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59.933 Aktuelle Fachpublikationen aus der Branche Medizin

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Montagna Symposium 2014|[mdash]|Skin Aging: Molecular Mechanisms and Tissue Consequences

01.04.2015 | Barbara A Gilchrest; Judith Campisi; Howard Y Chang; Gary J Fisher; Molly F Kulesz-Martin, Journal of Investigative Dermatology, 2015

Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences Journal of Investigative Dermatology 135, 950 (April 2015). doi:10.1038/jid.2014.546 Authors: Barbara A Gilchrest, Judith Campisi, Howard Y Chang, Gary J Fisher & Molly F Kulesz-Martin

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Spatial cognition in bats and rats: from sensory acquisition to multiscale maps and navigation

01.04.2015 | Maya Geva-Sagiv; Liora Las; Yossi Yovel; Nachum Ulanovsky, Nature Reviews Neuroscience, 2015

Nature Reviews Neuroscience 16, 244 (2015). doi:10.1038/nrn3931 Author: Maya Geva-Sagiv, Liora Las, Yossi Yovel & Nachum Ulanovsky Nature Reviews Neuroscience16, 94–108 (2015)On page 97 of the above article, the final line of the text of Box 1 should have read 'The figure part ...

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Announcement: double-blind peer review

01.04.2015 | Nature Immunology, 2015

Nature Immunology 16, 327 (2015). doi:10.1038/ni.3129 Nature and its sister journals start offering anonymity to authors during the peer-review process.

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BJD Editor's Choice

01.04.2015 | Journal of Investigative Dermatology, 2015

BJD Editor's Choice Journal of Investigative Dermatology 135, 933 (April 2015). doi:10.1038/jid.2015.34

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Leonard C. Harber (1927|[ndash]|2014)

01.04.2015 | David R Bickers, Journal of Investigative Dermatology, 2015

Leonard C. Harber (1927–2014) Journal of Investigative Dermatology 135, 935 (April 2015). doi:10.1038/jid.2014.550 Author: David R Bickers

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Verbascoside down‐regulates some pro‐inflammatory signal transduction pathways by increasing the activity of tyrosine phosphatase SHP‐1 in the U937 cell line

22.03.2015 | Mirko Pesce, Sara Franceschelli, Alessio Ferrone, Maria Anna De Lutiis, Antonia Patruno, Alfredo Grilli, Mario Felac ..., Journal of Cellular and Molecular Medicine, 2015

Abstract Polyphenols are the major components of many traditional herbal remedies, which exhibit several beneficial effects including anti‐inflammation and antioxidant properties. Src homology region 2 domain‐containing phosphatase‐1 (SHP‐1) is a redox sensitive protein tyrosine phosphatase ...

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Oculoectodermal syndrome is a mosaic RASopathy associated with KRAS alterations

22.03.2015 | Jacqueline D. Peacock, Karl J. Dykema, Helga V. Toriello, Marie R. Mooney, Donald J. Scholten, Mary E. Winn, Andrew ..., American Journal of Medical Genetics Part A, 2015

Oculoectodermal syndrome (OES) is a rare disease characterized by a combination of congenital scalp lesions and ocular dermoids, with additional manifestations including non‐ossifying fibromas and giant cell granulomas of the jaw occurring during the first decade of life. To identify the ...

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Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene

22.03.2015 | Megan Beck, Jess F. Peterson, Juliann McConnell, Marianne McGuire, Miya Asato, Joseph E. Losee, Urvashi Surti, Sunee ..., American Journal of Medical Genetics Part A, 2015

Deletions spanning the MN1 gene (22q12.1) have recently been proposed as playing a role in craniofacial abnormalities that include cleft palate, as mouse studies have demonstrated that Mn1 haploinsufficiency results in skull abnormalities and secondary cleft palate. We report on four patients ...

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FLCN intragenic deletions in Chinese familial primary spontaneous pneumothorax

22.03.2015 | Yibing Ding, Chengchu Zhu, Wei Zou, Dehua Ma, Haiyan Min, Baofu Chen, Minhua Ye, Yanqing Pan, Lei Cao, Yueming Wan, ..., American Journal of Medical Genetics Part A, 2015

Primary spontaneous pneumothorax (PSP) is a significant clinical problem, affecting tens of thousands patients annually. Germline mutations in the FLCN gene have been implicated in etiology of familial PSP (FPSP). Most of the currently identified FLCN mutations are small indels or point ...

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De novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

22.03.2015 | Colin J McMahon, Colm Breathnach, David R Betts, Freddie H Sharkey, Marie T Greally, American Journal of Medical Genetics Part A, 2015

We describe a 6‐year‐old male, diagnosed at birth with double outlet right ventricle (DORV), anterior aorta, multiple ventricular septal defects, pulmonary stenosis, microcephaly and mildly dysmorphic craniofacial findings. Chromosomal analysis showed a normal male karyotype but on subsequent ...

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