Genome-wide identification of AOX family genes in Moso bamboo and functional analysis of PeAOX1b_2 in drought and salinity stress tolerance
X Wang, X Geng, X Bi, R Li, Y Chen, C Lu - Plant Cell Reports, 2022 - Springer
Key message Five PeAOX genes from Moso bamboo genome were identified. PeAOX1b_2-OE
improved tolerance to drought and salinity stress in Arabidopsis, indicating it is involved …
improved tolerance to drought and salinity stress in Arabidopsis, indicating it is involved …
Genome-Wide Identification, Evolutionary and Expression Analysis of Cyclin-Dependent Kinase Gene Family Members in Moso Bamboo (Phyllostachys edulis)
K Dong, L Lan, M Liu, B Ge, X Bi, Y Liu, X Geng… - Journal of Plant Growth …, 2024 - Springer
Cyclin-dependent kinase (CDK), the pivotal controller of cell cycle progression, is involved
in stress resistance and plant growth. Moso bamboo (Phyllostachys edulis) with surprisingly …
in stress resistance and plant growth. Moso bamboo (Phyllostachys edulis) with surprisingly …
Isolation and functional characterization of cold-induced gene (AmCIP) promoter from Ammopiptanthus mongolicus
B Ge, K Dong, R Li, X Bi, Q Liu, W Zhang, Y Chen, C Lu - Gene, 2024 - Elsevier
AmCIP is a dehydrin-like protein which involved in abiotic stress tolerance in xerophytes
evergreen woody plant A. mongolicus. AmCIP could be induced in the cotyledon and radicle …
evergreen woody plant A. mongolicus. AmCIP could be induced in the cotyledon and radicle …
[HTML][HTML] Resolution of disease phenotypes resulting from multilocus genomic variation
…, ZH Coban Akdemir, M Walkiewicz, W Bi… - … England Journal of …, 2017 - Mass Medical Soc
Background Whole-exome sequencing can provide insight into the relationship between
observed clinical phenotypes and underlying genotypes. Methods We conducted a …
observed clinical phenotypes and underlying genotypes. Methods We conducted a …
Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management
Importance While congenital malformations and genetic diseases are a leading cause of
early infant death, to our knowledge, the contribution of single-gene disorders in this group is …
early infant death, to our knowledge, the contribution of single-gene disorders in this group is …
[HTML][HTML] Reanalysis of clinical exome sequencing data
Reanalysis of Clinical Exome Data and Diagnostic Yield As knowledge about genetic
causes of disease improves, periodic reanalysis of clinical exome sequence could yield new …
causes of disease improves, periodic reanalysis of clinical exome sequence could yield new …
[HTML][HTML] Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder
Background Exome sequencing is now being incorporated into clinical care for pediatric
and adult populations, but its integration into prenatal diagnosis has been more limited. One …
and adult populations, but its integration into prenatal diagnosis has been more limited. One …
RIPK1 Binds MCU to Mediate Induction of Mitochondrial Ca2+ Uptake and Promotes Colorectal Oncogenesis
…, F Lu, X Sun, D Ma, Y Yuan, Z Li, N Hou, H Zhao, X Bi… - Cancer research, 2018 - AACR
The receptor-interacting protein kinase 1 (RIPK1) is an essential signaling molecule in
pathways for cell survival, apoptosis, and necroptosis. We report here that RIPK1 is upregulated …
pathways for cell survival, apoptosis, and necroptosis. We report here that RIPK1 is upregulated …
[HTML][HTML] A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing
Background Although mosaic variation has been known to cause disease for decades, high-throughput
sequencing technologies with the analytical sensitivity to consistently detect …
sequencing technologies with the analytical sensitivity to consistently detect …
Phenotypic expansion in DDX3X – a common cause of intellectual disability in females
…, W He, F Vetrini, MA Walkiewicz, W Bi… - Annals of clinical …, 2018 - Wiley Online Library
De novo variants in DDX 3X account for 1–3% of unexplained intellectual disability ( ID )
cases and are amongst the most common causes of ID especially in females. Forty‐seven …
cases and are amongst the most common causes of ID especially in females. Forty‐seven …