Protein-Serine-Threonine Kinases < Proteins < Proteomics

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 22.
[0-20] [0 - 20][0 - 22][20-21][20-40]

Ident.	Authors (with country if any)	Title
000424 (2001)	H. Ujike [Japon] ; M. Yamamoto ; A. Kanzaki ; K. Okumura ; M. Takaki ; S. Kuroda	Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease.
000437 (2001)	C S Lu [Taïwan] ; J C Wu ; C H Tsai ; R S Chen ; Y H Chou ; N. Hattori ; H. Yoshino ; Y. Mizuno	Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
000585 (2001)	A. Danek [Allemagne] ; F. Tison ; J. Rubio ; M. Oechsner ; W. Kalckreuth ; A P Monaco	The chorea of McLeod syndrome.
000A37 (2003)	Saeed Bohlega [Arabie saoudite] ; Adel Al-Jishi ; Carol Dobson-Stone ; Luca Rampoldi ; Parthasarathi Saha ; Hatem Murad ; Abid Kareem ; George Roberts ; Anthony P. Monaco	Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula.
000A41 (2003)	Haydeh Payami [États-Unis] ; John Nutt ; Steven Gancher ; Thomas Bird ; Melissa Gonzales Mcneal ; William K. Seltzer ; Jennifer Hussey ; Paul Lockhart ; Katrina Gwinn-Hardy ; Amanda A. Singleton ; Andrew B. Singleton ; John Hardy ; Matthew Farrer	SCA2 may present as levodopa-responsive parkinsonism.
000C95 (2004)	Paul J. Lockhart [États-Unis] ; Casey A. O'Farrell ; Matthew J. Farrer	It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG).
000C97 (2004)	Susan Hollán [Hongrie] ; Lászl Vécsei ; Kálmán Magyar	Adverse effects of dopamine potentiation by long-term treatment with selegiline.
000D61 (2004)	Anne Roubergue [France] ; Emmanuelle Apartis ; Marie Vidailhet ; Cyril Mignot ; Anna Tullio-Pelet ; Stanislas Lyonnet ; Thierry Billette De Villemeur	Myoclonus and generalized digestive dysmotility in triple A syndrome with AAAS gene mutation.
000E19 (2004)	Patrice Péran [France] ; Jean-François Démonet ; Cyril Pernet ; Dominique Cardebat	Verb and noun generation tasks in Huntington's disease.
000E26 (2004)	Alastair Wilkins [Royaume-Uni] ; Jerry M. Brown ; Roger A. Barker	SCA2 presenting as levodopa-responsive parkinsonism in a young patient from the United Kingdom: a case report.
000E87 (2004)	Igor Sibon [France] ; Imad Ghorayeb ; Pierre Arné ; François Tison	Distressing belching and neuroacanthocytosis.
000F51 (2004)	Din-E Shan [République populaire de Chine] ; Ren-Shyan Liu ; Chen-Ming Sun ; Shwn-Jen Lee ; Kwong-Kum Liao ; Bing-Wen Soong	Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications.
001308 (2005)	Jason D. Dapper [États-Unis] ; Monica J. Justice	Defining the breakpoints of the quaking(viable) mouse mutation reveals a duplication from a Parkin intron.
002075 (2008)	Shu-Shan Zhang ; Qin Chen ; Xue-Ping Chen ; Jian-Gang Wang ; Jean-Marc Burgunder ; Hui-Fang Shang ; Jean-Marc Burgunder ; Yuan Yang	Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.
002991 (2010)	Paola S. Denora ; Knut Brockmann ; Marianna Ciccolella ; Jeremy Truchetto ; Giovanni Stevanin ; Filippo M. Santorelli	Identification of a de novo mutation in SPG11.
002A76 (2010)	Ana Maria Cuervo [États-Unis] ; Esther S P. Wong ; Marta Martinez-Vicente	Protein degradation, aggregation, and misfolding.
002D61 (2010)	Emanuele Cereda [Italie] ; Michela Barichella ; Carlo Pedrolli ; Gianni Pezzoli	Low-protein and protein-redistribution diets for Parkinson's disease patients with motor fluctuations: a systematic review.
002D65 (2010)	Coro Paisán-Ruiz [Royaume-Uni] ; Rocio Guevara ; Monica Federoff ; Hasmet Hanagasi ; Fardaz Sina ; Elahe Elahi ; Susanne A. Schneider ; Petra Schwingenschuh ; Nin Bajaj ; Murat Emre ; Andrew B. Singleton ; John Hardy ; Kailash P. Bhatia ; Sebastian Brandner ; Andrew J. Lees ; Henry Houlden	Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
003016 (2011)	Arianna Guidubaldi [Italie] ; Carla Piano ; Filippo M. Santorelli ; Gabriella Silvestri ; Martina Petracca ; Alessandra Tessa ; Anna Rita Bentivoglio	Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism.
003746 (2012)	Sean O Owd [Irlande (pays)] ; Denis Curtin [Irlande (pays)] ; Adrian J. Waite [Royaume-Uni] ; Kinley Roberts [Irlande (pays)] ; Niall Pender [Irlande (pays)] ; Valerie Reid [Irlande (pays)] ; Martin O Onnell [Irlande (pays)] ; Nigel M. Williams [Royaume-Uni] ; Huw R. Morris [Royaume-Uni] ; Bryan J. Traynor [États-Unis] ; Timothy Lynch [Irlande (pays)]	C9ORF72 Expansion in Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Also Causes Parkinsonism
003860 (2012)	Brent L. Fogel [États-Unis] ; Mochtar Pribadi [États-Unis] ; Sarah Pi [États-Unis] ; Susan L. Perlman [États-Unis] ; Daniel H. Geschwind [États-Unis] ; Giovanni Coppola [États-Unis]	C9ORF72 Expansion is Not a Significant Cause of Sporadic Spinocerebellar Ataxia

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Ncbi/Checkpoint

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/Mesh.i -k "Proteins" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Checkpoint/Mesh.i  \
                -Sk "Proteins" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Checkpoint/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Ncbi
   |étape=   Checkpoint
   |type=    indexItem
   |index=    Mesh.i
   |clé=    Proteins
}}

---

This area was generated with Dilib version V0.6.23. Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024