Oncogenic KRAS is dependent upon an EFR3A-PI4KA signaling axis for potent tumorigenic activity von Adhikari, Hema, Kattan, Walaa E., Kumar, Shivesh, Zhou, Pei, Hancock, John F., Counter, Christopher M.

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Glycolysis regulates KRAS plasma membrane localization and function through defined glycosphingolipids von Liu, Junchen, van der Hoeven, Ransome, Kattan, Walaa E., Chang, Jeffrey T., Montufar-Solis, Dina, Chen, Wei, Wong, Maurice, Zhou, Yong, Lebrilla, Carlito B., Hancock, John F.

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Molecular Analysis of Congenital Hypothyroidism in Saudi Arabia: SLC26A7 Mutation Is a Novel Defect in Thyroid Dyshormonogenesis von Zou, Minjing, Alzahrani, Ali S, Al-Odaib, Ali, Alqahtani, Mohammad A, Babiker, Omer, Al-Rijjal, Roua A, BinEssa, Huda A, Kattan, Walaa E, Al-Enezi, Anwar F, Al Qarni, Ali, Al-Faham, Manar S A, Baitei, Essa Y, Alsagheir, Afaf, Meyer, Brian F, Shi, Yufei

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Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A von Demir, Korcan, Kattan, Walaa E, Zou, Minjing, Durmaz, Erdem, BinEssa, Huda, Nalbantoğlu, Özlem, Al-Rijjal, Roua A, Meyer, Brian, Özkan, Behzat, Shi, Yufei

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Clinical and genetic characteristics of 15 families with hereditary hypophosphatemia: Novel Mutations in PHEX and SLC34A3 von Acar, Sezer, BinEssa, Huda A, Demir, Korcan, Al-Rijjal, Roua A, Zou, Minjing, Çatli, Gönül, Anık, Ahmet, Al-Enezi, Anwar F, Özışık, Seçil, Al-Faham, Manar S A, Abacı, Ayhan, Dündar, Bumin, Kattan, Walaa E, Alsagob, Maysoon, Kavukçu, Salih, Tamimi, Hamdi E, Meyer, Brian F, Böber, Ece, Shi, Yufei

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RAS Function in cancer cells: translating membrane biology and biochemistry into new therapeutics von Kattan, Walaa E., Hancock, John F.

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Components of the phosphatidylserine endoplasmic reticulum to plasma membrane transport mechanism as targets for KRAS inhibition in pancreatic cancer von Kattan, Walaa E., Liu, Junchen, Montufar-Solis, Dina, Liang, Hong, Barathi, Bhargavi Brahmendra, van der Hoeven, Ransome, Zhou, Yong, Hancock, John F.

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Acylpeptide hydrolase is a novel regulator of KRAS plasma membrane localization and function von Tan, Lingxiao, Cho, Kwang-Jin, Kattan, Walaa E, Garrido, Christian M, Zhou, Yong, Neupane, Pratik, Capon, Robert J, Hancock, John F

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Scalable, compressed phenotypic screening using pooled perturbations von Liu, Nuo, Kattan, Walaa E, Mead, Benjamin E, Kummerlowe, Conner, Cheng, Thomas, Ingabire, Sarah, Cheah, Jaime H, Soule, Christian K, Vrcic, Anita, McIninch, Jane K, Triana, Sergio, Guzman, Manuel, Dao, Tyler T, Peters, Joshua M, Lowder, Kristen E, Crawford, Lorin, Amini, Ava P, Blainey, Paul C, Hahn, William C, Cleary, Brian, Bryson, Bryan, Winter, Peter S, Raghavan, Srivatsan, Shalek, Alex K

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Mutational analysis of PHEX, FGF23 and CLCN5 in patients with hypophosphataemic rickets von Guven, Ayla, Al‐Rijjal, Roua A., BinEssa, Huda A., Dogan, Durmuş, Kor, Yılmaz, Zou, Minjing, Kaya, Namik, Alenezi, Anwar F., Hancili, Suna, Tarım, Ömer, Baitei, Essa Y., Kattan, Walaa E, Meyer, Brian F., Shi, Yufei

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Targeting plasma membrane phosphatidylserine content to inhibit oncogenic KRAS function von Kattan, Walaa E, Chen, Wei, Ma, Xiaoping, Lan, Tien Hung, van der Hoeven, Dharini, van der Hoeven, Ransome, Hancock, John F

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Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets von Acar, Sezer, Al-Rijjal, Roua A, Meyer, Brian, Shi, Yufei, Demir, Korcan, Böber, Ece, Kattan, Walaa E, Çatlı, Gönül, Binessa, Huda, Abacı, Ayhan, Bumin Dündar, Zou, Minjing, Salih Kavukçu

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Clinical and Genetic Features of Our Patients with Hypophosphatemic Rickets von Acar, Sezer, Al-Rijjal, Roua A, Meyer, Brian, Shi, Yufei, Demir, Korcan, Bober, Ece, Kattan, Walaa E, Catli, Gonul, Binessa, Huda, Abaci, Ayhan, Dundar, Bumin, Zou, Minjing, Kavukcu, Salih

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Novel CYP27B1 Gene Mutations in Patients with Vitamin D-Dependent Rickets Type 1A: e0131376 von Demir, Korcan, Kattan, Walaa E, Zou, Minjing, Durmaz, Erdem, BinEssa, Huda, Nalbantoglu, Oezlem, Al-Rijjal, Roua A, Meyer, Brian, Oezkan, Behzat, Shi, Yufei

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Predictive Factors for Critical Weight Loss in Saudi Head and Neck Cancer Patients Undergoing (Chemo)Radiotherapy von Redwan, Alaa S, Kattan, Fayrooz A, Alidrisi, Maha A, Ali, Gayur A, Ghaith, Mazen M, Arbaeen, Ahmad F, Almasmoum, Hussain A, Almohmadi, Najlaa H, Alkholy, Sarah O, Alhassani, Walaa E, Abusudah, Wafaa F, Babateen, Abrar M, Ghabashi, Mai A, Obeidat, Ahmad A, Al Yacoub, Azzam N, Alazzeh, Awfa Y, Azzeh, Firas S

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