Results 161 to 170 of about 23,382 (212)

Lamin A/C loss promotes R-loop-mediated genomic instability and poor survival in small-cell lung cancer. [PDF]

Proc Natl Acad Sci U S A
Schultz CW, Saha S, Dhall A, Zhang Y, Desai P, Pongor LS, Scheiblin DA, Magidson V, Shuklah RP, Sebastian R, Vekariya UM, Ahmed S, Sun Y, Redon C, Kumar S, Krishnamurthy M, Dias HB, Aksenova V, Giordano E, Takahashi N, Nirula M, Arora M, Tabe C, Thomas MS, Kumar R, Arakawa Y, Jo U, Skorski T, Teicher BA, Shreshta R, Aladjem MI, Lockett S, Dasso M, Pommier Y, Sharma AK, Thomas A.   +35 more
europepmc   +1 more source

Severe cardiac valvular calcification in two Chinese brothers with mandibuloacral dysplasia type A: a case report. [PDF]

Front Cardiovasc Med
Guo Y, Zhang X, Meng Y, Guo Q, Wang X.
europepmc   +1 more source

Stem cell-associated osteogenic deficiency causes craniofacial deformities with progeroid accumulation of prelamin A. [PDF]

JCI Insight
Li K, Hsu T, Uchida H, Wu T, Michaelis S, Worman H, Hsu W.   +6 more
europepmc   +1 more source

Classic Protocadherin PCDH10 Functions as a Tumor Suppressive Scaffold Protein Antagonizing Oncogenic WNT/β-catenin Signaling in Breast Carcinogenesis. [PDF]

Int J Biol Sci
Wang X, Tan Y, Wang Y, Li L, Xiang T, Chen Y, Peng W, Qiu Z, Li H, Ren G, Tao Q.   +10 more
europepmc   +1 more source

Genetically Confirmed Familial Case of Nonsyndromic Cardiac Progeria Caused by the <i>LMNA</i> p.Asp300Asn Variant with Presumed Gonadal Mosaicism: Phenotypic Comparison with Previously Reported Patients. [PDF]

Genes (Basel)
Nuzhnaya E, Sharova M, Chubykina U, Orlova A, Vorontsova E, Vasiliev P.   +5 more
europepmc   +1 more source

Genotype-first approach reveals monogenic lipodystrophy is underdiagnosed, with health and mortality risks. [PDF]

EBioMedicine
Sharp LN, Colclough K, Murray Leech J, Evans AV, Hattersley AT, Weedon MN, Brown RJ, Patel KA.   +7 more
europepmc   +1 more source

Precise gene editing of pathogenic Lamin A mutations corrects cardiac disease. [PDF]

Proc Natl Acad Sci U S A
Caravia XM, Hayashi B, Li H, Gan P, Alzhanov D, Tan W, Chen K, McAnally JR, Xu L, Liu N, Olson EN.   +10 more
europepmc   +1 more source

Why and How Are Infants with Hutchinson-Gilford Progeria Syndrome Born Without Severe Manifestations? [PDF]

Med Sci (Basel)
Erokhina MA, Vorotelyak EA, Vasiliev AV, Abdyev VK.   +3 more
europepmc   +1 more source

Elucidating the function of novel genes and molecular mechanisms involved in accelerated ageing [PDF]

, 2017
Schotik, Maria
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