نتایج جستجو برای: costello method

تعداد نتایج: 1630635  

2015

This bulletin is based on research conducted by Associate Professor Steven Rowley and Associate Professor Greg Costello at the AHURI Research Centre—Curtin University, Associate Professor David Higgins at the AHURI Research Centre—RMIT University, and Professor Peter Phibbs at the AHURI Research Centre—The University of Sydney. This research explored how property finance decisions are made and ...

Journal: :Journal of Medical Genetics 2003

2017
Leila Vahedi Noushin Sorkhkoh Azari Mohsen Moradi Jalal Gharesouran Maryam Rezazadeh

Background: Costello syndrome as a complex multi organ system anomalies caused by heterozygous de novo missense mutations in the proto oncogene HRAS which its product involved in controlling cell division and growth. Typical features that characterize this phenotype include distinctive coarse facial features, craniofacial anomalies, macrocephaly, low body mass gain, delayed development, short s...

Journal: :CoRR 2011
Erik Agrell

This documents lists some errors found in the second edition of Error Control Coding by Shu Lin and Daniel J. Costello.

Journal: :American journal of medical genetics. Part A 2014
Alice F Goodwin Snehlata Oberoi Maya Landan Cyril Charles Jessica C Massie Cecilia Fairley Katherine A Rauen Ophir D Klein

Costello syndrome (CS) is a RASopathy characterized by a wide range of cardiac, musculoskeletal, dermatological, and developmental abnormalities. The RASopathies are defined as a group of syndromes caused by activated Ras/mitogen-activated protein kinase (MAPK) signaling. Specifically, CS is caused by activating mutations in HRAS. Although receptor tyrosine kinase (RTK) signaling, which is upst...

Journal: :American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2011

Journal: :Disease models & mechanisms 2009
Cristina Santoriello Gianluca Deflorian Federica Pezzimenti Koichi Kawakami Luisa Lanfrancone Fabrizio d'Adda di Fagagna Marina Mione

Constitutively active, 'oncogenic' H-RAS can drive proliferation and transformation in human cancer, or be a potent inducer of cellular senescence. Moreover, aberrant activation of the Ras pathway owing to germline mutations can cause severe developmental disorders. In this study we have generated transgenic zebrafish that constitutively express low levels, or can be induced to express high lev...

Journal: :Journal of Medical Genetics 1993

Journal: :Dermatology Online Journal 2013

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