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For example, type 2 diabetes risk alleles can be divided into those that more strongly affect insulin production (homeostatic model assessment (HOMA -B) or insulin resistance (HOMA -B), and it forlows that insulinuals with SNP presistanceased in either direction may have different subtypes of diandtes [ 106].
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The Upper Xiajiadian individuals of the late Bronze Age had different subtypes of O3a-M324, O3a3c-M117.
However, human atrial muscle has different subtypes of contractile and metabolic proteins compared with ventricular myocytes, which may alter the response to ischaemia of atrial muscle cells compared with those of ventricular myocytes.
Countries/regions have different histopathological subtypes of NPC of varied etiology.
So far, a number of groups have generated different subtypes of neurons by combining BAM with specific TFs that play an important role in the development of specific neuron subtypes (Caiazzo et al., 2011; Kim, 2011; Pang et al., 2011; Son et al., 2011).
On the other hand, several reports have demonstrated different subtypes of RET/PTC and different BRAF mutational statuses in individual PTC foci among patients with multifocal PTCs 7– 10.
We found that patients with DM on metformin, those with DM not on metformin and the control group of patients without DM had different molecular subtypes of BC: the luminal A subtype was found in 78%, 83% and 71%, the luminal B in 12.6%, 9% and 11%, HER-2 in 0.8%, 1.6% and 8%, and the triple-negative/basal-like subtype in 8.6%, 6.4% and 10%, respectively.
Patients with DM on metformin, with DM not on metformin and the control group had different molecular subtypes of BC (p = 0.01): the luminal A subtype was found in 78%, 83% and 71%, the luminal B in 12.6%, 9% and 11%, HER-2 in 0.8%, 1.6% and 8%, and the triple-negative/basal-like subtype in 8.6%, 6.4% and 10%, respectively.
Patients with DM on metformin, those with DM not on metformin and the control group had different molecular subtypes of BC (p = 0.01): the luminal A subtype was found in 78%, 83% and 71%, the luminal B in 12.6%, 9% and 11%, HER-2 in 0.8%, 1.6% and 8%, and the triple-negative/basal-like subtype in 8.6%, 6.4% and 10%, respectively.
Patients with DM and the control group had different molecular subtypes of BC (p = 0.01): the luminal A subtype was found in 80% and 71%, the luminal B in 11% and 11%, HER-2 in 1% and 8%, and the triple-negative/basal-like subtype in 7% and 10%, respectively.
Laboratory tests have identified three different subtypes of Legionella bacteria from the patients, indicating one common source is unlikely.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com