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American Journal of Medical Genetics. Part A
|
July 4, 2014
Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?
Davor Lessel, Bidisha Saha, Fuki Hisama, et al.
Molecular Genetics & Genomic Medicine
|
November 6, 2018
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
Forough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, et al.
Journal of Human Genetics
|
May 20, 2011
LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining
Junko Oshima, Jennifer A Lee, Amy M Breman, et al.
Geroscience
|
January 11, 2021
SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome
Renuka Kandhaya-Pillai, Deyin Hou, Jiaming Zhang, et al.
Scientific Reports
|
August 26, 2016
Werner syndrome through the lens of tissue and tumour genomics
Mari Tokita, Scott R Kennedy, Rosa Ana Risques, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2011
Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A
Fuki M Hisama, Davor Lessel, Dru Leistritz, et al.
Molecular Genetics & Genomic Medicine
|
August 13, 2013
Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry
Bidisha Saha, Davor Lessel, Sheela Nampoothiri, et al.
Internal Medicine (Tokyo, Japan)
|
December 21, 2018
Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C
Namiko Matsumoto, Yasuyuki Ohta, Kentaro Deguchi, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 18, 2008
Cigarette smoke induces cellular senescence via Werner's syndrome protein down-regulation
Toru Nyunoya, Martha M Monick, Aloysius L Klingelhutz, et al.
Aging Cell
|
January 19, 2022
DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome
Yosra Bejaoui, Aleem Razzaq, Noha A Yousri, et al.
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of 9
Search research articles
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Showing results (61-70 of 90) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics. Part A
|
July 4, 2014
Atypical Aicardi-Goutieres syndrome: is the WRN locus a modifier?
Davor Lessel, Bidisha Saha, Fuki Hisama, et al.
Molecular Genetics & Genomic Medicine
|
November 6, 2018
CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
Forough Sargolzaeiaval, Jiaming Zhang, Jennifer Schleit, et al.
Journal of Human Genetics
|
May 20, 2011
LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining
Junko Oshima, Jennifer A Lee, Amy M Breman, et al.
Geroscience
|
January 11, 2021
SMAD4 mutations and cross-talk between TGF-β/IFNγ signaling accelerate rates of DNA damage and cellular senescence, resulting in a segmental progeroid syndrome-the Myhre syndrome
Renuka Kandhaya-Pillai, Deyin Hou, Jiaming Zhang, et al.
Scientific Reports
|
August 26, 2016
Werner syndrome through the lens of tissue and tumour genomics
Mari Tokita, Scott R Kennedy, Rosa Ana Risques, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2011
Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A
Fuki M Hisama, Davor Lessel, Dru Leistritz, et al.
Molecular Genetics & Genomic Medicine
|
August 13, 2013
Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry
Bidisha Saha, Davor Lessel, Sheela Nampoothiri, et al.
Internal Medicine (Tokyo, Japan)
|
December 21, 2018
Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C
Namiko Matsumoto, Yasuyuki Ohta, Kentaro Deguchi, et al.
American Journal of Respiratory and Critical Care Medicine
|
November 18, 2008
Cigarette smoke induces cellular senescence via Werner's syndrome protein down-regulation
Toru Nyunoya, Martha M Monick, Aloysius L Klingelhutz, et al.
Aging Cell
|
January 19, 2022
DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome
Yosra Bejaoui, Aleem Razzaq, Noha A Yousri, et al.
Page
of 9