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Studies

29675 Unclassified

13852 Reviews

12390 Research

10012 Case Reports

5522 Other Trials

3555 Advanced Trials

2472 Early Trials

343 Meta-Analysis

Guidelines

170 Guidelines

97 Consensuses

64 Cochrane

Congresses

4358 Abstracts

1

Research

Ribosome-mediated specificity in Hox mRNA translation and vertebrate tissue patterning.

Kondrashov Nadya, Pusic Aya, Stumpf Craig R, Shimizu Kunihiko, Hsieh Andrew C ...

Cell Vol 145(3)

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Date 29 Apr 2011

Institutional score
13.65
Impact
3197.10

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Date 29 Apr 2011

Institutional score
13.65
Impact
3197.10
2

Research

Cryo-EM Structure of Chikungunya Virus in Complex with the Mxra8 Receptor.

Basore Katherine, Kim Arthur S, Nelson Christopher A, Zhang Rong, Smith Brittany K ...

Cell Vol 177(7)

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Date 13 Jun 2019

Institutional score
0.00
Impact
3197.10

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Date 13 Jun 2019

Institutional score
0.00
Impact
3197.10
3

Research

Estrogen prevents bone loss via estrogen receptor alpha and induction of Fas ligand in osteoclasts.

Nakamura Takashi, Imai Yuuki, Matsumoto Takahiro, Sato Shingo, Takeuchi Kazusane ...

Cell Vol 130(5)

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Date 07 Sep 2007

Institutional score
128.24
Impact
3197.10

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Date 07 Sep 2007

Institutional score
128.24
Impact
3197.10
4

Research

MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover.

Holmbeck K, Bianco P, Caterina J, Yamada S, Kromer M ...

Cell Vol 99(1)

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Date 01 Oct 1999

Institutional score
20.16
Impact
3197.10

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Date 01 Oct 1999

Institutional score
20.16
Impact
3197.10
5

Research

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.

Morello Roy, Bertin Terry K, Chen Yuqing, Hicks John, Tonachini Laura ...

Cell Vol 127(2)

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Date 20 Oct 2006

Institutional score
39.78
Impact
3197.10

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Date 20 Oct 2006

Institutional score
39.78
Impact
3197.10
6

Research

An endocytic pathway essential for renal uptake and activation of the steroid 25-(OH) vitamin D3.

Nykjaer A, Dragun D, Walther D, Vorum H, Jacobsen C ...

Cell Vol 96(4)

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Date 19 Feb 1999

Institutional score
0.00
Impact
3197.10

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Date 19 Feb 1999

Institutional score
0.00
Impact
3197.10
7

Research

Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.

Albagha Omar M E, Wani Sachin E, Visconti Micaela R, Alonso Nerea, Goodman Kirsteen ...

Nature genetics Vol 43(7)

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Date 29 May 2011

Institutional score
64.68
Impact
2459.31

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Date 29 May 2011

Institutional score
64.68
Impact
2459.31
8

Research

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Watts Giles D J, Wymer Jill, Kovach Margaret J, Mehta Sarju G, Mumm Steven ...

Nature genetics Vol 36(4)

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Date 01 Apr 2004

Institutional score
39.35
Impact
2459.31

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Date 01 Apr 2004

Institutional score
39.35
Impact
2459.31
9

Research

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

Albagha Omar M E, Visconti Micaela R, Alonso Nerea, Langston Anne L, Cundy Tim ...

Nature genetics Vol 42(6)

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Date 01 Jun 2010

Institutional score
64.68
Impact
2459.31

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Date 01 Jun 2010

Institutional score
64.68
Impact
2459.31
10

Research

Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.

Jenkins Zandra A, van Kogelenberg Margriet, Morgan Tim, Jeffs Aaron, Fukuzawa Ryuji ...

Nature genetics Vol 41(1)

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Date 01 Jan 2009

Institutional score
0.00
Impact
2459.31

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Date 01 Jan 2009

Institutional score
0.00
Impact
2459.31

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