نتائج البحث

Evaluation of the Idylla ctEGFR mutation assay to detect EGFR mutations in plasma from patients with non-small cell lung cancers.

• Authors : Gilson, Pauline¹ ; Saurel, Chloé²; Salleron, Julia³

• Source: Scientific Reports. 5/18/2021, Vol. 11 Issue 1, p1-11. 11p.

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Mutation Profiling of Premalignant Colorectal Neoplasia.

• Authors : Karczmarski, Jakub¹; Goryca, Krzysztof¹; Pachlewski, Jacek²

• Source: Gastroenterology Research & Practice. 11/12/2019, p1-9. 9p.

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Mutation characteristic of 103 haemophilia A patients in Vietnam: Identification of novel mutations.

• Authors : Luu, Dung Vu¹ (AUTHOR); Tran, Thinh Huy^1,2 (AUTHOR); Nguyen, Duc Hinh^1,2 (AUTHOR)

• Source: Haemophilia. Jul2019, Vol. 25 Issue 4, pe274-e277. 4p. 1 Chart.

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Dysplastic Foot with Soft-Tissue Hypertrophy: Radiographic Features Suggestive of Proteus Syndrome

• Authors : Debabrata Maitra

Subjects: Proteus syndrome; congenital dysplastic foot; localized overgrowth

• Source: Radiography Open, Vol 11, Iss 1 (2025)

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Somatic mutations of cell-free circulating DNA detected by targeted next-generation sequencing and digital droplet PCR in classical Hodgkin lymphoma.

• Authors : Bessi, Lucile¹; Viailly, Pierre-Julien¹; Bohers, Elodie¹

• Source: Leukemia & Lymphoma. Feb2019, Vol. 60 Issue 2, p498-502. 5p.

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Gene analysis and clinical features of 22 GNE myopathy patients.

• Authors : Guo, Xuan¹ (AUTHOR); Zhao, Zhe¹ (AUTHOR); Shen, Hongrui¹ (AUTHOR)

• Source: Neurological Sciences. Aug2022, Vol. 43 Issue 8, p5049-5056. 8p. 1 Color Photograph, 1 Black and White Photograph, 2 Charts.

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Genetic alterations in patients with chronic leucocytosis and persistent thrombocytosis.

• Authors : Mori, Naoki^1,2 (AUTHOR) ; Ohwashi-Miyazaki, Mari¹ (AUTHOR); Yoshinaga, Kentaro¹ (AUTHOR)

• Source: Journal of Genetics. Jun2022, Vol. 101 Issue 1, p1-5. 5p.

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Differential transmission of the molecular signature of RBSP3, LIMD1 and CDC25A in basal/ parabasal versus spinous of normal epithelium during head and neck tumorigenesis: A mechanistic study.

• Authors : Sarkar, Shreya¹; Alam, Neyaz²; Mandal, Syam Sundar³

• Source: PLoS ONE. 4/19/2018, Vol. 13 Issue 3, p1-19. 19p.

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Disrupted myelin lipid metabolism differentiates frontotemporal dementia caused by GRN and C9orf72 gene mutations.

• Authors : Marian, Oana C.^1,2 (AUTHOR); Teo, Jonathan D.^1,2 (AUTHOR); Lee, Jun Yup^1,2 (AUTHOR)

• Source: Acta Neuropathologica Communications. 3/27/2023, Vol. 11 Issue 1, p1-18. 18p.

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Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

• Authors : Werheid, Friederike^1,2; Azzedine, Hamid²; Zwerenz, Eva^1,2

• Source: Brain & Behavior. Apr2016, Vol. 6 Issue 4, pn/a-N.PAG. 14p.

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