A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region

[Yield of xenodiagnosis and PCR in the evaluation of specific chemotherapy of Chagas' disease in children].

Boletin chileno de parasitologia·1998

[Percutaneous suprapubic bladder lithotripsy].

Annales d'urologie·1998

Factors associated with outcome in major depression: a 6-month prospective study.

Social psychiatry and psychiatric epidemiology·1998

[Simultaneous transplantation of fetal mesencephalic cells to the striatum and globus pallidus of rats with lesions induced by 6-hydroxydopamine].

Revista de neurologia·1998

Signs of glaucoma in rhesus monkeys from a restricted gene pool.

Journal of glaucoma·1998

The Bcl-2 gene is differentially regulated by IL-2 and IL-4: role of the transcription factor NF-AT.

Oncogene·1998

Unlocking the epigenetic code: future Frontiers in predictive biomarkers for intellectual disability in fragile X syndrome.

Human molecular genetics·2026

Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts.

Human molecular genetics·2026

CRISPR/dCas9-mediated tuning of DMPK transcription reveals a quantitative relationship between toxic repeat RNA expression and MBNL1 activity in myotonic dystrophy.

Human molecular genetics·2026

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

Human molecular genetics·2026

PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors.

Human molecular genetics·2026

N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

Human molecular genetics·2026

Using High-Dimensional Environmental Covariates to Study Genotype by Environment Interaction for Reproductive Traits in Duroc Boars.

Journal of animal science·2026

Toward comprehensive cellular characterization of H&E slides.

Journal of pathology informatics·2026

A Genome-Wide Association Study of Premenstrual Symptoms in Two Nordic Populations.

Biological psychiatry global open science·2026

Predicting gene compensation in disease with graph embedding techniques.

Artificial intelligence in medicine·2026

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

Mutation research·2026

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Epilepsia·2026

Related Experiment Videos

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region

Related Concept Videos

[Yield of xenodiagnosis and PCR in the evaluation of specific chemotherapy of Chagas' disease in children].

[Percutaneous suprapubic bladder lithotripsy].

Factors associated with outcome in major depression: a 6-month prospective study.

[Simultaneous transplantation of fetal mesencephalic cells to the striatum and globus pallidus of rats with lesions induced by 6-hydroxydopamine].

Signs of glaucoma in rhesus monkeys from a restricted gene pool.

The Bcl-2 gene is differentially regulated by IL-2 and IL-4: role of the transcription factor NF-AT.

Unlocking the epigenetic code: future Frontiers in predictive biomarkers for intellectual disability in fragile X syndrome.

Mitochondrial dysfunction, metabolic quiescence and premature senescence in CMT4B3 fibroblasts.

CRISPR/dCas9-mediated tuning of DMPK transcription reveals a quantitative relationship between toxic repeat RNA expression and MBNL1 activity in myotonic dystrophy.

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors.

N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

Using High-Dimensional Environmental Covariates to Study Genotype by Environment Interaction for Reproductive Traits in Duroc Boars.

Toward comprehensive cellular characterization of H&E slides.

A Genome-Wide Association Study of Premenstrual Symptoms in Two Nordic Populations.

Predicting gene compensation in disease with graph embedding techniques.

In silico analysis of missense variants in functional domains of PWWP2A and PWWP2B proteins.

Correlation of polygenic risk score and clinical phenotype in patients with genetic generalized epilepsy.

Related Experiment Videos

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region

Related Concept Videos

Related Articles