Ankyloblepharon-ectodermal defects-cleft lip-palate syndrome due to a novel missense mutation in the SAM domain of the TP63 gene von Tajir, M, Lyahyai, J, Guaoua, S, El Alloussi, M, Sefiani, A

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Comparative study of equine bone marrow and adipose tissue-derived mesenchymal stromal cells von RANERA, B., ORDOVÁS, L., LYAHYAI, J., BERNAL, M. L., FERNANDES, F., REMACHA, A. R., ROMERO, A., VÁZQUEZ, F. J., OSTA, R., CONS, C., VARONA, L., ZARAGOZA, P., MARTÍN-BURRIEL, I., RODELLAR, C.

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Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic features von Smaili, W., Elalaoui, S. Chafai, Zrhidri, A., Raymond, L., Egéa, G., Taoudi, M., Mouatassim, S.E.L., Sefiani, A., Lyahyai, J.

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Clinical and molecular report of novel GALC mutations in Moroccan patient with Krabbe disease: case report von Zerkaoui, M, Ratbi, I, Castellotti, B, Gellera, C, Lyahyai, J, Kriouile, Y, Sefiani, A

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CALR gene mutational profile in myeloproliferative neoplasms with non-mutated JAK2 in Moroccan patients: A case series and germline in-frame deletion von Smaili, W., Doubaj, Y., Laarabi, F.Z., Lyahyai, J., Kerbout, M., Mikdame, M., Sefiani, A.

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Myeloperoxidase Modulates Inflammation in Generalized Pustular Psoriasis and Additional Rare Pustular Skin Diseases von Haskamp, Stefan, Bruns, Heiko, Hahn, Madelaine, Hoffmann, Markus, Gregor, Anne, Löhr, Sabine, Hahn, Jonas, Schauer, Christine, Ringer, Mark, Flamann, Cindy, Frey, Benjamin, Lesner, Adam, Thiel, Christian T., Ekici, Arif B., von Hörsten, Stephan, Aßmann, Gunter, Riepe, Claudia, Euler, Maximilien, Schäkel, Knut, Philipp, Sandra, Prinz, Jörg C., Mößner, Rotraut, Kersting, Florina, Sticherling, Michael, Sefiani, Abdelaziz, Lyahyai, Jaber, Sondermann, Wiebke, Oji, Vinzenz, Schulz, Peter, Wilsmann-Theis, Dagmar, Sticht, Heinrich, Schett, Georg, Reis, André, Uebe, Steffen, Frey, Silke, Hüffmeier, Ulrike

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Report of the First Clinical Case of a Moroccan Kabuki Patient with a Novel MLL2 Mutation von Ratbi, I., Fejjal, N., Micale, L., Augello, B., Fusco, C., Lyahyai, J., Merla, G., Sefiani, A.

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First nonsense variant of MED12 gene in a female with complete Maat-Kievit-Brunner phenotype of Ohdo syndrome: A case report von Amllal, N., Lyahyai, J., Elalaoui, S.C., Sefiani, A., Ratbi, I.

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PRNP haplotype distribution in Moroccan goats von Serrano, C, Hammouchi, M, Benomar, A, Lyahyai, J, Ranera, B, Acín, C, el Hamidi, M, Monzón, M, Badiola, J.J, Tligui, N, Zaragoza, P, Martín-Burriel, I

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Polymorphisms of the prnp gene in Moroccan sheep breeds von Serrano, C., Martín-Burriel, I., Lyahyai, J., Monzón, M., El Hamidi, M., Acín, C., Badiola, J. J., Tligui, N., Zaragoza, P.

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La fibromatose hyaline juvénile : une nouvelle observation von Guerouaz, N., Benhiba, H., Lamchaheb, F.Z., Rimani, M., Lyahyai, J., Ratbi, I., Sefiani, A., Senouci, K., Hassam, B.

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Assignment of the bovine B-cell CLL/lymphoma 2 gene (BCL2) to BTA24q27 and the bovine BCL2-like 1 gene (BCL2L1) to BTA13q22 by in situ hybridization von Goldammer, T, Brunner, R M, Lyahyai, J, Zaragoza, P, Martín-Burriel, I

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Spinal muscular atrophy carrier frequency and estimated prevalence of the disease in Moroccan newborns von Lyahyai, Jaber, Sbiti, Aziza, Barkat, Amina, Ratbi, Ilham, Sefiani, Abdelaziz

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Positional and functional characterisation of apoptosis related genes belonging to the BCL2 family in sheep von Lyahyai, J., Goldammer, T., Beattie, A.E., Zaragoza, P., Martín-Burriel, I.

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Prion protein gene polymorphisms in healthy and scrapie-affected Spanish sheep von Acin, C, Martin-Burriel, I, Goldmann, W, Lyahyai, J, Monzon, M, Bolea, R, Smith, A, Rodellar, C, Badiola, J.J, Zaragoza, P

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Assignment of the bovine BCL2-like 2 gene (BCL2L2) to BTA10q15→q21 by in situ hybridization and with somatic cell hybrids von Martín-Burriel, I., Lyahyai, J., Zaragoza, P., Brunner, R.M., Womack, J.E., Goldammer, T.

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Novel nonsense mutation of BRCA2 gene in a Moroccan man with familial breast cancer von Guaoua, Soukaina, Ratbi, Ilham, Lyahyai, Jaber, El Alaoui, Siham Chafai, Laarabi, Fatima-Zahra, Sefiani, Abdelaziz

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Correlation between Bax overexpression and prion deposition in medulla oblongata from natural scrapie without evidence of apoptosis von Lyahyai, Jaber, Bolea, Rosa, Serrano, Carmen, Monleón, Eva, Moreno, Carlos, Osta, Rosario, Zaragoza, Pilar, Badiola, Juan J, Martín-Burriel, Inmaculada

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Differential expression and protein distribution of Bax in natural scrapie von Lyahyai, Jaber, Bolea, Rosa, Serrano, Carmen, Vidal, Enric, Pumarola, Martí, Badiola, Juan J, Zaragoza, Pilar, Martín-Burriel, Inmaculada

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Structural and Functional Analysis of the HSP90AA1 Gene: Distribution of Polymorphisms among Sheep with Different Responses to Scrapie von Marcos-Carcavilla, Ane, Calvo, Jorge H., González, Carmen, Moazami-Goudarzi, Katayoun, Laurent, Pascal, Bertaud, Maud, Hayes, Hélène, Beattie, Anne E., Serrano, Carmen, Lyahyai, Jaber, Martín-Burriel, Inmaculada, Serrano, Magdalena

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