Zobrazeno 1 - 10
of 6 277
pro vyhledávání: '"chromosome 21."'
Publikováno v:
International Journal of General Medicine, Vol Volume 17, Pp 1337-1347 (2024)
Biniam Endale Geleta, Girma Seyoum Department of Anatomy, Addis Ababa University, Addis Ababa, EthiopiaCorrespondence: Biniam Endale Geleta, Email benjaminbig12@gmail.comBackground: Children with DS are at higher risk of developing congenital anomali
Externí odkaz:
https://doaj.org/article/18d650d021bf4abe97472b944fe16397
Autor:
Bala, Usman1,2,3, Leong, Melody Pui-Yee2,4, Lim, Chai Ling1,2, Shahar, Hayati Kadir5, Othman, Fauziah1,2, Lai, Mei-I2,6, Law, Zhe-Kang7, Ramli, Khairunnisa8, Htwe, Ohnmar9, Ling, King-Hwa2,4, Cheah, Pike-See1,2 cheahpikesee@upm.edu.my
Publikováno v:
PLoS ONE. 5/24/2018, Vol. 13 Issue 5, p1-13. 13p.
Autor:
Peiris, Heshan1, Keating, Damien J.1 damien.keating@flinders.edu.au
Publikováno v:
Clinical & Experimental Pharmacology & Physiology. Apr2018, Vol. 45 Issue 4, p377-383. 7p. 2 Diagrams.
Autor:
Naomi Michels, Femke M. Hormann, Aurélie Boeree, Edwin Sonneveld, Anthony V. Moorman, Gabriele Escherich, Rosemary Sutton, H. Berna Beverloo, Rob Pieters, C. Michel Zwaan, Monique L. den Boer, Judith M. Boer
Publikováno v:
EJC Paediatric Oncology, Vol 3, Iss , Pp 100140- (2024)
Background: Chromosome 21 is affected in ∼60% of paediatric B-cell precursor acute lymphoblastic leukaemia (BCP-ALL) patients and includes somatic and constitutional gains, intrachromosomal amplification of chromosome 21 (iAMP21), and the transloca
Externí odkaz:
https://doaj.org/article/ecb1e835fb504ce692dbd72007e10a05
Autor:
Bălan, Valeria1
Publikováno v:
International Multidisciplinary Scientific Conference on Social Sciences & Arts SGEM. 2015, p646-653. 8p.
Autor:
Jakob Schuy, Kristine Bilgrav Sæther, Jasmin Lisfeld, Marlene Ek, Christopher M. Grochowski, Ming Yin Lun, Alex Hastie, Susanne Rudolph, Sigrid Fuchs, Kornelia Neveling, Maja Hempel, Alexander Hoischen, Maria Pettersson, Claudia M.B. Carvalho, Jesper Eisfeldt, Anna Lindstrand
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101863- (2024)
Purpose: Although chromosome 21 is the smallest human chromosome, it is highly relevant in the pathogenicity of both cancer and congenital diseases, including Alzheimer disease and trisomy 21 (Down syndrome). In addition, cases with rare structural v
Externí odkaz:
https://doaj.org/article/70b601806d7c45679087a28418058b52
Autor:
Ahmed, Md. Mahiuddin1, Dhanasekaran, A. Ranjitha1, Block, Aaron1, Tong, Suhong2, Costa, Alberto C. S.3, Stasko, Melissa3, Gardiner, Katheleen J.1,4,5 katheleen.gardiner@ucdenver.edu
Publikováno v:
PLoS ONE. Mar2015, Vol. 10 Issue 3, p1-25. 25p.
Publikováno v:
Molecular Medicine Reports. 2015, Vol. 11 Issue 2, p1235-1239. 5p.
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103204- (2023)
Down syndrome (DS) is caused by trisomy of Homo sapiens chromosome 21 (HSA21) and is by far the most common chromosomal disorder accompanied by neurodevelopmental disorders and congenital heart disease. Here, we generated two induced pluripotent stem
Externí odkaz:
https://doaj.org/article/60f483027ebe48f6987814d9995df5d4
Autor:
Yasin, S. R.1, Tahtamouni, L. H.1, Najeeb, N. S.1, Issa, N. M.1, Al–Mazaydeh, Z. A.1, Alfaouri, A. A.1
Publikováno v:
Andrologia. Sep2014, Vol. 46 Issue 7, p770-776. 7p.