Results 91 to 100 of about 53,826 (301)

Molecular Profiling of Genes Associated With Methylphenidate Pathway Therapy and Discovery of New Variants in Amazonian Amerindian Populations

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT In Attention Deficit Hyperactivity Disorder (ADHD), methylphenidate is one of the most widely used drugs, in which patient response significantly impacts prognosis. This study aimed to characterize the molecular profile of 10 genes associated with methylphenidate therapy.
Aline Pasquini Santos, Tatiane Carinta de Souza, Kaio Evandro Cardoso Aguiar, Ana Caroline Alves da Costa, Natasha Monte, Juliana Carla Gomes Rodrigues, Giovanna Gilioli da Costa Nunes, Rita de Cássia Calderaro Coelho, Ândrea Ribeiro‐dos‐Santos, André Maurício Ribeiro dos Santos, Sandro José de Souza, Sidney Emanuel Batista dos Santos, Rommel Mario Rodriguez Burbano, Marianne Rodrigues Fernandes, Ney Pereira Carneiro dos Santos   +14 more
wiley   +1 more source

Oceanus. [PDF]

, 1973
v.
Woods Hole Oceanographic Institution.
core   +1 more source

Genetic Risk and High Burden of Depression and Suicide in the Maya‐Mestizo Population of Yucatán, México

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT Major depression and suicide are critical public health concerns, particularly in underrepresented populations with unique genetic and sociocultural contexts. The Maya‐mestizo population presents the highest suicide rates in the country but remains understudied in psychiatric genetics. This study evaluated the association between three genetic
Marta Menjivar, Erandi Bravo, Margarita Rivera‐Balancan, Barbara Itzel Pena Espinoza   +3 more
wiley   +1 more source

Deep-water macroalgae from the Canary Islands: new records and biogeographical relationships [PDF]

, 1993
Due to the geographical location and paleobiogeography of the Canary Islands, the seaweed flora contains macroalgae with different distributional patterns.
A. B. Joly, A. M. Breeman, A. Vickers, C. A. Maggs, C. D. Amsler, C. Hoek van den, C. W. Schneider, C. W. Schneider, D. G. Müller, E. Serrao, F. Børgesen, F. Børgesen, F. Børgesen, F. Børgesen, F. Børgesen, F. Børgesen, G. J. Vermeij, G. J. Vermeij, G. W. Lawson, H. Rietema, J. Afonso-Carrillo, J. Afonso-Carrillo, J. Feldmann, J. H. Price, K. Lüning, L. Ballantine, M. C. Gil-Rodríguez, M. D. Hanisak, M. J. Wynne, M. Kajimura, M. M. Littler, M. Sansón, P. A. J. Audiffred, P. Huvé, R. B. Searles, R. B. Searles, R. B. Searles, R. E. Norris, R. Herrera, R. J. Haroun, S. Fredericq, S. Hiscock, W. F. Prud'homme van Reine, W. F. Prud'homme van Reine, W. F. Prud'homme van Reine, W. F. Prud'homme van Reine, W. R. Taylor, W. R. Taylor, W. R. Taylor   +48 more
core   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Oceans governance in the Arctic [PDF]

, 2008
Global warming is bringing rapid change to the Arctic. The melting of sea ice and glaciers is increasing faster than scientists predicted even a year ago.
de La Fayette, Louise Angélique
core   +1 more source

Genome Sequencing in 19 Families With Bladder Exstrophy and Epispadias Complex Indicates Involvement of the ADGR‐Gene Family

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Bladder exstrophy and epispadias complex (BEEC) is one of the most severe congenital malformations of the urogenital tract, significantly impacting continence, sexual function, and renal function. To date, the only recurrent genetic aberration identified is the 22q.11.2 microduplication, but several candidate regions and genes including ...
Agneta Nordenskjöld, Samara Alm, Jesper Eisfeldt, Jia Cao, Magnus Anderberg, Gillian Barker, Hans Matsson, Gundela Holmdahl, Anna Lindstrand, Kristina Lagerstedt‐Robinson   +9 more
wiley   +1 more source

Neurodevelopmental and Psychiatric Studies in Children and Adolescents With Neurofibromatosis Type I: A Comprehensive Scoping Review

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT A comprehensive synthesis of the broad range of neurodevelopmental and psychiatric manifestations in NF1 is needed to identify knowledge gaps and future directions for NF1 research. In the following scoping review, we identify and summarize the scope of research that examines neurodevelopmental and psychiatric manifestations, both as ...
Meera Chopra, Tin‐Suet Joan Lee, Jacob Vorstman, Patricia Parkin, Louise Gallagher, Aneta Krakowski   +5 more
wiley   +1 more source

Anatomy and origin of authochthonous late Pleistocene forced regression deposits, east Coromandel inner shelf, New Zealand: implications for the development and definition of the regressive systems tract [PDF]

, 2004
High-resolution seismic reflection data from the east Coromandel coast, New Zealand, provide details of the sequence stratigraphy beneath an autochthonous, wave dominated inner shelf margin during the late Quaternary (0-140 ka). Since c.
Bard E., Bard E., Bond G., Bradshaw B. E., Bradshaw B. E., Browne G. H., Chappell J., Chiocci F. L., Dansgaard W., Davis R. A., Emery D., Hart B. S., Haywick D. W., Hernández‐Molina F. J., Hunt D., Hunt D., Kitamura A., Kolla V., Kolla V., Marks G. P., Marshall J. F., Martinson D. G., Mellere D., Mitchum R. M., Morton R. A., Naish T., Nummedal D., Plint A. G., Plint A. G., Plint A. G., Plint A. G., Pomar L., Posamentier H. W., Posamentier H. W., Posamentier H. W., Roy P. S., Roy P. S., Saul G., Schofield J. C., Shackleton N. J., Tesson M. R., Thom B. G., Thom B. G., Thom B. G., Thrasher G. P., Trincardi F., Vail P. R., Van Wagoner J. C., Van Wagoner J. C., Wright I. C., Wright I. C.   +50 more
core   +2 more sources

Participatory Policy Development: Reflections on Designing the Strong Roots for Our Futures Program in Victoria

Australian Journal of Social Issues, EarlyView.
ABSTRACT In this paper, we trace the journey to create the Strong Roots for our Futures Program, a government program to resource and support Traditional Owners to undertake a range of activities in areas where no state recognition existed. We provide a background to state recognition in Victoria before considering the program design, leading to an ...
Nell Reidy, Bhiamie Williamson, Jesse Williams   +2 more
wiley   +1 more source