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    1. Carlson, JA; Scott, D; Wharton, J; Sell, S
      Incidental histopathologic patterns: Possible evidence of 'field cancerization' surrounding skin tumors

      AMERICAN JOURNAL OF DERMATOPATHOLOGY
    2. Ishiko, A; Akiyama, M; Takizawa, Y; Nishikawa, T; Shimizu, Y; Shimizu, H
      A novel leucine to valine mutation in residue 7 of the helix initiation motif of keratin 10 leads to bullous congenital ichthyosiform erythroderma

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    3. Arin, MJ; Longley, MA; Wang, XJ; Roop, DR
      Focal activation of a mutant allele defines the role of stem cells in mosaic skin disorders

      JOURNAL OF CELL BIOLOGY
    4. Presland, RB; Kuechle, MK; Lewis, SP; Fleckman, P; Dale, BA
      Regulated expression of human filaggrin in keratinocytes results in cytoskeletal disruption, loss of cell-cell adhesion, and cell cycle arrest

      EXPERIMENTAL CELL RESEARCH
    5. Whittock, NV; Ashton, GHS; Griffiths, WAD; Eady, RAJ; McGrath, JA
      New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens

      BRITISH JOURNAL OF DERMATOLOGY
    6. Mahdi, F; Shariat-Madar, Z; Todd, RF; Figueroa, CD; Schmaier, AH
      Expression and colocalization of cytokeratin 1 and urokinase plasminogen activator receptor on endothelial cells

      BLOOD
    7. Nomura, K; Umeki, K; Hatayama, I; Kuronuma, T
      Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma - Possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband

      ARCHIVES OF DERMATOLOGY
    8. Paller, AS
      Expanding our concepts of mosaic disorders of skin

      ARCHIVES OF DERMATOLOGY
    9. Guardiano, RA; Ryan, M; Liotta, EA
      Bullae in a 20-year old man

      ARCHIVES OF DERMATOLOGY
    10. Ishida-Yamamoto, A; Takahashi, H; Iizuka, H
      Immunoelectron microscopy links molecules and morphology in the studies ofkeratinization

      EUROPEAN JOURNAL OF DERMATOLOGY
    11. Williams, ML; Elias, PM
      Ichthyosis: Where we have been disorders of cornification: Where we are going

      CURRENT PROBLEMS IN DERMATOLOGY-US
    12. Berg, J; Grace, E; Teik, KW; Hammond, H; Tidman, M; FitzPatrick, D
      Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A

      CLINICAL DYSMORPHOLOGY
    13. Mayuzumi, N; Shigihara, T; Ikeda, S; Ogawa, H
      Recurrent R156H mutation of KRT10 in a Japanese family with bullous congenital ichthyosiform erythroderma

      JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
    14. Arin, MJ; Longley, MA; Epstein, EH; Rothnagel, JA; Roop, DR
      Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis

      EXPERIMENTAL DERMATOLOGY
    15. Magin, TM; Hesse, M; Schroder, R
      Novel insights into intermediate-filament function from studies of transgenic and knockout mice

      PROTOPLASMA
    16. Jensen, JM; Schutze, S; Neumann, C; Proksch, E
      Impaired cutaneous permeability barrier function, skin hydration, and sphingomyelinase activity in keratin 10 deficient mice

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    17. Xia, JH; Yang, YF; Deng, H; Tang, BS; Tang, DS; He, YG; Xia, K; Chen, SX; Li, YX; Pan, Q; Long, ZG; Dai, HP; Liao, XD; Xiao, JF; Liu, ZR; Lu, CY; Yu, KP; Deng, HX
      Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    18. Terrinoni, A; Puddu, P; Didona, B; De Laurenzi, V; Candi, E; Smith, FJD; McLean, WHI; Melino, G
      A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    19. Elias, P; Man, MQ; Williams, ML; Feingold, KR; Magin, T
      Barrier function in K-10 heterozygote knockout mice

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    20. Takizawa, Y; Akiyama, M; Nagashima, M; Shimizu, H
      A novel asparagine -> aspartic acid mutation in the rod 1A domain in keratin 2e in a Japanese family with ichthyosis bullosa of Siemens

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    21. Shariat-Madar, Z; Schmaier, AH
      Kininogen-cytokeratin 1 interactions in endothelial cell biology

      TRENDS IN CARDIOVASCULAR MEDICINE
    22. Bierkamp, C; Schwarz, H; Huber, O; Kemler, R
      Desmosomal localization of beta-catenin in the skin of plakoglobin null-mutant mice

      DEVELOPMENT
    23. Miller, AB; Breen, M; Murphy, KE
      Chromosomal localization of acidic and basic keratin genes of the domesticdog

      MAMMALIAN GENOME
    24. Yang, JM; Nam, K; Kim, SW; Jung, SY; Min, HG; Yeo, UC; Park, KB; Lee, JH; Suhr, KB; Park, JK; Lee, ES
      Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis

      JOURNAL OF DERMATOLOGICAL SCIENCE
    25. Michael, EJ; Schneiderman, P; Grossman, ME; Christiano, AM
      Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene

      EXPERIMENTAL DERMATOLOGY
    26. Lin, MTS; Levy, ML; Bowden, PE; Magro, C; Baden, L; Baden, HP; Roop, DR
      Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot

      EXPERIMENTAL DERMATOLOGY
    27. McLean, WHI; Morley, SM; Higgins, C; Bowden, PE; White, M; Leigh, IM; Lane, EB
      Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma

      EXPERIMENTAL DERMATOLOGY
    28. Arin, MJ; Longley, MA; Kuster, W; Huber, M; Hohl, D; Rothnagel, JA; Roop, DR
      An asparagine to threonine substitution in the 1A domain of keratin 1: a novel mutation that causes epidermolytic hyperkeratosis

      EXPERIMENTAL DERMATOLOGY
    29. Moraru, R; Cserhalmi-Friedman, PB; Grossman, ME; Schneiderman, P; Christiano, AM
      Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene

      CLINICAL AND EXPERIMENTAL DERMATOLOGY
    30. Wojcik, SM; Imakado, S; Seki, T; Longley, MA; Petherbridge, L; Bundman, DS; Bickenbach, JR; Rothnagel, JA; Roop, DR
      Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle

      DIFFERENTIATION
    31. Moss, C
      Cytogenetic and molecular evidence for cutaneous mosaicism: The ectodermalorigin of Blaschko lines

      AMERICAN JOURNAL OF MEDICAL GENETICS
    32. Arin, MJ; Longley, MA; Anton-Lamprech, I; Kurze, G; Huber, M; Hohl, D; Rothnagel, JA; Roop, DR
      A novel substitution in keratin 10 in epidermolytic hyperkeratosis

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    33. Yang, JM; Nam, K; Kim, HC; Lee, JH; Park, JK; Wu, K; Lee, ES; Steinert, PM
      A novel glutamic acid to aspartic acid mutation near the end of the 2B roddomain in the keratin 1 chain in epidermolytic hyperkeratosis

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    34. Arin, MJ; Longley, MA; Epstein, EH; Scott, G; Goldsmith, LA; Rothnagel, JA; Roop, DR
      A novel mutation in the 1A domain of keratin 2e in ichthyosis bullosa of Siemens

      JOURNAL OF INVESTIGATIVE DERMATOLOGY
    35. Swensson, O
      Pachyonychia congenita. Keratin gene mutations with pleiotropic effect

      HAUTARZT
    36. Maytin, EV; Lin, JC; Krishnamurthy, R; Batchvarova, N; Ron, D; Mitchell, PJ; Habener, JF
      Keratin 10 gene expression during differentiation of mouse epidermis requires transcription factors C/EBP and AP-2

      DEVELOPMENTAL BIOLOGY
    37. Smith, LT; Underwood, RA; McLean, WHI
      Ontogeny and regional variability of keratin 2e (K2e) in developing human fetal skin: a unique spatial and temporal pattern of keratin expression in development

      BRITISH JOURNAL OF DERMATOLOGY
    38. Basarab, T; Smith, FJD; Jolliffe, VML; McLean, WHI; Neill, S; Rustin, MHA; Eady, RAJ
      Ichthyosis bullosa of Siemens: report of a family with evidence of a keratin 2e mutation, and a review of the literature

      BRITISH JOURNAL OF DERMATOLOGY
    39. AMMIRATI CT; MALLORY SB
      THE MAJOR INHERITED DISORDERS OF CORNIFICATION - NEW ADVANCES IN PATHOGENESIS

      Dermatologic clinics
    40. SHIRAISHI A; KAO CWC; ISHIZAKI M; ZHANG Z; CONVERSE RL; TSENG SCG; SVOBODA KKH; KAO WWY
      CHARACTERIZATION OF BSK MICE - I - THE BSK MUTATION DOES NOT INVOLVE A RECOMBINATION OF CORNEA-SPECIFIC KERATIN 12 AND SKIN-SPECIFIC HAIR KERATIN GENES

      Current eye research
    41. EKANAYAKEMUDIYANSELAGE S; ASCHAUER H; SCHMOOK FP; JENSEN JM; MEINGASSNER JG; PROKSCH E
      EXPRESSION OF EPIDERMAL KERATINS AND THE CORNIFIED ENVELOPE PROTEIN INVOLUCRIN IS INFLUENCED BY PERMEABILITY BARRIER DISRUPTION

      Journal of investigative dermatology
    42. PORTER RM; REICHELT J; LUNNY DP; MAGIN TM; LANE EB
      THE RELATIONSHIP BETWEEN HYPERPROLIFERATION AND EPIDERMAL THICKENING IN A MOUSE MODEL FOR BCIE

      Journal of investigative dermatology
    43. CHOATE KA; WILLIAMS ML; KHAVARI PA
      ABNORMAL TRANSGLUTAMINASE-1 EXPRESSION PATTERN IN A SUBSET OF PATIENTS WITH ERYTHRODERMIC AUTOSOMAL RECESSIVE ICHTHYOSIS

      Journal of investigative dermatology
    44. OPITZ OG; JENKINS TD; RUSTGI AK
      TRANSCRIPTIONAL REGULATION OF THE DIFFERENTIATION-LINKED HUMAN K4 PROMOTER IS DEPENDENT UPON ESOPHAGEAL-SPECIFIC NUCLEAR FACTORS

      The Journal of biological chemistry
    45. AKIYAMA M
      SEVERE CONGENITAL ICHTHYOSIS OF THE NEONATE

      International journal of dermatology
    46. YANG JM; LEE ES; KANG HJ; CHOI GS; YONEDA K; JUNG SY; PARK KB; STEINERT PM; LEE ES
      A GLUTAMATE TO LYSINE MUTATION AT THE END OF 2B ROD DOMAIN OF KERATIN2E GENE IN ICHTHYOSIS BULLOSA OF SIEMENS

      Acta dermato-venereologica
    47. WASEEM A; WHITE K; WASEEM NH
      IDENTIFICATION OF A NOVEL KERATIN EPITOPE - EVIDENCE FOR ASSOCIATION BETWEEN NON-HELICAL SUB-DOMAINS L12 DURING FILAMENT ASSEMBLY

      International journal of biochemistry & cell biology
    48. DENG H; LIN Q; KHAVARI PA
      SUSTAINABLE CUTANEOUS GENE DELIVERY

      Nature biotechnology
    49. MENON G; GHADIALLY R
      MORPHOLOGY OF LIPID ALTERATIONS IN THE EPIDERMIS - A REVIEW

      Microscopy research and technique
    50. HOHL D
      STEATOCYSTOMA MULTIPLEX AND OLIGOSYMPTOMATIC PACHYONYCHIA-CONGENITA OF THE JACKSON-SERTOLI TYPE

      Dermatology
    51. NOMURA K; MENG XM; UMEKI K; TAMAI K; SAWAMURA D; HASHIMOTO I; KIKUCHI T
      A KERATIN K10 GENE MUTATION IN A JAPANESE PATIENT WITH EPIDERMOLYTIC HYPERKERATOSIS

      Japanese journal of human genetics
    52. QUINN TR; YOUNG RH
      EPIDERMOLYTIC HYPERKERATOSIS IN THE LOWER FEMALE GENITAL-TRACT - AN UNCOMMON SIMULANT OF MUCOCUTANEOUS PAPILLOMAVIRUS INFECTION - A REPORT OF 2 CASES

      International journal of gynecological pathology
    53. MAGRO CM; BADEN LA; CROWSON AN; BOWDEN PE; BADEN HP
      A NOVEL NONEPIDERMOLYTIC PALMOPLANTAR KERATODERMA - A CLINICAL AND HISTOPATHOLOGIC STUDY OF 6 CASES

      Journal of the American Academy of Dermatology
    54. COULOMBE PA
      TRANSGENIC MICE AS A MODEL FOR THE STUDY OF INHERITED SKIN BULLOUS DISEASES

      Annales de dermatologie et de venereologie
    55. YANG JM; LEE S; BANG HD; KIM WS; LEE ES; STEINERT PM
      A NOVEL THREONINE-]PROLINE MUTATION AT THE END OF 2B ROD DOMAIN IN THE KERATIN-2E CHAIN IN ICHTHYOSIS BULLOSA OF SIEMENS

      Journal of investigative dermatology
    56. JONES DO; WATTS C; MILLS C; SHARPE G; MARKS R; BOWDEN PE
      A NEW KERATIN 2E MUTATION IN ICHTHYOSIS BULLOSA OF SIEMENS

      Journal of investigative dermatology
    57. REICHELT J; BAUER C; PORTER RM; LANE EB; HERZOG V; MAGIN TM
      OUT OF BALANCE - CONSEQUENCES OF A PARTIAL KERATIN-10 KNOCKOUT

      Journal of Cell Science
    58. METZLER G; SONNICHSEN K
      DISSEMINATED EPIDERMOLYTIC ACANTHOMAS

      Hautarzt
    59. RATNAVEL RC; GRIFFITHS WAD
      THE INHERITED PALMOPLANTAR KERATODERMAS

      British journal of dermatology
    60. HAPPLE R
      A RULE CONCERNING THE SEGMENTAL MANIFESTATION OF AUTOSOMAL-DOMINANT SKIN DISORDERS - REVIEW OF CLINICAL EXAMPLES PROVIDING EVIDENCE FOR DICHOTOMOUS TYPES OF SEVERITY

      Archives of dermatology
    61. LENZNER U; HAPPLE R; KREMER H; MENSING H; REINEL D; STEIJLEN PM; ULRICH R
      ICHTHYOSIS BULLOSA OF SIEMENS - A DISTINCT TYPE OF EPIDERMOLYTIC HYPERKERATOSIS

      EJD. European journal of dermatology
    62. STUURMAN N; SASSE B; FISHER PA
      INTERMEDIATE FILAMENT PROTEIN POLYMERIZATION - MOLECULAR ANALYSIS OF DROSOPHILA NUCLEAR LAMIN HEAD-TO-TAIL BINDING

      Journal of structural biology
    63. KORGE BP; KRIEG T
      THE MOLECULAR-BASIS FOR INHERITED BULLOUS DISEASES

      Journal of molecular medicine
    64. MILISAVLJEVIC V; FREEDBERG IM; BLUMENBERG M
      CLOSE LINKAGE OF THE 2 KERATIN GENE CLUSTERS IN THE HUMAN GENOME

      Genomics
    65. BIDDLE D; SPANDAU DF
      EXPRESSION OF VIMENTIN IN CULTURED HUMAN KERATINOCYTES IS ASSOCIATED WITH CELL-EXTRACELLULAR MATRIX JUNCTIONS

      Archives of dermatological research
    66. WILLIAMS BT; BARR RJ
      EPIDERMOLYTIC HYPERKERATOSIS IN NEVI - A POSSIBLE MARKER FOR ATYPIA

      The American journal of dermatopathology
    67. WILLIAMSON TL; MARSZALEK JR; VECHIO JD; BRUIJN LI; LEE MK; XU Z; BROWN RH; CLEVELAND DW
      NEUROFILAMENTS, RADIAL GROWTH OF AXONS, AND MECHANISMS OF MOTOR-NEURON DISEASE

      Cold Spring Harbor Symposia on Quantitative Biology
    68. BIERKAMP C; MCLAUGHLIN KJ; SCHWARZ H; HUBER O; KEMLER R
      EMBRYONIC HEART AND SKIN DEFECTS IN MICE LACKING PLAKOGLOBIN

      Developmental biology
    69. LI LW; TUCKER RW; HENNINGS H; YUSPA SH
      INHIBITORS OF THE INTRACELLULAR CA2-ATPASE IN CULTURED MOUSE KERATINOCYTES REVEAL COMPONENTS OF TERMINAL DIFFERENTIATION THAT ARE REGULATEDBY DISTINCT INTRACELLULAR CA2+ COMPARTMENTS()

      Cell growth & differentiation
    70. CADRIN M; MARTINOLI MG
      ALTERATIONS OF INTERMEDIATE FILAMENTS IN VARIOUS HISTOPATHOLOGICAL CONDITIONS

      Biochemistry and cell biology
    71. PEKNY M; LEVEEN P; PEKNA M; ELIASSON C; BERTHOLD CH; WESTERMARK B; BETSHOLTZ C
      MICE LACKING GLIAL FIBRILLARY ACIDIC PROTEIN DISPLAY ASTROCYTES DEVOID OF INTERMEDIATE FILAMENTS BUT DEVELOP AND REPRODUCE NORMALLY

      EMBO journal
    72. ROTEN SV; BHAWAN J
      ISOLATED DYSKERATOTIC ACANTHOMA - A VARIANT OF ISOLATED EPIDERMOLYTICACANTHOMA

      The American journal of dermatopathology
    73. MOSS C; JONES DO; BLIGHT A; BOWDEN PE
      BIRTHMARK DUE TO CUTANEOUS MOSAICISM FOR KERATIN-10 MUTATION

      Lancet
    74. PERKINS EB; CUNNINGHAM JG; BRACETE AM; ZEHNER ZE
      2 HOMOLOGOUS ENHANCER ELEMENTS IN THE CHICKEN VIMENTIN GENE MAY BIND A NUCLEAR FACTOR IN COMMON WITH A NEARBY SILENCER ELEMENT

      The Journal of biological chemistry
    75. KUSTER W; ZEHENDER D; MENSING H; HENNIES HC; REIS A
      EPIDERMOLYTIC PALMOPLANTAR KERATODERMA OF VORNER - CLINICAL-FEATURES,FORMAL GENETICS, AND MOLECULAR BIOLOGICAL FINDINGS IN 22 FAMILIES

      Hautarzt
    76. ROTHNAGEL JA; TRAUPE H; WOJCIK S; HUBER M; HOHL D; PITTELKOW MR; SAEKI H; ISHIBASHI Y; ROOP DR
      MUTATIONS IN THE ROD DOMAIN OF KERATIN 2E IN PATIENTS WITH ICHTHYOSISBULLOSA OF SIEMENS

      Nature genetics
    77. MORGAN PR; SU L
      INTERMEDIATE FILAMENTS IN ORAL NEOPLASIA .1. ORAL-CANCER AND EPITHELIAL DYSPLASIA

      European journal of cancer. Part B, Oral oncology
    78. ELLIS A; FIELD JK; FIELD EA; FRIEDMANN PS; FRYER A; HOWARD P; LEIGH IM; RISK J; SHAW JM; WHITTAKER J
      TYLOSIS ASSOCIATED WITH CARCINOMA OF THE ESOPHAGUS AND ORAL LEUKOPLAKIA IN A LARGE LIVERPOOL FAMILY - A REVIEW OF 6 GENERATIONS

      European journal of cancer. Part B, Oral oncology
    79. HEINS S; AEBI U
      MAKING HEADS AND TAILS OF INTERMEDIATE FILAMENT ASSEMBLY, DYNAMICS AND NETWORKS

      Current opinion in cell biology
    80. SINGH S; GUPTA PD
      TAMPERING WITH CYTOKERATIN EXPRESSION RESULTS IN CELL DYSFUNCTION

      Epithelial cell biology
    81. CHAN YM; ANTONLAMPRECHT I; YU QC; JACKEL A; ZABEL B; ERNST JP; FUCHS E
      A HUMAN KERATIN-14 KNOCKOUT - THE ABSENCE OF K14 LEADS TO SEVERE EPIDERMOLYSIS-BULLOSA SIMPLEX AND A FUNCTION FOR AN INTERMEDIATE FILAMENT PROTEIN

      Genes & development
    82. STOSIEK N; ULMER R; VONDENDRIESCH P; CLAUSSEN U; HORNSTEIN OP; ROTT HD
      CHROMOSOMAL MOSAICISM IN 2 PATIENTS WITH EPIDERMAL VERRUCOUS NEVUS - DEMONSTRATION OF CHROMOSOMAL BREAKPOINT

      Journal of the American Academy of Dermatology
    83. MING ME; DARYANANI HA; ROBERTS LP; BADEN HP; KVEDAR JC
      BINDING OF KERATIN INTERMEDIATE FILAMENTS (K10) TO THE CORNIFIED ENVELOPE IN MOUSE EPIDERMIS - IMPLICATIONS FOR BARRIER FUNCTION

      Journal of investigative dermatology
    84. BONIFAS JM; MATSUMURA K; CHEN MA; BERTHJONES J; HUTCHINSON PE; ZLOCZOWER M; FRITSCH PO; EPSTEIN EH
      MUTATIONS OF KERATIN-9 IN 2 FAMILIES WITH PALMOPLANTAR EPIDERMOLYTIC HYPERKERATOSIS

      Journal of investigative dermatology
    85. MCLEAN WHI; MORLEY SM; LANE EB; EADY RAJ; GRIFFITHS WAD; PAIGE DG; HARPER JI; HIGGINS C; LEIGH IM
      ICHTHYOSIS BULLOSA OF SIEMENS - A DISEASE INVOLVING KERATIN 2E

      Journal of investigative dermatology
    86. STEIJLEN PM; KREMER H; VAKILZADEH F; HAPPLE R; LAVRIJSEN APM; ROPERS HH; MARIMAN ECM
      GENETIC-LINKAGE OF THE KERATIN TYPE-II GENE-CLUSTER WITH ICHTHYOSIS BULLOSA OF SIEMENS AND WITH AUTOSOMAL-DOMINANT ICHTHYOSIS EXFOLIATIVA

      Journal of investigative dermatology
    87. KREMER H; ZEEUWEN P; MCLEAN WHI; MARIMAN ECM; LANE EB; VANDEKERKHOF PCM; ROPERS HH; STEIJLEN PM
      ICHTHYOSIS BULLOSA OF SIEMENS IS CAUSED BY MUTATIONS IN THE KERATIN 2E GENE

      Journal of investigative dermatology
    88. ELDER JT; NAIR RP; VOORHEES JJ
      EPIDEMIOLOGY AND THE GENETICS OF PSORIASIS

      Journal of investigative dermatology
    89. BALE SJ; DOYLE SZ
      THE GENETICS OF ICHTHYOSIS - A PRIMER FOR EPIDEMIOLOGISTS

      Journal of investigative dermatology
    90. HUBER M; SCALETTA C; BENATHAN M; FRENK E; GREENHALGH DA; ROTHNAGEL JA; ROOP DR; HOHL D
      ABNORMAL KERATIN-1 AND KERATIN-10 CYTOSKELETON IN CULTURED KERATINOCYTES FROM EPIDERMOLYTIC HYPERKERATOSIS CAUSED BY KERATIN-10 MUTATIONS

      Journal of investigative dermatology
    91. MCLEAN WHI; EADY RAJ; DOPPINGHEPENSTAL PJC; MCMILLAN JR; LEIGH IM; NAVSARIA HA; HIGGINS C; HARPER JI; PAIGE DG; MORLEY SM; LANE EB
      MUTATIONS IN THE ROD 1A DOMAIN OF KERATIN-1 AND KERATIN-10 IN BULLOUSCONGENITAL ICHTHYOSIFORM ERYTHRODERMA (BCIE)

      Journal of investigative dermatology
    92. SYDER AJ; YU QC; PALLER AS; GIUDICE G; PEARSON R; FUCHS E
      GENETIC MUTATIONS IN THE K1 AND K10 GENES OF PATIENTS WITH EPIDERMOLYTIC HYPERKERATOSIS - CORRELATION BETWEEN LOCATION AND DISEASE SEVERITY

      The Journal of clinical investigation
    93. TAKEDA S; OKABE S; FUNAKOSHI T; HIROKAWA N
      DIFFERENTIAL DYNAMICS OF NEUROFILAMENT-H PROTEIN AND NEUROFILAMENT-L PROTEIN IN NEURONS

      The Journal of cell biology
    94. LI H; CHOUDHARY SK; MILNER DJ; MUNIR MI; KUISK IR; CAPETANAKI Y
      INHIBITION OF DESMIN EXPRESSION BLOCKS MYOBLAST FUSION AND INTERFERESWITH THE MYOGENIC REGULATORS MYOD AND MYOGENIN

      The Journal of cell biology
    95. ROGAEV EI; ROGAEVA EA; GINTER EK; KOROVAITSEVA GI; FARRER LA; SHLENSKII AB; PRYTKOV AN; STGEORGEHYSLOP P
      IS THE GENE FOR PALMOPLANTARIS HYPERKERAT OSIS ASSOCIATED WITH ONE OFTHE TYPE-1 KERATIN LOCI

      Genetika
    96. PAIGE DG; MORSEFISHER N; HARPER JI
      QUANTIFICATION OF STRATUM-CORNEUM CERAMIDES AND LIPID ENVELOPE CERAMIDES IN THE HEREDITARY ICHTHYOSES

      British journal of dermatology
    97. BRUSASCO A; CAVALLI R; CAMBIAGHI S; TADINI G; BERTI E; CAPUTO R
      ICHTHYOSIS CURTH-MACKLIN - A NEW SPORADIC CASE WITH IMMUNOHISTOCHEMICAL STUDY OF KERATIN EXPRESSION

      Archives of dermatology
    98. ELDER JT; NAIR RP; GUO SW; HENSELER T; CHRISTOPHERS E; VOORHEES JJ
      THE GENETICS OF PSORIASIS

      Archives of dermatology
    99. NIELSEN PG
      HEREDITARY PALMOPLANTAR KERATODERMA AND DERMATOPHYTOSIS IN THE NORTHERNMOST COUNTY OF SWEDEN (NORRBOTTEN)

      Acta dermato-venereologica
    100. GEISLER N; HEIMBURG T; SCHUNEMANN J; WEBER K
      PEPTIDES FROM THE CONSERVED ENDS OF THE ROD DOMAIN OF DESMIN DISASSEMBLE INTERMEDIATE FILAMENTS AND REVEAL UNEXPECTED STRUCTURAL FEATURES -A CIRCULAR-DICHROISM, FOURIER-TRANSFORM INFRARED, AND ELECTRON-MICROSCOPIC STUDY

      Journal of structural biology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 03/06/20 alle ore 02:12:43