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    1. Wilkie, AOM; Morriss-Kay, GM
      Genetics of craniofacial development and malformation

      NATURE REVIEWS GENETICS
    2. Ribatti, D; De Falco, G; Vacca, A; Nico, B; Errede, M; Roccaro, AM; Roncali, L; Dammacco, F
      Coordinate immunoreactivity to vascular endothelial growth factor receptor-2 and its ligand suggests a paracrine regulation during the development ofthe vascular system in the chick embryo bursa of Fabricius

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    3. Newman, L; Xia, WY; Yang, HY; Sahin, A; Bondy, M; Lukmanji, F; Hung, MC; Lee, MH
      Correlation of p27 protein expression with HER-2/neu expression in breast cancer

      MOLECULAR CARCINOGENESIS
    4. Lemonnier, J; Hay, E; Delannoy, P; Lomri, A; Modrowski, D; Caverzasio, J; Marie, PJ
      Role of N-cadherin and protein kinase C in osteoblast gene activation induced by the S252W fibroblast growth factor receptor 2 mutation in apert craniosynostosis

      JOURNAL OF BONE AND MINERAL RESEARCH
    5. Goldstrohm, AC; Greenleaf, AL; Garcia-Blanco, MA
      Co-transcriptional splicing of pre-messenger RNAs: considerations for the mechanism of alternative splicing

      GENE
    6. Kong, FM; Anscher, MS; Sporn, TA; Washington, MK; Clough, R; Barcellos-Hoff, MH; Jirtle, RL
      Loss of heterozygosity at the mannose 6-phosphate insulin-like growth factor 2 receptor (M6P/IGF2R) locus predisposes patients to radiation-induced lung injury

      INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
    7. Jones, RB; Carstens, RP; Luo, YD; McKeehan, WL
      5 '- and 3 '-terminal nucleotides in the FGFR2 ISAR splicing element core have overlapping roles in exon IIIb activation and exon IIIc repression

      NUCLEIC ACIDS RESEARCH
    8. Wagner, EJ; Garcia-Blanco, MA
      Polypyrimidine tract binding protein antagonizes exon definition

      MOLECULAR AND CELLULAR BIOLOGY
    9. Nishida, M; Nagata, K; Hachimori, Y; Horiuchi, M; Ogura, K; Mandiyan, V; Schlessinger, J; Inagaki, F
      Novel recognition mode between Vav and Grb2 SH3 domains

      EMBO JOURNAL
    10. Heike, C; Seto, M; Hing, A; Palidin, A; Hu, FZ; Preston, RA; Ehrlich, GD; Cunningham, M
      Century of Jackson-Weiss syndrome: Further definition of clinical and radiographic findings in "lost" descendants of the original kindred

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Cohen, MM
      Jackson-Weiss syndrome

      AMERICAN JOURNAL OF MEDICAL GENETICS
    12. Neuchrist, C; Erovic, BM; Handisurya, A; Steiner, GE; Rockwell, P; Gedlicka, C; Burian, M
      Vascular endothelial growth factor receptor 2 (VEGFR2) expression in squamous cell carcinomas of the head and neck

      LARYNGOSCOPE
    13. Jones, RB; Wang, F; Luo, YD; Yu, CD; Jin, CL; Suzuki, T; Kan, M; McKeehan, WL
      The nonsense-mediated decay pathway and mutually exclusive expression of alternatively spliced FGFR2IIIb and -IIIc mRNAs

      JOURNAL OF BIOLOGICAL CHEMISTRY
    14. Kearns, AE; Donohue, MM; Sanyal, B; Demay, MB
      Cloning and characterization of a novel protein kinase that impairs osteoblast differentiation in vitro

      JOURNAL OF BIOLOGICAL CHEMISTRY
    15. Le Guienr, C; Lejeune, F; Galiana, D; Kister, L; Breathnach, R; Stevenin, J; Del Gatto-Konczak, F
      TIA-1 and TIAR activate splicing of alternative exons with weak 5 ' splicesites followed by a U-rich stretch on their own pre-mRNAs

      JOURNAL OF BIOLOGICAL CHEMISTRY
    16. Genetta, T; Morisaki, H; Morisaki, T; Holmes, EW
      A novel bipartite intronic splicing enhancer promotes the inclusion of a mini-exon in the AMP deaminase 1 gene

      JOURNAL OF BIOLOGICAL CHEMISTRY
    17. Cote, J; Dupuis, S; Wu, JY
      Polypyrimidine track-binding protein binding downstream of caspase-2 alternative exon 9 represses its inclusion

      JOURNAL OF BIOLOGICAL CHEMISTRY
    18. Hosoya, K; Tomi, M; Ohtsuki, S; Takanaga, H; Ueda, M; Yanai, N; Obinata, M; Terasaki, T
      Conditionally immortalized retinal capillary endothelial cell lines (TR-iBRB) expressing differentiated endothelial cell functions derived from a transgenic rat

      EXPERIMENTAL EYE RESEARCH
    19. Revest, JM; Spencer-Dene, B; Kerr, K; De Moerlooze, L; Rosewell, I; Dickson, C
      Fibroblast growth factor receptor 2-IIIb acts upstream of Shh and Fgf4 andis required for limb bud maintenance but not for the induction of Fgf8, Fgf10, Msx1, or Bmp4

      DEVELOPMENTAL BIOLOGY
    20. Gill, M; Dias, S; Hattori, K; Rivera, ML; Hicklin, D; Witte, L; Girardi, L; Yurt, R; Himel, H; Rafii, S
      Vascular trauma induces rapid but transient mobilization of VEGFR2(+)AC133(+) endothelial precursor cells

      CIRCULATION RESEARCH
    21. Biscardi, JS; Ishizawar, RC; Silva, CM; Parsons, SJ
      Tyrosine kinase signalling in breast cancer - Epidermal growth factor receptor and c-Src interactions in breast cancer

      BREAST CANCER RESEARCH
    22. DaCosta, SA; Schumaker, LM; Elli, MJ
      Mannose 6-phosphate/insulin-like growth factor 2 receptor, a Bona fide tumor suppressor gene or just a promising candidate?

      JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA
    23. Rousseau, S; Houle, F; Huot, J
      Integrating the VEGF signals leading to actin-based motility in vascular endothelial cells

      TRENDS IN CARDIOVASCULAR MEDICINE
    24. Yang, ZW; Mooney, MP; Ferrell, RE
      Cloning and sequencing of the rabbit FGFR2 cDNA

      DNA SEQUENCE
    25. Seki, M; Toi, M; Kobayashi, K; Shitara, K; Umezawa, K; Seon, BK; Kan, M; Rhim, JS
      Differential behavior of VEGF receptor expression and response to TNP-470 in two immortalized human endothelial cell lines

      INTERNATIONAL JOURNAL OF ONCOLOGY
    26. Johnson, D; Wall, SA; Mann, S; Wilkie, AOM
      A novel mutation, Ala315Ser, in FGFR2: a gene-environment interaction leading to craniosynostosis?

      EUROPEAN JOURNAL OF HUMAN GENETICS
    27. De Moerlooze, L; Spencer-Dene, B; Revest, JM; Hajihosseini, M; Rosewell, I; Dickson, C
      An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis

      DEVELOPMENT
    28. Krasner, A; Wallace, L; Thiagalingam, A; Jones, C; Lengauer, C; Minahan, L; Ma, YK; Kalikin, L; Feinberg, AP; Jabs, EW; Tunnacliffe, A; Baylin, SB; Ball, DW; Nelkin, BD
      Cloning and chromosomal localization of the human BARX2 homeobox protein gene

      GENE
    29. Kanellis, J; Fraser, S; Katerelos, M; Power, DA
      Vascular endothelial growth factor is a survival factor for renal tubular epithelial cells

      AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
    30. Kress, W; Collmann, H; Busse, M; Halliger-Keller, B; Mueller, CR
      Clustering of FGFR2 gene mutations in patients with Pfeiffer and Crouzon syndromes (FGFR2-associated craniosynostoses)

      CYTOGENETICS AND CELL GENETICS
    31. Mathijssen, IMJ; van Leeuwen, JPTM; Vermeij-Keers, C
      Simultaneous induction of apoptosis, collagen type I expression and mineralization in the developing coronal suture following FGF4 and FGF2 application

      JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY
    32. Roscioli, T; Flanagan, S; Kumar, P; Masel, J; Gattas, M; Hyland, VJ; Glass, IA
      Clinical findings in a patient with FGFR1 P252R mutation and comparison with the literature

      AMERICAN JOURNAL OF MEDICAL GENETICS
    33. Brown, RE; Bernath, AM; Levis, GO
      HER-2/neu protein-receptor-positive breast carcinoma: An immunologic perspective

      ANNALS OF CLINICAL AND LABORATORY SCIENCE
    34. Steiner, MS; Gingrich, JR
      Gene therapy for prostate cancer: Where are we now?

      JOURNAL OF UROLOGY
    35. Illi, B; Puri, P; Morgante, L; Capogrossi, MC; Gaetano, C
      Nuclear factor-kappa B and cAMP response element binding protein mediate opposite transcriptional effects on the Flk-1/KDR gene promoter

      CIRCULATION RESEARCH
    36. Bruns, CJ; Liu, WB; Davis, DW; Shaheen, RM; McConkey, DJ; Wilson, MR; Bucana, CD; Hicklin, DJ; Ellis, LM
      Vascular endothelial growth factor is an in vivo survival factor for tumorendothelium in a murine model of colorectal carcinoma liver metastases

      CANCER
    37. Hehr, U; Muenke, M
      Craniosynostosis syndromes: From genes to premature fusion of skull bones

      MOLECULAR GENETICS AND METABOLISM
    38. Everett, ET; Britto, DA; Ward, RE; Hartsfield, JK
      A novel FGFR2 gene mutation in Crouzon syndrome associated with apparent nonpenetrance

      CLEFT PALATE-CRANIOFACIAL JOURNAL
    39. Sakaguchi, K; Lorenzi, MV; Matsushita, H; Miki, T
      Identification of a novel activated form of the keratinocyte growth factorreceptor by expression cloning from parathyroid adenoma tissue

      ONCOGENE
    40. Kern, JA; Wakita, R; Sliwkowski, MX
      Neuregulin receptor-mediated gene transfer by human epidermal growth factor receptor 2-targeted antibodies and neuregulin-1

      CANCER GENE THERAPY
    41. Ting, K; Vastardis, H; Mulliken, JB; Soo, C; Tieu, A; Do, H; Kwong, E; Bertolami, CN; Kawamoto, H; Kuroda, S; Longaker, MT
      Human NELL-1 expressed in unilateral coronal synostosis

      JOURNAL OF BONE AND MINERAL RESEARCH
    42. Lajeunie, E; Catala, M; Renier, D
      Craniosynostosis: from a clinical description to an understanding of bone formation of the skull

      CHILDS NERVOUS SYSTEM
    43. Kelly, DL; Rizzino, A
      Growth regulatory factors and carcinogenesis: The roles played by transforming growth factor beta, its receptors and signaling pathways

      ANTICANCER RESEARCH
    44. Waggoner, DJ; Chow, CK; Dowton, SB; Watson, MS
      Partial monosomy of distal 10q: Three new cases and a review

      AMERICAN JOURNAL OF MEDICAL GENETICS
    45. Shroyer, NF; Lewis, RA; Allikmets, R; Singh, N; Dean, M; Leppert, M; Lupski, JR
      The rod photoreceptor ATP-binding cassette transporter gene, ABCR, and retinal disease: from monogenic to multifactorial

      VISION RESEARCH
    46. Robin, NH
      Molecular genetic advances in understanding craniosynostosis

      PLASTIC AND RECONSTRUCTIVE SURGERY
    47. Kolb, C; Mauch, S; Krawinkel, U; Sedlacek, R
      Matrix metalloproteinase-19 in capillary endothelial cells: Expression in acutely, but not in chronically, inflamed synovium

      EXPERIMENTAL CELL RESEARCH
    48. Higashimoto, T; Yano, S; Ito, M; Clark-Sheehan, NC; Cowan, L; Boles, RG
      Rapid detection of FGFR mutations in syndromic craniosynostosis by temporal temperature gradient gel electrophoresis

      CLINICAL CHEMISTRY
    49. Oldridge, M; Zackai, EH; McDonald-McGinn, DM; Iseki, S; Morriss-Kay, GM; Twigg, RF; Johnson, D; Wall, SA; Jiang, W; Theda, C; Jabs, EW; Wilkie, AOM
      De novo Alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome

      AMERICAN JOURNAL OF HUMAN GENETICS
    50. CARLTON MBL; COLLEDGE WH; EVANS MJ
      CROUZON-LIKE CRANIOFACIAL DYSMORPHOLOGY IN THE MOUSE IS CAUSED BY AN INSERTIONAL MUTATION AT THE FGF3 FGF4 LOCUS/

      Developmental dynamics
    51. NAGASE T; NAGASE M; HIROSE S; OHMORI K
      MUTATIONS IN FIBROBLAST GROWTH-FACTOR RECEPTOR 2 GENE AND CRANIOSYNOSTOTIC SYNDROMES IN JAPANESE CHILDREN

      The Journal of craniofacial surgery
    52. ANDERSON PJ; HALL CM; EVANS RD; JONES BM; HAYWARD RD
      THE FEET IN PFEIFFERS-SYNDROME

      The Journal of craniofacial surgery
    53. KIM HJ; RICE DPC; KETTUNEN PJ; THESLEFF I
      FGF-MEDIATED, BMP-MEDIATED AND SHH-MEDIATED SIGNALING PATHWAYS IN THEREGULATION OF CRANIAL SUTURE MORPHOGENESIS AND CALVARIAL BONE-DEVELOPMENT

      Development
    54. ZIMMERMANN B; MOEGELIN A; DESOUZA P; BIER J
      MORPHOLOGY OF THE DEVELOPMENT OF THE SAGITTAL SUTURE OF MICE

      Anatomy and embryology
    55. Barni, T; Fantoni, G; Gloria, L; Maggi, M; Peri, A; Balsi, E; Grappone, C; Vannelli, GB
      Role of endothelin in the human craniofacial morphogenesis

      JOURNAL OF CRANIOFACIAL GENETICS AND DEVELOPMENTAL BIOLOGY
    56. OATES AJ; SCHUMAKER LM; JENKINS SB; PEARCE AA; DACOSTA SA; ARUN B; ELLIS MJC
      THE MANNOSE 6-PHOSPHATE INSULIN-LIKE GROWTH-FACTOR-2 RECEPTOR (M6P/IGF2R), A PUTATIVE BREAST-TUMOR SUPPRESSOR GENE/

      Breast cancer research and treatment
    57. GRIPP KW; STOLLE CA; MCDONALDMCGINN DM; MARKOWITZ RI; BARTLETT SP; KATOWITZ JA; MUENKE M; ZACKAI EH
      PHENOTYPE OF THE FIBROBLAST-GROWTH-FACTOR RECEPTOR-2 SER351CYS MUTATION - PFEIFFER-SYNDROME TYPE-III

      American journal of medical genetics
    58. CHUN K; SIEGELBARTELT J; CHITAYAT D; PHILLIPS J; RAY PN
      FGFR2 MUTATION ASSOCIATED WITH CLINICAL MANIFESTATIONS CONSISTENT WITH ANTLEY-BIXLER-SYNDROME

      American journal of medical genetics
    59. KREPELOVA A; BAXOVA A; CALDA P; PLAVKA R; KAPRAS J
      FGFR2 GENE MUTATION (TYR375CYS) IN A NEW CASE OF BEARE-STEVENSON-SYNDROME

      American journal of medical genetics
    60. PLOMP AS; HAMEL BCJ; COBBEN JM; VERLOES A; OFFERMANS JPM; LAJEUNIE E; FRYNS JP; DEDIESMULDERS CEM
      PFEIFFER SYNDROME TYPE-2 - FURTHER DELINEATION AND REVIEW OF THE LITERATURE

      American journal of medical genetics
    61. LEVINE JP; BRADLEY JP; ROTH DA; MCCARTHY JG; LONGAKER MT
      STUDIES IN CRANIAL SUTURE BIOLOGY - REGIONAL DURA-MATER DETERMINES OVERLYING SUTURE BIOLOGY

      Plastic and reconstructive surgery
    62. FLANAGAN N; BOYADJIEV SA; HARPER J; KYNE L; EARLEY M; WATSON R; JABS EW; GERAGHTY MT
      FAMILIAL CRANIOSYNOSTOSIS, ANAL ANOMALIES, AND POROKERATOSIS - CAP SYNDROME

      Journal of Medical Genetics
    63. PASSOSBUENO MR; RICHIERICOSTA A; SERTIE AL; KNEPPERS A
      PRESENCE OF THE APERT CANONICAL S252W FGFR2 MUTATION IN A PATIENT WITHOUT SEVERE SYNDACTYLY

      Journal of Medical Genetics
    64. DU YZ; DICKERSON C; AYLSWORTH AS; SCHWARTZ CE
      A SILENT MUTATION, C924T (G308G), IN THE L1CAM GENE RESULTS IN X-LINKED HYDROCEPHALUS (HSAS)

      Journal of Medical Genetics
    65. LOMRI A; LEMONNIER J; HOTT M; DEPARSEVAL N; LAJEUNIE E; MUNNICH A; RENIER D; MARIE PJ
      INCREASED CALVARIA CELL-DIFFERENTIATION AND BONE-MATRIX FORMATION INDUCED BY FIBROBLAST GROWTH-FACTOR RECEPTOR 2 MUTATIONS IN APERT-SYNDROME

      The Journal of clinical investigation
    66. JABS EW
      TOWARD UNDERSTANDING THE PATHOGENESIS OF CRANIOSYNOSTOSIS THROUGH CLINICAL AND MOLECULAR CORRELATES

      Clinical genetics
    67. PAZNEKAS WA; CUNNINGHAM ML; HOWARD TD; KORF BR; LIPSON MH; GRIX AW; FEINGOLD M; GOLDBERG R; BOROCHOWITZ Z; ALECK K; MULLIKEN J; YIN MF; JABS EW
      GENETIC-HETEROGENEITY OF SAETHRE-CHOTZEN-SYNDROME, DUE TO TWIST AND FGFR MUTATIONS

      American journal of human genetics
    68. RICE DPC; KIM HJ; THESLEFF I
      DETECTION OF GELATINASE-B EXPRESSION REVEALS OSTEOCLASTIC BONE-RESORPTION AS A FEATURE OF EARLY CALVARIAL BONE-DEVELOPMENT

      Bone
    69. DIXON MJ
      TWIST AND SHOUT

      Nature genetics
    70. HOWARD TD; PAZNEKAS WA; GREEN ED; CHIANG LC; MA N; DELUNA RIO; DELGADO CG; GONZALEZRAMOS M; KLINE AD; JABS EW
      MUTATIONS IN TWIST, A BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTOR, INSAETHRE-CHOTZEN SYNDROME

      Nature genetics
    71. MAROTEAUX P; LEMERRER M
      CLINICAL APPROACH STILL HAS AN IMPORTANT ROLE IN CONSTITUTIONAL BONE-DISEASES

      Journal of pediatric orthopedics. Part B
    72. KREBS I; WEIS I; HUDLER M; ROMMENS JM; ROTH H; SCHERER SW; TSUI LC; FUCHTBAUER EM; GRZESCHIK KH; TSUJI K; KUNZ J
      TRANSLOCATION BREAKPOINT MAPS 5 KB 3' FROM TWIST IN A PATIENT AFFECTED WITH SAETHRE-CHOTZEN-SYNDROME

      Human molecular genetics
    73. GLADWIN A; DONNAI D; METCALFE K; SCHRANDERSTUMPEL C; BRUETON L; VERLOES A; AYLSWORTH A; TORIELLO H; WINTER R; DIXON M
      LOCALIZATION OF A GENE FOR OCULODENTODIGITAL SYNDROME TO HUMAN-CHROMOSOME 6Q22-Q24

      Human molecular genetics
    74. DONNENFELD AE
      FETAL DYSMORPHOLOGY

      Ultrasound in obstetrics & gynecology
    75. MULLER U; STEINBERGER D; KUNZE S
      MOLECULAR-GENETICS OF CRANIOSYNOSTOTIC SYNDROMES

      Graefe's archive for clinical and experimental ophthalmology
    76. SERGI C; STEIN H; HEEP JG; OTTO HF
      A 19-WEEK-OLD FETUS WITH CRANIOSYNOSTOSIS, RENAL AGENESIS AND GASTROSCHISIS - CASE-REPORT AND DIFFERENTIAL-DIAGNOSIS

      Pathology research and practice
    77. CALLEA F
      A 19-WEEK-OLD FETUS WITH CRANIOSYNOSTOSIS, RENAL AGENSIS AND GASTROSCHISIS - CRITICAL COMMENTARY

      Pathology research and practice
    78. TARTAGLIA M; DIROCCO C; LAJEUNIE E; VALERI S; VELARDI F; BATTAGLIA PA
      JACKSON-WEISS-SYNDROME - IDENTIFICATION OF 2 NOVEL FGFR2 MISSENSE MUTATIONS SHARED WITH CROUZON AND PFEIFFER CRANIOSYNOSTOTIC DISORDERS

      Human genetics
    79. WOLF U
      IDENTICAL MUTATIONS AND PHENOTYPIC VARIATION

      Human genetics
    80. COHEN MM
      SHORT-LIMB SKELETAL DYSPLASIAS AND CRANIOSYNOSTOSIS - WHAT DO THEY HAVE IN COMMON

      Pediatric radiology
    81. MARZELLA R; KOKKINAKI MA; KAPSETAKI M; RICCO A; ARGYROKASTRITIS A; KAMAKARI S; SARAFIDOU T; ARCHIDIACONO N; ROUSSOU A; PASPARAKI A; ROCCHI M; MOSCHONAS NK
      MAP INTEGRATION AT HUMAN-CHROMOSOME-10 - MOLECULAR AND CYTOGENETIC ANALYSIS OF A CHROMOSOME-SPECIFIC SOMATIC-CELL HYBRID PANEL AND GENOMIC CLONES, BASED ON A WELL-SUPPORTED GENETIC-MAP

      Cytogenetics and cell genetics
    82. WOLFF RK
      POSITIONAL CLONING - A REVIEW AND PERSPECTIVE

      Drug development research
    83. ANDERSON PJ; HALL CM; EVANS RD; JONES BM; HAYWARD RD
      THE FEET IN CROUZON-SYNDROME

      Journal of craniofacial genetics and developmental biology
    84. WEBSTER MK; DONOGHUE DJ
      FGFR ACTIVATION IN SKELETAL DISORDERS - TOO MUCH OF A GOOD THING

      Trends in genetics
    85. PASSOSBUENO MR; SERTIE AL; ZATZ M; RICHIERICOSTA A
      PFEIFFER MUTATION IN AN APERT PATIENT - HOW WIDE IS THE SPECTRUM OF VARIABILITY DUE TO MUTATIONS IN THE FGFR2 GENE

      American journal of medical genetics
    86. BRADLEY JP; LEVINE JP; MCCARTHY JG; LONGAKER MT
      STUDIES IN CRANIAL SUTURE BIOLOGY - REGIONAL DURA-MATER DETERMINES IN-VITRO CRANIAL SUTURE FUSION

      Plastic and reconstructive surgery
    87. REARDON W; WILKES D; RUTLAND P; PULLEYN LJ; MALCOLM S; DEAN JCS; EVANS RD; JONES BM; HAYWARD R; HALL CM; NEVIN NC; BARAITSER M; WINTER RM
      CRANIOSYNOSTOSIS ASSOCIATED WITH FGFR3 PRO250ARG MUTATION RESULTS IN A RANGE OF CLINICAL PRESENTATIONS INCLUDING UNISUTURAL SPORADIC CRANIOSYNOSTOSIS

      Journal of Medical Genetics
    88. STEINBERGER D; COLLMANN H; SCHMALENBERGER B; MULLER U
      A NOVEL MUTATION (A886G) IN EXON-5 OF FGFR2 IN MEMBERS OF A FAMILY WITH CROUZON PHENOTYPE AND PLAGIOCEPHALY

      Journal of Medical Genetics
    89. SIEGFRIED S; PEKONEN F; NYMAN T; AMMALA M; RUTANEN EM
      DISTINCT PATTERNS OF EXPRESSION OF KERATINOCYTE GROWTH-FACTOR AND ITSRECEPTOR IN ENDOMETRIAL CARCINOMA

      Cancer
    90. CHAPPELL SA; WALSH T; WALKER RA; SHAW JA
      LOSS OF HETEROZYGOSITY AT THE MANNOSE 6-PHOSPHATE INSULIN-LIKE-GROWTH-FACTOR-2 RECEPTOR GENE CORRELATES WITH POOR DIFFERENTIATION IN EARLY BREAST CARCINOMAS

      British Journal of Cancer
    91. BANSAL GS; COX HC; MARSH S; GOMM J; YIANGOU C; LUQMANI Y; COOMBES RC; JOHNSTON CL
      EXPRESSION OF KERATINOCYTE GROWTH-FACTOR AND ITS RECEPTOR IN HUMAN BREAST-CANCER

      British Journal of Cancer
    92. STEINBERGER D; MULLIKEN JB; MULLER U
      CROUZON SYNDROME - PREVIOUSLY UNRECOGNIZED DELETION, DUPLICATION, ANDPOINT MUTATION WITHIN FGFR2 GENE

      Human mutation
    93. LACOMBE D
      CLINICAL DYSMORPHOLOGY AND HUMAN DEVELOPM ENTAL GENES

      MS. Medecine sciences
    94. STEINBERGER D; REINHARTZ T; UNSOLD R; MULLER U
      FGFR2 MUTATION IN CLINICALLY NONCLASSIFIABLE AUTOSOMAL-DOMINANT CRANIOSYNOSTOSIS WITH PRONOUNCED PHENOTYPIC VARIATION

      American journal of medical genetics
    95. WILKES D; RUTLAND P; PULLEYN LJ; REARDON W; MOSS C; ELLIS JP; WINTER RM; MALCOLM S
      A RECURRENT MUTATION, ALA391GLU, IN THE TRANSMEMBRANE REGION OF FGFR3CAUSES CROUZON SYNDROME AND ACANTHOSIS NIGRICANS

      Journal of Medical Genetics
    96. FLEISCHMAN RA; GALLARDO T; MI XF
      MUTATIONS IN THE LIGAND-BINDING DOMAIN OF THE KIT RECEPTOR - AN UNCOMMON SITE IN HUMAN PIEBALDISM

      Journal of investigative dermatology
    97. BONINI JA; COLCA JR; DAILEY C; WHITE M; HOFMANN C
      COMPENSATORY ALTERATIONS FOR INSULIN SIGNAL-TRANSDUCTION AND GLUCOSE-TRANSPORT IN INSULIN-RESISTANT DIABETES

      American journal of physiology: endocrinology and metabolism
    98. SUZUKI T; TSUDA T; HARUMA K; YOSHIHARA M; SUMII K; KAJIYAMA G
      GROWTH OF HUMAN GASTRIC CARCINOMAS AND EXPRESSION OF EPIDERMAL GROWTH-FACTOR, TRANSFORMING GROWTH FACTOR-A, EPIDERMAL GROWTH-FACTOR RECEPTOR AND P185(C-ERB-2)

      Oncology
    99. GIORGETTIPERALDI S; PEYRADE F; BARON V; VANOBBERGHEN E
      INVOLVEMENT OF JANUS KINASES IN THE INSULIN SIGNALING PATHWAY

      European journal of biochemistry
    100. LABOSKY PA; BARLOW DP; HOGAN BLM
      MOUSE EMBRYONIC GERM (EG) CELL-LINES - TRANSMISSION THROUGH THE GERMLINE AND DIFFERENCES IN THE METHYLATION IMPRINT OF INSULIN-LIKE GROWTH-FACTOR 2 RECEPTOR (IGF2R) GENE COMPARED WITH EMBRYONIC STEM (ES) CELL-LINES

      Development


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Documento generato il 10/08/20 alle ore 08:59:32