Zobrazeno 1 - 10
of 102
pro vyhledávání: '"Haiming Yuan"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-7 (2024)
Abstract According to the atmospheric scattering model (ASM), the object signal’s attenuation diminishes exponentially as the imaging distance increases. This imposes limitations on ASM-based methods in situations where the scattering medium one wi
Externí odkaz:
https://doaj.org/article/1676b59211dc4f4a866e367d8732c801
Autor:
Fang Zhang, Hongmei Guo, Xinlong Zhou, Zhengxi Deng, Qiuhong Xu, Qingming Wang, Haiming Yuan, Jianhua Luo
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-6 (2024)
Abstract Background Biallelic pathogenic variants in PIP5K1C (MIM #606,102) lead to lethal congenital contractural syndrome 3 (LCCS3, MIM #611,369), a rare autosomal recessive genetic disorder characterized by small gestational age, severe multiple j
Externí odkaz:
https://doaj.org/article/1673822b10b24bc984cdab1d1191d105
Autor:
Zhentian Guo, Zongming Zhang, Limin Liu, Yue Zhao, Zhuo Liu, Chong Zhang, Hui Qi, Jinqiu Feng, Peijie Yao, Haiming Yuan
Publikováno v:
Bioengineering, Vol 11, Iss 9, p 927 (2024)
(1) Background: This study seeks to employ a machine learning (ML) algorithm to forecast the risk of distant metastasis (DM) in patients with T1 and T2 gallbladder cancer (GBC); (2) Methods: Data of patients diagnosed with T1 and T2 GBC was obtained
Externí odkaz:
https://doaj.org/article/68aa32f67e3e437eb4a676a4e7c9576b
Publikováno v:
Journal of High Energy Physics, Vol 2023, Iss 8, Pp 1-25 (2023)
Abstract We represent the first investigation of pole-skipping on both the gravity and field theory sides. In contrast to the higher dimensional models, there is no momentum degree of freedom in (1 + 1)−dimensional bulk theory. Thus, we then consid
Externí odkaz:
https://doaj.org/article/7f53f5b94a4b4e96a6d60ad8aa48aab8
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 11, Pp n/a-n/a (2023)
Abstract Background Biallelic pathogenic variants in the KCNJ16 gene result in hypokalemic tubulopathy and deafness (HKTD) (MIM #619406), which is a rare autosomal recessive disease characterized by hypokalemic tubulopathy with renal salt wasting, di
Externí odkaz:
https://doaj.org/article/daf6c71dfdee49ee9ed4a6bdc20f6492
Autor:
Haiming Yuan, Qingming Wang, Xiumei Zeng, Peiqing He, Wanfang Xu, Hongmei Guo, Yanhui Liu, Yangyang Lin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-7 (2022)
Abstract Background Homozygous or compound heterozygous variants in the KLHL40 gene cause nemaline myopathy 8 (NEM8), a severe autosomal recessive muscle disorder characterized by prenatal polyhydramnios, fetal akinesia or hypokinesia, joint contract
Externí odkaz:
https://doaj.org/article/4598ef6e0e2a477cb4372aedb3b12794
Autor:
Haiming Yuan, Xian-Hui Ge
Publikováno v:
European Physical Journal C: Particles and Fields, Vol 82, Iss 2, Pp 1-9 (2022)
Abstract The pole-skipping phenomenon is a special property of the retarded Green’s function of black hole perturbations. We turn to its analog in acoustic black holes, which may relate to experiments. The frequencies of these special points are lo
Externí odkaz:
https://doaj.org/article/29fa7cc0cd9e47ab959d798e9982536d
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Pathogenic variants in the RASopathy-causing SHOC2 gene have been suggested to cause Noonan syndrome-like with loose anagen hair (NS/LAH). This condition is characterized by facial features resembling Noonan syndrome (NS), short stature, growth hormo
Externí odkaz:
https://doaj.org/article/ef564abc0a0f4454845b8d13e89cf04c
Autor:
Haiming Yuan, Xian-Hui Ge
Publikováno v:
Journal of High Energy Physics, Vol 2021, Iss 6, Pp 1-27 (2021)
Abstract The “pole-skipping” phenomenon reflects that the retarded Green’s function is not unique at a pole-skipping point in momentum space (ω, k). We explore the universality of pole-skipping in different geometries. In holography, near hori
Externí odkaz:
https://doaj.org/article/264567157db54afcafcb76589f016f6a
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background:ZEB2 gene mutations or deletions cause Mowat-Wilson syndrome (MWS), which is characterized by distinctive facial features, global developmental delay, intellectual disability, epilepsy, friendly and happy personalities, congenital heart di
Externí odkaz:
https://doaj.org/article/5ff2400927254d0dac5a95e63c16bc11