Bulimia research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Bulimia treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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9771 Abstracts
Research
Transgenic expression of syndecan-1 uncovers a physiological control of feeding behavior by syndecan-3.
Reizes O, Lincecum J, Wang Z, Goldberger O, Huang L ...
Cell Vol 106(1)
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Date 13 Jul 2001
Research
KSR2 mutations are associated with obesity, insulin resistance, and impaired cellular fuel oxidation.
Pearce Laura R, Atanassova Neli, Banton Matthew C, Bottomley Bill, van der Klaauw Agatha A ...
Cell Vol 155(4)
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Date 07 Nov 2013
Research
Targeted disruption of the melanocortin-4 receptor results in obesity in mice.
Huszar D, Lynch C A, Fairchild-Huntress V, Dunmore J H, Fang Q ...
Cell Vol 88(1)
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Date 10 Jan 1997
Research
Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.
Mundlos S, Otto F, Mundlos C, Mulliken J B, Aylsworth A S ...
Cell Vol 89(5)
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Date 30 May 1997
Research
Mitofusin 2 in POMC neurons connects ER stress with leptin resistance and energy imbalance.
Schneeberger Marc, Dietrich Marcelo O, Sebastián David, Imbernón Mónica, Castaño Carlos ...
Cell Vol 155(1)
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Date 26 Sep 2013
Research
Decoding neural circuits that control compulsive sucrose seeking.
Nieh Edward H, Matthews Gillian A, Allsop Stephen A, Presbrey Kara N, Leppla Christopher A ...
Cell Vol 160(3)
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Date 29 Jan 2015
Research
Dopamine is required for hyperphagia in Lep(ob/ob) mice.
Szczypka M S, Rainey M A, Palmiter R D
Nature genetics Vol 25(1)
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Date 01 May 2000
Research
Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.
Hurvitz J R, Suwairi W M, Van Hul W, El-Shanti H, Superti-Furga A ...
Nature genetics Vol 23(1)
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Date 01 Sep 1999
Research
Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Lerner-Ellis Jordan P, Tirone Jamie C, Pawelek Peter D, Doré Carole, Atkinson Janet L ...
Nature genetics Vol 38(1)
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Date 01 Jan 2006
Research
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch.
Bielinska B, Blaydes S M, Buiting K, Yang T, Krajewska-Walasek M ...
Nature genetics Vol 25(1)
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Date 01 May 2000
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