Results 141 to 150 of about 2,137 (185)

Epizootological Survey and Identification of Helminth Fauna in Golden Jackals (<i>Canis aureus</i>) from Southern Kazakhstan. [PDF]

Biology (Basel)
Suleimenov M, Uakhit R, Berkinbay O, Omarov B, Zhanteliyeva L, Jussupbekova N, Baimukhanbetov Y, Khamchukova A, Manapov N, Alash A, Kiyan V.   +10 more
europepmc   +1 more source

Indigenous knowledge, forest landscape modeling, and the cumulative effects of environmental changes. [PDF]

Ecol Appl
Bélisle AC, Mantyka-Pringle C, Boulanger Y, Croteau B, Wapachee A, Drapeau LJ, Desrochers M, Asselin H.   +7 more
europepmc   +1 more source

Genetic variability and population structure analysis of Protostrongylus oryctolagi (Nematoda: Protostrongylidae) in Lepus europaeus from Central and Northern Italy. [PDF]

PLoS One
Guarniero I, Stancampiano L, Franch R, Armaroli E, Macchioni F, Negrisolo E.   +5 more
europepmc   +1 more source

Case Report With Biallelic Variants in GCNT2 Implicates Exon 1B in Congenital Cataracts

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT GCNT2‐related cataracts is a disorder characterized by bilateral congenital cataracts (CC) of various types (with or without the adult i blood phenotype) and is caused by biallelic variants in GCNT2, which has 3 major isoforms, differentiated by alternative splicing of the first exon (known as exon 1A, B, and C).
Audrey O'Neill, Cindy Bayer, Emily McQuillen, Erica D. Smith, Meghan Towne, Dallas Reed   +5 more
wiley   +1 more source

Blackfoot legal traditions, treaty-making, and non-territorial forms of settler jurisdiction? Niitsitapi oral histories of Treaty 7. [PDF]

Environ Plan D
Fabris M.
europepmc   +1 more source

A Systematic Review of Adverse Childhood Experiences and Epigenetic Age Acceleration in Later Adult Life Measured With Second and Third‐Generation Epigenetic Clocks

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT We examined the relationship between adverse childhood experiences (ACEs) and epigenetic age acceleration (EAA) in adulthood as measured by second and third generation epigenetic clocks by performing a systematic review of the literature. The electronic databases MEDLINE and EMBASE were searched on 17 July 2023.
Matthew Green, Laura Horsfall, Azam Saied   +2 more
wiley   +1 more source

Brucella suis in feral pigs in Australia: what is the risk? [PDF]

Aust Vet J
Kneipp CC, Marshall D, Westman ME, Malik R, Stevenson MA, Mor SM, Wiethoelter AK.   +6 more
europepmc   +1 more source

Genetic and Phenotypic Features of the Five Known Polyaminopathies: A Critical Narrative Review

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Polyaminopathies are a recently described family of rare genetic neurodevelopmental disorders. Polyaminopathies disrupt the biosynthesis of the primary polyamines: putrescine, spermidine, and spermine. Snyder–Robinson syndrome results from hemizygous loss‐of‐function variants in the spermine synthase (SMS) gene, resulting in decreased or ...
Elizabeth A. VanSickle, Sara M. Sarasua, Tracy Lowe, Christopher L. Farrell, Luigi Boccuto, Charles Schwartz, Anthony E. Pegg, Angela Peron, Victor Faundes, Mythily Ganapathi, Wendy K. Chung, Alban Ziegler, Floris Hofstede, Clément Prouteau, Katharina Steindl, Colleen Olson, Orrin Devinsky, Teresa L. Mastracci, Robert A. Casero Jr., Tracy Murray Stewart, Susan Gilmour, Teri Koerner, Mary Jo Kutler, Surender Rajasekaran, Julianne Michael, André S. Bachmann, Caleb P. Bupp   +26 more
wiley   +1 more source

Inheritance of Material Wealth in a Natural Population. [PDF]

Ecol Lett
Ålund M, McFarlane SE, Husby A, Knape J, Pärt T, Sirkiä P, Weissing FJ, Wheatcroft D, Zhu Y, Qvarnström A.   +9 more
europepmc   +1 more source

Marfan Syndrome Associated With Intellectual Disability and Behavioral Anomalies: Further Evidence for the Effect of Compound Heterozygous Variants in FBN1 on Phenotypic Severity

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Marfan syndrome (MFS) is a rare connective tissue disorder characterized by involvement of the cardiovascular, ocular, and musculoskeletal systems. Pathogenic variants in FBN1 cause most of the MFS cases; however, intellectual disability (ID) is rarely observed. A non‐consanguineous Pakistani family with four affected individuals was recruited.
Azmatullah Khan, Naseebullah Kakar, Ainullah Kakar, Malte Spielmann, Sajid Malik   +4 more
wiley   +1 more source