Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Mariem Ben-Said"'
Autor:
Mariem Ben-Said
Publikováno v:
Ecological Processes, Vol 10, Iss 1, Pp 1-23 (2021)
Abstract Background Ecological processes such as seedling establishment, biotic interactions, and mortality can leave footprints on species spatial structure that can be detectable through spatial point-pattern analysis (SPPA). Being widely used in p
Externí odkaz:
https://doaj.org/article/b516911a8f9d41cfa553342840a126b0
Autor:
Mariem BEN-SAID, Abdelilah GHALLAB, Farida BERRAD, Abdallah AOUADI, Fadoua ASRAOUI, Majida EL ALAMI EL MOUTAOUAKIL
Publikováno v:
Revue Nature et Technologie, Vol 14, Iss 02 (2022)
La dégradation accélérée des forêts est un défi majeur pour les gestionnaires. Le reboisement constitue alors une solution importante pour l’amélioration des services écosystémiques voire la survie des écosystèmes. Comparée à d’autre
Externí odkaz:
https://doaj.org/article/f06d7b7cbfd04dee9367cd2769ecaa98
Autor:
Mariem Ben-Said
Publikováno v:
Mediterranean Botany, Vol 43 (2022)
Western Mediterranean firs are endemic and illustrate the Tertiary flora heritage in the Mediterranean basin. Due to their morphological and anatomical similarities, the classification of certain relict firs still debated especially those belonging t
Externí odkaz:
https://doaj.org/article/66893938d809490793df7a419b7fa962
Autor:
Mariem Ben-Said, Abdelilah Ghallab, Hajar Lamrhari, José Antonio Carreira, Juan Carlos Linares, Lahcen Taïqui
Publikováno v:
Forest Systems, Vol 29, Iss 2, Pp e014-e014 (2020)
Aim of study: Understanding small-scale patterns caused by stochastic factors or community interactions driving forest structure and diversity of Moroccan fir Abies marocana Trab. Area of study: Talassemtane fir forest, Talassemtane National Park, R
Externí odkaz:
https://doaj.org/article/d7bf3a5cdd3c4606a2ea18c4ed7de12e
Autor:
Abir Ben Issa, Ikhlas Ben Ayed, Olfa Jallouli, Amal Souissi, Wafa Bouchaalla, Mariem Ben Said, Salma Mallouli, Saber Masmoudi, Chahnez Charfi Triki, Hassen Hadj Kacem, Fatma Kammoun
Publikováno v:
International Journal of Developmental Neuroscience.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e8cc47fecb46b3815d89d91866ea2df8
https://doi.org/10.1002/jdn.10266
https://doi.org/10.1002/jdn.10266
Autor:
Mariem Ben-Said
Publikováno v:
Biology and Environment: Proceedings of the Royal Irish Academy. :39-52
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::926eb5ce28df475f72f4e6cda3e4777f
https://doi.org/10.1353/bae.2022.0002
https://doi.org/10.1353/bae.2022.0002
Autor:
Dina Ben Mohamed, Zacharia Saied, Samia Ben Sassi, Mariem Ben Said, Fatma Nabli, Afef Achouri, Cyrine Jeridi, Saber Masmoudi, Rim Amouri
Publikováno v:
Clinical Case Reports. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::939eda6cd1929edd154cfe14279a3ffb
https://doi.org/10.1002/ccr3.6737
https://doi.org/10.1002/ccr3.6737
Publikováno v:
Genetic Testing and Molecular Biomarkers. 25:528-539
Background: Variants in the HARS2 gene have been reported to be associated with nonsyndromic hearing loss (HL) and Perrault syndrome (PS), a rare recessive disorder marked by bilateral sensorineura...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99f81a1f412dfffa6f2373cad4f087ba
https://doi.org/10.1089/gtmb.2021.0092
https://doi.org/10.1089/gtmb.2021.0092
Autor:
Mariem Ben Said, Abdelaziz Tlili, Saber Masmoudi, Ikhlas Ben Ayed, Amal Bouzid, Hassen Kamoun, Malek Belcadhi, Amal Souissi, Mohamed Ali Mosrati, Abdullah A.Y. Gibriel, Mehdi Hasnaoui, Ines Elloumi, Nabil Idriss, N. Gharbi
Publikováno v:
Journal of Advanced Research, Vol 31, Iss, Pp 13-24 (2021)
Journal of Advanced Research
Journal of Advanced Research
Graphical abstract
Introduction Hearing impairment (HI) is characterized by complex genetic heterogeneity. The evolution of next generation sequencing, including targeted enrichment panels, has revolutionized HI diagnosis. Objectives In this stu
Introduction Hearing impairment (HI) is characterized by complex genetic heterogeneity. The evolution of next generation sequencing, including targeted enrichment panels, has revolutionized HI diagnosis. Objectives In this stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49b22b0998b87a76309abc3face7c791
http://www.sciencedirect.com/science/article/pii/S2090123221000126
http://www.sciencedirect.com/science/article/pii/S2090123221000126
Autor:
Marwa, Mahdouani, Slim, Ben Ahmed, Fahmi, Hmila, Henda, Rais, Rihab, Ben Sghaier, Hanene, Saad, Mariem, Ben Said, Saber, Masmoudi, Dorra, Hmida, Angela, Brieger, Stefan, Zeuzem, Ali, Saad, Moez, Gribaa, Guido, Plotz
Publikováno v:
PloS one. 17(12)
Lynch syndrome is a heritable condition caused by a heterozygous germline inactivating mutation of the DNA mismatch repair (MMR) genes, most commonly the MLH1 gene. However, one third of the identified alterations are missense variants, for which the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4cddfd466c7ac5cf55bd37256a2ca1ff
https://pubmed.ncbi.nlm.nih.gov/36454741
https://pubmed.ncbi.nlm.nih.gov/36454741