These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 887325)

  • 81. Familial cutaneous photosensitivity and colitis with lethal outcome.
    Labrune P; Huguet P; Alagille D; Odievre M
    J Med Genet; 1991 Feb; 28(2):114-6. PubMed ID: 2002480
    [TBL] [Abstract][Full Text] [Related]  

  • 82. CACHECTIC DWARFISM RESEMBLING THE COCKAYNE-NEILL TYPE.
    SPARK H
    J Pediatr; 1965 Jan; 66():41-7. PubMed ID: 14250055
    [No Abstract]   [Full Text] [Related]  

  • 83. Dwarfism with skin manifestations.
    SZALAY GC
    J Pediatr; 1963 May; 62():686-95. PubMed ID: 13979851
    [No Abstract]   [Full Text] [Related]  

  • 84. A Rare Case of Cockayne Syndrome-MRI Features.
    Mundaganur P
    J Clin Diagn Res; 2012 Nov; 6(9):1582-3. PubMed ID: 23285467
    [TBL] [Abstract][Full Text] [Related]  

  • 85. [Cockayne syndrome].
    Serrano CA; MorĂ¡n V; Diez P
    Bol Med Hosp Infant Mex; 2015; 72(4):276-283. PubMed ID: 29421148
    [No Abstract]   [Full Text] [Related]  

  • 86. Adult diagnosis of Cockayne syndrome.
    Neurology; 2020 Oct; 95(17):802. PubMed ID: 32938791
    [No Abstract]   [Full Text] [Related]  

  • 87. Cockayne syndrome.
    Khan F; Chemmanam T; Mathuranath PS
    Ann Indian Acad Neurol; 2008 Apr; 11(2):125-6. PubMed ID: 19893654
    [No Abstract]   [Full Text] [Related]  

  • 88. Dwarfism with Mental Defect.
    Tallerman KH
    Proc R Soc Med; 1931 Mar; 24(5):568-9. PubMed ID: 19988008
    [No Abstract]   [Full Text] [Related]  

  • 89. HiPSC-derived 3D neural models reveal neurodevelopmental pathomechanisms of the Cockayne Syndrome B.
    Kapr J; Scharkin I; Ramachandran H; Westhoff P; Pollet M; Dangeleit S; Brockerhoff G; Rossi A; Koch K; Krutmann J; Fritsche E
    Cell Mol Life Sci; 2024 Aug; 81(1):368. PubMed ID: 39179905
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Cutaneous Manifestations and Neurological Diseases.
    Lahoti A; Singh A; Bisen YT; Bakshi AM
    Cureus; 2023 Oct; 15(10):e47024. PubMed ID: 37965391
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations.
    Chikhaoui A; Kraoua I; Calmels N; Bouchoucha S; Obringer C; Zayoud K; Montagne B; M'rad R; Abdelhak S; Laugel V; Ricchetti M; Turki I; Yacoub-Youssef H
    Orphanet J Rare Dis; 2022 Mar; 17(1):121. PubMed ID: 35248096
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Cockayne Syndrome: The many challenges and approaches to understand a multifaceted disease.
    Vessoni AT; Guerra CCC; Kajitani GS; Nascimento LLS; Garcia CCM
    Genet Mol Biol; 2020; 43(1 suppl. 1):e20190085. PubMed ID: 32453336
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Cockayne Syndrome Misdiagnosed as Cerebral Palsy.
    Vafaee A; Baghdadi T; Norouzzadeh S
    Iran J Child Neurol; 2018; 12(4):162-168. PubMed ID: 30279719
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Deep intronic variation in splicing regulatory element of the ERCC8 gene associated with severe but long-term survival Cockayne syndrome.
    Schalk A; Greff G; Drouot N; Obringer C; Dollfus H; Laugel V; Chelly J; Calmels N
    Eur J Hum Genet; 2018 Apr; 26(4):527-536. PubMed ID: 29422660
    [TBL] [Abstract][Full Text] [Related]  

  • 95. A ubiquitylation site in Cockayne syndrome B required for repair of oxidative DNA damage, but not for transcription-coupled nucleotide excision repair.
    Ranes M; Boeing S; Wang Y; Wienholz F; Menoni H; Walker J; Encheva V; Chakravarty P; Mari PO; Stewart A; Giglia-Mari G; Snijders AP; Vermeulen W; Svejstrup JQ
    Nucleic Acids Res; 2016 Jun; 44(11):5246-55. PubMed ID: 27060134
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Global contributions to the understanding of DNA repair and skin cancer.
    Kraemer KH; DiGiovanna JJ
    J Invest Dermatol; 2014 Oct; 134(e1):E8-17. PubMed ID: 25302472
    [No Abstract]   [Full Text] [Related]  

  • 97. Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease.
    Wang Y; Chakravarty P; Ranes M; Kelly G; Brooks PJ; Neilan E; Stewart A; Schiavo G; Svejstrup JQ
    Proc Natl Acad Sci U S A; 2014 Oct; 111(40):14454-9. PubMed ID: 25249633
    [TBL] [Abstract][Full Text] [Related]  

  • 98. DNA repair diseases: What do they tell us about cancer and aging?
    Menck CF; Munford V
    Genet Mol Biol; 2014 Mar; 37(1 Suppl):220-33. PubMed ID: 24764756
    [TBL] [Abstract][Full Text] [Related]  

  • 99. The role of genetics in the establishment and maintenance of the epigenome.
    Huidobro C; Fernandez AF; Fraga MF
    Cell Mol Life Sci; 2013 May; 70(9):1543-73. PubMed ID: 23474979
    [TBL] [Abstract][Full Text] [Related]  

  • 100.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.