Generation and Maintenance of Homogeneous Human Midbrain Organoids

per Renner, Henrik, Grabos, Martha, Schöler, Hans R., Bruder, Jan M.
Publicat a Bio Protoc (2021)

Chronic Myeloid Leukemia Associated Hypercalcemia: A Case Report and Literature Review

per Toro-Tobón, David, Agosto, Sarimar, Ahmadi, Sara, Koops, Maureen, Bruder, Jan M.
Publicat a Am J Case Rep (2017)

Giant Prolactinoma Causing Proptosis and Stroke

per Wortham, Joy, Sandoval, Brenda, Koops, Maureen, Granda-Rodriguez, Ramona, Bruder, Jan M
Publicat a J Endocr Soc (2021)

Fluorescence-based Single-cell Analysis of Whole-mount-stained and Cleared Microtissues and Organoids for High Throughput Screening

per Renner, Henrik, Otto, Mandy, Grabos, Martha, Schöler, Hans R., Bruder, Jan M.
Publicat a Bio Protoc (2021)

SAT-183 Right Adrenal Mass: An Unusual Presentation

per Gondin-Hernandez, Lyan, Trejo, Jonathan, Sandoval, Brenda, Bruder, Jan M, Granda-Rodriguez, Ramona
Publicat a J Endocr Soc (2020)

Rate of bone loss is greater in young Mexican American men than women: The San Antonio Family Osteoporosis Study

per Shaffer, John R., Kammerer, Candace M., Dressen, Amy S., Bruder, Jan M., Bauer, Richard L., Mitchell, Braxton D.
Publicat 2010

Large Invasive Adrenal Cortical Carcinoma in a Patient With Neurofibromatosis Type I

per Sandoval, Brenda G, Morales, Maria Del Mar Felix, Wortham, Joy, Koops, Maureen, Granda-Rodriguez, Ramona, Bruder, Jan M
Publicat a J Endocr Soc (2021)

Melanosomal Dynamics Assessed with a Live-Cell Fluorescent Melanosomal Marker

per Bruder, Jan M., Pfeiffer, Zachary A., Ciriello, Jonathan M., Horrigan, Diana M., Wicks, Nadine L., Flaherty, Benjamin, Oancea, Elena
Publicat 2012

Cell-Type-Specific High Throughput Toxicity Testing in Human Midbrain Organoids

per Renner, Henrik, Becker, Katharina J., Kagermeier, Theresa E., Grabos, Martha, Eliat, Farsam, Günther, Patrick, Schöler, Hans R., Bruder, Jan M.
Publicat a Front Mol Neurosci (2021)

Enhanced RANK ligand expression and responsivity of bone marrow cells in Paget’s disease of bone

per Menaa, Cheikh, Reddy, Sakamuri V., Kurihara, Noriyoshi, Maeda, Hidefumi, Anderson, Dirk, Cundy, Tim, Cornish, Jillian, Singer, Frederick R., Bruder, Jan M., Roodman, G. David
Publicat 2000

MON-925 A Wolf in Sheep’s Clothing: Intermittent Hypercalcemia from an Intrathyroidal Parathyroid Carcinoma

per Trejo, Jonathan, Hernandez, Lyan Gondin, Wortham, Joy, Sandoval, Brenda, Armaiz-Pena, Gustavo R, Bruder, Jan M, Koops, Maureen, Solis-Herrera, Carolina, Granda-Rodriguez, Ramona
Publicat a J Endocr Soc (2020)

Quantitative trait locus on chromosome 1q influences bone loss in young Mexican American adults

per Shaffer, John R., Kammerer, Candace M., Bruder, Jan M., Cole, Shelley A., Dyer, Thomas D., Almasy, Laura, MacCluer, Jean W., Blangero, John, Bauer, Richard L., Mitchell, Braxton D.
Publicat 2008

Genetic influences on bone loss in the San Antonio Family Osteoporosis Study

per Shaffer, John R., Kammerer, Candace M., Bruder, Jan M., Cole, Shelley A., Dyer, Thomas D., Almasy, Laura, MacCluer, Jean W., Blangero, John, Bauer, Richard L., Mitchell, Braxton D.
Publicat 2008

A fully automated high-throughput workflow for 3D-based chemical screening in human midbrain organoids

per Renner, Henrik, Grabos, Martha, Becker, Katharina J, Kagermeier, Theresa E, Wu, Jie, Otto, Mandy, Peischard, Stefan, Zeuschner, Dagmar, TsyTsyura, Yaroslav, Disse, Paul, Klingauf, Jürgen, Leidel, Sebastian A, Seebohm, Guiscard, Schöler, Hans R, Bruder, Jan M
Publicat a eLife (2020)

Derivation and Expansion Using Only Small Molecules of Human Neural Progenitors for Neurodegenerative Disease Modeling

per Reinhardt, Peter, Glatza, Michael, Hemmer, Kathrin, Tsytsyura, Yaroslav, Thiel, Cora S., Höing, Susanne, Moritz, Sören, Parga, Juan A., Wagner, Lydia, Bruder, Jan M., Wu, Guangming, Schmid, Benjamin, Röpke, Albrecht, Klingauf, Jürgen, Schwamborn, Jens C., Gasser, Thomas, Schöler, Hans R., Sterneckert, Jared
Publicat 2013

Correction: Derivation and Expansion Using Only Small Molecules of Human Neural Progenitors for Neurodegenerative Disease Modeling

per Reinhardt, Peter, Glatza, Michael, Hemmer, Kathrin, Tsytsyura, Yaroslav, Thiel, Cora S., Höing, Susanne, Moritz, Sören, Parga, Juan A., Wagner, Lydia, Bruder, Jan M., Wu, Guangming, Schmid, Benjamin, Röpke, Albrecht, Klingauf, Jürgen, Schwamborn, Jens C., Gasser, Thomas, Schöler, Hans R., Sterneckert, Jared
Publicat 2013

Genotype-Phenotype Features of Germline Variants of the TMEM127 Pheochromocytoma Susceptibility Gene: A 10-Year Update

per Armaiz-Pena, Gustavo, Flores, Shahida K, Cheng, Zi-Ming, Zhang, Xhingyu, Esquivel, Emmanuel, Poullard, Natalie, Vaidyanathan, Anusha, Liu, Qianqian, Michalek, Joel, Santillan-Gomez, Alfredo A, Liss, Michael, Ahmadi, Sara, Katselnik, Daniel, Maldonado, Enrique, Salgado, Sarimar Agosto, Jimenez, Camilo, Fishbein, Lauren, Hamidi, Oksana, Else, Tobias, Lechan, Ron, Tischler, Art S, Benn, Diana E, Dwight, Trisha, Clifton-Bligh, Rory, Sanso, Gabriela, Barontini, Marta, Vincent, Deepa, Aronin, Neil, Biondi, Bernadette, Koops, Maureen, Bowhay-Carnes, Elizabeth, Gimenez-Roqueplo, Anne-Paule, Alvarez-Eslava, Andrea, Bruder, Jan M, Kitano, Mio, Burnichon, Nelly, Ding, Yanli, Dahia, Patricia L M
Publicat a J Clin Endocrinol Metab (2020)