issue 1. 2018-05-10. PMID:28835241. |
neurofibromatosis type 1 (nf1) is an autosomally dominant inherited disorder characterized by multiple pigmented skin spots (café-au-lait spots) and neurofibroma. |
2018-05-10 |
2023-08-13 |
Not clear |
| Delphine Raffin, Julia Zaragoza, Gabriella Georgescou, Youssef Mourtada, Annabel Maruani, Frédéric Ossant, Frédéric Patat, Loïc Vaillant, Laurent Mache. High-frequency ultrasound imaging for cutaneous neurofibroma in patients with neurofibromatosis type I. European journal of dermatology : EJD. vol 27. issue 3. 2018-04-12. PMID:28524060. |
high-frequency ultrasound imaging for cutaneous neurofibroma in patients with neurofibromatosis type i. neurofibromas (nfs) are benign tumours arising from a nerve sheath, which are present in nearly all patients with neurofibromatosis type 1 (nf1). |
2018-04-12 |
2023-08-13 |
Not clear |
| Haizea Iribar, Ane Jaka, Nerea Ormaechea, Anna Tuneu, Ander Izeta, Araika Gutiérrez-River. Does Schwann cell dedifferentiation originate dermal neurofibromas? Experimental dermatology. vol 25. issue 11. 2018-01-30. PMID:27303947. |
dermal neurofibromas are characteristic of neurofibromatosis type one (nf1), and their developmental origin still unsolved. |
2018-01-30 |
2023-08-13 |
Not clear |
| Haizea Iribar, Ane Jaka, Nerea Ormaechea, Anna Tuneu, Ander Izeta, Araika Gutiérrez-River. Does Schwann cell dedifferentiation originate dermal neurofibromas? Experimental dermatology. vol 25. issue 11. 2018-01-30. PMID:27303947. |
although nf1 loss is required for neurofibroma initiation, some features of these benign tumors resemble a skin injury state and cutaneous trauma or other insults might support tumor development. |
2018-01-30 |
2023-08-13 |
Not clear |
| Chung-Ping Liao, Sanjay Pradhan, Zhiguo Chen, Amish J Patel, Reid C Booker, Lu Q L. The role of nerve microenvironment for neurofibroma development. Oncotarget. vol 7. issue 38. 2018-01-30. PMID:27517146. |
there is increasing evidences that neurofibroma initiates through loss of nf1 function in the schwann cell lineage, followed by a cascade of interactions with other cell types in the surrounding tumor microenvironment. |
2018-01-30 |
2023-08-13 |
Not clear |
| Chung-Ping Liao, Sanjay Pradhan, Zhiguo Chen, Amish J Patel, Reid C Booker, Lu Q L. The role of nerve microenvironment for neurofibroma development. Oncotarget. vol 7. issue 38. 2018-01-30. PMID:27517146. |
in nf1 patients, neurofibromas always develop along peripheral nerves and do not migrate to distant organs, including the central nervous system. |
2018-01-30 |
2023-08-13 |
Not clear |
| Mark Bigder, Paul Szelemej, Neil Berringto. Extensive Mirror-Image Neurofibromas of Entire Spine Resulting in Spastic Tetraplegia. World neurosurgery. vol 108. 2017-12-27. PMID:28867317. |
neurofibromatosis 1 (nf1) is associated with increased incidence of spinal tumors including neurofibromas. |
2017-12-27 |
2023-08-13 |
Not clear |
| Mark Bigder, Paul Szelemej, Neil Berringto. Extensive Mirror-Image Neurofibromas of Entire Spine Resulting in Spastic Tetraplegia. World neurosurgery. vol 108. 2017-12-27. PMID:28867317. |
we present a 21-year-old male diagnosed with nf1 in infancy and followed for multiple mirror-image neurofibromas involving the entire spine. |
2017-12-27 |
2023-08-13 |
Not clear |
| Kairong Li, Ashley N Turner, Min Chen, Stephanie N Brosius, Trenton R Schoeb, Ludwine M Messiaen, David M Bedwell, Kurt R Zinn, Corina Anastasaki, David H Gutmann, Bruce R Korf, Robert A Kesterso. Mice with missense and nonsense NF1 mutations display divergent phenotypes compared with human neurofibromatosis type I. Disease models & mechanisms. vol 9. issue 7. 2017-12-04. PMID:27482814. |
mice with one nf1(arg681*) allele in combination with a conditional floxed nf1 allele and the dhhcre transgene (nf1(4f/arg681*); dhhcre) display disorganized nonmyelinating axons and neurofibromas along the spinal column, which leads to compression of the spinal cord and paralysis. |
2017-12-04 |
2023-08-13 |
mouse |
| Yassine Abaloun, Yousra Ajhou. [Lisch nodule in neurofibromatosis type 1]. The Pan African medical journal. vol 27. 2017-10-23. PMID:28979620. |
neurofibromatosis type 1 (nf1) or von recklinghausen disease manifests as cutaneous café-au-lait spots and neurofibromas. |
2017-10-23 |
2023-08-13 |
Not clear |
| Azadeh Amirnasr, Rob M Verdijk, Patricia F van Kuijk, Walter Taal, Stefan Sleijfer, Erik A C Wieme. Expression and inhibition of BRD4, EZH2 and TOP2A in neurofibromas and malignant peripheral nerve sheath tumors. PloS one. vol 12. issue 8. 2017-10-13. PMID:28813519. |
the transcript levels of brd4, ezh2 and top2a were determined in paired formalin-fixed paraffin-embedded (ffpe) neurofibroma/mpnst samples derived from the same nf1 patient and in a set of plexiform neurofibromas, atypical neurofibromas and mpnst. |
2017-10-13 |
2023-08-13 |
human |
| A Hernández-Martín, A Duat-Rodrígue. An Update on Neurofibromatosis Type 1: Not Just Café-au-Lait Spots and Freckling. Part II. Other Skin Manifestations Characteristic of NF1. NF1 and Cancer. Actas dermo-sifiliograficas. vol 107. issue 6. 2017-10-02. PMID:26956402. |
by contrast, the presence of multiple cutaneous neurofibromas or at least 1 plexiform neurofibroma is a very specific indication of nf1. |
2017-10-02 |
2023-08-13 |
Not clear |
| Verena Stahn, Inga Nagel, Susan Fischer-Huchzermeyer, Florian Oyen, Reinhard Schneppenheim, Stefan Gesk, Axel Bohring, Levan Chikobava, Peter Young, Burkhard Gess, Mathias Werner, Volker Senner, Anja Harde. Molecular Analysis of Hybrid Neurofibroma/Schwannoma Identifies Common Monosomy 22 and α-T-Catenin/CTNNA3 as a Novel Candidate Tumor Suppressor. The American journal of pathology. vol 186. issue 12. 2017-09-20. PMID:27765635. |
neurofibromas in nf1 and schwannomas in nf2 or schwannomatosis are defined by distinctive molecular hits. |
2017-09-20 |
2023-08-13 |
Not clear |