نتایج جستجو برای: memory de duplication

تعداد نتایج: 1802836  

Journal: :Journal of Information Processing and Management 2003

2010
Naomi R. Stevens Jeroen Dobbelaere Kathrin Brunk Anna Franz Jordan W. Raff

In Caenorhabditis elegans, five proteins are required for centriole duplication: SPD-2, ZYG-1, SAS-5, SAS-6, and SAS-4. Functional orthologues of all but SAS-5 have been found in other species. In Drosophila melanogaster and humans, Sak/Plk4, DSas-6/hSas-6, and DSas-4/CPAP-orthologues of ZYG-1, SAS-6, and SAS-4, respectively-are required for centriole duplication. Strikingly, all three fly prot...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه فردوسی مشهد - دانشکده ادبیات و علوم انسانی دکتر علی شریعتی 1391

ce memoire presente une etude du theme de la solitude de lhomme dans trois oeuvres noires de jean anouilh: antigone, la sauvage, le voyageur sans bagage. lobjectif est dexpliquer les approches de jean anouilh sur les conditions sociales de lhomme daujourdhui qui se revelent par le theme de la solitude. cette etude comprend cinq chapitres: le premier explique la solitude volontaire et egalement ...

بسکابادی, علی, حشمتی فر, نرجس, خامنه باقری, آرش, علیخواه, لیلا, منصوری, مسلم,

Complete duplication of the bladder and urethra is a very rare congenital anomaly which is diagnosed either shortly after birth or during early childhood. These rare malformations are usually seen by other concomitant anomalies, especially in the genital area, large intestine and skeletal system. Complete duplication often occurs in the coronal and sagittal planes and may emerge as complete or ...

Journal: :Revue italienne d’études françaises 2012

2017
Anne Benoit Aurélien Cavelan Franck Cappello Padma Raghavan Yves Robert Hongyang Sun

This paper provides a model and an analytical study of replication as a technique to detect and correct silent errors, as well as to cope with both silent and fail-stop errors on large-scale platforms. Fail-stop errors are immediately detected, unlike silent errors for which a detection mechanism is required. To detect silent errors, many application-specific techniques are available, either ba...

Ali Babaei, Attiyeh Vasaghi Mojtaba Habibagahi Tahereh Talaei-Khozani, Zahra Vojdani

Objective(s): Umbilical cord blood is a good source of the mesenchymal stem cells that can be banked, expanded and used in regenerative medicine.  The objective of this study was to test whether amniotic membrane extract, as a rich source of growth factors such as basic-fibroblast growth factor, can promote the proliferation potential of the umbilical cord mesenchymal stem cells. Materials and ...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تبریز 1390

le mythe gémellaire a pour fonction de montrer la dualité dans l’homme. dualité qui est la conséquence de rivalité, de jalousie, d’amour et de haine, mais cette dualité constitue les notions de la mortalité et l’immortalité. michel tournier actualise le thème de la dualité et lui procure un contenu nouveau. prise dans les paradigmes astreignants, l’histoire de jean-paul commençait par de sombre...

2013
Nora Urraca Julie Cleary Victoria Brewer Eniko K Pivnick Kathryn McVicar Ronald L Thibert N Carolyn Schanen Carmen Esmer Dustin Lamport Lawrence T Reiter

Chromosomal copy number variants (CNV) are the most common genetic lesion found in autism. Many autism-associated CNVs are duplications of chromosome 15q. Although most cases of interstitial (int) dup(15) that present clinically are de novo and maternally derived or inherited, both pathogenic and unaffected paternal duplications of 15q have been identified. We performed a phenotype/genotype ana...

2014
Carolina Sanchez-Jimeno Ana Bustamante-Aragonés Fernando Infantes-Barbero Marta Rodriguez De Alba Carmen Ramos María Jose Trujillo-Tiebas Isabel Lorda-Sánchez

KEY CLINICAL MEASSAGE Patients with rare deletions in 16q12 and a duplication of 17p, both interstitial and de novo. Only seven cases have been described with these deletions and none of them presented other chromosomal abnormalities. The proband showed a complex phenotype with features found in patients with dup17p11.2 syndrome, deletions in 16q12.

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