Xiangmin Xu

[An improved PCR-based megaprimer method for site-directed mutagenesis].

Static and dynamic views of visual cortical organization.

Are primate lateral geniculate nucleus (LGN) cells really sensitive to orientation or direction?

[Prevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of Guangxi].

Optical imaging reveals retinotopic organization of dorsal V3 in New World owl monkeys.

Modeling receptive-field structure of koniocellular, magnocellular, and parvocellular LGN cells in the owl monkey (Aotus trivigatus).

De novo synthesis of PCR templates for the development of SARS diagnostic assay.

A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family.

Optical imaging of visually evoked responses in prosimian primates reveals conserved features of the middle temporal visual area.

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.

Functional organization of visual cortex in the owl monkey.

[Rapid detection of three common deletional alpha thalassemias in Chinese by single-tube multiplex PCR].

Optical imaging of visually evoked responses in the middle temporal area after deactivation of primary visual cortex in adult primates.

Functional organization of visual cortex in the prosimian bush baby revealed by optical imaging of intrinsic signals.

Mouse cortical inhibitory neuron type that coexpresses somatostatin and calretinin.

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.

Unequal representation of cardinal vs. oblique orientations in the middle temporal visual area.

A simple method for the preparation of containing Sb nano- and microcrystallines via an ultrasound agitation.

How do functional maps in primary visual cortex vary with eccentricity?

Electrochemical detection of point mutation based on surface ligation reaction and biometallization.

Enzymatic amplification detection of DNA based on "molecular beacon" biosensors.

Identification of a novel frameshift mutation at codon 53 (-T) in the beta-globin gene causing dominantly inherited beta-thalassemia in a Chinese Miao family.

Catechol determination in compost bioremediation using a laccase sensor and artificial neural networks.

Fidelity genotyping of point mutation by enhanced melting point difference using DNA ligase.

Laminar specificity of functional input to distinct types of inhibitory cortical neurons.

Highly specific and sensitive electrochemical genotyping via gap ligation reaction and surface hybridization detection.

Immunochemical characterization of inhibitory mouse cortical neurons: three chemically distinct classes of inhibitory cells.

Generation and characterization of human delta-globin-specific monoclonal antibodies.

High precision and fast functional mapping of cortical circuitry through a novel combination of voltage sensitive dye imaging and laser scanning photostimulation.

Direct fluorescence detection of point mutations in human genomic DNA using microbead-based ligase chain reaction.

The molecular basis of beta-thalassemia intermedia in southern China: genotypic heterogeneity and phenotypic diversity.

Analysis of alpha-hemoglobin-stabilizing protein (AHSP) gene as a genetic modifier to the phenotype of beta-thalassemia in Southern China.

Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy.

Novel use of matched filtering for synaptic event detection and extraction.

Extraction of prostatic lumina and automated recognition for prostatic calculus image using PCA-SVM.

Oligodendrocytes as regulators of neuronal networks during early postnatal development.

A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validation.

Characterization of a weak allele of zebrafish cloche mutant.

Cell-type specific regulation of cortical excitability through the allatostatin receptor system.