FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Anne-Marie Lamhonwah

Research Profile

Chemicals & Drugs

Living Beings

Physiology

Mutation

Anatomy

Concepts & Ideas

Molecular Sequence Data

Disorders

Co-author Network

Publications

TOP 3
Zarazuela Zolkipli; Anne-Marie Lamhonwah; Lydia Mai; Ingrid Tein
The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophy.
Anne-Marie Lamhonwah; Lydia Mai; Cilla Chung; Daniel Lamhonwah; Cameron Ackerley; Ingrid Tein
Upregulation of mammary gland OCTNs maintains carnitine homeostasis in suckling infants.
Zarazuela Zolkipli; Christina B Pedersen; Anne-Marie Lamhonwah; Niels Gregersen; Ingrid Tein
Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants.

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 Anne-Marie Lamhonwah (preview)

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

Flash Player Required

All Publications

2012: Zarazuela Zolkipli; Anne-Marie Lamhonwah; Lydia Mai; Ingrid Tein
The mdx mouse as a model for carnitine deficiency in the pathogenesis of Duchenne muscular dystrophy.
Muscle & nerve 2012;46(5):767-72.
2011: Anne-Marie Lamhonwah; Lydia Mai; Cilla Chung; Daniel Lamhonwah; Cameron Ackerley; Ingrid Tein
Upregulation of mammary gland OCTNs maintains carnitine homeostasis in suckling infants.
Biochemical and biophysical research communications 2011;404(4):1010-5.
2011: Zarazuela Zolkipli; Christina B Pedersen; Anne-Marie Lamhonwah; Niels Gregersen; Ingrid Tein
Vulnerability to oxidative stress in vitro in pathophysiology of mitochondrial short-chain acyl-CoA dehydrogenase deficiency: response to antioxidants.
PloS one 2011;6(4):e17534.
2010: Anne-Marie Lamhonwah; Christine E Bear; Ling Jun Huan; Patrick Kim Chiaw; Cameron Ackerley; Ingrid Tein
Cystic fibrosis transmembrane conductance regulator in human muscle: Dysfunction causes abnormal metabolic recovery in exercise.
Annals of neurology 2010;67(6):802-8.
2009: Anne-Marie Lamhonwah; Jeannie Wong; Carolyn Tam; Lydia Mai; Ingrid Tein
Organic cation/carnitine transporter family expression patterns in adult murine heart.
Pathology, research and practice 2009;205(6):395-402.
2008: Ingrid Tein; Orly Elpeleg; Bruria Ben-Zeev; Stanley H Korman; Alexander Lossos; Dorit Lev; Tally Lerman-Sagie; Esther Leshinsky-Silver; Jerry Vockley; Gerard T Berry; Anne-Marie Lamhonwah; Dietrich Matern; Charles R Roe; Niels Gregersen
Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin.
Molecular genetics and metabolism 2008;93(2):179-89.
2008: Anne-Marie Lamhonwah; Cynthia E Hawkins; Carolyn Tam; Jeannie Wong; Lydia Mai; Ingrid Tein
Expression patterns of the organic cation/carnitine transporter family in adult murine brain.
Brain & development 2008;30(1):31-42.
2006: Anne-Marie Lamhonwah; Ingrid Tein
Novel localization of OCTN1, an organic cation/carnitine transporter, to mammalian mitochondria.
Biochemical and biophysical research communications 2006;345(4):1315-25.
2005: Anne-Marie Lamhonwah; Cameron Ackerley; Aina Tilups; Vernon D Edwards; Ronald J Wanders; Ingrid Tein
OCTN3 is a mammalian peroxisomal membrane carnitine transporter.
Biochemical and biophysical research communications 2005;338(4):1966-72.
2005: Anne-Marie Lamhonwah; Cameron Ackerley; Russell Onizuka; Aina Tilups; Daniel Lamhonwah; Cilla Chung; Ke Sheng Tao; Raymond Tellier; Ingrid Tein
Epitope shared by functional variant of organic cation/carnitine transporter, OCTN1, Campylobacter jejuni and Mycobacterium paratuberculosis may underlie susceptibility to Crohn's disease at 5q31.
Biochemical and biophysical research communications 2005;337(4):1165-75.
2004: Anne-Marie Lamhonwah; Russell Onizuka; Simon E Olpin; F Muntoni; Ingrid Tein
OCTN2 mutation (R254X) found in Saudi Arabian kindred: recurrent mutation or ancient founder mutation?
Journal of inherited metabolic disease 2004;27(4):473-6.
2003: Wanli Xuan; Anne-Marie Lamhonwah; Clifford Librach; Keith Jarvi; Ingrid Tein
Characterization of organic cation/carnitine transporter family in human sperm.
Biochemical and biophysical research communications 2003;306(1):121-8.
2003: Anne-Marie Lamhonwah; Jennifer Skaug; Stephen W Scherer; Ingrid Tein
A third human carnitine/organic cation transporter (OCTN3) as a candidate for the 5q31 Crohn's disease locus (IBD5).
Biochemical and biophysical research communications 2003;301(1):98-101.
2002: Anne-Marie Lamhonwah; Simon E Olpin; Rodney J Pollitt; Christine Vianey-Saban; Priscille Divry; Nathalie Guffon; G T N Besley; Russell Onizuka; Linda De Meirleir; Ljerka Cvitanovic-Sojat; Ivo Baric; Carlo Dionisi Vici; Ksenija Fumic; Miljenka Maradin; Ingrid Tein
Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy.
American journal of medical genetics 2002;111(3):271-84.
1999: Anne-Marie Lamhonwah; Ingrid Tein
GFP-Human high-affinity carnitine transporter OCTN2 protein: subcellular localization and functional restoration of carnitine uptake in mutant cell lines with the carnitine transporter defect.
Biochemical and biophysical research communications 1999;264(3):909-14.
1999: Katherine A Siminovitch; Anne-Marie Lamhonwah; AK Somani; Robert Cardiff; Gordon B Mills
Involvement of the SHP-1 tyrosine phosphatase in regulating B lymphocyte antigen receptor signaling, proliferation and transformation.
Current topics in microbiology and immunology 1999;246():291-7; discussion 298.
1998: Anne-Marie Lamhonwah; Ingrid Tein
Carnitine uptake defect: frameshift mutations in the human plasmalemmal carnitine transporter gene.
Biochemical and biophysical research communications 1998;252(2):396-401.
1995: R Kolluri; A Shehabeldin; M Peacocke; Anne-Marie Lamhonwah; K Teichert-Kuliszewska; S M Weissman; Katherine A Siminovitch
Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus.
Human molecular genetics 1995;4(7):1119-26.