نتایج جستجو برای: chromosome 14

تعداد نتایج: 471848  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Laksana Kantama Timothy F Sharbel M Eric Schranz Thomas Mitchell-Olds Sacco de Vries Hans de Jong

We conducted a cytogenetic study of sexual lines of Boechera stricta and Boechera holboellii (2n = 14) and seven diploid apomictic accessions of their interspecific hybrid Boechera divaricarpa and B. holboellii (2n = 14 or 15). By studying chromosome morphology, rDNA repeats, genome painting, male meiosis, pollen morphology, and flow-cytometry seed screens, we revealed an unexpected plethora of...

Journal: :The Journal of heredity 1989
N S Ma D C Page T S Harris

Probe pDP1007, which contains highly conserved DNA sequences from the sex-determining region of the human Y chromosome, cross-hybridized with owl monkey EcoRI restriction fragments of 1.8 kb and 6.6 kb. Southern transfer analysis of owl monkey (karyotype VI)--rodent somatic cell hybrids localized the 1.8-kb fragment on the owl monkey X chromosome and the 6.6-kb fragment, which is male specific,...

Journal: :Blood 1978
R Levitt R V Pierre W L White R G Siekert

We observed two sisters with ataxia telangiectasia, one of whom developed an atypical subacute lymphocytic leukemia characterized by atypical lymphocytes and absence of palpable lymphadenopathy or hepatosplenomegaly. The lack of organomegaly in this patient may have been due to the underlying ataxia telangiectasia, which was associated with lymphoid hypoplasia. Cytogenetic studies showed a mark...

Journal: :Cancer research 2002
Linda M Sargent Jamie R Senft David T Lowry Amy M Jefferson Frederick L Tyson Alvin M Malkinson Allen E Coleman Steven H Reynolds

Although adenocarcinoma is rapidly becoming the most common form of lung cancer in the United States, the difficulty in obtaining lung cancer families and representative samples of the various stages of adenocarcinoma progression has led to intense study of mouse models. As a powerful approach to delineating molecular changes, we have analyzed 15 early-passage mouse cell lines by spectral karyo...

Journal: :Genome research 2013
Giuliana Giannuzzi Michele Pazienza John Huddleston Francesca Antonacci Maika Malig Laura Vives Evan E Eichler Mario Ventura

Ape chromosomes homologous to human chromosomes 14 and 15 were generated by a fission event of an ancestral submetacentric chromosome, where the two chromosomes were joined head-to-tail. The hominoid ancestral chromosome most closely resembles the macaque chromosome 7. In this work, we provide insights into the evolution of human chromosomes 14 and 15, performing a comparative study between mac...

2012
Oleg S. Alexandrov Mikhail G. Divashuk Nikolay A. Yakovin Gennady I. Karlov

Humulus japonicus Siebold et Zucc (Japanese hop) is a dioecious species of the family Cannabaceae. The chromosome number is 2n = 16 = 14 + XX for females and 2n = 17 = 14 + XY1Y2 for male. To date, no fluorescence in situ hybridization (FISH) markers have been established for the identification of Humulus japonicus sex chromosomes. In this paper, we report a method for the mitotic and meiotic s...

2017
Berardo Rinaldi Alessandro Vaisfeld Sergio Amarri Chiara Baldo Giuseppe Gobbi Pamela Magini Erto Melli Giovanni Neri Francesca Novara Tommaso Pippucci Romana Rizzi Annarosa Soresina Laura Zampini Orsetta Zuffardi Marco Crimi

BACKGROUND Ring chromosome 14 syndrome is a rare chromosomal disorder characterized by early onset refractory epilepsy, intellectual disability, autism spectrum disorder and a number of diverse health issues. RESULTS The aim of this work is to provide recommendations for the diagnosis and management of persons affected by ring chromosome 14 syndrome based on evidence from literature and exper...

Journal: :Haematologica 2003
Sophie Gazzo Lucile Baseggio Lionel Coignet Chantal Poncet Dominique Morel Bertrand Coiffier Pascale Felman Françoise Berger Gilles Salles Evelyne Callet-Bauchu

BACKGROUND AND OBJECTIVES Whole or partial trisomy 3 represents the most recurrent chromosomal abnormality occurring in marginal zone B-cell lymphoma (MZBCL), a distinct subtype of B-cell non-Hodgkin's lymphoma (NHL). By conventional cytogenetic analysis, unbalanced translocations involving chromosome 3 and leading to a partial trisomy 3q were identified in a series of 14 MZBCL patients. Fluore...

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