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 …

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 …

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 …

[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 …

Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management

…, R Xiao, P Liu, C Shaw, M Walkiewicz, W Bi… - JAMA …, 2017 - jamanetwork.com
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 …

[HTML][HTML] Reanalysis of clinical exome sequencing data

…, A Braxton, P Ward, H Dai, BO Yuan, W Bi… - … England Journal of …, 2019 - Mass Medical Soc
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 …

[HTML][HTML] Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

…, H Dai, L Meng, X Wang, R Xiao, P Liu, W Bi… - Genome medicine, 2018 - Springer
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 …

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 …

[HTML][HTML] A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing

…, PA Ward, A Braxton, X Wang, L Meng, R Xiao, W Bi… - Genome Medicine, 2019 - Springer
Background Although mosaic variation has been known to cause disease for decades, high-throughput
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 …