Lack of lymphocytes impairs macrophage polarization and angiogenesis in diabetic wound healing von Seraphim, Patricia M., Leal, Ermelindo C., Moura, João, Gonçalves, Pedro, Gonçalves, Jenifer P., Carvalho, Eugénia

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The cancer cell-derived extracellular vesicle glycocode in immunoevasion von Goncalves, Jenifer P., Deliwala, Vatsal J., Kolarich, Daniel, Souza-Fonseca-Guimaraes, Fernando, Wolfram, Joy

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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort von Guran, Tulay, Buonocore, Federica, Saka, Nurcin, Ozbek, Mehmet Nuri, Aycan, Zehra, Bereket, Abdullah, Bas, Firdevs, Darcan, Sukran, Bideci, Aysun, Guven, Ayla, Demir, Korcan, Akinci, Aysehan, Buyukinan, Muammer, Aydin, Banu Kucukemre, Turan, Serap, Agladioglu, Sebahat Yilmaz, Atay, Zeynep, Abali, Zehra Yavas, Tarim, Omer, Catli, Gonul, Yuksel, Bilgin, Akcay, Teoman, Yildiz, Metin, Ozen, Samim, Doger, Esra, Demirbilek, Huseyin, Ucar, Ahmet, Isik, Emregul, Ozhan, Bayram, Bolu, Semih, Ozgen, Ilker Tolga, Suntharalingham, Jenifer P, Achermann, John C

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A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development von Bashamboo, Anu, Donohoue, Patricia A, Vilain, Eric, Rojo, Sandra, Calvel, Pierre, Seneviratne, Sumudu N, Buonocore, Federica, Barseghyan, Hayk, Bingham, Nathan, Rosenfeld, Jill A, Mulukutla, Surya Narayan, Jain, Mahim, Burrage, Lindsay, Dhar, Shweta, Balasubramanyam, Ashok, Lee, Brendan, Dumargne, Marie-Charlotte, Eozenou, Caroline, Suntharalingham, Jenifer P, de Silva, Ksh, Lin, Lin, Bignon-Topalovic, Joelle, Poulat, Francis, Lagos, Carlos F, McElreavey, Ken, Achermann, John C

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Transforming undergraduate laboratory courses with interlinked real-world challenges von Iannotta, Dalila, Goncalves, Jenifer P, Ghebosu, Raluca E, Gopalakrishnan, Aswathi, Cooper-White, Justin, Wolfram, Joy

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New Observation on Cesaro Summability in Neutrosophic n-Normed Linear Spaces von Jenifer, P, Jeyaraman, M

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Characterization of Turner Syndrome-associated diabetes mellitus von Cameron-Pimblett, Antoinette, La Rosa, Clementina, Davies, Melanie C, Suntharalingham, Jenifer P, Ishida, Miho, Achermann, John C, Conway, Gerard S

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Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans von Buonocore, Federica, Kühnen, Peter, Suntharalingham, Jenifer P, Del Valle, Ignacio, Digweed, Martin, Stachelscheid, Harald, Khajavi, Noushafarin, Didi, Mohammed, Brady, Angela F, Blankenstein, Oliver, Procter, Annie M, Dimitri, Paul, Wales, Jerry K H, Ghirri, Paolo, Knöbl, Dieter, Strahm, Brigitte, Erlacher, Miriam, Wlodarski, Marcin W, Chen, Wei, Kokai, George K, Anderson, Glenn, Morrogh, Deborah, Moulding, Dale A, McKee, Shane A, Niemeyer, Charlotte M, Grüters, Annette, Achermann, John C

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Biocompatible gum arabic-gold nanorod composite as an effective therapy for mistreated melanomas von Gonçalves, Jenifer P., da Cruz, Anderson F., Nunes, Ábner M., Meneghetti, Mario R., de Barros, Heloise R., Borges, Beatriz S., de Medeiros, Lia C.A.S., Soares, Maurilio J., dos Santos, Mayara P., Grassi, Marco T., Rossi, Gustavo R., Bellan, Daniel L., Biscaia, Stellee M.P., Cristal, Aline M., Buzzo, João L.A., Ribeiro, Yasmin C., Acco, Alexandra, Cardoso, Mateus B., Simas, Fernanda F., Trindade, Edvaldo S., Riegel-Vidotti, Izabel C., de Oliveira, Carolina C.

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Hyaluronic acid: An overlooked extracellular vesicle contaminant von Goncalves, Jenifer P, Ghebosu, Raluca E, Tan, Xuan Ning Sharon, Iannotta, Dalila, Koifman, Na'ama, Wolfram, Joy

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Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome von Suntharalingham, Jenifer P, Ishida, Miho, Del Valle, Ignacio, Stalman, Susanne E, Solanky, Nita, Wakeling, Emma, Moore, Gudrun E, Achermann, John C, Buonocore, Federica

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Long-term outcome of partial P450 side-chain cleavage enzyme deficiency in three brothers: the importance of early diagnosis von Kallali, Wafa, Gray, Ewan, Mehdi, Muhammad Zain, Lindsay, Robert, Metherell, Louise A, Buonocore, Federica, Suntharalingham, Jenifer P, Achermann, John C, Donaldson, Malcolm

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Analysis of genetic variability in Turner syndrome linked to long-term clinical features von Suntharalingham, Jenifer P, Ishida, Miho, Cameron-Pimblett, Antoinette, McGlacken-Byrne, Sinead M, Buonocore, Federica, Del Valle, Ignacio, Madhan, Gaganjit Kaur, Brooks, Tony, Conway, Gerard S, Achermann, John C

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β-Cyclodextrins alter the energy metabolism-related enzyme activities in rats von Ianiski, Francine R, Oliveira, Amanda L DE, Mezzomo, Nathana Jamille, Franceschi, Itiane D DE, Carmo, Guilherme M DO, Cremonese, Camila R, Baldissera, Matheus D, Zanon, Jenifer P, Kolling, Jenifer, Friederich, Jordana Daniela, Silva, Ivana Z, Giongo, Janice L, Feksa, Luciane R, Vaucher, Rodrigo A, Wannmacher, Clovis Milton D, Rech, Virginia C

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DNA Barcoding and Phylogenetic Analysis of Indian Medicinal Plant Piper longum von Shaji, Sneha Mariam, Udhaya P, Jenifer

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DAX-1 (NR0B1) and steroidogenic factor-1 (SF-1, NR5A1) in human disease von Suntharalingham, Jenifer P., BSc, Buonocore, Federica, PhD, Duncan, Andrew J., PhD, Achermann, John C., MB, MD, PhD, FRCP, FRCPCH

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A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development von Bashamboo, Anu, Donohoue, Patricia A, Vilain, Eric, Rojo, Sandra, Calvel, Pierre, Seneviratne, Sumudu N, Buonocore, Federica, Barseghyan, Hayk, Bingham, Nathan, Rosenfeld, Jill A, Mulukutla, Surya Narayan, Jain, Mahim, Burrage, Lindsay, Dhar, Shweta, Balasubramanyam, Ashok, Lee, Brendan, Dumargne, Marie-Charlotte, Eozenou, Caroline, Suntharalingham, Jenifer P, de Silva, Ksh, Lin, Lin, Bignon-Topalovic, Joelle, Poulat, Francis, Lagos, Carlos F, McElreavey, Ken, Achermann, John C

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Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD von Buonocore, Federica, Clifford-Mobley, Oliver, King, Tom F J, Striglioni, Niccolò, Man, Elim, Suntharalingham, Jenifer P, Del Valle, Ignacio, Lin, Lin, Lagos, Carlos F, Rumsby, Gill, Conway, Gerard S, Achermann, John C

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An integrated single-cell analysis of human adrenal cortex development von Del Valle, Ignacio, Young, Matthew D, Kildisiute, Gerda, Ogunbiyi, Olumide K, Buonocore, Federica, Simcock, Ian C, Khabirova, Eleonora, Crespo, Berta, Moreno, Nadjeda, Brooks, Tony, Niola, Paola, Swarbrick, Katherine, Suntharalingham, Jenifer P, McGlacken-Byrne, Sinead M, Arthurs, Owen J, Behjati, Sam, Achermann, John C

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Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency von McGlacken-Byrne, Sinéad M, Del Valle, Ignacio, Quesne Stabej, Polona Le, Bellutti, Laura, Garcia-Alonso, Luz, Ocaka, Louise A, Ishida, Miho, Suntharalingham, Jenifer P, Gagunashvili, Andrey, Ogunbiyi, Olumide K, Mistry, Talisa, Buonocore, Federica, Crespo, Berta, Moreno, Nadjeda, Niola, Paola, Brooks, Tony, Brain, Caroline E, Dattani, Mehul T, Kelberman, Daniel, Vento-Tormo, Roser, Lagos, Carlos F, Livera, Gabriel, Conway, Gerard S, Achermann, John C

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