Výsledky vyhledávání - "Willy, Renier"

Supplementary Figure Legends from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Autor: Richard Marais, Willeke A.M. Blokx, Pieter Wesseling, Benno Küsters, Caroline J. Springer, Ion Niculescu-Duvaz, Jolanda Schieving, Willy Renier, Ilse A. van Engen-van Grunsven, Jacobus H. Gilhuis, Berta Sanchez-Laorden, Patricia J.T.A. Groenen, Amaya Viros, Heidi V.N. Küsters-Vandevelde, Malin Pedersen

Supplementary Figure Legends PDF file - 92K, This file contains the Figure legends to Supplementary Figures 1-5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0aa9f1d1988d8356a6d76064cd6a7c7
https://doi.org/10.1158/2159-8290.22529580

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Supplementary Figure 2 from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Supplementary Figure 2 PDF file - 394K,Data are presented to show that congenital expression of NRASG12D in mouse melanocytes does not affect eyes or heart development

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51c6a44f19cebe45fc8ea000571a436d
https://doi.org/10.1158/2159-8290.22529592.v1

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Supplementary Figure 4 from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Supplementary Figure 4 PDF file - 39K, Sequencing of RT-PCR amplified cDNA is presented to show that NRASG12D is expressed in the CNS tumors of our mice

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2741ff69ad00be20cc3114449000de66
https://doi.org/10.1158/2159-8290.22529586.v1

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Supplementary Figure 5 from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Supplementary Figure 5 PDF file - 1328K, Histopathology is shown to confirm that the tumors from patients 1 and 2 are melanoma of the CNS and that the congenital nevus from patient 2 expresses NRASQ61K

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72edd5c6effee2a6c1efb87a9da744f7
https://doi.org/10.1158/2159-8290.22529583.v1

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Supplementary Figure 1 from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Supplementary Figure 1 PDF file - 795K, Data are presented to show that NRASG12D does not induce melanoma when expressed in the melanocytes of adult mice

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a8703c189596c2be9bdd440c1d9c66d
https://doi.org/10.1158/2159-8290.22529595.v1

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Supplementary Figure 3 from Primary Melanoma of the CNS in Children Is Driven by Congenital Expression of Oncogenic NRAS in Melanocytes

Supplementary Figure 3 PDF file - 498K, Histopathology data are presented to confirm that CNS tumors in our mice are malignant melanomas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5e2505da9c1b2ca1590ca6cd653a41d
https://doi.org/10.1158/2159-8290.22529589.v1

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Severe fatigue in narcolepsy with cataplexy

Autor: Hal A, Droogleever Fortuyn, Rolf, Fronczek, Mirjan, Smitshoek, Sebastiaan, Overeem, Martijn, Lappenschaar, Joke, Kalkman, Willy, Renier, Jan, Buitelaar, Gert Jan, Lammers, Gijs, Bleijenberg

Publikováno v: Journal of sleep research. 21(2)

Excessive daytime sleepiness (EDS) is the core symptom of narcolepsy. However, there have been indications that fatigue - which should be separated from EDS--is also a frequent complaint. We determined the prevalence of severe fatigue in a group of n

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::eaba2a1c7ed0f3298f0f50604f7fe1c9
https://pubmed.ncbi.nlm.nih.gov/21848801

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Development and Developmental Disorders of the Cerebral Cortex

Autor: Hans J. ten Donkelaar, Martin Lammens, Willy Renier, Ben Hamel, Akira Hori, Berit Verbist

Publikováno v: Clinical Neuroembryology ISBN: 9783540291404

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c60affcafe24f899be4309d13055a047
https://doi.org/10.1007/3-540-34659-7_10

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Klippel-Trenaunay syndrome and Sturge-Weber syndrome: variations on a theme?

Autor: Wynand, Vissers, Maurice, Van Steensel, Peter, Steijlen, Willy, Renier, Peter, Van De Kerkhof, Carine, Van Der Vleuten

Publikováno v: European journal of dermatology : EJD. 13(3)

We describe a patient with a complex neurocutaneous syndrome of congenital vascular malformations, abnormalities of brain and bones, and soft tissue hypertrophy of one leg. According to eponymous classification schemes, the patient can be assigned to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1e2c7f4dff1f2870330da9956226b693
https://pubmed.ncbi.nlm.nih.gov/12804977

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