Results 141 to 150 of about 272,419 (371)
Classical swine fever and foot-and-mouth disease in Lao PDR [PDF]
Approximately 75% of the population of Lao PDR is engaged in agriculture and the vast majority (approximately 90%) of these producers are in the smallholder sector.
Conlan, J., Khounsy, S.
core +1 more source
Construction of New Genetically Engineered Vaccine Strain for O-type Foot-and-Mouth Disease of Pig [PDF]
Foot-and-mouth disease is an acute and highly contagious viral infectious disease. Although the foot and mouthdisease vaccine has been applied in some parts of the world since the beginning of the 20th century, the currentepidemic of foot and mouth ...
Feifei, Liu
core +2 more sources
ABSTRACT SETD2 has an essential role in epigenetic regulation. SETD2 pathogenic variants cause neurodevelopmental disorders (SETD2‐NDDs) that most commonly include various degrees of intellectual disability and behavioral disorders, macrocephaly, brain malformations, and generalized overgrowth.
Marie Lucain+11 more
wiley +1 more source
Snap and Diagnose: An Advanced Multimodal Retrieval System for Identifying Plant Diseases in the Wild [PDF]
Plant disease recognition is a critical task that ensures crop health and mitigates the damage caused by diseases. A handy tool that enables farmers to receive a diagnosis based on query pictures or the text description of suspicious plants is in high demand for initiating treatment before potential diseases spread further.
arxiv
The survival of foot-and-mouth disease virus in meat and offal [PDF]
W. M. Henderson, J. B. Brooksby
openalex +1 more source
Hubungan Antara Pengetahuan Dengan Sikap Pencegahan Hand, Foot and Mouth Disease (Hfmd) Pada Ibu Balita Di Perengdawe Desa Balaicatur Gamping Sleman [PDF]
Latar Belakang:Menurut data WHO,2012 penyebaran HFMD (hand, foot and mouth disease) pada Balita terjadi di beberapa negara,penyakit ini menginfeksi 104 anak-anak dalam 3,5 bulan.
Handayani, S. (Sri)
core
A New EP300‐Related Syndrome With Prominent Developmental and Immune Phenotypes
ABSTRACT Rubinstein Taybi syndrome (RTS) is a disorder of chromatin remodeling and transcriptional regulation caused by heterozygous pathogenic variants in CREBBP and EP300. RTS is characterized by a distinct facial gestalt, intellectual disability, structural kidney and heart differences, feeding difficulties, and broad thumbs and great toes ...
Devi Priyanka Maripuri+3 more
wiley +1 more source
STUDIES ON THE PHYSICAL AND CHEMICAL PROPERTIES OF THE VIRUS OF FOOT-AND-MOUTH DISEASE [PDF]
Peter K. Olitsky, Louis Boëz
openalex +1 more source
ABSTRACT Prader‐Willi syndrome (PWS) is a neurodevelopmental disorder typically caused by large deletions or imprinting defects on chromosome 15q11.2, encompassing multiple genes. While the contribution of individual genes to the PWS phenotype remains unclear, previous studies suggested that isolated deletions of MAGEL2, NDN, and MKRN3, excluding the ...
Jannis Buecking+6 more
wiley +1 more source