نتایج جستجو برای: q14

تعداد نتایج: 206  

Journal: :Haematologica 2002
Josep F Nomdedéu Adriana Lasa Josep Ubeda Giuseppe Saglio Mar Bellido Sílvia Casas Maria J Carnicer Anna Aventín Anna Sureda Jorge Sierra Montserrat Baiget

BACKGROUND AND OBJECTIVES Deletions at the long arm of chromosome 13, mostly at the q14, and monosomy of chromosome 13 are described to be common in multiple myeloma (MM). 13q- has been associated with an adverse outcome and it has been proposed as one of the most important prognostic factors for MM patients. Deletions of 13q14 are rare in monoclonal gammopathy of undetermined significance (MGU...

2017
Osamu Imataki Makiko Uemura Shumpei Uchida Shigeyuki Yokokura Akihiro Takeuchi Ryo Ishikawa Akihiro Kondo Kayoko Seo Norimitsu Kadowaki

BACKGROUND A small number of rhabdomyosarcoma (RMS) cases involve the bone marrow. A leukemic presentation of RMS has been reported in a few case series, although almost all cases of leukemic RMS are not completely mimicking leukemia. We encountered a case with RMS cell infiltration of the bone marrow that resembled floating hematological cells. CASE PRESENTATION We encountered a rare case of...

2016
David Chisnall Justus Matthiesen Kayvan Memarian Peter Sewell Robert N. M. Watson

2 Abstract Pointers 7 2.1 Pointer Provenance . . . . . . . . . . . . . 7 2.1.1 Q1. Must the pointer used for a memory access have the right provenance, i.e. be derived from the pointer to the original allocation (with undefined behaviour otherwise)? (This lets compilers do provenance-based alias analysis) . . 7 2.1.2 Q2. Can equality testing on pointers be affected by pointer provenance informa...

2009
Conrad S. Tucker Harrison M. Kim Douglas E. Barker Yuanhui Zhang

Q1 Should RELIEFF be set as ReliefF as in other sources? See throughout article. Q2 Please supply date of meeting, place of publication, name of publisher and page numbers. Q3 Please supply date and place of symposium, place of publication and name of publisher. Q4 Please clarify publication details. Q5 Please supply place of publication. Q6 Please supply place of publication. Q7 Please supply ...

2015
Jian Li Chongguang Li Jean-Paul Chavas Jean Paul Chavas

The last decade has witnessed different price trajectories in the international and Chinese agricultural commodity markets. This paper compares and contrasts these dynamic patterns between markets from the perspective of price bubbles. A newly developed right-tailed unit root testing procedure is applied to detect price bubbles in the CBOT and Chinese agricultural futures market during the peri...

2012
Christopher John Jackson Meilang Xue

Protein C is a vitamin K–dependent zymogen, discovered in 1976 in bovine plasma (Stenflo, 1976). It is derived from the human PROC gene on chromosome 2 (2q13-q14) which contains 9 exons (Rezaie, 1993). Post-translational modifications include -hydroxylation at Asp71, N-linked glycosylation at residues 97, 248, 313 and 329 and ┛-carboxylation of 9 glutamic acid residues which forms the Gla doma...

2017
Hye-Young Lee Chan-Jeoung Park Enkyung You Young-Uk Cho Seongsoo Jang Eul-Ju Seo

Dear Editor, The association of CLL with hematologic malignancies such as AML is relatively rare [1, 2], with mostly associated with prior cytotoxic chemotherapy [3]. Few reports of untreated CLL manifesting with or followed by AML suggested that each tumor probably evolved from simultaneous expansion of two independent clones, not a common clone [1]. Concomitant AML and CLL having a common clo...

2016
Andrew D. Hollenbach

a disease that afflicts individuals regardless of age. It may occur in children, adolescents, or young adults who are born with genetic mutations that predispose them to the disease. It also occurs in the elderly where a lifetime of exposure to environmental or age-related stressors facilitates the acquisition of oncogenic mutations. Regardless of the age of onset, cancer is a multifaceted and ...

Journal: :Journal of medical genetics 2002
M G Butler D Bittel Z Talebizadeh

Prader-Willi syndrome (PWS) is characterised by infantile hypotonia, feeding difficulties, hypogonadism, small hands and feet, mental deficiency, obesity in early childhood, a particular facial appearance, and a paternally derived 15q11-q13 deletion (approximately 4 million bp in size) in about 70% of subjects, maternal disomy 15 (both 15s from the mother) in 25% of subjects, or an imprinting m...

2010
Dale S Cannon Judith S Miller Reid J Robison Michele E Villalobos Natalie K Wahmhoff Kristina Allen-Brady William M McMahon Hilary Coon

BACKGROUND It has been suggested that efforts to identify genetic risk markers of autism spectrum disorder (ASD) would benefit from the analysis of more narrowly defined ASD phenotypes. Previous research indicates that 'insistence on sameness' (IS) and 'repetitive sensory-motor actions' (RSMA) are two factors within the ASD 'repetitive and stereotyped behavior' domain. The primary aim of this s...

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