نتائج البحث

Computational analysis of non-synonymous SNPs in the human LCN2 gene.

• Authors : Sivakumar, Kaniha¹ (AUTHOR); Subbiah, Usha¹ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 8/20/2024, Vol. 25 Issue 1, p1-13. 13p.

تفاصيل العنوان

In silico analysis of missense SNPs in GABRA1, GABRB1, and GABRB3 genes associated with some diseases in neurodevelopmental disorders.

• Authors : Manaz, Mehmet¹ (AUTHOR); Karasakal, Ömer Faruk² (AUTHOR) ; Özkan Oktay, Ebru³ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 10/25/2023, Vol. 24 Issue 1, p1-12. 12p.

تفاصيل العنوان

In silico analysis of missense SNPs in GABRA1, GABRB1, and GABRB3 genes associated with some diseases in neurodevelopmental disorders

• Authors : Mehmet Manaz; Ömer Faruk Karasakal; Ebru Özkan Oktay

Subjects: GABRA1; GABRB1; GABRB3

• Source: Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-12 (2023)

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Investigating pathogenic SNPs in androgen receptor with direct influence on polycystic ovary syndrome (PCOS) in women.

• Authors : Ramadhan, Rehab S.¹ (AUTHOR); Algafari, Rebah N.² (AUTHOR) ; Jarallah, Aziz Latif¹ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 4/9/2022, Vol. 23 Issue 1, p1-10. 10p.

تفاصيل العنوان

In-silico analysis unravels the structural and functional consequences of non-synonymous SNPs in the human IL-10 gene.

• Authors : Das, Shuvo Chandra¹ (AUTHOR); Rahman, Md. Anisur¹ (AUTHOR); Das Gupta, Shipan¹ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 1/23/2022, Vol. 23 Issue 1, p1-14. 14p.

تفاصيل العنوان

In-silico analysis unravels the structural and functional consequences of non-synonymous SNPs in the human IL-10 gene

• Authors : Shuvo Chandra Das; Md. Anisur Rahman; Shipan Das Gupta

Subjects: Interleukin-10; JAK-STAT pathway; nsSNPs

• Source: Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-14 (2022)

تفاصيل العنوان

Protein secondary structure prediction (PSSP) using different machine algorithms.

• Authors : Afify, Heba M.¹ (AUTHOR); Abdelhalim, Mohamed B.² (AUTHOR); Mabrouk, Mai S.³ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. Dec2021, Vol. 22 Issue 1, p1-10. 10p.

تفاصيل العنوان

Chanarin–Dorfman syndrome: clinical/genetic features and natural history in six Pakistani patients.

• Authors : Waheed, Nadia¹ (AUTHOR) ; Ijaz, Sadaqat² (AUTHOR); Fayyaz, Zafar³ (AUTHOR)

• Source: Egyptian Journal of Medical Human Genetics. 8/25/2021, Vol. 22 Issue 1, p1-10. 10p.

تفاصيل العنوان

Chanarin–Dorfman syndrome: clinical/genetic features and natural history in six Pakistani patients

• Authors : Nadia Waheed; Sadaqat Ijaz; Zafar Fayyaz

Subjects: Chanarin–Dorfman syndrome; Genetic mutation; Phenotype

• Source: Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-10 (2021)

تفاصيل العنوان

Chanarin–Dorfman syndrome: clinical/genetic features and natural history in six Pakistani patients

• Authors : Sadaqat Ijaz; Nadia Waheed; Zafar Fayyaz

Subjects: medicine.medical_specialty; Mutation; Medicine (General)

• Source: Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-10 (2021)

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