Sentence examples for molecular defect causes from inspiring English sources

In the respiratory tract, this molecular defect causes obstruction of the airways by mucus and chronic endobronchial infection.

The sctt maternal-/zygotic- germ cell phenotype suggested that the molecular defect causing this phenotype represents a severe loss of function.

We observed reduced telomeric overhang lengths in the affected cells, providing an insight into the molecular defect causing the disease in this family and possibly also in other DC and HHS patients.

Our elucidation of the molecular defect caused by mutations in Rab7 illustrates an alternative mechanism: toxic misregulation of native function.

Has there been any attempt to do it, considering the potential help provided by the localization of the N/C-terminal tags? 1) They should provide further evidence for the molecular defect caused when binding of Orc6 to the rest of the complex is disrupted, or at the very least discuss the ambiguities remaining from their current analysis.

We suggest that FRG1 misregulation in a specific window of muscle differentiation may contribute to FSHD, although it cannot be considered the only molecular defect causing the FSHD phenotype: for example, the transcription of DUX4 recently observed in FSHD myoblasts [ 14, 16] may contribute to the manifestation of FSHD.

When the authors submit a revised manuscript, they must address the following points: 1) They should provide further evidence for the molecular defect caused when binding of Orc6 to the rest of the complex is disrupted, or at the very least discuss the ambiguities remaining from their current analysis.

Moreover, it will allow the design of innovative therapeutic strategies for these pathologies based on the specific molecular defects causing the disease.

We conclude that several different molecular defects cause the Kell null phenotype.

In conclusion, the present study demonstrates the heterogeneity of molecular defects causing beta-thalassemia in Thai children.

Ongoing candidate gene/protein analyses in radiosensitive cancer patients are expected to yield further examples of the range of molecular defects causing human radiosensitivity.