Showing 1–7 of 7 results
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Research | | Open
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Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome
- Kirk Mykytyn
- , Darryl Y. Nishimura
- , Charles C. Searby
- , Mythreyi Shastri
- , Hsan-jan Yen
- , John S. Beck
- , Terry Braun
- , Luan M. Streb
- , Alberto S. Cornier
- , Gerald F. Cox
- , Anne B. Fulton
- , Rivka Carmi
- , Güven Lüleci
- , Settara C. Chandrasekharappa
- , Francis S. Collins
- , Samuel G. Jacobson
- , John R. Heckenlively
- , Richard G. Weleber
- , Edwin M. Stone
- & Val C. Sheffield
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Somatic mutation of the MEN1 gene in parathyroid tumours
- Christina Heppner
- , Mary Beth Kester
- , Sunita K. Agarwal
- , Larisa V. Debelenko
- , Michael R. Emmert-Buck
- , Siradanahalli C. Guru
- , Pachiappan Manickam
- , Shodimu-Emmanuel Olufemi
- , Monica C. Skarulis
- , John L. Doppman
- , Richard H. Alexander
- , Young S. Kim
- , Suraj K. Saggar
- , Irina A. Lubensky
- , Zhengping Zhuang
- , Lance A. Liotta
- , Settara C. Chandrasekharappa
- , Francis S. Collins
- , Alien M. Spiegel
- , A. Lee Burns
- & Stephen J. Marx
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Loss-of-function mutations in TNFAIP3 leading to A20 haploinsufficiency cause an early-onset autoinflammatory disease
- Qing Zhou
- , Hongying Wang
- , Daniella M Schwartz
- , Monique Stoffels
- , Yong Hwan Park
- , Yuan Zhang
- , Dan Yang
- , Erkan Demirkaya
- , Masaki Takeuchi
- , Wanxia Li Tsai
- , Jonathan J Lyons
- , Xiaomin Yu
- , Claudia Ouyang
- , Celeste Chen
- , David T Chin
- , Kristien Zaal
- , Settara C Chandrasekharappa
- , Eric P Hanson
- , Zhen Yu
- , James C Mullikin
- , Sarfaraz A Hasni
- , Ingrid E Wertz
- , Amanda K Ombrello
- , Deborah L Stone
- , Patrycja Hoffmann
- , Anne Jones
- , Beverly K Barham
- , Helen L Leavis
- , Annet van Royen-Kerkof
- , Cailin Sibley
- , Ezgi D Batu
- , Ahmet Gül
- , Richard M Siegel
- , Manfred Boehm
- , Joshua D Milner
- , Seza Ozen
- , Massimo Gadina
- , JaeJin Chae
- , Ronald M Laxer
- , Daniel L Kastner
- & Ivona Aksentijevich
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