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31,771 Newest Publications of WILEY
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Upper‐Room Ultraviolet Germicidal Irradiation (UVGI) for Air Disinfection A Symposium in Print
18-05-2013 | Edward Nardell, Richard Vincent, David H. Sliney, Photochemistry and Photobiology, 2013
This issue contains nine papers on the subject of upper‐room ultraviolet germicidal irradiation (UVGI) for control of hazards to health from airborne bio‐aerosols. These contributions originated from a two‐day “Symposium on Upper Room UVGI ‐ Toward International Application Guidelines” held ...
Oxidation of tyrosine photoinduced by pterin in aqueous solution
18-05-2013 | Carolina Castaño, M. Laura Dántola, Esther Oliveros, Andrés H. Thomas, Carolina Lorente, Photochemistry and Photobiology, 2013
Abstract Pterins, heterocyclic compounds widespread in biological systems, accumulate in the skin of patients suffering from vitiligo, a chronic depigmentation disorder. Pterins have been previously identified as good photosensitizers under UV‐A irradiation. In this work, we have ...
Cloning and characterization of luciferase from a Fijian luminous click beetle
18-05-2013 | Yasuo Mitani, Ryo Futahashi, Kazuki Niwa, Nobuyoshi Ohba, Yoshihiro Ohmiya, Photochemistry and Photobiology, 2013
Abstract Luminous click beetle is distributed almost exclusively in Central and South America with a single genus in Melanesia. Among these click beetles, the description of Melanesian species has been fragmentary, and its luciferase gene and phylogenetic relation to other click beetles ...
Commercial landscape of noninvasive prenatal testing in the United States
18-05-2013 | Ashwin Agarwal, Lauren C. Sayres, Mildred K. Cho, Robert Cook‐Deegan, Subhashini Chandrasekharan, Prenatal Diagnosis, 2013
ABSTRACT Cell‐free fetal DNA‐based noninvasive prenatal testing (NIPT) could significantly change the paradigm of prenatal testing and screening. Intellectual property (IP) and commercialization promise to be important components of the emerging debate about clinical implementation of ...
Fetal aneuploidy detection by maternal plasma DNA sequencing: a technology assessment
18-05-2013 | Judith M. E. Walsh, James D. Goldberg, Prenatal Diagnosis, 2013
ABSTRACT The American College of Obstetricians and Gynecologists currently recommends that all pregnant women be offered screening for chromosomal abnormalities, regardless of maternal age. Traditional screening tests have detection rates ranging from 85% to 90% and false‐positive rates ...
Severe Obstructive Sleep Apnea in Loeys–Dietz Syndrome Successfully Treated Using Continuous Positive Airway Pressure
18-05-2013 | Toshiki Takenouchi, Hideyuki Saito, Ryo Maruoka, Naoki Oishi, Chiharu Torii, Jun Maeda, Takao Takahashi, Kenjiro Kosaki, American Journal of Medical Genetics Part A, 2013
Abstract Loeys–Dietz syndrome is a recently recognized connective tissue disorder characterized by severe craniofacial and skeletal abnormalities as well as arterial tortuosity with aggressive aneurysm formation. Marfan syndrome, a classic connective tissue disorder, is known to be ...
Genome‐wide Association Mapping of Natural Variation in Odor‐guided Behavior in Drosophila
18-05-2013 | Elizabeth B. Brown, John E. Layne, Cheng Zhu, Anil G. Jegga, Stephanie M. Rollmann, Genes, Brain and Behavior, 2013
Abstract A defining goal in the field of behavioral genetics is to identify the key genes or genetic networks that shape behavior. A corollary to this goal is the goal of identifying genetic variants that are responsible for variation in the behavior. These goals are achieved by measuring ...
Characterization of X‐linked Hypohidrotic Ectodermal Dysplasia (XL‐HED) Hair and Sweat Gland Phenotypes Using Phototrichogram Analysis and Live Confocal Imaging
18-05-2013 | Kyle B. Jones, Alice F. Goodwin, Maya Landan, Kerstin Seidel, Dong‐Kha Tran, Jacob Hogue, Miquella Chavez, Mary Fete ..., American Journal of Medical Genetics Part A, 2013
Abstract Hypohidrotic ectodermal dysplasia (HED) is the most common type of ectodermal dysplasia (ED), which encompasses a large group of syndromes that share several phenotypic features such as missing or malformed ectodermal structures, including skin, hair, sweat glands, and teeth. ...
Genetic Heterogeneity in Type III Familial Cutaneous Syndactyly and Linkage to Chromosome 7q36
18-05-2013 | Mohammad M. Al‐Qattan, Hanan E. Shamseldin, Mohammed Al Mazyad, Saud Al Deghaither, Fowzan S. Alkuraya, American Journal of Medical Genetics Part A, 2013
Abstract The ZRS (zone of polarizing activity regulatory sequence) is a long‐range limb‐specific Sonic Hedgehog (SHH) enhancer. In humans, the ZRS is located in chromosome 7q36 within intron 5 of LMBR1; approximately 1 Mb telomeric of SHH. Point mutations and duplications of the ZRS lead ...
Mosaic Isochromosome 15q and Maternal Uniparental Isodisomy for Chromosome 15 in a Patient With Morbid Obesity and Variant PWS‐Like Phenotype
17-05-2013 | Jia‐Chi Wang, Mary Vaccarello‐Cruz, Leslie Ross, Renius Owen, Victoria M. Pratt, Katherine Lightman, Yan Liu, Katayo ..., American Journal of Medical Genetics Part A, 2013
Abstract Angelman and Prader–Willi syndromes are reciprocal imprinting disorders caused by loss of maternally or paternally expressed genes, respectively, within 15q11.2–q13. Angelman syndrome (AS; OMIM 105830) is a neurodevelopmental disorder and is due to the loss of maternally ...
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