Results 151 to 160 of about 9,936 (203)
Progerin-induced nuclear envelope remodeling is shaped by cell division and NUP153. [PDF]
J Cell SciTurkmen AM, Wang J, Frost A, Ullman KS.
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Mechanics and mechanobiology of arterial development. [PDF]
Biomech Model MechanobiolHumphrey JD, Schwarz EL.
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Farnesylated prelamin A induces fibroblast polarity defects in premature aging disorders by inhibiting nesprin-2-SUN2 LINC complex function. [PDF]
J Cell SciLio C +9 more
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Surgical Aortic Valve Replacement Combined With Coronary Artery Bypass Grafting in a Patient With Progeria. [PDF]
JACC Case RepAnquetil S +3 more
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Archives of Dermatology, 1989
Progeria, also known as the Hutchinson-Gilford syndrome, is an extremely rare condition that was initially reported by Johnathan Hutchinson in 1886 and further described by Hastings Gilford in 1904. Transmission is most likely from a sporadic autosomal dominant mutation.
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Progeria, also known as the Hutchinson-Gilford syndrome, is an extremely rare condition that was initially reported by Johnathan Hutchinson in 1886 and further described by Hastings Gilford in 1904. Transmission is most likely from a sporadic autosomal dominant mutation.
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Journal of Anti-Aging Medicine, 2003
Abstract In a book on cell senescence in human disease, it is negligent not to discuss progerias, yet from what perspective? Does cell senescence cause progerias? Do the progerias cause cell senescence? Are “progcroid syndromes” (Brown, 1995) related to cell senescence at all (Greally et al., 1992)?
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Abstract In a book on cell senescence in human disease, it is negligent not to discuss progerias, yet from what perspective? Does cell senescence cause progerias? Do the progerias cause cell senescence? Are “progcroid syndromes” (Brown, 1995) related to cell senescence at all (Greally et al., 1992)?
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Pediatrics, 1956
A typical case of progeria (Hutchinson-Gilford syndrome) is reported including the findings of the necropsy. Death occurred at the age of 11 years as the result of an accident. Analysis of cephalometric roentgenograms of this patient revealed that the characteristic facies of progeria results from marked retardation of facial growth in the presence of ...
Ira M. Rosenthal +4 more
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A typical case of progeria (Hutchinson-Gilford syndrome) is reported including the findings of the necropsy. Death occurred at the age of 11 years as the result of an accident. Analysis of cephalometric roentgenograms of this patient revealed that the characteristic facies of progeria results from marked retardation of facial growth in the presence of ...
Ira M. Rosenthal +4 more
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Clinical Radiology, 1976
Progeria or 'prematurely old' is an autosomal recessive trait that appears insidiously at or after the age of 6 months. Two affected siblings are reported showing radiologically progressive attenuation of the clavicles and terminal phalanges, widening of cranial sutures and mandibular hypoplasia. Scleroderma was also present.
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Progeria or 'prematurely old' is an autosomal recessive trait that appears insidiously at or after the age of 6 months. Two affected siblings are reported showing radiologically progressive attenuation of the clavicles and terminal phalanges, widening of cranial sutures and mandibular hypoplasia. Scleroderma was also present.
openaire +2 more sources