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 *

198 related articles for article (PubMed ID: 35104372)

  • 21. Deletions of the steroid sulphatase gene in "classical" X-linked ichthyosis and in X-linked ichthyosis associated with Kallmann syndrome.
    Ballabio A; Sebastio G; Carrozzo R; Parenti G; Piccirillo A; Persico MG; Andria G
    Hum Genet; 1987 Dec; 77(4):338-41. PubMed ID: 3480263
    [TBL] [Abstract][Full Text] [Related]  

  • 22. X-linked ichthyosis and Crigler-Najjar syndrome I: Coexistence in a male patient with two copy number variable regions of 2q37.1 and Xp22.3.
    Bai J; Qu Y; Cao Y; Li Y; Zhang W; Jin Y; Wang H; Song F
    Mol Med Rep; 2016 Feb; 13(2):1135-40. PubMed ID: 26676689
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X-linked ichthyosis and ichthyosis vulgaris: comparison of their clinical features based on biochemical analysis.
    Okano M; Kitano Y; Yoshikawa K; Nakamura T; Matsuzawa Y; Yuasa T
    Br J Dermatol; 1988 Dec; 119(6):777-83. PubMed ID: 3203072
    [TBL] [Abstract][Full Text] [Related]  

  • 24. X-linked ichthyosis: Molecular findings in four pedigrees with inconspicuous clinical manifestations.
    Zhang M; Huang H; Lin N; He S; An G; Wang Y; Chen M; Chen L; Lin Y; Xu L
    J Clin Lab Anal; 2020 May; 34(5):e23201. PubMed ID: 31944387
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis].
    Liu A; Xiao SX; Tan SS; Jiao T; Liu Y; Li XL; Zhou SN
    Di Yi Jun Yi Da Xue Xue Bao; 2005 Aug; 25(8):1023-5. PubMed ID: 16109567
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Xp22.3 interstitial deletion: a recognizable chromosomal abnormality encompassing VCX3A and STS genes in a patient with X-linked ichthyosis and mental retardation.
    Ben Khelifa H; Soyah N; Ben-Abdallah-Bouhjar I; Gritly R; Sanlaville D; Elghezal H; Saad A; Mougou-Zerelli S
    Gene; 2013 Sep; 527(2):578-83. PubMed ID: 23791652
    [TBL] [Abstract][Full Text] [Related]  

  • 27. X-linked ichthyosis: Clinical and molecular findings in 35 Italian patients.
    Diociaiuti A; Angioni A; Pisaneschi E; Alesi V; Zambruno G; Novelli A; El Hachem M
    Exp Dermatol; 2019 Oct; 28(10):1156-1163. PubMed ID: 29672931
    [TBL] [Abstract][Full Text] [Related]  

  • 28. End-stage renal failure in a child with X-linked ichthyosis.
    Matsukura H; Fuchizawa T; Ohtsuki A; Higashiyama H; Higuchi O; Higuchi A; Miyawaki T
    Pediatr Nephrol; 2003 Mar; 18(3):297-300. PubMed ID: 12644929
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The detection of steroid sulfatase gene deletion (STS) in Egyptian males with X-linked ichthyosis.
    Abdel-Hamed MF; Hussein HA; Helmy NA; Elsaie ML
    J Drugs Dermatol; 2010 Oct; 9(10):1192-6. PubMed ID: 20941942
    [TBL] [Abstract][Full Text] [Related]  

  • 30. STS gene in a pedigree with X-linked ichthyosis.
    Liu A; Xiao S; Tan S; Lei X; Zhang J; Jiao T; Liu Y
    J Huazhong Univ Sci Technolog Med Sci; 2005; 25(4):468-9. PubMed ID: 16196306
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis.
    Valdes-Flores M; Kofman-Alfaro SH; Jimenez-Vaca AL; Cuevas-Covarrubias SA
    Am J Med Genet; 2001 Aug; 102(2):146-8. PubMed ID: 11477606
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Deletion of distal promoter of VCXA in a patient with X-linked ichthyosis associated with borderline mental retardation.
    Hosomi N; Oiso N; Fukai K; Hanada K; Fujita H; Ishii M
    J Dermatol Sci; 2007 Jan; 45(1):31-6. PubMed ID: 17113756
    [TBL] [Abstract][Full Text] [Related]  

  • 33. X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient.
    Hernández-Martín A; Cuadrado-Corrales N; Ciria-Abad S; Arias-Palomo D; Mascaró-Galy JM; Escámez MJ; García M; Del Río M; Torrelo A; González-Sarmiento R
    Dermatology; 2010; 221(2):113-6. PubMed ID: 20523032
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic Heterogeneity of X-Linked Ichthyosis in the Republic of North Ossetia-Alania, Case Series Report.
    Vasilyeva TA; Marakhonov AV; Tebieva IS; Kadyshev VV; Borovikov AO; Markova ZG; Chukhrova AL; Ginter EK; Kutsev SI; Zinchenko RA
    Int J Mol Sci; 2023 Feb; 24(5):. PubMed ID: 36901946
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Analysis of the STS gene in 40 patients with recessive X-linked ichthyosis: a high frequency of partial deletions in a Spanish population.
    Cañueto J; Ciria S; Hernández-Martín A; Unamuno P; González-Sarmiento R
    J Eur Acad Dermatol Venereol; 2010 Oct; 24(10):1226-9. PubMed ID: 20236202
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Microsomal sulfatase deficiency in X chromosome-linked ichthyosis].
    Meyer JC; Schnyder UW
    Hautarzt; 1982 Feb; 33(2):82-8. PubMed ID: 6951821
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Atypical X-linked ichthyosis in a patient with a large deletion involving the steroid sulfatase (STS) gene.
    Gonzalez-Huerta L; Mendiola-Jimenez J; Del Moral-Stevenel M; Rivera-Vega M; Cuevas-Covarrubias S
    Int J Dermatol; 2009 Feb; 48(2):142-4. PubMed ID: 19200188
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Unraveling the molecular mechanisms of cell migration impairment and apoptosis associated with steroid sulfatase deficiency: Implications for X-linked ichthyosis.
    Kwon TU; Kwon YJ; Baek HS; Park H; Lee H; Chun YJ
    Biochim Biophys Acta Mol Basis Dis; 2024 Mar; 1870(3):167004. PubMed ID: 38182070
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A model of corrective gene transfer in X-linked ichthyosis.
    Freiberg RA; Choate KA; Deng H; Alperin ES; Shapiro LJ; Khavari PA
    Hum Mol Genet; 1997 Jun; 6(6):927-33. PubMed ID: 9175741
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A clinical and genetic study of X-linked recessive ichthyosis and contiguous gene defects.
    Paige DG; Emilion GG; Bouloux PM; Harper JI
    Br J Dermatol; 1994 Nov; 131(5):622-9. PubMed ID: 7999591
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.