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Studies

30309 Unclassified

14204 Reviews

12684 Research

11581 Case Reports

5543 Other Trials

3618 Advanced Trials

2509 Early Trials

344 Meta-Analysis

Guidelines

170 Guidelines

99 Consensuses

64 Cochrane

Congresses

4450 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)

Read

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

Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome.

Sousa Sérgio B, Jenkins Dagan, Chanudet Estelle, Tasseva Guergana, Ishida Miho ...

Nature genetics Vol 46(1)

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Date 01 Jan 2014

Institutional score
323.39
Impact
2459.31

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Date 01 Jan 2014

Institutional score
323.39
Impact
2459.31
8

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
9

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
10

Research

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia.

Nürnberg P, Thiele H, Chandler D, Höhne W, Cunningham M L ...

Nature genetics Vol 28(1)

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Date 01 May 2001

Institutional score
0.00
Impact
2459.31

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Date 01 May 2001

Institutional score
0.00
Impact
2459.31

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