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Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP
Fragile X mGluR MPEP audiogenic seizures open field fmr1
2015/8/3
Fragile X Syndrome is the most common form of inherited mental retardation worldwide. A Fragile X mouse model, fmr1, with a disruption in the X-linked Fmr1 gene, has three substantial deficits observe...
Association Between Sarcopenia-Related Phenotypes and Aerobic Capacity Indexes of Older Women
Sarcopenia VO peak muscle strength elderly cardiorespiratory fitness peak torque
2015/4/23
The purpose of the present study was to examine the association between fat-free mass (FFM), quadriceps strength and sarcopenia with aerobic fitness indexes of elderly women. A total of 189 volunteers...
Macrophage phenotypes correspond with remodeling outcomes of various acellular dermal matrices
Acellular Dermal Matrix Derma Matrix AlloDerm Integra Derm Acell
2013/1/31
Macrophages have recently been characterized as having an M1 or M2 phenotype based on receptor expression, mechanism of activation and function. The effects of macrophage phenotype upon tissue remodel...
DIFFERENT PHENOTYPES OF INTERMITTENT AND PERSISTENT RESPIRATORY ALLERGY IN ZAGREB, CROATIA
airborne pollen allergic rhinitis asthma prevalence
2010/12/22
Allergic rhinitis (AR) is a major chronic respiratory disease because of its
prevalence, its impacts on the quality of life, economic burden and links with asthma.A signifi cant relationship between ...
Adiponectin and adiponectin receptor gene variants in relation to resting metabolic rate, respiratory quotient, and adiposity-related phenotypes in the Québec Family Study1,2,3
Adiponectin adiponectin receptor resting metabolic rate respiratory quotient obesity abdominal obesity
2008/12/12
Background: Despite adiponectin's presumed role in fatty acid oxidation and energy homeostasis, little is known about the effect of gene variants on substrate oxidation, energy expenditure, and adipos...
Omenn Syndrome—Review of Several Phenotypes of Omenn Syndrome and RAG1/RAG2 Mutations in Japan
immunodeficiency Japan Omenn syndrome RAG1 RAG2 mutation
2010/11/18
Omenn syndrome (OS) is a form of severe combined immunodeficiency (SCID) characterized by erythrodermia, hepatosplenomegaly, lymphadenopathy, and alopecia. In patients with OS, B cells are mostly abse...
Study of α1-Antitrypsin Phenotypes Frequencies in Patients with Primary Antibody Deficiency
Allele Alpha-1-Antitrypsin Antibody Deficiency Bronchiectasis
2010/2/3
Primary antibody deficiencies are the most frequent primary immunodeficiency disorders. Bronchiectasis as a feature of these disorders may be developed due to some factors such α-1-antitrypsin deficie...
Arsenic Trioxide Compound Modulates Multiple Myeloma Phenotypes: Assessment on Cell Line Models
Multiple myeloma Karpas 707 MMP-2 Angiogenesis Apoptosis Cytotoxicity Arsenic trioxide
2010/2/3
Recent evidences suggest that multiple myeloma phenotypes (MMPs) are involved in the infiltration of multiple myeloma-affected marrow foci. In this study, the effects of arsenic trioxide on the invasi...
Chronic Mucocutaneous Candidiasis; Report of Three Cases with Different Phenotypes
Candidia Chronic Mucocutaneous Candidiasis Immunologic Deficiency Syndromes
2010/2/3
Despite the fact that higher BMI is a risk factor for, wheeze ever, wheeze and dyspnea in the last 12 months, and diagnosed asthma, higher BMI is not a risk factor for obstructive pattern in pulmonary...