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Author/Creator Khan, Muhammad Ismail

1. Absence of CD74 Isoform at 41kDa Prevents the Heterotypic Associations between CD74 and CD44 in Human Lung Adenocarcinoma-derived Cells. (17th November 2021)

Authors:
Al Abdulmonem, Waleed; Rasheed, Zafar; Aljohani, Abdullah S. M.; Omran, Ola M.; Rasheed, Naila; Alkhamiss, Abdullah; A. M. Al Salloom, Abdulaziz; Alhumaydhi, Fahad; Alblihed, Mohamd A.; Al Ssadh, Hussain; Khan, Muhammad Ismail; Fernández, Nelson
Journal:
Immunological investigations
Issue:
Volume 50:Number 8(2021)
Page Start:
891
Record Type:
Journal Article
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3. Whole exome sequencing identified a novel missense alteration in CC2D2A causing Joubert syndrome 9 in a Pakhtun family. (27th October 2020)

Authors:
Khan, Muhammad Ismail; Latif, Muhammad; Saif, Maria; Ahmad, Hilal; Khan, Atta Ullah; Naseer, Muhammad Imran; Hussain, Hafiz Muhammad Jafar; Jelani, Musharraf
Journal:
Journal of gene medicine
Issue:
Volume 23:Number 1(2021)
Page Start:
n/a
Record Type:
Journal Article
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4. Whole exome sequencing identifies a novel compound heterozygous GFM1 variant underlying developmental delay, dystonia, polymicrogyria, and severe intellectual disability in a Pakhtun family. Issue 9 (15th June 2022)

Authors:
Khan, Atta Ullah; Khan, Ibrar; Khan, Muhammad Ismail; Latif, Muhammad; Siddiqui, Muhammad Imran; Khan, Shafi Ullah; Htar, Thet Thet; Wahid, Ghazala; Ullah, Ikram; Bibi, Fehmida; Khan, Asifullah; Naseer, Muhammad Imran; Seo, Go Hun; Jelani, Musharraf
Journal:
American journal of medical genetics
Issue:
Volume 188:Issue 9(2022)
Page Start:
2693
Record Type:
Journal Article
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