[Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example]

Brand vs generic adverse event reporting patterns: An authorized generic-controlled evaluation of cardiovascular medications.

Journal of clinical pharmacy and therapeutics·2017

Mutational and biochemical findings in adults with persistent hypophosphatasemia.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2017

Comparison of Outcomes Following a Switch From a Brand to an Authorized Versus Independent Generic Drug.

Clinical pharmacology and therapeutics·2016

The relationship between childhood BMI and adult serum cholesterol, LDL, and ankle brachial index.

Clinical medicine & research·2014

Characterization of statin dose response in electronic medical records.

Clinical pharmacology and therapeutics·2013

Acute hypophosphatasemia.

Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2013

[Developing forensic reference database by 18 autosomal STR for DNA identification in Republic of Belarus].

Genetika·2018

[Assessment of the genetic distances between some species of the family Bradybaenidae (Mollusca, Pulmonata)].

Genetika·2018

[Molecular phylogenetic analysis of Diacyclops and Acanthocyclops (Copepoda: Cyclopoida) from Lake Baikal].

Genetika·2018

[Genetic diversity of the Pacific walrus (Odobenus rosmarus divergens) in the western part of the Chukchi Sea].

Genetika·2018

[The genetic diversity of burbot (Lota lota L., 1758) of Western Siberia (the analysis of the mtDNA control region polymorphism)].

Genetika·2018

[Fish growth hormone genes: Divergence of coding sequences in salmonid fishes].

Genetika·2018

QTL mapping.

Genetics·2026

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Case reports in ophthalmological medicine·2026

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Related Experiment Videos

[Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example]

Related Concept Videos

Brand vs generic adverse event reporting patterns: An authorized generic-controlled evaluation of cardiovascular medications.

Mutational and biochemical findings in adults with persistent hypophosphatasemia.

Comparison of Outcomes Following a Switch From a Brand to an Authorized Versus Independent Generic Drug.

The relationship between childhood BMI and adult serum cholesterol, LDL, and ankle brachial index.

Characterization of statin dose response in electronic medical records.

Acute hypophosphatasemia.

[Developing forensic reference database by 18 autosomal STR for DNA identification in Republic of Belarus].

[Assessment of the genetic distances between some species of the family Bradybaenidae (Mollusca, Pulmonata)].

[Molecular phylogenetic analysis of Diacyclops and Acanthocyclops (Copepoda: Cyclopoida) from Lake Baikal].

[Genetic diversity of the Pacific walrus (Odobenus rosmarus divergens) in the western part of the Chukchi Sea].

[The genetic diversity of burbot (Lota lota L., 1758) of Western Siberia (the analysis of the mtDNA control region polymorphism)].

[Fish growth hormone genes: Divergence of coding sequences in salmonid fishes].

QTL mapping.

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Related Experiment Videos

[Population-genetic approach to studying the mutation process using 4 forms of myopathy as an example]

Related Concept Videos

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