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Identification of hereditary breast and ovarian cancer germline variants in Granada (Spain): NGS perspective.
Molina-Zayas M, Garrido-Navas C, García-Puche JL, Barwell J, Pedrinaci S, Atienza MM, García-Linares S, de Haro-Muñoz T, Lorente JA, Serrano MJ, Poyatos-Andújar A. Molina-Zayas M, et al. Among authors: garcia linares s. Mol Genet Genomics. 2022 May;297(3):859-871. doi: 10.1007/s00438-022-01891-5. Epub 2022 Apr 22. Mol Genet Genomics. 2022. PMID: 35451682 Free PMC article.
New mutation associated with autosomal dominant polycystic kidney disease with founder effect located in the alpujarra region of granada.
García-Rabaneda C, Martínez-Atienza M, Morales-García AI, Poyatos-Andújar A, García-Linares S, Bellido-Díaz ML, Argüelles-Toledo I, García-Valverde M, Bravo-Soto JA, Esteban-de-la-Rosa RJ. García-Rabaneda C, et al. Nefrologia (Engl Ed). 2020 Sep-Oct;40(5):536-542. doi: 10.1016/j.nefro.2020.03.003. Epub 2020 Jun 3. Nefrologia (Engl Ed). 2020. PMID: 32505451 Free article. English, Spanish.
Variation genetics and disease: the answer is in the clinical and in the family.
Morales-García AI, García-Rabaneda C, García-Linares S, Prados-Garrido MD, Esteban-de la Rosa RJ. Morales-García AI, et al. Nefrologia (Engl Ed). 2021 Feb 15:S0211-6995(21)00004-7. doi: 10.1016/j.nefro.2020.10.004. Online ahead of print. Nefrologia (Engl Ed). 2021. PMID: 33602562 Free article. English, Spanish. No abstract available.
Study of Human Leukocyte Antigen (HLA) in 13 cases of familial frontal fibrosing alopecia: CYP21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA-A*33:01; B*14:02; C*08:02 as a genetic marker.
Porriño-Bustamante ML, López-Nevot MÁ, Aneiros-Fernández J, Casado-Ruiz J, García-Linares S, Pedrinacci-Rodríguez S, García-Lora E, Martín-Casares MA, Fernández-Pugnaire MA, Arias-Santiago S. Porriño-Bustamante ML, et al. Australas J Dermatol. 2019 Aug;60(3):e195-e200. doi: 10.1111/ajd.12985. Epub 2019 Jan 17. Australas J Dermatol. 2019. PMID: 30656636
The interaction of the ribotoxin α-sarcin with complex model lipid vesicles.
García-Montoya C, García-Linares S, Heras-Márquez D, Majnik M, Laxalde-Fernández D, Amigot-Sánchez R, Martínez-Del-Pozo Á, Palacios-Ortega J. García-Montoya C, et al. Among authors: garcia linares s. Arch Biochem Biophys. 2024 Jan;751:109836. doi: 10.1016/j.abb.2023.109836. Epub 2023 Nov 23. Arch Biochem Biophys. 2024. PMID: 38000493
Sticholysin recognition of ceramide-phosphoethanolamine.
García-Montoya C, Heras-Márquez D, Amigot-Sánchez R, García-Linares S, Martínez-Del-Pozo Á, Palacios-Ortega J. García-Montoya C, et al. Among authors: garcia linares s. Arch Biochem Biophys. 2023 Jul 1;742:109623. doi: 10.1016/j.abb.2023.109623. Epub 2023 May 18. Arch Biochem Biophys. 2023. PMID: 37207934
Variation genetics and disease: The answer is in the clinical and in the family.
Morales-García AI, García-Rabaneda C, García-Linares S, Prados-Garrido MD, Esteban-de la Rosa RJ. Morales-García AI, et al. Among authors: garcia linares s. Nefrologia (Engl Ed). 2022 Nov-Dec;42(6):731-733. doi: 10.1016/j.nefroe.2023.02.002. Epub 2023 Mar 14. Nefrologia (Engl Ed). 2022. PMID: 36925326 Free article. No abstract available.
33 results