نتایج جستجو برای: chromosome anomaly

تعداد نتایج: 157750  

Journal: :The Yale Journal of Biology and Medicine 1978
Margretta R. Sseashore

Convention terminology. There follows a compilation of numerical abnormalities of chromosome constitution, again in order 1 to 22, X and Y. There is a table of syndromes associated with breakage syndromes. Associations of chromosome anomalies and cancer cell lines have been excluded. The preface contains seven tables, listing chromosome involved in polymorphisms, breakage, and aneuploidy syndro...

Journal: :Environmental Health Perspectives 1979
Liane B. Russell

Since trisomies produce adverse effects relatively late in development or even postnatally, they are an important component of the array of genetic damages that might be caused by environmental agents. Whole-chromosome aneuploidy (as opposed to breakage-derived aneuploidy) might come about secondarily from crossover depression, or could follow damage to the meiotic spindle or to kinetochores. F...

Journal: :The Yale Journal of Biology and Medicine 1978
Margretta R. Seashore

Convention terminology. There follows a compilation of numerical abnormalities of chromosome constitution, again in order 1 to 22, X and Y. There is a table of syndromes associated with breakage syndromes. Associations of chromosome anomalies and cancer cell lines have been excluded. The preface contains seven tables, listing chromosome involved in polymorphisms, breakage, and aneuploidy syndro...

Journal: :Cancer research 1987
J S Lee S Pathak V Hopwood B Tomasovic T D Mullins F L Baker G Spitzer J A Neidhart

By using the newly developed adhesive tumor cell culture system, we analyzed the chromosomal constitutions of primary lung tumor and nonmalignant normal lung tissue from 10 previously untreated patients with non-small cell lung cancer. Chromosomal analyses were successfully carried out in banded chromosome preparations from 10 tumor and 8 normal lung tissue samples. All analyzed tumor and norma...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
G Kovacs R Erlandsson F Boldog S Ingvarsson R Müller-Brechlin G Klein J Sümegi

Renal cell carcinoma (RCC) and normal kidney tissues have been examined from 34 patients with sporadic, nonhereditary RCC. Eighteen of the 21 cytogenetically examined tumors (86%) had a detectable anomaly of chromosome arm 3p distal to band 3p11.2-p13, manifested as a deletion, combined with the nonreciprocal translocation of a segment from another chromosome or monosomy 3. Restriction-fragment...

Journal: :Genetics 2007
Ayako Oka Toshihiro Aoto Yoshikazu Totsuka Riichi Takahashi Masatsugu Ueda Akihiko Mita Noriko Sakurai-Yamatani Hiromi Yamamoto Satoshi Kuriki Nobuo Takagi Kazuo Moriwaki Toshihiko Shiroishi

Reproductive isolation that initiates speciation is likely caused by incompatibility among multiple loci in organisms belonging to genetically diverging populations. Laboratory C57BL/6J mice, which predominantly originated from Mus musculus domesticus, and a MSM/Ms strain derived from Japanese wild mice (M. m. molossinus, genetically close to M. m. musculus) are reproductively isolated. Their F...

Journal: :gene, cell and tissue 0
maryam sadat daneshpour cellular and molecular endocrine research center, obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran; cellular and molecular endocrine research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran. tel: +98-2122432500, fax: +98-2122416264 massoud houshmand department of medical genetics, national institute for genetic engineering and biotechnology, tehran, ir iran suad alfadhli department of medical laboratory sciences, faculty of allied health sciences, kuwait university, kuwait city, kuwait maryam zarkesh cellular and molecular endocrine research center, obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran sirous zeinali biotechnology research centre, pasteur institute of iran, teheran, ir iran mehdi hedayati cellular and molecular endocrine research center, obesity research center, research institute for endocrine sciences, shahid beheshti university of medical sciences, tehran, ir iran

conclusions this study revealed allele frequency of some strs on chromosome 12 and 16 for the first time in iran, and indicated differences between subjects with metabolic syndrome and subjects in the control group. results there was no significant deviation in allelic frequencies from hardy-weinberg equilibrium for all the studied markers except for d12s1632 and d12s329. the long alleles in d1...

Journal: :Journal of clinical and diagnostic research : JCDR 2013
Mot Yee Yik Murizah Mohd Zain Zubaidah Zakaria Narazah Mohd Yusoff

The premature ovarian failures with underlying chromosomal abnormalities are normally X-linked, although their associations with the autosomal and the Robertsonian translocations are also possible. Here, we are reporting a case of premature ovarian failure which was associated with a translocation between the long arm of chromosome 7 at q11.23 and the short arm of chromosome 5 at p15.3. The pro...

Journal: :Cancer genetics and cytogenetics 1996
M M Mostert M van de Pol D Olde Weghuis R F Suijkerbuijk A Geurts van Kessel J van Echten J W Oosterhuis L H Looijenga

Comparative genomic hybridization (CGH) was carried out on 15 primary testicular germ cell tumors (TGCT) of adolescents and adults and two metastatic residual tumors after chemotherapeutic treatment. The results were compared with karyotypic data obtained form the same tumor specimens after direct harvesting of metaphases or short-term in vitro culture. Both techniques revealed that the most co...

2005
Sonal R. Bakshi Shambhu K. Roy Pina J. Trivedi Manisha M. Brahmbhatt Shwetal M. Rawal Purvi M. Kakadia Samarth S. Bhatt

Total or partial duplication of chromosome 1q and whole arm translocation can result from unbalanced translocation of chromosomes, isochromosomes or jumping translocations. These structural rearrangements are reported as secondary aberrations associated with tumor progression, and advanced disease. Partial duplication of 1q resulting from der(18)t(1;18)(q12;p11) has been reported in Fanconi ane...

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