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2023
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Fetal cardiac troponin isoforms rescue the increased Ca2+ sensitivity produced by a novel double deletion in cardiac troponin T linked to restrictive cardiomyopathy: a clinical, genetic, and functional approach.
Not available
S-EPMC3121488
|
biostudies-literature
Cite
Peroxisome disruption alters lipid metabolism and potentiates antitumor response with MAPK-targeted therapy in melanoma.
Not available
S-EPMC10575734
|
biostudies-literature
Cite
GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome.
Not available
S-EPMC3789886
|
biostudies-literature
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Yunis-Varon syndrome caused by biallelic VAC14 mutations.
Not available
S-EPMC5558182
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biostudies-literature
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Postinduction dexamethasone and individualized dosing of Escherichia Coli L-asparaginase each improve outcome of children and adolescents with newly diagnosed acute lymphoblastic leukemia: results from a randomized study--Dana-Farber Cancer Institute ALL Consortium Protocol 00-01.
Not available
S-EPMC3595424
|
biostudies-literature
Cite
High recombination rates and hotspots in a Plasmodium falciparum genetic cross.
Not available
S-EPMC3218859
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biostudies-literature
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Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.
Not available
S-EPMC141043
|
biostudies-literature
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Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation.
Not available
S-EPMC4542621
|
biostudies-literature
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Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study.
Not available
S-EPMC9202717
|
biostudies-literature
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Effects of eight neuropsychiatric copy number variants on human brain structure.
Not available
S-EPMC8292542
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biostudies-literature
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