Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tiiu Ilus"'
Autor:
Christiaan H. Righolt, Sabine Mai, Tiiu Ilus, Adebayo Olujohungbe, Ludger Klewes, Mari Punab, Pille Tammur, Chirawadee Sathitruangsak, Anu Tamm
Publikováno v:
Journal of Cellular Biochemistry, 116 (5), 2015
Journal of Cellular Biochemistry
Journal of Cellular Biochemistry
The mammalian nucleus has a distinct substructure that cannot be visualized directly by conventional microscopy. In this study, the organization of the DNA within the nucleus of multiple myeloma (MM) cells, their precursor cells (monoclonal gammopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902fb3fa37c3060eaab35d3938577e74
http://resolver.tudelft.nl/uuid:01395c2e-d0bb-44c7-9565-0502447e57a4
http://resolver.tudelft.nl/uuid:01395c2e-d0bb-44c7-9565-0502447e57a4
Publikováno v:
American Journal of Medical Genetics Part A. :434-438
We report a newborn girl with intrachromosomal triplication of 3q25.3 --> q29 (mosaicism) who died at the age of 3.5 weeks due to her malformations. She demonstrated disproportionate short stature with short limbs, a prominent and hairy forehead, thi
Publikováno v:
Paediatric and perinatal epidemiology. 20(6)
The aim of the study was to investigate the livebirth prevalence of Down's syndrome (DS) in Estonia during the past 14 years, create a DS database and observe the effectiveness of prenatal screening. This is a population-based descriptive study. The
Autor:
Haide Põder, Tiina Talvik, Elve Raukas, Tiina Kahre, Marja-Leena Väisänen, Gunnar Tasa, Oliver Bartsch, Tiiu Ilus, Katrin Õunap, Riina Zordania, Eve Õiglane-Shlik
Publikováno v:
American journal of medical genetics. Part A. 140(18)
In 2000-2004, we performed a focused search for individuals with Angelman syndrome (AS) and Prader-Willi syndrome (PWS) aiming to establish the prevalence data for the individuals born between 1984 and 2004 in Estonia. All persons with probable AS or
Publikováno v:
American journal of medical genetics. Part A. (3)
We report on a pure duplication of the proximal chromosome 2q in a 6.5-year-old boy with V-shaped midline cleft palate and bifid uvula, posteriorly located tongue, and micrognathia (Pierre Robin sequence), celiac disease, failure to thrive, and devel
Publikováno v:
American journal of medical genetics. Part A. 134(4)
We report a newborn girl with intrachromosomal triplication of 3q25.3 --q29 (mosaicism) who died at the age of 3.5 weeks due to her malformations. She demonstrated disproportionate short stature with short limbs, a prominent and hairy forehead, thick
Publikováno v:
American journal of medical genetics. 93(5)
We describe a 2(1/2)-year-old boy with a ring chromosome 13 with distal deletion of 13q32-->qter and celiac disease.
Publikováno v:
Human Genetics. 41
The chromosomes of 102 normal newborn babies (51 boys and 51 girls) born at term, their parents, and 45 nonrelated children with mental retardation at the level of imbecility were investigated by fluorescence microscopy using propyl quinacrine mustar
Autor:
Rhea Vallente, Mari Punab, Carolin Brand, Pille Tammur, Amanda Guffei, Alexandra Kuzyk, Eric Dupas, Morel Rubinger, Sabine Mai, Anu Tamm, Dietrich Grün, Julius Adebayo Awe, Tiiu Ilus, Ludger Klewes, Chirawadee Sathitruangsak, Adebayo Olujohungbe, Daniel Lichtensztejn
Publikováno v:
Translational Oncology. (6):749-IN36
Multiple myeloma (MM) is preceded by monoclonal gammopathy of undetermined significance (MGUS). Up to date, it is difficult to predict an individual's time to disease progression and the treatment response. To examine whether the nuclear telomeric ar