Zobrazeno 1 - 10
of 179
pro vyhledávání: '"Liang, Liang"'
Autor:
Liang L; Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences, Fourth Military Medical University, Xi'an 710032, China., Liang SQ; Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences, Fourth Military Medical University, Xi'an 710032, China., Qin HY; Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences, Fourth Military Medical University, Xi'an 710032, China., Ji Y; School of Basic Medical Sciences, Fourth Military Medical University, Xi'an 710032, China., Han H; Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences, Fourth Military Medical University, Xi'an 710032, China.
Publikováno v:
Yi chuan = Hereditas [Yi Chuan] 2015 Jun; Vol. 37 (6), pp. 599-604.
Publikováno v:
Hereditas, Vol 160, Iss 1, Pp 1-6 (2023)
Abstract Interstitial lung diseases (ILDs), or diffuse pulmonary lung disease, are a subset of lung diseases that primarily affect lung alveoli and the space around interstitial tissue and bronchioles. It clinically manifests as progressive dyspnea,
Externí odkaz:
https://doaj.org/article/7250b4a81b98494fbbce83abe0123b05
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 8, Iss 10, Pp 1067-1070 (2023)
Lanmaoa macrocarpa is a boletoid mushroom from the family Boletaceae and was named after its relatively larger basidiocarp and bluish color change when bruised. At present, its mitochondrial genome and phylogenetic relationships with other boletes re
Externí odkaz:
https://doaj.org/article/ce847c5d89b246c0b4870d412471700b
Autor:
Xiao-guo Wang, Shi-yan Wei, Liang-liang Qi, Zai-feng Yang, Jun Tang, Zeng-liang Liu, Sheng-jin Wu
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 8, Iss 10, Pp 1109-1113 (2023)
Auricularia delicata (Mont.) Henn. 1893 is an edible and medicinal jelly mushroom popular in China. Here, we report the assembly and annotation of a complete A. delicata mitochondrial genome based on data sequenced using an Illumina NovaSeq 6000 plat
Externí odkaz:
https://doaj.org/article/9ff727b76acf4f99a69511ffca3b3569
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Prenatal diagnosis and genetic counseling play an important role in preventing and controlling birth defects. No reports were found of prenatal diagnosis of couples carrying both the thalassemia and deafness genes. In this study, we prese
Externí odkaz:
https://doaj.org/article/18f491a70d3c45a79a0dc166ae655f91
New insight of obesity-associated NAFLD: Dysregulated 'crosstalk' between multi-organ and the liver?
Autor:
Ya-Di Wang, Liang-Liang Wu, Xiao-Yan Qi, Yuan-Yuan Wang, Zhe-Zhen Liao, Jiang-Hua Liu, Xin-Hua Xiao
Publikováno v:
Genes and Diseases, Vol 10, Iss 3, Pp 799-812 (2023)
Obesity plays a crucial role in the development of non-alcoholic fatty liver disease (NAFLD). However, the underlying mechanism for the pathogenesis of obesity-associated NAFLD remains largely obscure. Although the “multiple hit” theory provides
Externí odkaz:
https://doaj.org/article/f9406fc7a469423781108b2a412ed59c
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Hereditary spastic paraplegia (HSP) is a progressive upper-motor neurodegenerative disease. Mutations in the WASHC5 gene are associated with autosomal dominant HSP, spastic paraplegia 8 (SPG8). However, due to the small number of reported
Externí odkaz:
https://doaj.org/article/55cc1d209ccd43ff8639f3b1e7ef910f
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Heterozygous mutations in the dehydrodolichol diphosphate synthase (DHDDS) gene are one of the causes generating developmental and epileptic encephalopathies. So far, only eleven mutations in the DHDDS gene have been identified. The mutat
Externí odkaz:
https://doaj.org/article/eb91288c84b6487ab96717e43fdeb2e8
Autor:
Yingying Cao, Shanshan Zhai, Zhuxin Li, Zhengtuan Huang, Liang Liang, Junyu Tao, Jian Xiao, Jing Leng, Haibo Tang
Publikováno v:
Mitochondrial DNA. Part B. Resources, Vol 8, Iss 3, Pp 402-404 (2023)
The tree shrew (Tupaia belangeri) is currently placed in the order Scandentia. Owing to their unique characteristics, such as small body size, high brain-to-body mass ratio, short reproductive cycle and life span, and low maintenance costs in laborat
Externí odkaz:
https://doaj.org/article/43c3b400202e421caa9414194652208a
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Objective Roberts syndrome (RBS), also known as Roberts‐SC phocomelia syndrome, is a rare autosomal recessive developmental disorder caused by mutations in the ESCO2 gene. Cardinal clinical manifestations are pre‐ and postnatal growth re
Externí odkaz:
https://doaj.org/article/3631a4e68aa84e38b3731296e20bfad5