FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Shobbir Hussain

Research Profile

Chemicals & Drugs

Disorders

Fanconi's Anemia

Procedures

Living Beings

Anatomy

Tumor Cell Line

Genes & Molecular Sequences

Concepts & Ideas

Molecular Sequence Data

Co-author Network

Publications

TOP 3
Shobbir Hussain; Nobuaki R Kudo; Frank Lyko; Suraj Menon; Francesca Tuorto; Stephen Watt; Sandra Blanco; Claire Cox; Joana V Flores; Michaela Frye
The mouse cytosine-5 RNA methyltransferase NSun2 is a component of the chromatoid body and required for testis differentiation.
Muzammil Ahmad Khan; Roland Malli; Abdul Noor; Muhammad Arshad Rafiq; Verena Rupp; Akshita K Vincent; Rosanna Weksberg; Christian Windpassinger; Ghazanfar Ali; Muhammad Ansar; Muhammad Ayub; Dan Doherty; Joana Vieira Flores; Michaela Frye; Shobbir Hussain; Shahnaz Ibrahim; Gisele E Ishak; Falak Sher Khan; John B Vincent
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.
Elisabete M Nascimento; Jennifer Nichols; Duncan T Odom; Menon Suraj; Matthew Trotter; Salvador Aznar Benitah; Sandra Blanco; Claire L Cox; Brian Hendrich; Shobbir Hussain; Bernd Kübler; Stewart MacArthur; Michaela Frye
The opposing transcriptional functions of Sin3a and c-Myc are required to maintain tissue homeostasis.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Shobbir Hussain (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Shobbir Hussain; Nobuaki R Kudo; Frank Lyko; Suraj Menon; Francesca Tuorto; Stephen Watt; Sandra Blanco; Claire Cox; Joana V Flores; Michaela Frye
The mouse cytosine-5 RNA methyltransferase NSun2 is a component of the chromatoid body and required for testis differentiation.
Molecular and cellular biology 2013;33(8):1561-70.
2012: Muzammil Ahmad Khan; Roland Malli; Abdul Noor; Muhammad Arshad Rafiq; Verena Rupp; Akshita K Vincent; Rosanna Weksberg; Christian Windpassinger; Ghazanfar Ali; Muhammad Ansar; Muhammad Ayub; Dan Doherty; Joana Vieira Flores; Michaela Frye; Shobbir Hussain; Shahnaz Ibrahim; Gisele E Ishak; Falak Sher Khan; John B Vincent
Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.
American journal of human genetics 2012;90(5):856-63.
2011: Elisabete M Nascimento; Jennifer Nichols; Duncan T Odom; Menon Suraj; Matthew Trotter; Salvador Aznar Benitah; Sandra Blanco; Claire L Cox; Brian Hendrich; Shobbir Hussain; Bernd Kübler; Stewart MacArthur; Michaela Frye
The opposing transcriptional functions of Sin3a and c-Myc are required to maintain tissue homeostasis.
Nature cell biology 2011;13(12):1395-405.
2009: Shobbir Hussain; Sandra Blanco Benavente; Elisabete Nascimento; Ilaria Dragoni; Agata Kurowski; Astrid Gillich; Peter Humphreys; Michaela Frye
The nucleolar RNA methyltransferase Misu (NSun2) is required for mitotic spindle stability.
The Journal of cell biology 2009;186(1):27-40.
2008: James B Wilson; K Yamamoto; A S Marriott; Shobbir Hussain; P Sung; Maureen Hoatlin; Christopher G Mathew; M Takata; Larry H Thompson; G M Kupfer; Nigel Jones
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.
Oncogene 2008;27(26):3641-52.
2007: Ravi K Nookala; Shobbir Hussain; Luca Pellegrini
Insights into Fanconi Anaemia from the structure of human FANCE.
Nucleic acids research 2007;35(5):1638-48.
2006: Shobbir Hussain; James B Wilson; Eric Blom; Larry H Thompson; Patrick Sung; Susan M Gordon; Gary M Kupfer; Hans Joenje; Christopher G Mathew; Nigel Jones
Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.
DNA repair 2006;5(5):629-40.
2005: Marieke Levitus; Quinten Waisfisz; Barbara C Godthelp; Yne de Vries; Shobbir Hussain; Wouter W Wiegant; Elhaam Elghalbzouri-Maghrani; Jûrgen Steltenpool; Martin A Rooimans; Gerard Pals; Fré Arwert; Christopher G Mathew; Malgorzata Z Zdzienicka; Kevin Hiom; Johan P de Winter; Hans Joenje
The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.
Nature genetics 2005;37(9):934-5.
2004: Shobbir Hussain; James B Wilson; Annette L Medhurst; James Hejna; Emily Witt; Sahana Ananth; Adelina Davies; Jean-Yves Masson; Robb Moses; Stephen C West; Johan P de Winter; Alan Ashworth; Nigel Jones; Christopher G Mathew
Direct interaction of FANCD2 with BRCA2 in DNA damage response pathways.
Human molecular genetics 2004;13(12):1241-8.
2003: Shobbir Hussain; Emily Witt; Pia A J Huber; Annette L Medhurst; Alan Ashworth; Christopher G Mathew
Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
Human molecular genetics 2003;12(19):2503-10.