نتایج جستجو برای: chromosome 10q

تعداد نتایج: 119424  

Journal: :iranian journal of public health 0
rahil mashhadi 1. urology research center, tehran university of medical sciences , tehran, iran. gholamreza pourmand 1. urology research center, tehran university of medical sciences , tehran, iran. abdolrasou mehrsai 1. urology research center, tehran university of medical sciences , tehran, iran. saeed pakdel 2. dept. of urology, kermanshah university of medical sciences , kermanshah, iran. hossein dialameh 1. urology research center, tehran university of medical sciences , tehran, iran. ayat ahmadi 3. dept. of pathobiology, school of medicine, tehran university of medical sciences , tehran, iran.

bladder cancer is the most frequent genitourinary malignancy in iran. environmental and genetic factors are the two factors linked with bladder cancer expansion. the aim of this study was to investigate the role of pten gene and environmental risk factors on the progression and prognosis of bladder cancer.we evaluated 55 tumor specimens and 66 bladder mucosa samples of non-cancerous patients be...

Journal: :Cancer research 1997
S I Wang J Puc J Li J N Bruce P Cairns D Sidransky R Parsons

Alterations of the PTEN gene occur in glioblastoma multiforme. To determine the frequency of PTEN alteration, 34 consecutive glioblastomas were studied in detail. Sequencing each of the nine exons amplified from tumor DNA revealed 11 mutations. Analysis of polymorphic markers within and surrounding the PTEN gene identified an additional four homozygous deletion mutations. Loss of heterozygosity...

Journal: :Journal of medical genetics 1996
C James A Jauch L Robson N Watson A Smith

A 3 1/2 year old girl was evaluated because of developmental delay. Short stature was evident with height between the 3rd and 10th centiles, while weight and head circumference were on the 50th centile. Dysmorphic features consisted of a high bossed forehead, pointed short ear lobes, small nose, bilateral convergent strabismus, left simian crease, a gap between the first and second toes bilater...

2014
EMMANOUIL MANOLAKOS ANNALISA VETRO ANTONIOS GARAS LORETTA THOMAIDIS KONSTANTINOS KEFALAS GEORGE KITSOS MONIKA ZIEGLER THOMAS LIEHR ORSETTA ZUFFARDI IOANNIS PAPOULIDIS

Proximal 10q duplication is a well-defined but rare genetic syndrome. Duplication of proximal segments of the long arm of chromosome 10 results in a pattern of malformations, which are distinct from those of the more common distal 10q trisomy syndrome. The present study describes the case of a boy with phenotypic abnormalities (severe central hypotonia, mild ataxia, moderate developmental delay...

2016
Laura Fontana Silvia Tabano Eleonora Bonaparte Giovanni Marfia Chiara Pesenti Rossella Falcone Claudia Augello Nicole Carlessi Rosamaria Silipigni Silvana Guerneri Rolando Campanella Manuela Caroli Silvia Maria Sirchia Silvano Bosari Monica Miozzo

Several molecular markers drive diagnostic classification, prognostic stratification, and/or prediction of response to therapy in patients with gliomas. Among them, IDH gene mutations are valuable markers for defining subtypes and are strongly associated with epigenetic silencing of the methylguanine DNA methyltransferase (MGMT) gene. However, little is known about the percentage of MGMT-methyl...

Journal: :Archives of disease in childhood 1997
N Mitsufuji S Tokuda H Nakanoin H Yoshioka T Sawada

A case of partial trisomy 10q with partial monosomy 12q is reported. The chromosomal abnormalities resulted from a paternal balanced, reciprocal translocation involving chromosomes 10 and 12, which, to the best of our knowledge, has not been previously described.

Aliakbar Rahbarimanesh, Amirhassan Barkhordari, Pupak Derakhshandeh-Peykar, Reza Ebrahimzadeh-Vesal, Soja Shamizadeh Kalkhoran,

Background: Here we describe a new case of partial distal 10q trisomy in a 6-year-old Iranian girl from healthy parents with mental, growth, and psychomotor retardations. Methods: Additional clinical features include dysmorphic craniofacial features, microcephaly, bilateral hydronephrosis without heart problems, small and rotated low-set ears, bow-shaped mouth, abnormal teeth, short neck, an...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1987
J Kagan J Finan J Letofsky E C Besa P C Nowell C M Croce

Human leukemic T cells carrying a t(10;14)(q24;q11) chromosome translocation were fused with mouse leukemic T cells, and the hybrids were examined for genetic markers of human chromosomes 10 and 14. Hybrids containing the human 10q+ chromosome had the human genes for terminal deoxynucleotidyltransferase that has been mapped at 10q23-q25 and for C alpha [the constant region of TCRA (the alpha-ch...

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