[Hereditary progressive sensorineural deafness--report of 30 cases in 12 families]

Familial aggregation of low birth weight among whites and blacks in the United States.

The New England journal of medicine·1995

Identification of a species specific regulatory site in human pancreatic cholesterol esterase.

Biochemistry·1995

Fibronectin peptide DRVPHSRNSIT and fibronectin receptor peptide DLYYLMDL arrest gastrulation of Rana pipiens.

Experientia·1995

Remodelling of hand representation in adult cortex determined by timing of tactile stimulation.

Nature·1995

Factors responsible for the Ca(2+)-dependent inactivation of calcineurin in brain.

FEBS letters·1995

Autoregulation of zonal glomerular filtration rate and renal blood flow in spontaneously hypertensive rats.

The American journal of physiology·1995

[The application value of neuroelectrophysiological monitoring in posterior spinal corrective surgery for patients with osteochondrodysplasia complicated by kyphoscoliosis].

Zhonghua yi xue za zhi·2026

[Mechanism of growth differentiation factor 15 in curcumin-induced ferroptosis in triple-negative breast cancer].

Zhonghua yi xue za zhi·2026

[Study on the relationship between ultrasound-based response evaluation and pathological outcomes in neoadjuvant therapy for HER2-positive breast cancer].

Zhonghua yi xue za zhi·2026

[Predictive accuracy of different risk stratification strategies for prognosis in patients with acute pulmonary embolism].

Zhonghua yi xue za zhi·2026

[Construction and validation of a prognosis prediction model for patients with high-frequency predominant sudden sensorineural hearing loss with concomitant middle- and low-frequency involvement].

Zhonghua yi xue za zhi·2026

[Association of proton pump inhibitor management strategies with clinical outcomes in patients with hospital-acquired acute kidney injury].

Zhonghua yi xue za zhi·2026

Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.

bioRxiv : the preprint server for biology·2026

Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.

bioRxiv : the preprint server for biology·2026

Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.

bioRxiv : the preprint server for biology·2026

Single-nucleus transcriptome-wide association study of human brain disorders.

Nature·2026

A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals.

Liver international : official journal of the International Association for the Study of the Liver·2026

Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases.

Molecular genetics & genomic medicine·2026

Related Experiment Videos

[Hereditary progressive sensorineural deafness--report of 30 cases in 12 families]

Related Concept Videos

Familial aggregation of low birth weight among whites and blacks in the United States.

Identification of a species specific regulatory site in human pancreatic cholesterol esterase.

Fibronectin peptide DRVPHSRNSIT and fibronectin receptor peptide DLYYLMDL arrest gastrulation of Rana pipiens.

Remodelling of hand representation in adult cortex determined by timing of tactile stimulation.

Factors responsible for the Ca(2+)-dependent inactivation of calcineurin in brain.

Autoregulation of zonal glomerular filtration rate and renal blood flow in spontaneously hypertensive rats.

[The application value of neuroelectrophysiological monitoring in posterior spinal corrective surgery for patients with osteochondrodysplasia complicated by kyphoscoliosis].

[Mechanism of growth differentiation factor 15 in curcumin-induced ferroptosis in triple-negative breast cancer].

[Study on the relationship between ultrasound-based response evaluation and pathological outcomes in neoadjuvant therapy for HER2-positive breast cancer].

[Predictive accuracy of different risk stratification strategies for prognosis in patients with acute pulmonary embolism].

[Construction and validation of a prognosis prediction model for patients with high-frequency predominant sudden sensorineural hearing loss with concomitant middle- and low-frequency involvement].

[Association of proton pump inhibitor management strategies with clinical outcomes in patients with hospital-acquired acute kidney injury].

Synergistic Variants in C-terminal Binding Protein 1 and Alkaline Phosphatase Lead to Mandibular Hypoplasia Through Impaired Wnt Signaling: An Oligogenic Model.

Point mutations and complex variants impact gene expression and addiction-related behaviors in Heterogeneous Stock rats.

Developmental Cerebellar Pathology in Mouse Models of SCN2A Premature Termination Codon Variants.

Single-nucleus transcriptome-wide association study of human brain disorders.

A Genetic Risk Variant Associated With the Risk of Primary Biliary Cholangitis Is Inherited From Neanderthals.

Clinical and Genetic Analysis of Pediatric Neurodevelopmental Disorders With Complex Chromosomal Rearrangements in Two Cases.

Related Experiment Videos

[Hereditary progressive sensorineural deafness--report of 30 cases in 12 families]

Related Concept Videos

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