Sarcolemmal ATPase activities in normal and BIO 14.6 dystrophic hamster skeletal muscle

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Molecular psychiatry·2015

Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.

Neuromuscular disorders : NMD·2001

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy.

Neurology·2001

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).

Neuromuscular disorders : NMD·2000

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).

Human molecular genetics·1999

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

American journal of human genetics·1998

Purification and characterization of dihydrofolate reductase from Walker 256 carcinosarcoma.

Canadian journal of biochemistry·1982

Structure of the glycopeptides of a human gamma 1-immunoglobulin G (Tem) myeloma protein as determined by 360-megahertz nuclear magnetic resonance spectroscopy.

Canadian journal of biochemistry·1982

Phosphorylated and unphosphorylated forms of cardiac tropomyosin.

Canadian journal of biochemistry·1982

Glycerol-induced adenine nucleotide catabolism in rat liver cells.

Canadian journal of biochemistry·1982

Large-scale production of citrate synthase from a cloned gene.

Canadian journal of biochemistry·1982

Analysis of the expression of cloned genes using an Escherichia coli cell-free system.

Canadian journal of biochemistry·1982

Validation of the AViTA upper arm blood pressure monitor BPM636 in a combined pediatric and adult population according to the American National Standards Institute/Association for the Advancement of Medical Instrumentation/International Organization for Standardization 81060-2:2018/Amd2:2024.

Blood pressure monitoring·2026

Transfer-workflow optimization in a regional chest pain center network reduces door-in-door-out time in ST-segment elevation myocardial infarction: An interrupted time-series study with spectral validation.

International journal of cardiology. Heart & vasculature·2026

Radiographic changes in retroperitoneal corridor dimensions during staged positioning for prone transpsoas lateral lumbar interbody fusion.

North American Spine Society journal·2026

Objective assessment of transition hyperactivated motility in 10-μm chambers: a functional predictor of sperm recovery in assisted reproduction.

Frontiers in endocrinology·2026

The Impact of Blood Gas Sample Waiting Time on Laboratory Parameters in Intensive Care Patients.

Enfermeria clinica·2026

A Physiology- and Measurement-Informed Framework for Evaluating PPG Features in Cuffless Blood Pressure Estimation.

Physiological measurement·2026

Related Experiment Videos

Sarcolemmal ATPase activities in normal and BIO 14.6 dystrophic hamster skeletal muscle

Related Concept Videos

X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes.

Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.

Identical dysferlin mutation in limb-girdle muscular dystrophy type 2B and distal myopathy.

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).

Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).

A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Purification and characterization of dihydrofolate reductase from Walker 256 carcinosarcoma.

Structure of the glycopeptides of a human gamma 1-immunoglobulin G (Tem) myeloma protein as determined by 360-megahertz nuclear magnetic resonance spectroscopy.

Phosphorylated and unphosphorylated forms of cardiac tropomyosin.

Glycerol-induced adenine nucleotide catabolism in rat liver cells.

Large-scale production of citrate synthase from a cloned gene.

Analysis of the expression of cloned genes using an Escherichia coli cell-free system.

Validation of the AViTA upper arm blood pressure monitor BPM636 in a combined pediatric and adult population according to the American National Standards Institute/Association for the Advancement of Medical Instrumentation/International Organization for Standardization 81060-2:2018/Amd2:2024.

Transfer-workflow optimization in a regional chest pain center network reduces door-in-door-out time in ST-segment elevation myocardial infarction: An interrupted time-series study with spectral validation.

Radiographic changes in retroperitoneal corridor dimensions during staged positioning for prone transpsoas lateral lumbar interbody fusion.

Objective assessment of transition hyperactivated motility in 10-μm chambers: a functional predictor of sperm recovery in assisted reproduction.

The Impact of Blood Gas Sample Waiting Time on Laboratory Parameters in Intensive Care Patients.

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Related Experiment Videos

Sarcolemmal ATPase activities in normal and BIO 14.6 dystrophic hamster skeletal muscle

Related Concept Videos

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