Results 161 to 170 of about 469,727 (275)

Editorial

International Journal of Racket Sports Science, 2020
Adrian Lees
doaj  

Editorial: Multidisciplinary aspects and performance in racket sports, volume II. [PDF]

Front Psychol
Martínez-Gallego R, Sánchez-Alcaraz Martínez BJ, Vuckovic G, Ramón-Llin J.   +3 more
europepmc   +1 more source

IKAROS Associated Immunodeficiency and Thrombotic Thrombocytopenic Purpura

Pediatric Blood &Cancer, Volume 73, Issue 2, February 2026.
ABSTRACT Pathogenic variants in IKZF1 (IKAROS) are linked to immunodeficiency, malignancy, and immune dysregulation. We describe a family with a rare IKZF1 variant presenting with humoral immunodeficiency and thrombotic thrombocytopenic purpura (TTP). A non‐consanguineous family was clinically monitored; clinical, immunological, and genetic data (exome
Ilia Spivak, Daniella Magen, Karin Weiss, Tamar Paperna, Suhair Hanna, Amos Etzioni, Adi Miller‐Barmak, Yonatan Butbul Aviel   +7 more
wiley   +1 more source

Diagenetic and Hydrothermal Processes Produce Heavy Molybdenum Isotope Signatures in Pelagic Sediments of the North and South Pacific

Geochemistry, Geophysics, Geosystems, Volume 27, Issue 2, February 2026.
Abstract Molybdenum isotopes (δ98Mo) have been used for more than two decades to investigate past‐ocean redox conditions due to the distinct behavior of this element in oxic and anoxic environments. The oxic sink is generally accepted to have a near‐constant δ98Mo value of −0.7‰, a value derived primarily from the δ98Mo signatures of Fe–Mn crusts and ...
P. L. Fraga‐Ferreira, C. Siebert, M. Frank, F. Scholz   +3 more
wiley   +1 more source

Missense Variants in the Second Transmembrane Domain of TMEM17 Disrupt Its Stability and Function and Lead to a Wide Phenotypic Spectrum of Ciliopathies

Clinical Genetics, Volume 109, Issue 2, Page 305-315, February 2026.
Missense variants in TMEM17 disrupt its localization and function at the ciliary transition zone, leading to a wide range of ciliopathy phenotypes, from OFD6 and Joubert syndromes to Meckel syndrome. ABSTRACT Ciliopathies are rare genetic disorders characterized by significant genetic and phenotypic variability.
Lucile Boutaud, Chunmei Li, Candice Moncler, Laure Verlin, Meriem Garfa‐Traoré, Nicolas Bourgon, Dhruvin Akbari, Jeanne Porée, Valentina Serpieri, Marine Panza, Lynda Haddad, Patrick Nitschké, Jacqueline Aziza, Cristina Matt, Enza Maria Valente, Patricia Gargallo, Charlotte Dubucs, Tania Attié‐Bitach, Michel R. Leroux, Sophie Thomas   +19 more
wiley   +1 more source

Internet corporate blackmail: a growing problem [PDF]

, 2004
Griffiths, MD
core  

Rethinking the Rule of Reason: From Professional Engineers to NCAA [PDF]

, 1984
Wertheimer, Barry
core   +1 more source

Is knee extension strength a key factor in badminton-specific agility among elite players? [PDF]

Front Sports Act Living
Nakashima H, Ando R, Kameda M, Tamai S, Iizuka T, Hoshikawa Y, Nakamura M.   +6 more
europepmc   +1 more source

Pelvis-Trunk coordination strategies differ a cross preparatory court movement distances during the tennis forehand. [PDF]

PeerJ
Meng X, Kim Y, Wang S, Kim S, Li M.
europepmc   +1 more source

Table Tennis in Physical Education: Teachers' Perceptions of Health-Related Aspects in School-Age Children. [PDF]

Behav Sci (Basel)
Ortega-Zayas MÁ, Patanè P, Peñarrubia-Lozano C, Pradas F.   +3 more
europepmc   +1 more source