Results 71 to 80 of about 3,804 (178)
Individual variation in animal communication: from species averages to unique voices
Biological Reviews, Volume 100, Issue 6, Page 2625-2640, December 2025.ABSTRACT The comparative study of communicative behaviour in non‐human animals, especially primates, has yielded crucial insights into the evolution of human language. This research, mostly focused on the species and population level, has improved our understanding of the various socio‐ecological factors that shape communication systems.
Angèle Lombrey, Marlen Fröhlich
wiley +1 more source
Molecular Ecology, Volume 34, Issue 24, December 2025.ABSTRACT Humans have relied on animal fur for centuries, yet fur farming only began recently during the mid‐19th Century. Little is known about this incipient domestication or the genomic processes involved. Domestication may involve founder effects, population bottlenecks and low population size, which, when combined with intense artificial selection,
Christopher A. Cockerill +22 more
wiley +1 more source
International Medical Case Reports Journal, 2023 Kartika Ruchiatan, Noer Olivy Alifiar, Diah Puspitosari, Reti Hindritiani Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran - Dr.
Ruchiatan K +3 more
doaj
PTPN11 Mutations in LEOPARD Syndrome: Report of Four Cases in Taiwan
Journal of the Formosan Medical Association, 2009 LEOPARD syndrome (LS) is a rare, autosomal dominant disorder. The typical clinical presentation includes multiple lentigines and cardiac defects. Mutation analysis of the PTPN11 gene is feasible.
I-Shou Lin +4 more
doaj +1 more source
, 2017 LEOPARD syndrome is an autosomal dominantly inherited multiple congenital anomaly syndrome with high penetrance and a markedly variable expression.
정기양, 조영훈
core
The culture of JACMP, the sanctity of editorial independence, and why your ego is not your amigo
Journal of Applied Clinical Medical Physics, Volume 26, Issue 12, December 2025.
Michael D. Mills
wiley +1 more source
, 2010 SummaryThe tyrosine phosphatase SHP2 (PTPN11) regulates cellular proliferation, survival, migration, and differentiation during development. Germline mutations in PTPN11 cause Noonan and LEOPARD syndromes, which have overlapping clinical features ...
Hurley, Aeron D. +10 more
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Severe, early onset hypertrophic cardiomyopathy in a family with LEOPARD syndrome [PDF]
, 2008 LEOPARD syndrome (multiple Lentigines, Electrocardiographic conduction abnormalities, Ocular hypertelorism, Pulmonic stenosis, Abnormal genitalia, Retardation of growth, and sensorineural Deafness) is a rare inherited disease. Mutations in the PTPN11 and
Anna Sarkozy +20 more
core
Syndrome de Leopard, distúrbio da crista neural: relato de um caso
Arquivos de Neuro-Psiquiatria, 1981 A síndrome de Leopard é uma condição autosoma dominante de variável expressão fenotípica. Uma minoria apenas dos pacientes apresenta todos os componentes da síndrome, ou seja, lentigenes múltiplas (L), alterações eletrocardiográficos (E), hipertelorismo ...
Marco Aurelio Lana Peixoto +4 more
doaj +1 more source
Juvenile Patient with LEOPARD Syndrome: Clinical Profile of a Genetically Confirmed Case. [PDF]
Ann Dermatol, 2023 Wan P, Cheng Y, Chen Z, Chen J.
europepmc +1 more source