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Your search keyword '"Uddin, K. M. Furkan"' showing total 18 results

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18 results on '"Uddin, K. M. Furkan"'

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1. Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population

2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

3. An Exploration of Physical and Phenotypic Characteristics of Bangladeshi Children with Autism Spectrum Disorder

4. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11–q13 imprinting region

5. An Exploration of Physical and Phenotypic Characteristics of Bangladeshi Children with Autism Spectrum Disorder

6. Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders

7. Novel mutations in actionable breast cancer genes by targeted sequencing in an ethnically homogenous cohort

8. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

9. A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

10. Author Correction: A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection (Nature Immunology, (2022), 23, 2, (159-164), 10.1038/s41590-021-01030-z)

11. Studying severe long COVID to understand post-infectious disorders beyond COVID-19

12. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

13. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

14. An Exploration of Physical and Phenotypic Characteristics of Bangladeshi Children with Autism Spectrum Disorder

15. AnANKRD26nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome)

16. An ANKRD26 nonsense somatic mutation in a female with epidermodysplasia verruciformis (Tree Man Syndrome).

17. Analyzing single cell transcriptome data from severe COVID-19 patients.

18. Single-cell transcriptome identifies FCGR3B upregulated subtype of alveolar macrophages in patients with critical COVID-19.

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