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1 . Academic Journal
Cancer stem cells: a challenging paradigm for designing targeted drug therapies
저자
by
Khan, Ishaq N.
;
Al-Karim, Saleh
;
Bora, Roop S.
;
Chaudhary, Adeel G.
;
Saini, Kulvinder S.
.
소스
In
Drug Discovery Today
October 2015 20(10):1205-1216
Full Text (ScienceDirect)
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7 . Academic Journal
Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia.
저자
by
Alharazy, Shatha
;
Alissa, Eman
;
Lanham-New, Susan
;
Naseer, Muhammad Imran
;
Chaudhary, Adeel G.
, et al.
소스
BMC Endocrine Disorders
. 8/12/2021, Vol. 21 Issue 1, p1-10. 10p.
Open Access (BioMed Central)
Web of Science
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7 . Academic Journal
Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia.
저자
by
Alharazy, Shatha
;
Naseer, Muhammad Imran
;
Alissa, Eman
;
Robertson, M. Denise
;
Lanham-New, Susan
, et al.
소스
Saudi Journal of Biological Sciences; Aug2021, Vol. 28 Issue 8, p4626-4632, 7p
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7 . Academic Journal
Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.
저자
by
Alharazy, Shatha
;
Naseer, Muhammad Imran
;
Alissa, Eman
;
Robertson, Margaret Denise
;
Lanham-New, Susan
, et al.
소스
Frontiers in Genetics; 6/8/2021, Vol. 11, p1-10, 10p
Web of Science
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7 . Academic Journal
Exome sequencing reveled a compound heterozygous mutations in RTTN gene causing developmental delay and primary microcephaly.
저자
by
Imran Naseer, Muhammad
;
Abdulrahman Abdulkareem, Angham
;
Yousef Muthaffar, Osama
;
Chaudhary, Adeel G.
.
소스
Saudi Journal of Biological Sciences; May2021, Vol. 28 Issue 5, p2824-2829, 6p
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6 . Academic Journal
Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly.
저자
by
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrahman
;
Jan, Mohammed M.
;
Chaudhary, Adeel G.
;
Alharazy, Shatha
, et al.
소스
Saudi Journal of Biological Sciences; Nov2020, Vol. 27 Issue 11, p3125-3131, 7p
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7 . Academic Journal
Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family.
저자
by
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrahman
;
Jan, Mohammed Mohammed
;
Chaudhary, Adeel G.
;
Al-Qahtani, Mohammad H.
.
소스
Pakistan Journal of Medical Sciences
. 2020, Vol. 36 Issue 6, p1425-1428. 4p.
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7 . Academic Journal
Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis.
저자
by
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrahman
;
Guzmán-Vega, Francisco J.
;
Arold, Stefan T.
;
Pushparaj, Peter Natesan
, et al.
소스
Frontiers in Genetics; 5/7/2020, Vol. 11, p1-6, 6p
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7 . Academic Journal
Exome Analysis Identified Novel Homozygous Splice Site Donor Alteration in NT5C2 Gene in a Saudi Family Associated With Spastic Diplegia Cerebral Palsy, Developmental Delay, and Intellectual Disability.
저자
by
Naseer, Muhammad Imran
;
Abdulkareem, Angham Abdulrahman
;
Pushparaj, Peter Natesen
;
Bibi, Fehmida
;
Chaudhary, Adeel G.
.
소스
Frontiers in Genetics; 2/21/2020, p1-6, 6p
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7 . Academic Journal
Molecular and enzoinformatics perspectives of targeting Polo-like kinase 1 in cancer therapy.
저자
by
Shakil, Shazi
;
Baig, Mohammad H.
;
Tabrez, Shams
;
Rizvi, Syed M. Danish
;
Zaidi, Syed K.
, et al.
소스
Seminars in Cancer Biology
. Jun2019, Vol. 56, p47-55. 9p.
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