Restriction maps of plasmids pUB110 and pBD9

Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.

Human molecular genetics·2010

CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease.

Human molecular genetics·2001

Neuronal trafficking of palmitoyl protein thioesterase provides an excellent model to study the effects of different mutations which cause infantile neuronal ceroid lipofuscinocis.

Molecular and cellular neurosciences·2001

Molecular pathogenesis of a disease: structural consequences of aspartylglucosaminuria mutations.

Human molecular genetics·2001

Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL).

Human molecular genetics·2001

CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain.

The Journal of comparative neurology·2000

Interplay of βPS and βν integrins in Drosophila muscle functioning.

Gene·2026

Targeting the gut-joint axis: Ferrostatin-1 alleviates Collagen-Induced arthritis and is associated with alterations in microbiota-derived metabolites.

Gene·2026

Antagonistic regulation by mango MiSPL9a and MiSPL9b regulates flowering time, drought and salt stress in Arabidopsis.

Gene·2026

Integrative single‑cell and bulk transcriptomic profiling reveals MMP1 as a core effector and CTSB as a putative collaborator in ATBC‑aggravated pulmonary fibrosis.

Gene·2026

A novel PKHD1 missense variant disrupting splicing in a fetus with Caroli disease.

Gene·2026

An oxidative stress - and immunotherapy-related six-gene signature defines immune subtypes and predicts prognosis and immunotherapy response in hepatocellular carcinoma.

Gene·2026

Lessons from a systematic review of family-based studies in ALS.

Amyotrophic lateral sclerosis & frontotemporal degeneration·2026

Spadmiss with basal ganglia calcification and multilocus genetic disease: a novel phenotypic expansion.

Annals of medicine and surgery (2012)·2026

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Biology-informed neural networks learn nonlinear representations from omics data to improve genomic prediction and biological discovery.

The Plant journal : for cell and molecular biology·2026

The causal role of plasma protein ratios in ulcerative colitis: insights from mendelian randomization and single-cell sequencing.

Open medicine (Warsaw, Poland)·2026

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

Human mutation·2026

Related Experiment Videos

Restriction maps of plasmids pUB110 and pBD9

Related Concept Videos

Expression and lysosomal targeting of CLN7, a major facilitator superfamily transporter associated with variant late-infantile neuronal ceroid lipofuscinosis.

CLN3 protein is targeted to neuronal synapses but excluded from synaptic vesicles: new clues to Batten disease.

Neuronal trafficking of palmitoyl protein thioesterase provides an excellent model to study the effects of different mutations which cause infantile neuronal ceroid lipofuscinocis.

Molecular pathogenesis of a disease: structural consequences of aspartylglucosaminuria mutations.

Palmitoyl protein thioesterase (PPT) localizes into synaptosomes and synaptic vesicles in neurons: implications for infantile neuronal ceroid lipofuscinosis (INCL).

CLN-1 and CLN-5, genes for infantile and variant late infantile neuronal ceroid lipofuscinoses, are expressed in the embryonic human brain.

Interplay of βPS and βν integrins in Drosophila muscle functioning.

Targeting the gut-joint axis: Ferrostatin-1 alleviates Collagen-Induced arthritis and is associated with alterations in microbiota-derived metabolites.

Antagonistic regulation by mango MiSPL9a and MiSPL9b regulates flowering time, drought and salt stress in Arabidopsis.

Integrative single‑cell and bulk transcriptomic profiling reveals MMP1 as a core effector and CTSB as a putative collaborator in ATBC‑aggravated pulmonary fibrosis.

A novel PKHD1 missense variant disrupting splicing in a fetus with Caroli disease.

An oxidative stress - and immunotherapy-related six-gene signature defines immune subtypes and predicts prognosis and immunotherapy response in hepatocellular carcinoma.

Lessons from a systematic review of family-based studies in ALS.

Spadmiss with basal ganglia calcification and multilocus genetic disease: a novel phenotypic expansion.

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

Biology-informed neural networks learn nonlinear representations from omics data to improve genomic prediction and biological discovery.

The causal role of plasma protein ratios in ulcerative colitis: insights from mendelian randomization and single-cell sequencing.

Molecular Characterization of TSC1 and TSC2 Variants in a Greek Cohort of Tuberous Sclerosis Complex Patients.

Related Experiment Videos

Restriction maps of plasmids pUB110 and pBD9

Related Concept Videos

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