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Aberrant expression of IL-22 receptor 1 and autocrine IL-22 stimulation contribute to tumorigenicity in ALK+ anaplastic large cell lymphomaDIEN BARD, J; GELEBART, P; ANAND, M et al.Leukemia. 2008, Vol 22, Num 8, pp 1595-1603, issn 0887-6924, 9 p.Article

Potential involvement of IL-22 and IL-22-producing cells in the inflamed salivary glands of patients with Sjögren's syndromeCICCIA, Francesco; GUGGINO, Giuliana; RIZZO, Aroldo et al.Annals of the rheumatic diseases. 2012, Vol 71, Num 2, pp 295-301, issn 0003-4967, 7 p.Article

Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13NARKIS, Ginat; LANDAU, Daniella; MANOR, Esther et al.American journal of medical genetics. 2004, Vol 130A, Num 3, pp 272-276, issn 0148-7299, 5 p.Article

Structural and mutational analysis of a conserved gene (DGSI) from the minimal DiGeorge syndrome critical regionGONG, W; EMANUEL, B. S; GALILI, N et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 267-276, issn 0964-6906Article

Anesthesia in a patient with chromosome 11;22 translocation : a case report and literature reviewDRUM, Elizabeth T; HERLICH, Andrew; LEVINE, Bruce et al.Paediatric anaesthesia (Paris). 2005, Vol 15, Num 11, pp 985-987, issn 1155-5645, 3 p.Article

Cannabinoid Receptor 1 Gene Polymorphism and Irritable Bowel Syndrome in the Korean Population: A Hypothesis-generating StudyJAE MYUNG PARK; CHOI, Myung-Gyu; YU KYUNG CHO et al.Journal of clinical gastroenterology. 2011, Vol 45, Num 1, pp 45-49, issn 0192-0790, 5 p.Article

Different phenotypes in Muir-Torre syndrome : clinical and biomolecular characterization in two Italian familiesPONTI, G; PONZ DE LEON, M; SEIDENARI, S et al.British journal of dermatology (1951). 2005, Vol 152, Num 6, pp 1335-1338, issn 0007-0963, 4 p.Article

Elejalde syndrome- : A case reportSIHANOVA, Eva; PLEVOVA, Pavlina; CURIK, Romuald et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 20, pp 2223-2226, issn 1552-4825, 4 p.Article

Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDSMÄKLTIE, O; ELLIS, L; DURIE, P. R et al.Clinical genetics. 2004, Vol 65, Num 2, pp 101-112, issn 0009-9163, 12 p.Article

Syndromes de délétion en 22q11 : fin d'enquête en vue ? = Syndromes associated with a 22q11 deletion : the end of the road ?LIPINSKI, M.MS. Médecine sciences. 1999, Vol 15, Num 8-9, pp 999-1002, issn 0767-0974Article

UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromePIZZUTI, A; NOVELLI, G; OTTOLENGHI, S et al.Human molecular genetics (Print). 1997, Vol 6, Num 2, pp 259-265, issn 0964-6906Article

Impaired TH17 responses in patients with chronic mucocutaneous candidiasis with and without autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophyNG, Wan-Fai; VON DELWIG, Alexei; CARMICHAEL, Andrew J et al.Journal of allergy and clinical immunology. 2010, Vol 126, Num 5, pp 1006-1015, issn 0091-6749, 10 p.Article

Vertebral Fusion in a Patient With Supernumerary-der(22)t(11;22) SyndromeTOYOSHIMA, Mitsuo; YONEE, Chihiro; MAEGAKI, Yoshihiro et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 8, pp 1722-1726, issn 1552-4825, 5 p.Article

Association of serotonin transporter gene polymorphism with obstructive sleep apnea syndromeYILMAZ, Metin; BAYAZIT, Yildirim A; ULUKAVAK CIFTCI, Tansu et al.The Laryngoscope. 2005, Vol 115, Num 5, pp 832-836, issn 0023-852X, 5 p.Article

DiGeorge syndrome: the use of model organisms to dissect complex geneticsBALDINI, Antonio.Human molecular genetics (Print). 2002, Vol 11, Num 20, pp 2363-2369, issn 0964-6906Article

Leptin and Leptin Receptor Gene Polymorphisms in Obstructive Sleep Apnea SyndromeHANAOKA, Masayuki; XIUJUN YU; URUSHIHATA, Kazuhisa et al.Chest. 2008, Vol 133, Num 1, pp 79-85, issn 0012-3692, 7 p.Article

Catch 22 : Microdeletion 22q11 screening in patients with congenital heart defectsVON BEUST, G; BARTMUS, D; BARTELS, I et al.Genetic counseling. 1998, Vol 9, Num 3, pp 223-227, issn 1015-8146Conference Paper

Fat chance: genetic syndromes with obesityDELRUE, M-A; MICHAUD, J. L.Clinical genetics. 2004, Vol 66, Num 2, pp 83-93, issn 0009-9163, 11 p.Article

Stage 3 immature human natural killer cells found in secondary lymphoid tissue constitutively and selectively express the TH17 cytokine interleukin-22HUGHES, Tiffany; BECKNELL, Brian; MCCLORY, Susan et al.Blood. 2009, Vol 113, Num 17, pp 4008-4010, issn 0006-4971, 3 p.Article

Description and molecular analysis of SRY and AR genes in a patient with 46,XY pure gonadal dysgenesis (Swyer syndrome)ILIOPOULOS, Dimitrios; VOLAKAKIS, Nikolaos; TSIGA, Alexandra et al.Annales de génétique (Paris). 2004, Vol 47, Num 2, pp 185-190, issn 0003-3995, 6 p.Article

Anesthetic management of a child with chromosome 22q11 deletion syndromeYOTSUI-TSUCHIMOCHI, Hiroe; HIGA, Kazuo; MATSUNAGA, Matsuko et al.Paediatric anaesthesia (Paris). 2006, Vol 16, Num 4, pp 454-457, issn 1155-5645, 4 p.Article

IL-22 : A critical mediator in mucosal host defenseAUJLA, S. J; KOLLS, J. K.Journal of molecular medicine (Berlin. Print). 2009, Vol 87, Num 5, pp 451-454, issn 0946-2716, 4 p.Article

Pseudoisodicentric bisatellited extra marker chromosome (tetrasomy 22pter→q11, trisomy Yqh), derived from a maternal Y/22 translocation. Association between this tetrasomy and Cat eyë phenotypical featuresGABARRON, J; GLOVER, G; JIMENEZ, A et al.Clinical genetics. 1985, Vol 28, Num 6, pp 509-515, issn 0009-9163Article

Double trisomie et inversion péricentrique transmise [48,XXY, +21, inv(22)] effet interchrosomique = Double trisomy and inherited pericentric inversion [48,XXY, +21, inv(22)] interchromosomal effectSAURA, R; LONGY, M; SAUTAREL, M et al.Annales de génétique (Paris). 1983, Vol 26, Num 3, pp 180-182, issn 0003-3995Article

Nucleotide and deduced amino acid sequences of bacteriophage T4 gene 22MARUSICH, E. I; MESYANZHINOV, V. V.Nucleic acids research. 1989, Vol 17, Num 21, issn 0305-1048, 8865 [1 p.]Article

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