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Shaheen Khan

Research Profile

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Pakistan

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Mesenchymal Stromal Cells

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TOP 3
Nadia Wajid; Fazal-ur-Rehman Bhatti; Shaheen N Khan; Azra Mehmood; Sheikh Riazuddin
Lovastatin protects chondrocytes derived from Wharton's jelly of human cord against hydrogen-peroxide-induced in vitro injury.
Zil-e-Huma Bashir; Inna A Belyantseva; Thomas B Friedman; Farheena Iqbal; Shaheen N Khan; Noreen Latief; Sheikh Riazuddin; Sheikh Amer Riazuddin; Saima Riazuddin
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.
Muhammad Tariq; Shaheen N Khan; Muhammad Sharif Masoud; Azra Mehmood; Sheikh Riazuddin
Stromal cell derived factor-1alpha protects stem cell derived insulin-producing cells from glucotoxicity under high glucose conditions in-vitro and ameliorates drug induced diabetes in rats.

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2013: Nadia Wajid; Fazal-ur-Rehman Bhatti; Shaheen N Khan; Azra Mehmood; Sheikh Riazuddin
Lovastatin protects chondrocytes derived from Wharton's jelly of human cord against hydrogen-peroxide-induced in vitro injury.
Cell and tissue research 2013;351(3):433-43.
2013: Zil-e-Huma Bashir; Inna A Belyantseva; Thomas B Friedman; Farheena Iqbal; Shaheen N Khan; Noreen Latief; Sheikh Riazuddin; Sheikh Amer Riazuddin; Saima Riazuddin
Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.
Journal of human genetics 2013;58(2):102-8.
2013: Muhammad Tariq; Shaheen N Khan; Muhammad Sharif Masoud; Azra Mehmood; Sheikh Riazuddin
Stromal cell derived factor-1alpha protects stem cell derived insulin-producing cells from glucotoxicity under high glucose conditions in-vitro and ameliorates drug induced diabetes in rats.
Journal of translational medicine 2013;11():115.
2013: Ghazanfar Ali Nasir; Sulaiman Shams; Gibran Ali; Mohsin Khan; Shaheen N Khan; Sadia Mohsin; Sheikh Riazuddin
Mesenchymal stem cells and Interleukin-6 attenuate liver fibrosis in mice.
Journal of translational medicine 2013;11():78.
2012: Mahmood S Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Sadia Mohsin; Shoaib Akhtar; Fatima Ali; Sheikh Amer Riazuddin
Mesenchymal stem cells conditioned with glucose depletion augments their ability to repair-infarcted myocardium.
Journal of cellular and molecular medicine 2012;16(10):2518-29.
2012: Mahmood Saba Choudhery; Mohsin Khan; Shaheen N Khan; Ruhma Mahmood; Azra Mehmood; Sheikh Amer Riazuddin
Bone marrow derived mesenchymal stem cells from aged mice have reduced wound healing, angiogenesis, proliferation and anti-apoptosis capabilities.
Cell biology international 2012;36(8):747-53.
2012: Muhammad Asif Naeem; Saima Riazuddin; Sheikh Riazuddin; Shahbaz Ali; Radha Ayyagari; Venkata R M Chavali; J Fielding Hejtmancik; Tayyab Husnain; Muhammad Iqbal; Shaheen N Khan; Paul Sieving; Sheikh Amer Riazuddin
GNAT1 associated with autosomal recessive congenital stationary night blindness.
Investigative ophthalmology & visual science 2012;53(3):1353-61.
2012: Muhammad Shareef Masoud; Azra Mehmood; Muhammad Zeeshan Afzal; Sanam Saiqa Anwar; Shaheen N Khan; Sheikh Riazuddin
Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment.
Journal of translational medicine 2012;10():243.
2012: Gibran Ali; Mohsin Khan; Shaheen N Khan; Sadia Mohsin; Ghazanfar Ali Nasir; Sulaiman Shams; Sheikh Amer Riazuddin
Nitric oxide augments mesenchymal stem cell ability to repair liver fibrosis.
Journal of translational medicine 2012;10():75.
2011: Atteeq U Rehman; Saima Riazuddin; Sheikh Amer Riazuddin; Mohsin Shahzad; Wasim Ahmad; Zubair M Ahmed; Rana A Ali; Paula B Andrade; Carmen C Brewer; Khitab Gul; Ateeq-Ul Jaleel; Saadullah Khan; Shaheen N Khan; Suzanne M Leal; Kwanghyuk Lee; Robert J Morell; Thomas B Friedman
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p.
Human genetics 2011;130(6):759-65.
2011: Muhammad Iqbal; Shaheen N Khan; Muhammad Asif Naeem; Zaheeruddin A Qazi; Saima Riazuddin; Shahbaz Ali; Tahir Farooq; J Fielding Hejtmancik; Tayyab Husnain; Sheikh Amer Riazuddin; Paul A Sieving; Sheikh Riazuddin
Association of pathogenic mutations in TULP1 with retinitis pigmentosa in consanguineous Pakistani families.
Archives of ophthalmology 2011;129(10):1351-7.
2011: Ali M Waryah; Munir A Bhinder; Mohsin Shahzad; Robert A Sisk; Zubair M Ahmed; Munir A Binder; Daniel I Choo; Thomas B Friedman; Shaheen N Khan; Sheikh Amer Riazuddin; Saima Riazuddin
Molecular and clinical studies of X-linked deafness among Pakistani families.
Journal of human genetics 2011;56(7):534-40.
2011: Sadaf Naz; Sheikh Amer Riazuddin; Paul A Sieving; Ahmad U Zafar; Shahbaz Ali; Nadeem H Butt; Tahir Farooq; J Fielding Hejtmancik; Tayyab Husnain; Shaheen N Khan; Ian M MacDonald; Sheikh Riazuddin
Mutations in RLBP1 associated with fundus albipunctatus in consanguineous Pakistani families.
The British journal of ophthalmology 2011;95(7):1019-24.
2011: Mohsin Khan; Shaheen N Khan; Sadia Mohsin; Sheikh Amer Riazuddin
Repair of senescent myocardium by mesenchymal stem cells is dependent on the age of donor mice.
Journal of cellular and molecular medicine 2011;15(7):1515-27.
2011: Zubair M Ahmed; Rizwan Yousaf; Byung Cheon Lee; Shaheen N Khan; Sue Lee; Kwanghyuk Lee; Tayyab Husnain; Atteeq Ur Rehman; Sarah Bonneux; Muhammad Ansar; Wasim Ahmad; Suzanne M Leal; Vadim N Gladyshev; Inna A Belyantseva; Guy Van Camp; Sheikh Amer Riazuddin; Thomas B Friedman; Saima Riazuddin
Functional null mutations of MSRB3 encoding methionine sulfoxide reductase are associated with human deafness DFNB74.
American journal of human genetics 2011;88(1):19-29.
2011: Usman Ali Ashfaq; Shaheen N Khan; Zafar Nawaz; Sheikh Amer Riazuddin
In-vitro model systems to study Hepatitis C Virus.
Genetic vaccines and therapy 2011;9():7.
2011: Sadia Mohsin; Sulaiman Shams; Ghazanfar Ali Nasir; Mohsin Khan; Sana Javaid Awan; Shaheen N Khan; Sheikh Amer Riazuddin
Enhanced hepatic differentiation of mesenchymal stem cells after pretreatment with injured liver tissue.
Differentiation; research in biological diversity 2011;81(1):42-8.
2010: Sheikh Amer Riazuddin; Amber Shahzadi; Christina Zeitz; Zubair M Ahmed; Radha Ayyagari; Venkata R M Chavali; Virgilio G Ponferrada; Isabelle Audo; Christelle Michiels; Marie-Elise Lancelot; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Xiaodong Jiao; Ian M MacDonald; Sheikh Riazuddin; Paul Sieving; Nicholas Katsanis; J Fielding Hejtmancik
A mutation in SLC24A1 implicated in autosomal-recessive congenital stationary night blindness.
American journal of human genetics 2010;87(4):523-31.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Ectopia lentis in a consanguineous pakistani family and a novel locus on chromosome 8q.
Archives of ophthalmology 2010;128(8):1046-9.
2010: Amber Shahzadi; Sheikh Amer Riazuddin; Shahbaz Ali; David Li; Shaheen N Khan; Tayyab Husnain; Javed Akram; Paul Sieving; J Fielding Hejtmancik; Sheikh Riazuddin
Nonsense mutation in MERTK causes autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family.
The British journal of ophthalmology 2010;94(8):1094-9.
2010: Atteeq Ur Rehman; Robert J Morell; Inna A Belyantseva; Shahid Y Khan; Erich T Boger; Mohsin Shahzad; Zubair M Ahmed; Saima Riazuddin; Shaheen N Khan; Sheikh Amer Riazuddin; Thomas B Friedman
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.
American journal of human genetics 2010;86(3):378-88.
2010: Namerah Sabir; Sheikh Amer Riazuddin; Haiba Kaul; Farheena Iqbal; Idrees A Nasir; Ahmad U Zafar; Zaheeruddin A Qazi; Nadeem H Butt; Shaheen N Khan; Tayyab Husnain; J Fielding Hejtmancik; Sheikh Riazuddin
Mapping of a novel locus associated with autosomal recessive congenital cataract to chromosome 8p.
Molecular vision 2010;16():2911-5.
2010: Namerah Sabir; Sheikh Amer Riazuddin; Tariq Butt; Farheena Iqbal; Idrees A Nasir; Ahmad U Zafar; Zaheeruddin A Qazi; Nadeem H Butt; Shaheen N Khan; Tayyab Husnain; J Fielding Hejtmancik; Sheikh Riazuddin
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3q.
Molecular vision 2010;16():2634-8.
2010: Afshan Yasmeen; Sheikh Amer Riazuddin; Haiba Kaul; Sadia Mohsin; Mohsin Khan; Zaheeruddin A Qazi; Idrees A Nasir; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1.
Molecular vision 2010;16():682-8.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Mariam Shahid; Samra Kousar; Nadeem H Butt; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family.
Molecular vision 2010;16():511-7.
2010: Haiba Kaul; Sheikh Amer Riazuddin; Afshan Yasmeen; Sadia Mohsin; Mohsin Khan; Idrees A Nasir; Shaheen N Khan; Tayyab Husnain; Javed Akram; J Fielding Hejtmancik; Sheikh Riazuddin
A new locus for autosomal recessive congenital cataract identified in a Pakistani family.
Molecular vision 2010;16():240-5.
2009: Julie M Schultz; Shaheen N Khan; Zubair M Ahmed; Saima Riazuddin; Ali M Waryah; Dhananjay Chhatre; Matthew F Starost; Barbara Ploplis; Stephanie Buckley; David Velásquez; Madhulika Kabra; Kwanghyuk Lee; Muhammad J Hassan; Ghazanfar Ali; Muhammad Ansar; Manju Ghosh; Edward R Wilcox; Wasim Ahmad; Glenn Merlino; Suzanne M Leal; Sheikh Amer Riazuddin; Thomas B Friedman; Robert J Morell
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
American journal of human genetics 2009;85(1):25-39.
2009: Mohsin Khan; Sobia Manzoor; Sadia Mohsin; Shaheen N Khan; Fridoon Jawad Ahmad
IGF-1 and G-CSF complement each other in BMSC migration towards infarcted myocardium in a novel in vitro model.
Cell biology international 2009;33(6):650-7.
2009: Zubair M Ahmed; Sheikh Amer Riazuddin; Shaheen N Khan; P L Friedman; S Riazuddin; Thomas B Friedman
USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23.
Clinical genetics 2009;75(1):86-91.
2008: Sheikh Amer Riazuddin; Sabiha Nazli; Zubair M Ahmed; Yi Yang; Fareeha Zulfiqar; Rehan S Shaikh; Ahmed U Zafar; Shaheen N Khan; Farooq Sabar; Fouzia T Javid; Edward R Wilcox; Ekaterini Tsilou; Erich T Boger; James R Sellers; Inna A Belyantseva; Sheikh Riazuddin; Thomas B Friedman
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual function.
Human mutation 2008;29(4):502-11.
2008: Sabika Firasat; Sheikh Amer Riazuddin; Shaheen N Khan; Sheikh Riazuddin
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.
Molecular vision 2008;14():2002-9.
2007: Quratul Ain; Sabiha Nazli; Saima Riazuddin; Ateeq-ul Jaleel; Sheikh Amer Riazuddin; Ahmad U Zafar; Shaheen N Khan; Tayyab Husnain; Andrew J Griffith; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3.
Human genetics 2007;122(5):445-50.
2007: Shahid Y Khan; Zubair M Ahmed; Muhammad I Shabbir; Shin-ichiro Kitajiri; Saeeda Kalsoom; Saba Tasneem; Sara Shayiq; Arabandi Ramesh; Srikumari Srisailpathy; Shaheen N Khan; Richard J H Smith; Sheikh Amer Riazuddin; Thomas B Friedman; Sheikh Riazuddin
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus.
Human mutation 2007;28(5):417-23.
2007: Shahid Y Khan; Saima Riazuddin; Muhammad Tariq; Saima Anwar; Muhammad I Shabbir; Sheikh Amer Riazuddin; Shaheen N Khan; Tayyab Husnain; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.
Human genetics 2007;120(6):789-93.
2006: Sheikh Amer Riazuddin; Zubair M Ahmed; Alan S Fanning; Ayala Lagziel; Shin-ichiro Kitajiri; Khushnooda Ramzan; Shaheen N Khan; Parna Chattaraj; Penelope L Friedman; James M Anderson; Inna A Belyantseva; Andrew Forge; Sheikh Riazuddin; Thomas B Friedman
Tricellulin is a tight-junction protein necessary for hearing.
American journal of human genetics 2006;79(6):1040-51.
2006: Muhammad I Shabbir; Zubair M Ahmed; Shahid Y Khan; Sheikh Amer Riazuddin; A M Waryah; Shaheen N Khan; R D Camps; M Ghosh; M Kabra; Inna A Belyantseva; Thomas B Friedman; Sheikh Riazuddin
Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.
Journal of medical genetics 2006;43(8):634-40.
2006: Sheikh Amer Riazuddin; Shaheen N Khan; Zubair M Ahmed; Manju Ghosh; Kyle Caution; Sabiha Nazli; Madhulika Kabra; Ahmad U Zafar; Kevin Chen; Sadaf Naz; Anthony Antonellis; William J Pavan; Eric Green; Edward R Wilcox; Penelope L Friedman; Robert J Morell; Sheikh Riazuddin; Thomas B Friedman
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
American journal of human genetics 2006;78(1):137-43.
2005: Rehan Sadiq Shaikh; Khushnooda Ramzan; Sabiha Nazli; Sameera Sattar; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.
American journal of medical genetics. Part A 2005;138(4):392-5.
2005: Jamil Ahmad; Shaheen N Khan; Shahid Y Khan; Khushnooda Ramzan; Sheikh Amer Riazuddin; Zubair M Ahmed; Edward R Wilcox; Thomas B Friedman; Sheikh Riazuddin
DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1.
Human genetics 2005;116(5):407-12.
2005: Khushnooda Ramzan; Rehan S Shaikh; Jamil Ahmad; Shaheen N Khan; Sheikh Amer Riazuddin; Zubair M Ahmed; Thomas B Friedman; Edward R Wilcox; Sheikh Riazuddin
A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1.
Human genetics 2005;116(1-2):17-22.
2004: Sadaf Naz; Andrew J Griffith; S Riazuddin; Lori L Hampton; James F Battey; Shaheen N Khan; Sheikh Amer Riazuddin; Edward R Wilcox; Thomas B Friedman
Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction.
Journal of medical genetics 2004;41(8):591-5.
2003: Zubair M Ahmed; Robert J Morell; Sheikh Amer Riazuddin; Andrea Gropman; Shahzad Shaukat; Mussaber M Ahmad; Saidi Mohiddin; Lameh Fananapazir; Rafael C Caruso; Tayyab Husnain; Shaheen N Khan; Sheikh Riazuddin; Andrew J Griffith; Thomas B Friedman; Edward R Wilcox
Mutations of MYO6 are associated with recessive deafness, DFNB37.
American journal of human genetics 2003;72(5):1315-22.
2001: Julie M Bork; Linda M Peters; S Riazuddin; Steven L Bernstein; Z M Ahmed; Seth L Ness; R Polomeno; Arabandi Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Zubair M Ahmed; Shaheen N Khan; V M Kaloustian; XC Li; Anil K Lalwani; Sheikh Amer Riazuddin; Maria Bitner-Glindzicz; Walter E Nance; Xue Zhong Liu; G Wistow; Richard J H Smith; Andrew J Griffith; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
American journal of human genetics 2001;68(1):26-37.