نتایج جستجو برای: insertional translocation

تعداد نتایج: 49544  

2012
Neveen Ashaat Ahmed Husseiny

BACKGROUND Missed abortion (Silent miscarriage) is defined as intrauterine fetal death before twenty weeks gestation. One of the most common causes of early missed abortions (before 10 weeks gestation) is cytogenetic abnormalities. OBJECTIVE To asses if there is a correlation between chromosomal aberrations (especially in chromosome 7) and missed abortion among at least two generations. MAT...

Journal: :Journal of virology 2005
Daniel G Miller Grant D Trobridge Lisa M Petek Michael A Jacobs Rajinder Kaul David W Russell

The integration sites of viral vectors used in human gene therapy can have important consequences for safety and efficacy. However, an extensive evaluation of adeno-associated virus (AAV) vector integration sites has not been completed, despite the ongoing use of AAV vectors in clinical trials. Here we have used a shuttle vector system to isolate and analyze 977 unique AAV vector-chromosome int...

Journal: :Cancer research 2007
Christopher Slape Helge Hartung Ying-Wei Lin Juraj Bies Linda Wolff Peter D Aplan

The t(2;11)(q31;p15) chromosomal translocation results in a fusion between the NUP98 and HOXD13 genes and has been observed in patients with myelodysplastic syndrome (MDS) or acute myelogenous leukemia. We previously showed that expression of the NUP98-HOXD13 (NHD13) fusion gene in transgenic mice results in an invariably fatal MDS; approximately one third of mice die due to complications of se...

Journal: :Human molecular genetics 2008
Takema Kato Hidehito Inagaki Hiroshi Kogo Tamae Ohye Kouji Yamada Beverly S Emanuel Hiroki Kurahashi

Regions containing palindromic sequence are known to be susceptible to genomic rearrangement in prokaryotes and eukaryotes. Palindromic AT-rich repeats (PATRR) are hypervariable in the human genome, manifesting size polymorphisms and a propensity to rearrange. Size variations are mainly the result of internal deletions, while two PATRRs on 11q23 and 22q11 (PATRR11 and 22) contribute to generati...

Journal: :Blood 2007
Emmanuelle Clappier Wendy Cuccuini Anna Kalota Antoine Crinquette Jean-Michel Cayuela Willem A Dik Anton W Langerak Bertrand Montpellier Bertrand Nadel Pierre Walrafen Olivier Delattre Alain Aurias Thierry Leblanc Hervé Dombret Alan M Gewirtz André Baruchel Francois Sigaux Jean Soulier

The C-Myb transcription factor is essential for hematopoiesis, including in the T-cell lineage. The C-Myb locus is a common site of retroviral insertional mutagenesis, however no recurrent genomic involvement has been reported in human malignancies. Here, we identified 2 types of genomic alterations involving the C-MYB locus at 6q23 in human T-cell acute leukemia (T-ALL). First, we found a reci...

Journal: :Genetics 1972
D D Perkins

In strain T(I-->II)39311 a long interstitial segment is transposed from IL to IIR, where it is inserted in reversed order with respect to the centromere. In crosses of T x T essentially all asci have eight viable, black spores, and all progeny are phenotypically normal. When T(I-->II)39311 is crossed by Normal sequence (N), the expected duplication class is viable while the corresponding defici...

Journal: :Journal of medical genetics 1999
A Utkus I Sorokina V Kucinskas B Röthlisberger D Balmer L Brecevic A Schinzel

A moderately mentally retarded 3 year old boy showed minor anomalies including a prominent forehead and flat occiput, exophthalmos, large and prominent ears, high arched palate, umbilical hernia, sacral dimple, and irregular position of the toes. Cardiac sonography disclosed a chorda running through the left ventricle. Cytogenetic investigation of the family showed a balanced insertional transl...

Journal: :American journal of medical genetics. Part A 2012
Shane C Quinonez Peter Hedera Mason Barr Todd Ackley Cindy Lam Anjali Purkayastha Thomas W Glover Jeffrey W Innis

We identified a novel 6.33 Mb deletion of 1q21.3q23.3 (hg18; chr1: 153035245-159367106) in two siblings presenting with blepharophimosis, ptosis, microbrachycephaly, severe psychomotor, and intellectual disability. Additional common features include small corpus callosum, normal birth length and head circumference, postnatal growth restriction, low anterior hairline, upturned nose, bilateral pr...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید