WRN

LE WE PMID CA

WRN

7129

WRN

ABCC8 SUR1

Anemia (megaloblastic thiamine responsive)

Bererdinelli Seip congenital lipodystrophy

BLM

BSCL1 AGPAT2

BSCL2 Seipin

Cell cylce (BASKET)

Diabetes mellitus (Hereditary MODY)

Diabetes mellitus (hereditary)

Diabetes mellitus (neonatal)

DNA (helicase)

DNA (Repair and Toxicology)

DNA (Replication)

Donohue s syndrome Leprechaunism

EIF2AK3 PERK

FRDA1 Frataxin

Friedreich ataxia

Genetic instability

Glucokinase

GLUD1

Insulin resistance type a

KCNJ11 Kir6 2

Lipodystrophy

OMIM_601487

OMIM_x600937

Persistent hyperinsulinemic hypoglycemia of infancy

Persistent neonatal hypoglycemia

Pot1

Rabson Mendenhall s syndrome

Receptor (Insulin)

Receptor (PPAR gamma)

RECQ1

RECQ4

RECQ5

SLC19A2 THTR1

Telomere

TNDM29locus

TRF1

TRF2

Werner s syndrome

Wfs1 Wolframin

Wfs2

Wolcott Rallison syndrome

Wolfram s syndrome DIDMOAD

WRN

2011 1	The Werner syndrome protein: linking the replication checkpoint response to genome stability. [21389352] Aging (Albany NY) 3(3): 311-8 (2011)
2007 2	WRN at telomeres: implications for aging and cancer. [17314245] J Cell Sci 120(Pt 5): 713-21 (2007)
2010 3	Distinct roles of RECQ1 in the maintenance of genomic stability. [20061189] DNA Repair (Amst) 9(3): 315-24 (2010)
2010 4	Roles of Werner syndrome protein in protection of genome integrity. [20075015] DNA Repair (Amst) 9(3): 331-44 (2010)
2008 5	Roles of the Werner syndrome RecQ helicase in DNA replication. [18722555] DNA Repair (Amst) 7(11): 1776-86 (2008)
2005 6	Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure. [15772126] J Med Genet 42(12): 893-902 (2005)
2010 7	Unwinding protein complexes in ALTernative telomere maintenance. [19911388] J Cell Biochem 109(1): 7-15 (2010)

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